Abstract
Hydroxide exchange membrane fuel cells (HEMFCs) have the advantages of using cost-effective materials, but hindered by the sluggish anodic hydrogen oxidation reaction (HOR) kinetics. Here, we report an atomically dispersed Ir on Mo2C nanoparticles supported on carbon (IrSA-Mo2C/C) as highly active and stable HOR catalysts. The specific exchange current density of IrSA-Mo2C/C is 4.1 mA cm−2ECSA, which is 10 times that of Ir/C. Negligible decay is observed after 30,000-cycle accelerated stability test. Theoretical calculations suggest the high HOR activity is attributed to the unique Mo2C substrate, which makes the Ir sites with optimized H binding and also provides enhanced OH binding sites. By using a low loading (0.05 mgIr cm−2) of IrSA-Mo2C/C as anode, the fabricated HEMFC can deliver a high peak power density of 1.64 W cm−2. This work illustrates that atomically dispersed precious metal on carbides may be a promising strategy for high performance HEMFCs.
Similar content being viewed by others
Introduction
Utilizing hydrogen energy presents a viable solution to reduce the dependence on fossil fuels and tackle environmental concerns1,2. In the pursuit of establishing hydrogen economy, fuel cells play crucial roles3,4. Hydroxide exchange membrane fuel cells (HEMFCs), which are analogs of proton exchange membrane fuel cells (PEMFCs) but using hydroxide exchange membranes, are promising due to their cost-effectiveness coming from the possibility to use platinum group metals (PGMs) free cathode electrocatalysts (e.g., Ag, Mn-Co oxides and Fe-N-C) and Ni-based bipolar plates5,6. However, high-performance anodes for HEMFCs still rely on PGMs7. Moreover, the pH effect on PGMs (e.g., Pt, Rh, Pd and Ir) leads to a significant slowdown of the hydrogen oxidation reaction (HOR) kinetics by approximately 2-3 orders of magnitude when changing the electrolyte from acid to alkaline, which results in high PGMs loadings on anode of HEMFCs8. Consequently, the anode cost in HEMFC substantially increases. Additionally, the poor stability of commonly used Pt-based catalysts necessitates higher catalyst loadings to enable a stable HEMFC, further increasing costs9. Hence, the development of highly efficient and stable catalysts with lower loading of PGMs for alkaline HOR is a pivotal target for the ongoing advancement of HEMFCs.
Significant efforts have been made to develop highly efficient catalysts for alkaline HOR10 and have shown that by tuning the microenvironment of active sites, the binding energies of HOR intermediates could be adjusted to improve the HOR kinetics11. Alloys, heterostructures and decorated catalysts have been reported with elevated HOR performance compared with the pristine metal catalysts by adjusting the H and OH binding energies12,13,14,15. Ir, which demonstrates enhanced OH bindings than Pt, has been shown to be a promising candidate for HOR in alkaline. Ir alloy (e.g., IrNi, IrMo and IrRu)16,17,18 and heterostructures (e.g., Ir/MoS2 and Ir/WOx)19,20 have been reported with enhanced HOR activities, even comparable to the state-of-the-art PtRu/C catalysts. The catalyst HOR stability is also strongly affected by the microenvironment of active sites9,21. Recent studies ascribed the poor stability of commercial carbon-supported Pt nanoparticle (NP) catalysts to the local carbon support corrosion22,23. Especially, PGMs can catalyze the carbon corrosion, making it especially serious at the interface of Pt NP and carbon support. Thus, a more stable substrate is desired to load the PGMs with less corrosion. Alternative supports, such as oxides, carbides, and nitrides, have been reported to improve the stability21,24. For example, TiO2-RuO2 was used as the support for Pt nanoparticles, and enhanced fuel cell stability was achieved25. Another method is to use a buffer to separate PGMs and the carbon substrates. For example, Dekel et. al.26 reported Pd/CeO2-C with enhanced stability, by using CeO2 as buffer substrate to load Pd nanoparticles, which could prevent the direct contact between Pd sites and the carbon support and thus mitigate the local carbon corrosion27. This work indicates that a rationally designed catalyst with a tailored microenvironment could also achieve high activity and stability.
Atomically dispersed metal catalysts show great potential for high-performance electrocatalysts due to their high atom-utilization and special microenvironment around the metal sites28,29. However, the commonly used M-N4-C type atomically dispersed catalysts do not show satisfactory performance for HOR, especially in HEMFC devices, because their significantly different metal microenvironments compared with those in pristine metal NPs may lead to improper binding to the HOR intermediates, such as adsorbed H (*H) and adsorbed OH (*OH)30,31,32. As a result, if a properly selected substrate can both host the atomically dispersed PGMs and achieve the optimized metal site microenvironment, it may simultaneously bring high HOR activity and stability.
Herein, we report an atomically dispersed Ir on Mo2C NPs supported on carbon (denoted as IrSA-Mo2C/C) as a highly active and stable HOR catalyst in alkaline electrolyte. Mo2C NPs are used as the hosts for Ir atoms. The Mo2C shows Pt-like electronic structure, enabling the guest Ir to have a unique binding property with intermediates33,34,35. Mo2C also has high stability and strong interaction with PGMs, making Ir atoms atomically dispersed in the hexagonal Mo2C matrix. The obtained IrSA-Mo2C/C catalyst achieves excellent activity for HOR, indicated by the high specific exchange current density of 4.1 mA cm-2ECSA and mass activity at 50 mV versus reversible hydrogen electrode (RHE, the same hereafter) of 17.9 A mg-1Ir, which are 10 and 12 times that of Ir/C, and 2.6 and 4.3 times that of the current state-of-the-art PtRu/C, respectively. By using a low anode PGM loading of only 50 μgIr cm-2, the fabricated IrSA-Mo2C/C HEMFC can deliver a high peak power density (PPD) of 1.64 W cm-2. The IrSA-Mo2C/C illustrates high stability as well. It can work stably in a 120-h continuous operation and 30,000 cycles of accelerated durability test (ADT). Density functional theory (DFT) calculations reveal that the d-orbital of IrSA-Mo2C is much different from that of the HOR inactive M-N4-C type atomically dispersed catalysts, and the high activity of IrSA-Mo2C/C comes from the enhanced hydroxide binding as well as the optimized hydrogen binding. The present study demonstrates the advantages of the atomically dispersed metal on carbides in electrocatalysis.
Results and Discussion
Catalyst synthesis and characterization
The IrSA-Mo2C/C catalyst was synthesized by a two-step approach (Fig. 1a). Firstly, MoOx was grown on pre-oxidized carbon black via the hydrolysis of MoCl5. Supplementary Fig. 1 shows the transmission electron microscopy (TEM) image and the corresponding energy-dispersive X-ray spectroscopy (EDS) mappings. It demonstrated that Mo was homogeneously dispersed on the carbon support. The broad shoulder peak in powder X-ray diffraction (PXRD) pattern (Supplementary Fig. 2) suggested the formation of amorphous MoOx. Subsequently, Ir was introduced by impregnation, followed by calcination at 900 °C under nitrogen environment. Under high temperature, carbon atoms would diffuse from carbon black to MoOx and produce the Mo2C NPs36. At the same time, Ir was atomically dispersed on it to form the IrSA-Mo2C/C catalyst because of the strong interaction between Ir atoms and Mo2C host.
Figure 1b shows the PXRD pattern of the IrSA-Mo2C/C. All the diffraction peaks were assigned to hexagonal Mo2C without any signal from Ir-derived species, such as Ir and IrO2. The TEM image of IrSA-Mo2C/C (Fig. 1c) clearly shows the well-dispersed NPs with an average size of 2.4 nm (inset of Fig. 1c) on the carbon supports. The aberration-corrected high-angle annular dark-field scanning TEM images (AC-HAADF-STEM, Fig. 1d) illustrated two sets of lattice with spacing of both 0.23 nm and angle of ca. 57°, which could be assigned to the (101) and (\(\bar{1}01\)) facets of hexagonal Mo2C37. Figure 1e exhibits the line intensity profile of the two areas in Fig. 1d. Isolated dots with particularly high intensity were observed, which was assigned to Ir atoms because of the higher atomic number of Ir than Mo15. It was confirmed that Ir substituted the Mo sites in Mo2C, and Ir were atomically isolated. Furthermore, the EDS mapping (Fig. 1f) verified the uniform dispersion of Ir and Mo. The Ir/Mo molar ratio in IrSA-Mo2C/C was ca. 1:11 from EDS spectra (Supplementary Fig. 3), which was consistent with the ratio of ca. 1:10 tested by inductively coupled plasma optical emission spectra (ICP-OES). The Ir loading in IrSA-Mo2C/C was ca. 3.1 wt% from ICP-OES.
Then, the electronic structures and coordination environments of Ir in IrSA-Mo2C/C were further investigated by X-ray absorption spectroscopy (XAS). The Ir L3-edge X-ray absorption near-edge structure (XANES, Fig. 2a) of IrSA-Mo2C/C exhibited the white line intensity between that of Ir foil and IrO2, revealing that the valence state of Ir in IrSA-Mo2C/C was between that of Ir and IrO238. The same conclusion was obtained from the Ir 4f X-ray photoelectron spectroscopy (XPS, Fig. 2d). The 4f7/2 peak of Ir/C could be deconvoluted into three peaks: Ir0 at 61.5 eV, Ir4+ at 62.4 eV and its satellite peak at 64.0 eV39,40. The existence of the Ir4+ species is likely from the surface oxidation of nanoparticles41. For IrO2, only the Ir4+ species and satellite peak were observed. The peak of IrSA-Mo2C/C was located in between of those for Ir0 and Ir4+, indicting its medium oxidation state. Supplementary Fig. 4 shows the Mo 3d XPS spectra of IrSA-Mo2C/C and Mo2C/C, indicating the proportion of Mo6+ species increased after introducing Ir. The Fourier-transformed k2-weighted extended X-ray absorption fine structure (EXAFS, Fig. 2b) shows that IrSA-Mo2C/C exhibits a major peak at ca. 1.75 Å, which comes from the Ir−C path. No Ir−Ir path (2.52 Å, reference Ir foil) or Ir−O path (1.62 Å, reference IrO2) was observed. We further performed the wavelet transform EXAFS (Fig. 2e) analysis to distinguish back-scattering atoms in the k-space. The IrSA-Mo2C/C revealed only one intensity maximum located at 4.1 Å−1, which was different from that of IrO2 (5.8 Å−1) and Ir foil (11.4 Å−1), suggesting the unique Ir−C scattering path in IrSA-Mo2C/C31. Furthermore, the FT-EXAFS fitting in the R-space (Fig. 2c) and the k-space (Supplementary Fig. 5) suggested the Ir−C scattering path of 2.10 Å after phase correction with the coordination number of ca. 3.1, which was reasonably close to the Mo−C path in Mo2C located at 2.11 Å with corresponding coordination number of 3. The fitting curves for Ir foil and IrO2 were shown in Supplementary Fig. 6, and results were summarized in Supplementary Table 1. Thus, the structure of IrSA-Mo2C was confirmed as the Ir atoms partially replaced the Mo atoms in the hexagonal Mo2C lattice and thus coordinated with C.
High HOR activity of the IrSA-Mo2C/C
The HOR electrocatalytic activity of the IrSA-Mo2C/C was firstly investigated by the rotating disk electrode (RDE) method in H2-saturated 0.1 M KOH using the standard three-electrode system. The commercial PtRu/C, Pt/C and IrO2 were tested at the same condition for comparison. The commonly used carbon-based Ir single atom catalysts (i.e., IrSA-N4-C, synthesized through the procedure reported in refs. 32,42. Ir/C (synthetic procedure shown in Methods, TEM images and XRD pattern shown in Supplementary Fig. 7), and Ir nanocluster on Mo2C supported on carbon (IrNC-Mo2C/C, synthetic procedure shown in Methods, TEM images and XRD pattern shown in Supplementary Fig. 8) were tested as control samples. Different from the negligible HOR activity of the IrSA-N4-C (Supplementary Fig. 9, similar performance was reported by Q. Wang et al.)43 the IrSA-Mo2C/C illustrated high HOR performance, indicated by the steeply increased anodic current density (Fig. 3a). The Mo2C/C support showed scarce HOR activity, suggesting that the high performance of IrSA-Mo2C/C came from the Ir sites. And the IrSA-Mo2C/C also displayed higher HOR activity than IrNC-Mo2C/C, indicating the benefit of the monoatomic dispersed Ir in Mo2C. The IrSA-Mo2C/C showed better performance than the other Ir-based catalysts, such as Ir/C and IrO2 (Fig. 3a and Supplementary Fig. 10), as well as the commonly used Pt-based catalysts, such as Pt/C and the state-of-the-art PtRu/C (Fig. 3a).
We further tested the polarization curves of IrSA-Mo2C/C at different rotating speeds (Fig. 3b). By fitting with the Koutecky-Levich equation (Fig. 3c), a slope of 4.70 cm2 mA−1 s−1/2 was obtained, which was reasonably close to the theoretical value of the 2e HOR process (4.87 cm2 mA−1 s−1/2) and suggested the anode current mainly derived from HOR44,45.
In order to quantitatively compare the HOR activity, we calculate the specific exchange current density (j0,ECSA) based on the electrochemical surface area (ECSA) and the mass activity at 0.05 V of the catalysts. The ECSA of the catalysts are determined by CO stripping voltammetry, and the same specific charge of 420 μC cm−2 is used for all the catalysts (Supplementary Fig. 11 and Supplementary Table 2). The IrSA-Mo2C/C exhibits an ECSA of 156 m2 g−1Ir, which was larger than the ECSA values of Ir/C (128 m2 g−1Ir), Pt/C (97 m2 g−1Pt) and PtRu/C (107 m2 g−1PtRu)46. The high ECSA was benefited from the atomically dispersion of Ir in IrSA-Mo2C/C, which brought high utilization of Ir. Figure 3d shows the ECSA normalized Tafel plots. By fitting with the Butler-Volmer equation according to Tafel-Volmer pathway45, the IrSA-Mo2C/C provides the greatest j0,ECSA of 4.1 ± 0.16 mA cm−2ECSA (Fig. 3e), which was 2.6, 7.7 and 10 times as high as that for PtRu/C (1.6 ± 0.07 mA cm−2ECSA), Pt/C (0.53 ± 0.041 mA cm−2ECSA) and Ir/C (0.41 ± 0.054 mA cm−2ECSA), respectively. The measured specific j0,ECSA of PtRu/C, Pt/C and Ir/C reproduced the literature data13,45,47, implying a reliable evaluation of HOR activity. The IrSA-Mo2C/C also exhibited a high mass activity at 50 mV of 17.9 ± 1.2 A mg−1Ir, which was 4.3, 13 and 12 times higher than that of PtRu/C (4.12 ± 0.16 A mg−1PtRu), Pt/C (1.37 ± 0.06 A mg−1Pt) and Ir/C (1.47 ± 0.08 A mg−1Ir), respectively. The more significant improvement of the mass activity is attributed to the higher Ir utilization of IrSA-Mo2C/C. IrSA-Mo2C/C also showed great advantages in both specific activity and mass activity compared with the previously reported high-performance HOR catalysts (summarized in Supplementary Fig. 12 and Supplementary Table 3).
Encouraged by the superior HOR activity of the obtained IrSA-Mo2C/C catalyst, we employed it as the anode catalyst to assemble the HEMFCs. The membrane electrode assembly (MEA) was made by using IrSA-Mo2C/C as anode catalyst with a low PGM loading of 0.05 mgIr cm−2 (confirmed by ICP-OES), commercial Pt/C (0.4 mgPt cm-2) as cathode catalyst and the PiperION™ A15 (Versogen) as the hydroxide exchange membrane. The control MEAs were fabricated by only replacing the anode catalyst to PtRu/C, Pt/C and Ir/C with the same loading of 0.05 mgPGM cm−2. Figure 3f displays the polarization and power density curves of the as-prepared HEMFCs under H2/O2 condition. The IrSA-Mo2C/C HEMFC exhibited excellent performance, which could deliver high PPD of 1.64 W cm−2, and is much better than the HEMFCs using PtRu/C (0.91 W cm−2), Pt/C (0.51 W cm−2) and Ir/C (0.60 W cm−2). The IrSA-Mo2C/C HEMFC achieved a high current density of 1.60 A cm−2 at the cell voltage of 0.65 V, which was also higher than that of PtRu/C HEMFC (0.76 A cm−2), Pt/C HEMFC (0.43 A cm−2) and Ir/C HEMFC (0.49 A cm-2). The IrSA-Mo2C/C HEMFC also showed high performance under H2/air(CO2-free) condition, which delivered a PPD of 0.90 W cm−2 and reached a current density of 1.11 A cm−2 at 0.65 V (Supplementary Fig. 13). Furthermore, we normalized the PPD of these MEAs to the anode catalyst loading to calculate the anode mass activity. As shown in Supplementary Fig. 14 and Supplementary Table 4, IrSA-Mo2C/C HEMFC delivered a high anode mass activity of 32.8 W mg−1Ir, which was superior to the previously reported HEMFCs.
Enhanced HOR stability of IrSA-Mo2C/C
The HOR stability of IrSA-Mo2C/C was evaluated by RDE method. Two techniques, chronoamperometry and cyclic voltammetry for ADT, were carried out. Figure 4a exhibits the chronoamperometry response of IrSA-Mo2C/C and the control catalysts in H2-saturated 0.1 M KOH at a constant potential of 50 mV. The current density of IrSA-Mo2C/C maintained ca. 95% of the initial value after continuously operating for 120 h. The polarization curves before and after 120 h operation (Supplementary Fig. 15) showed negligible decay. While for the IrNC-Mo2C/C, Ir/C, Pt/C and PtRu/C, the current density remained only 62 %, 45 %, 35 % and 33 % after a short test of 20 h, respectively. The decay rate of IrSA-Mo2C/C was 0.042 % h−1, much smaller than those of IrNC-Mo2C/C (1.9 % h−1), Ir/C (2.5 % h−1), Pt/C (2.9 % h−1) and PtRu/C (3.0 % h−1), showing nearly two order of magnitude slowdown of the catalyst decay. Supplementary Fig. 16 and Supplementary Table 5 summarize the decay rate of IrSA-Mo2C/C and the reported HOR catalysts, where IrSA-Mo2C/C showed great advantage.
The stable HOR performance of IrSA-Mo2C/C was also determined by ADT. After scanning at a potential window of 0 ~ 0.5 V with the scanning rate of 0.1 V s−1 for 30,000 cycles, IrSA-Mo2C/C did not show any decline (Fig. 4b). By comparison, PtRu/C, Pt/C, Ir/C and IrNC-Mo2C/C exhibited dramatic decline in kinetic current (Fig. 4b and Supplementary Fig. 17). To quantitatively compare the activity loss in ADT, the corresponding exchange currents of these catalysts were summarized in Fig. 4c. IrSA-Mo2C/C maintained its activity in the whole process of ADT without any decline, while PtRu/C, Pt/C, Ir/C and IrSA-Mo2C/C suffered from a decay of 65 %, 76 %,14 % and 45 % in j0 after scanning for 10,000 cycles, respectively. The TEM image of IrSA-Mo2C/C after ADT (Fig. 4d) showed the same structure with almost the same size distribution of NPs (ca. 2.5 nm) compared with the fresh catalyst. The HRTEM image (Supplementary Fig. 18) exhibited lattice spacing of 0.23 nm belonging to the Mo2C (101). The EDS mapping shows the homogenous dispersion of Ir and Mo atoms in the NPs after ADT. Overall, these results indicated the good stability and the IrSA-Mo2C/C maintained its microstructure during HOR process.
The IrSA-Mo2C/C was also stable under the HEMFC working conditions. Supplementary Fig. 19 shows the galvanostatic discharge curve at 500 mA cm−2 at 80 °C of the IrSA-Mo2C/C HEMFC under H2/O2 condition. It showed negligible voltage loss after 50 h of test.
Mechanism investigation
Based on the DFT calculations, electronic structures and reaction pathways of Mo2C (101) slab model with 10% of Mo atoms substituted by Ir (model shown in Supplementary Fig. 20 and cell parameter shown in Supplementary Table 6) were studied to deeply understand the origin of the high HOR activity of atomically dispersed IrSA-Mo2C/C catalyst at the atomistic level. The Ir (111) slab and the typical carbon-based IrSA-N4-C single-atom catalyst (model shown in Supplementary Fig. 21) were also studied for comparison. Bader charge analysis (Supplementary Fig. 22) suggests the electron transfer from surface Mo to the adjacent Ir in IrSA-Mo2C, consistent with the XPS results.The partial density of states (PDOS) plots (Fig. 5a) show that the Ir-5d orbitals of IrSA-N4-C are very localized. By contrast, the Ir-5d orbitals of the IrSA-Mo2C exhibit a large degree of delocalization, suggesting its metal-like electronic structure of Ir atoms in IrSA-Mo2C, which is similar to the 5d bands of Ir (111). Such maintained metallicity of Ir in IrSA-Mo2C was benefited from the Pt-like electronic structure of the Mo2C substrate, which makes the dispersed Ir sites behave more like single atom alloy and thus brings high HOR activity similar to Ir (111). Actually, it is noteworthy that almost all reported high-efficient HOR catalysts rely on the metallic sites48. Furthermore, the total density of states (DOS, Supplementary Fig. 23) of IrSA-Mo2C exhibits a higher occupation (with higher carrier concentration) at the Fermi level compared with IrSA-N4-C, suggesting a much better electron conductivity49.
The adsorption energies of the HOR intermediates control the activity of IrSA-Mo2C. Although the mechanism of alkaline HOR was still under debate, H and OH adsorptions were generally considered as the key step in the kinetics of alkaline hydrogen oxidation50,51,52. Figure 5b summarizes the calculated adsorption Gibbs free energy (∆G) of adsorbed H, OH. The ∆GH value is considered as the primary descriptor for the HOR kinetics. The H adsorptions on the different sites of IrSA-Mo2C were evaluated (Supplementary Fig. 24 and Supplementary Table 7), and it was found that the Ir-Mo hollow sites offer the suitable ∆GH of −0.25 eV. The IrSA-Mo2C illustrated slightly weaker H binding than Ir (111) surface (∆GH = − 0.27 eV), which was more optimized for the HOR process53. The slightly weakened H binding was indicated by the 14 mV of negatively shift of the Hupd peak as well (Fig. 5c). When an Ir cluster was placed on the Mo2C (101) substrate (IrNC-Mo2C, model shown in Supplementary Fig. 25), a stronger H adsorption with ∆GH = − 0.40 eV was found. Pure IrO2 (110) (∆GH = − 0.64 eV) and Mo2C (101) (∆GH = − 0.57 eV) also exhibited the too strong H bindings (shown in Supplementary Fig. 26–27), leading to the poorer HOR activity, which were consistent to the experimental results. In addition, although IrSA-N4-C demonstrated a stronger H binding (∆GH = − 0.33 eV) than Ir (111) surface, it did not remarkably deviate from the optimal value of H adsorption energy.
Besides ∆GH, the free energy of OH adsorption (∆GOH) is considered as another important indicator for activity in alkaline HOR. Markovic et al. considered that the *OH combined with *H to generate water through the bifunctional mechanism, and thus accelerating the H desorption11. While Chen et al. proposed stronger H-bond network among interfacial water molecules, which was important for the H transfer54. Both possible mechanisms suggested that the enhanced OH adsorption could improve HOR. Here, the IrSA-Mo2C, Ir and IrSA-N4-C catalysts illustrated much different values of ∆GOH (Fig. 5b). Based on the screening of the different sites of IrSA-Mo2C, it was found that the Mo sites were more favored to adsorb OH (Supplementary Fig. 28 and Supplementary Table 6). Compared with Ir (111) surface (∆GOH = 0.66 eV), IrSA-Mo2C (∆GOH = 0.01 eV) showed dramatic enhancement of OH adsorption, while IrSA-N4-C (∆GOH = 1.02 eV) possessed an increased ∆GOH value. The enhanced OH adsorption of IrSA-Mo2C could be concluded by the lower onset potential of IrSA-Mo2C/C than Ir/C in the CO-stripping voltammetry (Fig. 5d). The much weaker OH adsorption of the IrSA-N4-C catalyst should be the origin of its poor HOR performance.
Therefore, the calculated adsorption-free energies suggest the high HOR performance of the IrSA-Mo2C/C can be attributed to its optimized H binding and enhanced OH binding. The Gibbs free energy profiles of the HOR process on each catalyst are displayed in Fig. 5e. Due to the weak OH adsorption, the potential-determining steps on Ir (111) and IrSA-N4-C were both the OH− adsorption step (i.e., *H + * + OH− →*H + *OH + e−), and the energy barriers were 0.70 and 1.86 eV, respectively. Four reaction paths were considered on IrSA-Mo2C through different adsorption sites (Supplementary Fig. 29). Because of the enhanced OH adsorption on Mo sites, all the paths exhibited lower energy barrier for OH− adsorption step, giving the potential determining step of water generation step (i.e., *H + *OH → *H2O) on IrSA-Mo2C. The favorite path showed a lower energy barrier of 0.20 eV, indicating its fastest HOR kinetics. The Gibbs free energy profiles for IrNC-Mo2C, Mo2C (101) and IrO2 (110) were calculated as well (Supplementary Fig. 25–27), which showed higher energy barriers of 0.80, 1.57, and 1.03 eV, respectively.
In summary, we have developed an atomically dispersed Ir (i.e., IrSA-Mo2C/C) as a highly efficient and stable HOR catalyst in alkaline electrolyte to achieve high HEMFC performance using low anode PGM loading. The unique Mo2C substrate properly adjusts the Ir sites to achieve optimized H binding and enhanced OH binding, and thus significantly promotes the HOR kinetics on IrSA-Mo2C/C. The IrSA-Mo2C/C exhibits a high mass activity of 17.9 A mgIr−1 at 0.05 V, surpassing the state-of-the-art PtRu/C by 4.3 times. The high stability of the Mo2C substrate also promotes the durability of the IrSA-Mo2C/C, exhibiting a decay rate 72 times smaller than the PtRu/C. This work highlights that carbides can serve as an excellent substrate to host the atomically dispersed PGMs, and this type catalyst is promising in reducing the PGM requirement in electrocatalysis.
Methods
Materials
MoCl5 (99.99%), Ethanol (99.5%), HNO3 (65%) and KOH (99.999%) was purchased from Aladdin. IrCl3 · xH2O (99.9%) was obtained from Sigma Aldrich. Ketjen black EC-300J was purchased from Lion Corporation. Nafion solution, Pt/C (20%, Johnson Matthey), PtRu/C (40% Pt and 20% Ru, Johnson Matthey), IrO2 and gas diffusion layers (SGL 29BC) were obtained from Suzhou Sinero Technology Co., Ltd. The hydroxide exchange membrane (PiperION™ A15) and the ionomer were bought from Versogen. Ultrapure water (18.2 MΩ·cm, Mili-Q, Merck) was used in the synthesis of catalysts and electrochemical measurements.
Syntheses of the catalysts
Synthesis of the oxidized-carbon black
1 g of Ketjen black (EC-300J) was dispersed in 100 mL of 65% HNO3 solution through ultrasonication for 15 min. The mixture was then heated to 85 °C with vigorous stirring at refluxed state for 1 h. Then it was centrifuged and dispersed in water, followed by filtering and washing with plenty of water. Finally, the filter cake was dried by lyophilization.
Synthesis of the IrSA-Mo2C/C catalyst
Firstly, 200 mg of the as-prepared oxidized-carbon black and 380 mg of MoCl5 were dispersed in 30 mL of ethanol through ultrasonication for 15 min, followed by adding 5 mL of water. Then, the mixture was heat to 80 °C with vigorous stirring for 8 h. The product was centrifuged and dispersed in water, followed by filtering and washing with plenty of water. The MoOx/C was obtained by lyophilization. Secondly, 0.03 mM of IrCl3 · xH2O (12 mg) and 109 mg of the obtained MoOx/C were dispersed in 50 mL of water by ultrasonication for 1 h. The solvent was then evaporated using rotary evaporator at 50 °C. The residue was collected and dried overnight. Then, it was grinded and calcined at 900 °C under N2 atmosphere for 1 h to obtain IrSA-Mo2C/C catalyst. The Ir loading in the catalyst was ca. 3.1% determined by ICP-OES.
Synthesis of the IrNC-Mo2C/C catalyst
IrNC-Mo2C/C catalyst was prepared by the same method as IrSA-Mo2C/C catalyst, except using 3 times the amounts of IrCl3 · xH2O.
Synthesis of the Ir/C catalyst
0.03 mM of IrCl3 · xH2O (12 mg) and 109 mg of oxidized-carbon black were dispersed in 50 mL of water by ultrasonication for 1 h. The solvent was then evaporated using rotary evaporator at 50 °C. The residue was collected and dried overnight. Then, it was grinded and calcined at 900 °C under N2 atmosphere for 1 h to obtain Ir/C catalyst.
Synthesis of the IrSA-N4-C catalyst
The synthesis of IrSA-N4-C was followed by the procedure reported by Li et al.42. Typically, 2 mmol of Zn(NO3)2·6H2O (594 mg) and 0.2 mmol of Ir(acac)3 (98 mg) were simultaneously dissolved in 7.5 mL of methanol to form a uniform solution. Another solution was made by dissolving 8 mmol of 2-methyl imidazole (656 mg) to 15 mL of methanol. After rapidly mixing the two solutions and vigorously stirring for 5 min, the mixed solution was transferred into a 50 mL Telfon-lined stainless-steel autoclave. The sealed vessel was heated at 120 °C for 4 h before it was cooled to room temperature. Then it was separated by centrifugation, washed with methanol for four times, and dried under vacuum for 8 h. Finally, it was put into a tube furnace and pyrolyzed at 900 °C for 3 h under Ar atmosphere to obtain IrSA-N4-C catalyst.
Characterizations
Powder X-ray powder diffraction (PXRD) patterns were recorded on a Rigaku D/Max 2500 VB2 + /PC X-ray powder diffractometer equipped with Cu Kα radiation (λ = 0.154 nm). Transmission electron microscopy (TEM) images were obtained on a HITACHI HT7700 transmission electron microscope operating at 100 kV. Aberration-corrected high-angle annular dark-field scanning transmission electron microscopy (AC-HAADF-STEM) and energy dispersive X-ray spectrometry (EDS) elemental mapping were performed using FEI TITAN 80-300 operating at 300 kV. The X-ray photoelectron spectra (XPS) were measured using a Thermo Fisher ESCALAB 250Xi XPS system with a monochromatic Al Kα X-ray source. All binding energies were calibrated to the C 1 s peak (284.8 eV). Inductively coupled plasma optical emission spectroscopy (ICP-OES, Optima 7300 DV, Perkin Elmer) was used to determine the metal contents.
XAS measurements
X-ray absorption spectroscopy (XAS) at the Ir L3-edge (11215 eV) were measured at 1W1B station in Beijing Synchrotron Radiation Facility (BSRF, operated at 2.5 GeV with a maximum current of 250 mA). The XAS data of the samples were collected at room temperature in fluorescence excitation mode using a Lytle detector. All the samples were mixed with graphite and ground uniformly and then pressed into a 10 mm plate with a thickness of 1 mm.
The EXAFS data were processed by Athena and Artemis in the IFEFFIT packages. Firstly, the EXAFS spectra were obtained by Fourier transforming the \(\chi \left(k\right)\) data with Hanning windows (dk = 0.5 Å−1) to separate the contributions from different coordination shells. Then, quantitative structural parameters around the Ru atom were obtained by fitting with the following EXAFS equation using the Artemis module.
where \({S}_{0}^{2}\) is the amplitude reduction factor, \({F}_{j}\left(k\right)\) is the effective curved-wave backscattering amplitude, \({N}_{j}\) is the number of neighbor atoms from different coordination shells, \({R}_{j}\) is the distance between the core atom and neighbor atoms, \(\lambda \left(k\right)\) is the mean free path in Å, \({{\phi }_{j}}(k)\) is the phase shift (including the phase shift for each shell and the total central atom phase shift), \({\sigma }_{j}^{2}\) is the Debye-Waller parameter of the different atomic shells. The functions \({F}_{j}\left(k\right)\), \(\lambda \left(k\right)\) and \({\phi }_{j}\left(k\right)\) were calculated by the ab initio code FEFF 8.2. During the fitting process, \({S}_{0}^{2}\) was fixed, while R, \({\sigma }^{2}\) and the edge-energy shift \(\Delta {E}_{0}\) were allowed to run freely.
Electrochemical measurements
The electrochemical measurements were operated at room temperature in a standard three-electrode electrochemical system controlled by a potentialstat (V3, Princeton Applied Research). A homemade glass electrochemical cell equipped with three-electrode assembly was used. The cell and glassware were cleaned by 3:1 mixture of concentrated sulfuric acid and hydrogen peroxide (30%), rinsed thoroughly and boiled with ultrapure water before measurements. A catalyst thin film on glassy carbon (GC) rotating disk electrode RDE (5 mm in diameter, Pine Research Instrumentation) was used as the working electrode. The surface of GC was polished with 0.05 mm Al2O3 powder and cleaned with water under ultrasonic. The catalyst ink was made by ultrasonically dispersing 1 mg of as-prepared IrSA-Mo2C/C catalyst in a mixed solution containing 250 μL of distilled water, 750 μL of ethanol, and 5 μL of 5 wt % Nafion. Then 20 μL of the catalyst ink was transferred onto the GC substrate to yield a thin film electrode. The Ir loading was ca. 3.2 μgIr cm−2 according to the result of ICP-OES. The reversible hydrogen electrode (RHE, Phychemi Co., Ltd.) and a Pt wire (99.999%, Gaoss Union Co., Ltd.) were used as the reference and counter electrodes, respectively. The fresh 0.1 M KOH solution with the pH of ca. 12.8 ± 0.1, prepared by dissolving 2.81 g of KOH in 500 mL of water, was used as the electrolyte for all RDE measurements.
Cyclic voltammetry (CV) was carried out to analyze the electrochemical properties of the catalysts. The recorded potentials were iR-corrected. The solution resistance (R) was measured using AC-impendence from 200 kHz to 100 mHz with a voltage perturbation of 5 mV. The HOR activity was calculated using a positive-going direction polarization curves obtained in a H2-saturated 0.1 M KOH solution with the rotation rate of 1600 rpm and the scanning rate of 5 mV s−1. For the stability test, the catalyst loading was controlled at ca. 7 μgIr cm−2. A homemade fluorinated ethylene propylene electrochemical cell equipped was used. Two techniques were used to evaluated the stability. The rotation rate was change to 900 rpm to reduce the mechanical detachment of catalyst from the surface of RDE. Firstly, the chronoamperpmentry at a constant potential of 0.05 V was used. Secondly, the CV cycling was used for the accelerated durability test (ADT) by scanning the potential between 0 and 0.5 V with the scanning rate of 100 mV s−1. To eliminate the influence of CO2 from air, the electrolyte was refreshed each 50 h.
Evaluation of activity and ECSA
The HOR/HER activity was represented by the exchange current density (j0), which was obtained by fitting kinetic current (ik) with the Butler-Volmer equation:
where αa and αc are the transfer coefficients for HOR and HER, respectively, with αa + αc = 1 (Tafel-Volmer pathway). As is the electrochemical surface area (ECSA), and η is the overpotential. ik is calculated by the Koutecky-Levich equation:
where i is the measured current, ik is the kinetic current, and id is the diffusion limited current. id is defined from the following equation:
where η is the overpotential and il is the maximum current obtained from polarization curves.
The ECSA was evaluated by CO-stripping voltammetry. A monolayer of CO was firstly adsorbed onto the catalyst’s surface by holding at 0.1 V for 10 min. The electrolyte was then flushed with Ar for 10 min to remove dissolved CO completely. Then, the adsorbed CO was stripped by scanning between 0.1 and 1.2 V at a scan rate of 10 mV·s−1.
HEMFCs fabrications and tests
The synthesized IrSA-Mo2C/C or the control catalysts were used as the anode catalyst with the loading of 0.05 mgPGM cm−2. Pt/C (HiSpec 4000, 40 wt% Pt, Alfa Aesar) was used as the cathode catalyst with the loading of 0.4 mgPt cm−2. The catalyst ink was sprayed onto both sides of PiperION™ A15 membrane (17 µm) to fabricate a catalyst coated membrane (CCM) with the electrode area of 5 cm−2. All CCMs were immersed into 3 M NaOH solution overnight and then rinsed thoroughly with deionized water to remove all excess NaOH. The rinsed CCM was assembled with a fluorinated ethylene propylene (FEP) gasket, a GDL (SGL 29 BC), a graphite bipolar plate with 5 cm2 flow field and a metal current collector for each side to complete the full HEMFC. Fuel cell test system (Scribner 850 g) equipped with a backpressure module was used to evaluate the performance of the HEMFCs. The operating temperature was set as 95 °C. The H2 and O2 were humidified at 92 °C and 95 °C, respectively. The flow rates for both H2 and O2 were 1000 sccm. The back-pressure was set at 250 kPa.
DFT calculations
First-principles computations were performed using the projector augmented wave method (PAW) as implemented in the Vienna ab-initio simulation package (VASP). The generalized gradient approximation in the form of Perdew-Burke- Ernzerhof (PBE) for the exchange-correction potential and a cutoff energy of 500 eV for the plane-wave basis were adopted. For all calculations, spin polarization was adopted. To consider long-range van der Waals (vdW) interactions, Grimme’s DFT-D3 method was employed. Atomic structures were fully released with converging tolerance for forces on all atoms less than 0.02 eV Å−1, and the energy convergence criterion was set to 10-5 eV. 2×2, 5×5, 2×3, 2×3 and 3×2 unit cells of Ir (111), IrSA-N4-C, IrSA-Mo2C,IrNC-Mo2C and IrO2 (110) with 4 layers thickness was employed with 15 Å vacuum space in the vacuum-direction to avoid image interactions. The bottom two layers were fixed while the top two layers were relaxed during geometry optimization. 3×3×1, 2×1×2, 3×3×1, 3×3×1 and 3×2×1 Monkhorst–Pack k-meshes were used to sample the Brillouin zone for geometry relaxation. The computational hydrogen electrode model proposed by Nørskov et al.55. Was used to evaluate the activity of the catalyst. The Gibbs free energy change, ΔG, of each elementary step was obtained based on the following equation, in which the contributions of zero-point energy (ΔZPE) and entropy (TΔS) changes were considered:
Where ΔE was the calculated energy change of the intermediates, such as *H, *OH and *H2O, U was the applied electrode potential.
Data availability
The data generated in this study are provided in the Source Data file. Source data are provided with this paper.
References
Seh, Z. W. et al. Combining theory and experiment in electrocatalysis: insights into materials design. Science 355, eaad4998 (2017).
Cullen, D. A. et al. New roads and challenges for fuel cells in heavy-duty transportation. Nat. Energy 6, 462–474 (2021).
Kempler, P. A., Slack, J. J. & Baker, A. M. Research priorities for seasonal energy storage using electrolyzers and fuel cells. Joule 6, 280–285 (2022).
Yang, Y. et al. Anion-exchange membrane water electrolyzers and fuel cells. Chem. Soc. Rev. 51, 9620–9693 (2022).
Setzler, B. P., Zhuang, Z., Wittkopf, J. A. & Yan, Y. Activity targets for nanostructured platinum-group-metal-free catalysts in hydroxide exchange membrane fuel cells. Nat. Nanotech. 11, 1020–1025 (2016).
Wang, Y. et al. Synergistic Mn-Co catalyst outperforms Pt on high-rate oxygen reduction for alkaline polymer electrolyte fuel cells. Nat. Commun. 10, 1506 (2019).
Wang, T. et al. High-performance hydroxide exchange membrane fuel cells through optimization of relative humidity, backpressure and catalyst selection. J. Electrochem. Soc. 166, F3305 (2019).
Zheng, J., Sheng, W. C., Zhuang, Z. B., Xu, B. J. & Yan, Y. S. Universal dependence of hydrogen oxidation and evolution reaction activity of platinum-group metals on pH and hydrogen binding energy. Sci. Adv. 2, e1501602 (2016).
Zhao, T. et al. Pseudo-Pt Monolayer for robust hydrogen oxidation. J. Am. Chem. Soc. 145, 4088–4097 (2023).
Xue, Y. et al. Cost-effective hydrogen oxidation reaction catalysts for hydroxide exchange membrane fuel cells. Acta Phy.-Chim. Sin. 37, 2009103–2009100 (2020).
Strmcnik, D. et al. Improving the hydrogen oxidation reaction rate by promotion of hydroxyl adsorption. Nat. Chem. 5, 300–306 (2013).
Yao, Z.-C. et al. Electrocatalytic hydrogen oxidation in alkaline media: from mechanistic insights to catalyst design. ACS Nano 16, 5153–5183 (2022).
Xue, Y. et al. A highly-active, stable and low-cost platinum-free anode catalyst based on RuNi for hydroxide exchange membrane fuel cells. Nat. Commun. 11, 5651 (2020).
Zhan, C. et al. Subnanometer high-entropy alloy nanowires enable remarkable hydrogen oxidation catalysis. Nat. Commun. 12, 6261 (2021).
Tang, T. et al. Unconventional Bilateral Compressive Strained Ni–Ir Interface Synergistically Accelerates Alkaline Hydrogen Oxidation. J. Am. Chem. Soc. 145, 13805–13815 (2023).
Liu, D. et al. One-pot synthesis of IrNi@Ir core-shell nanoparticles as highly active hydrogen oxidation reaction electrocatalyst in alkaline electrolyte. Nano Energy 59, 26–32 (2019).
Fu, L. et al. IrMo nanocatalysts for efficient alkaline hydrogen electrocatalysis. ACS Catal 10, 7322–7327 (2020).
Wang, H. & Abruña, H. D. IrPdRu/C as H2 oxidation catalysts for Alkaline Fuel Cells. J. Am. Chem. Soc. 139, 6807–6810 (2017).
Liu, D.-Q. et al. Tailoring interfacial charge transfer of epitaxially grown Ir clusters for boosting hydrogen oxidation reaction. Adv. Energy Mater. 13, 2202913 (2023).
Fu, L. et al. Discrepant roles of adsorbed OH* species on IrWOx for boosting alkaline hydrogen electrocatalysis. Sci. Bull. 65, 1735–1742 (2020).
Zhou, Y. et al. Lattice-confined Ru clusters with high CO tolerance and activity for the hydrogen oxidation reaction. Nat. Catal. 3, 454–462 (2020).
Zadick, A., Dubau, L., Sergent, N., Berthomé, G. & Chatenet, M. Huge instability of Pt/C catalysts in alkaline medium. ACS Catal 5, 4819–4824 (2015).
Lafforgue, C., Chatenet, M., Dubau, L. & Dekel, D. R. Accelerated stress test of Pt/C nanoparticles in an Interface with an anion-exchange membrane—an identical-location transmission electron microscopy study. ACS Catal 8, 1278–1286 (2018).
Hamo, E. R. et al. Carbide-supported PtRu catalysts for hydrogen oxidation reaction in alkaline electrolyte. ACS Catal 11, 932–947 (2021).
Parrondo, J. et al. Platinum supported on titanium–ruthenium oxide is a remarkably stable electrocatayst for hydrogen fuel cell vehicles. Proc. Natl. Acad. Sci. USA. 111, 45–50 (2014).
Miller, H. A. et al. A Pd/C-CeO2 Anode vatalyst for high-performance platinum-free anion exchange membrane fuel cells. Angew. Chem. Int. Ed. 55, 6004–6007 (2016).
Singh, R. K. et al. Synthesis of CeOx-decorated Pd/C catalysts by controlled surface reactions for hydrogen oxidation in anion exchange membrane fuel cells. Adv. Funct. Mater. 30, 2002087 (2020).
Chen, Y. et al. Single-atom catalysts: synthetic strategies and electrochemical applications. Joule 2, 1242–1264 (2018).
Yang, J., Li, W., Wang, D. & Li, Y. Electronic metal–support interaction of single-atom catalysts and applications in electrocatalysis. Adv. Mate. 32, 2003300 (2020).
Han, L. et al. Design of Ru-Ni diatomic sites for efficient alkaline hydrogen oxidation. Sci. Adv. 8, eabm3779 (2022).
Yang, X. et al. CO-tolerant PEMFC anodes enabled by synergistic catalysis between iridium single-atom sites and nanoparticles. Angew. Chem. Int. Ed. 60, 26177–26183 (2021).
Wang, X. et al. Atomic-precision Pt6 nanoclusters for enhanced hydrogen electro-oxidation. Nat. Commun. 13, 1596 (2022).
Tackett, B. M., Sheng, W. & Chen, J. G. Opportunities and challenges in utilizing metal-modified transition metal carbides as low-cost electrocatalysts. Joule 1, 253–263 (2017).
Levy, R. B. & Boudart, M. Platinum-like behavior of tungsten carbide in surface catalysis. Science 181, 547–549 (1973).
Hunt, S. T. et al. Self-assembly of noble metal monolayers on transition metal carbide nanoparticle catalysts. Science 352, 974–978 (2016).
Gong, Q. et al. Ultrasmall and phase-pure W2C nanoparticles for efficient electrocatalytic and photoelectrochemical hydrogen evolution. Nat. Commun. 7, 13216 (2016).
Liu, W. et al. A durable and pH-universal self-standing MoC–Mo2C heterojunction electrode for efficient hydrogen evolution reaction. Nat. Commun. 12, 6776 (2021).
Zhang, B. et al. Lattice-Confined Ir Clusters on Pd Nanosheets with Charge Redistribution for the Hydrogen Oxidation Reaction under Alkaline Conditions. Adv. Mater. 33, 2105400 (2021).
Hao, S. et al. Torsion strained iridium oxide for efficient acidic water oxidation in proton exchange membrane electrolyzers. Nat. Nanotech. 16, 1371–1377 (2021).
Zhang, J. et al. OH spectator at IrMo intermetallic narrowing activity gap between alkaline and acidic hydrogen evolution reaction. Nat. Commun. 13, 5497 (2022).
Lee, W. H. et al. High crystallinity design of Ir-based catalysts drives catalytic reversibility for water electrolysis and fuel cells. Nat. Commun. 12, 4271 (2021).
Li, Z. et al. Iridium single-atom catalyst on nitrogen-doped carbon for formic acid oxidation synthesized using a general host–guest strategy. Nat. Chem. 12, 764–772 (2020).
Wang, Q. et al. Atomic metal–non-metal catalytic pair drives efficient hydrogen oxidation catalysis in fuel cells. Nat. Catal. 6, 916–926 (2023).
Tian, X., Zhao, P. & Sheng, W. Hydrogen evolution and oxidation: mechanistic studies and material advances. Adv. Mater. 31, e1808066 (2019).
Sheng, W., Gasteiger, H. A. & Shao-Horn, Y. Hydrogen Oxidation and Evolution Reaction Kinetics on Platinum: Acid vs Alkaline Electrolytes. J. Electrochem. Soc. 157, B1529 (2010).
Lee, G. R. et al. Efficient and sustainable water electrolysis achieved by excess electron reservoir enabling charge replenishment to catalysts. Nat. Commun. 14, 5402 (2023).
Li, M. et al. Revealing the regulation mechanism of Ir–MoO2 interfacial chemical bonding for improving hydrogen oxidation reaction. ACS Catal 11, 14932–14940 (2021).
Yang, Y. et al. Electrocatalysis in alkaline media and alkaline membrane-based energy technologies. Chem. Rev. 122, 6117–6321 (2022).
Wang, L. et al. Stabilizing low-valence single atoms by constructing metalloid Tungsten Carbide supports for efficient hydrogen oxidation and evolution. Angew. Chem. Int. Ed. 62, e202311937 (2023).
Su, L. et al. Electric-double-layer origin of the kinetic pH effect of hydrogen electrocatalysis revealed by a universal hydroxide adsorption-dependent inflection-point behavior. J. Am. Chem. Soc. 145, 12051–12058 (2023).
Men, Y. et al. Oxygen-inserted top-surface layers of Ni for boosting alkaline hydrogen oxidation electrocatalysis. J. Am. Chem. Soc. 144, 12661–12672 (2022).
McCrum, I. T. & Koper, M. T. M. The role of adsorbed hydroxide in hydrogen evolution reaction kinetics on modified platinum. Nat. Energy 5, 891–899 (2020).
Nørskov, J. K. et al. Trends in the exchange current for hydrogen evolution. J. Electrochem. Soc. 152, J23 (2005).
Li, P. et al. Hydrogen bond network connectivity in the electric double layer dominates the kinetic pH effect in hydrogen electrocatalysis on Pt. Nat. Catal. 5, 900–911 (2022).
Nørskov, J. K. et al. Origin of the overpotential for oxygen reduction at a fuel-cell. Cathode. J. Phys. Chem. B 108, 17886–17892 (2004).
Acknowledgements
This work was financially supported by the National Key Research and Development Program of China (2019YFA0210300, ZZ), the National Natural Science Foundation of China (22379004 ZZ, 22101016 WZ, 22288102 HL), Beijing Natural Science Foundation (Z210016, ZZ), and Fundamental Research Funds for the Central Universities (buctrc201916, ZZ). The authors appreciate the 1W2B in the Beijing Synchrotron Radiation Facility (BSRF) for help with XAFS experiments.
Author information
Authors and Affiliations
Contributions
Z.Z. supervised the project. Z.Z. and J.F. conceived the idea. J.F. and Hai.W synthesized and characterized the catalysts. J.P. and Z.X conducted the XAS experiments. J.F. and Hai.W carried out the electrochemical measurements. J.F. and X.W. assembled the HEMFCs. Q.D. and H.L. performed the DFT calculations. Hao.W., C.C., and W.Z. helped with data interpretation. J.F., H.L., Y.Y., and Z.Z. wrote the manuscript. All authors discussed the results and assisted with the manuscript preparation.
Corresponding authors
Ethics declarations
Competing interests
The authors declare no competing interests.
Peer review
Peer review information
Nature Communications thanks Li Li, and the other, anonymous, reviewer(s) for their contribution to the peer review of this work. A peer review file is available.
Additional information
Publisher’s note Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
Supplementary information
Source data
Rights and permissions
Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.
About this article
Cite this article
Fang, J., Wang, H., Dang, Q. et al. Atomically dispersed Iridium on Mo2C as an efficient and stable alkaline hydrogen oxidation reaction catalyst. Nat Commun 15, 4236 (2024). https://doi.org/10.1038/s41467-024-48672-9
Received:
Accepted:
Published:
DOI: https://doi.org/10.1038/s41467-024-48672-9
Comments
By submitting a comment you agree to abide by our Terms and Community Guidelines. If you find something abusive or that does not comply with our terms or guidelines please flag it as inappropriate.