Abstract
The carbon−carbon coupling at the Cu/Cu2O Schottky interface has been widely recognized as a promising approach for electrocatalytic CO2 conversion into value-added alcohols. However, the limited selectivity of C2+ alcohols persists due to the insufficient control over rectifying interface characteristics required for precise bonding of oxyhydrocarbons. Herein, we present an investigation into the manipulation of the coordination environment of Cu sites through an in-situ electrochemical reconstruction strategy, which indicates that the construction of low-coordinated Cu sites at the Cu/Cu2O interface facilitates the enhanced rectifying interfaces, and induces asymmetric electronic perturbation and faster electron exchange, thereby boosting C-C coupling and bonding oxyhydrocarbons towards the nucleophilic reaction process of *H2CCO-CO. Impressively, the low-coordinated Cu sites at the Cu/Cu2O interface exhibit superior faradic efficiency of 64.15 ± 1.92% and energy efficiency of ~39.32% for C2+ alcohols production, while maintaining stability for over 50 h (faradic efficiency >50%, total current density = 200 mA cm−2) in a flow-cell electrolyzer. Theoretical calculations, operando synchrotron radiation Fourier transform infrared spectroscopy, and Raman experiments decipher that the low-coordinated Cu sites at the Cu/Cu2O interface can enhance the coverage of *CO and adsorption of *CH2CO and CH2CHO, facilitating the formation of C2+ alcohols.
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Introduction
CO2 electrochemical reduction (CER) to produce value-added chemicals and fuel is an available strategy in response to the growing energy and environmental crisis1. C2+ alcohols are coveted outputs of CER owing to their extensive market potentials and remarkable energy densities2. Indubitably, the harmonious cooperation of biphasic Cu/Cu2O catalyst stands as an eminent contender in engendering C2+ alcohols owing to its heightened predilection towards *CO adsorbates on Cu+ and reduced energy barrier for C–C or C2–C coupling at the rectifying interface3,4. Nevertheless, owing to the precarious stability of oxyhydrocarbons intermediates (wherein, C2H3O* serves as the watershed of C2H4 or alcohols) and the oxidation state of Cu, the enduringly biphasic Cu/Cu2O catalyst continues to face significant obstacles in suppressing the desorption of C2H3O* and enhancing the yield of alcohols compared to hydrocarbons in the highly reductive environmental5. Therefore, the feasible strategies are demanded to develop the architectural blueprint of catalysts and electrolytic systems for preserving the oxidation state and bolstering the CO2 performance of copper-based catalysts, including but not limited to elemental doping6, interface engineering7,8, intermediate confinement9, and pulse CO2 electrolysis (P-eCO2R owing the straightforward and readily adjustable means of manipulating anodic potentials for facilitating the formation of Cu oxide species)10,11. Especially, the Mott−Schottky catalyst possesses the remarkable ability to hinder the accumulation of electrons, thereby safeguarding the integrity of Cu–O bonds, while simultaneously enabling swift electron transfer courtesy of its built-in electric field12,13. Therefore, it necessitates the employment of intricate catalyst configuration and fabrication techniques to elevate the rectifying interface effects of Cu/Cu2O for the purpose of bonding oxyhydrocarbons.
Several strategies can improve the selectivity of oxyhydrocarbons in CER, including the high concentration of local *CO around the active sites14,15, doping modification of copper catalysts with heteroatoms16,17, building of crystal defects and low coordination of copper12,18,19. Effectively, the coverage of *CO can be facilitated on the low-coordinated Cu sites of oxide-derived Cu, leading to its subsequent hydrogenation into *COH, which is essential for the coupling of OC−COH20,21. For example, Liang group reported a fragmented Cu catalyst with abundant low-coordinated sites by electrochemical reconstruction of B-doped Cu2O, which exhibited a C2+ products faradaic efficiency of 77.8% at 300 mA cm−2 (see ref. 19). Theoretical computations have demonstrated that the *CO bindings could be strengthened on low-coordinated copper sites and prefer to coupling with *COH instead of *CO dimerization22. Moreover, the incorporation of halide species and the creation of oxygen vacancy also contribute to the formation of low-coordinated metal and the controlled generation of intermediates23,24. Sun and co-worker intervened the behavior of low-coordination chloride ion (Cl−) adsorption on the surface of a silver hollow fiber (Ag HF) electrode in 3 M KCl electrolyte, which resulted in the high concentration of *CO on low-coordination Ag–Cl state for CER25. However, only few studies provide insight on the priority of enhanced rectifying interface effects for bonding oxyhydrocarbons on the low-coordinated Cu/Cu2O in comparison to the pure Cu/Cu2O Mott–Schottky catalyst. Thus, the mechanism exploration of low-coordinated Cu/Cu2O on stabilizing *CO and oxyhydrocarbons intermediates is significant.
Herein, we demonstrated a low-coordinated Cu/Cu2O Mott–Schottky catalyst with an enhanced rectifying interface (CuL/Cu2O). This catalyst adjusts the electron densities through interfacial charge exchange, leveraging the difference in Cu and Cu2O work functions, which can effectively form bonds between *CO and oxyhydrocarbons under CER conditions. Furthermore, CuL/Cu2O catalyst generated highly selective catalytic sites for the coupling reaction of *CO–COH and hydrogenation of C2H2O* intermediate to C2+ alcohols. Chlorine-doped cuprous oxide (Cl–Cu2O) and pure Cu2O were selected as the precursors and electrochemically reconstructed to unsaturated-coordinate CuL/Cu2O and pure CuP/Cu2O. The low-coordinated CuL/Cu2O achieved a C2+ alcohols faradic efficiency (FEalcohols) of 64.15 ± 1.92% with the corresponding energy efficiency of ~39.32%. In addition, a stable C2+ alcohols faradaic efficiency of >50% was also obtained during a continuous 50 h chronopotentiometry experiment. Our research provides a platform for the rational design of low-coordinated Cu–Cu2O Mott–Schottky catalysts and analyzes the key elements for efficient synthesis of C2+ alcohols.
Results
Synthesis and characterization of CuL/Cu2O nanoparticles
The CuL/Cu2O catalysts were synthesized using a simple electrochemical reconstruction strategy on Cl–Cu2O nanoparticles (see details in “Methods”, Supplementary Figs. 1–4). The CuL/Cu2O catalysts are designed to function as a Mott–Schottky catalyst of Cu/Cu2O, which generates enhanced rectifying interfaces between electron-deficient metal and electron-rich region because of the difference in work function (Fig. 1A). The rectifying interface effect of Cu–Cu2O Mott–Schottky catalyst adjusts the electronic densities through interfacial charge exchange, resulting in reduced adsorption resistance for intermediates This effect also leads to higher catalytic performance due to the electronic perturbation at both sides of the interface (Fig. 1B)26. Enhancement of the rectifying interface effect, however, can be achieved through the smaller size and defects of crystals27,28, which contributes to faster electron transfer and a denser asymmetric charge distribution (Fig. 1C). Furthermore, the accumulable electron density indicates that the d → 2π* back donation induce the transfer of electron density from Cu to the *CO intermediates29,30. The adsorption abilities for intermediates on different catalyst models are quantified by DFT calculation (Supplementary Figs. 5–8 and Supplementary Table 3). Figure 1D demonstrates that all these models exhibit a linear relationship between the adsorption energy and *CO coverage. Notably, the CuL/Cu2O model shows a higher stark tuning slope (−1.04), indicating an enhanced interaction between *CO and the catalyst surface, resulting in increased adsorption strength and coverage. In addition, the Cu2O model bonds more firmly with CO molecules than other models due to the presence of stepped sites, confirming the affinity for *CO adsorbates on Cu+ sites, as stated in previous literature31,32. Subsequently, the adsorption energy of CH2CHO (a branching intermediate for ethanol or ethylene) and CH2CO intermediates were calculated to assess the potential capacities for ethanol and C3 products (Fig. 1E, F). Both of them exhibit strong adsorption on the surface of CuL/Cu2O model. The *CH2CO molecular, with the C(2) end of H2C(1)C(2)O possessing a high positive charge, serves as a key intermediate for the C2–C coupling reaction, suggesting the C2–C coupling as a nucleophilic addition reaction process in the mixed-valence boundary region33. Thus, the low-coordinated CuL/Cu2O Mott–Schottky catalyst has an enhanced affinity for intermediates compared to pure CuP/Cu2O.
To verify the enhanced rectifying interfaces of CuL/Cu2O, a series of experiments were conducted. The sharp peaks of XRD patterns matched perfectly with the standard cubic Cu2O (JCPDS No. 99-0041) and Cu (JCPDS No. 89-2838), providing evidence for the coexistence of Cu+ and Cu0 (Fig. 2A). The SEM and TEM images show that the reconstructed CuL/Cu2O nanoparticles exhibit smaller particle sizes ranging from 200 to 300 nm compared to CuP/Cu2O, with no serious agglomeration (Supplementary Figs. 9 and 10). From the high-resolution TEM and SAED images of CuL/Cu2O (Fig. 2B and Supplementary Fig. 10C), the lattice fringes with interplanar spacing of 0.25 and 0.18 nm are classified to the d spacing of exposed Cu2O (111) and Cu (200) planes, respectively. The distortion of Cu(200) may be caused by the potential surface defect owing to the counter diffusion of lattice O from the Cu2O/Cu interface with low energy barriers34. The distorted Cu(200) can induce a low-coordinated Cu and reduce the barriers of intermediates adsorption35. Energy dispersive X-ray spectra (EDS) mapping analysis shows the presence of residual chlorine with a content of 1.14 at% and a homogeneous distribution among Cu, Cl, and O (Fig. 2C, Supplementary Fig. 10D and Supplementary Table S2). The enhanced rectifying interfaces of low-coordinated CuL/Cu2O result in an increased absorption edge in the ultraviolet–visible (UV–vis) diffuse reflectance spectrum across the entire wavelength range (inserted in Fig. 2D). Based on the Kubelka−Munk function, the optical bandgap of a semiconductor can be extrapolated from the Tauc plot (the curve of converted (αhν)1/n versus hν from the UV-vis spectrum, where α, h, and ν are the absorption coefficient, Planck constant, and frequency of the photon, respectively, and n is 1/2 for a direct bandgap semiconductor or 2 for an indirect bandgap semiconductor)33. The Tauc plot exhibits a well-matched linear fit with n = 1/2, which is in line with previous articles supporting Cu2O as a direct bandgap semiconductor (Supplementary Fig. 11)36. The Eg value of CuL/Cu2O is calculated to be 1.73 eV by measuring the x-axis intercept of an extrapolated line from the linear regime of the curve, which is smaller than that of CuP/Cu2O (1.85 eV). The CuL/Cu2O sample with a minimum band energy and highest conductivity is beneficial for enhancing the rectifying interface effect. Kelvin probe force microscopy (KPFM) was carried out to explore the internal electric field and work function of CuL/Cu2O (Fig. 2E). The contact potential difference (CPD) profile shows light and dark variations due to the different work functions of sample and substrate37. According to the CPD profiles, the work function of CuL/Cu2O was defined to be the lowest among the other samples (Supplementary Fig. 12). Figure 2E exhibits the contact potential difference (CPD) profiles for CuL/Cu2O, from which an estimate of the average surface potential of 0.037 V can be derived. These results are in accordance with the experimental expectations of Ultraviolet photoelectron spectroscopy (UPS). Importantly, UPS experiments were performed to calculate the work function (WF) of samples for estimating the electron binding factor (Fig. 2F). The experimental WF values for Cu2O, Cl-Cu2O, CuP/Cu2O, and CuL/Cu2O, calculated by recording the secondary electron cutoff and Fermi edge (Supplementary Fig. 13), are 5.23, 5.06, 4.57, and 4.18, respectively. These values suggest that CuL/Cu2O has a smaller escaping resistance for electrons from the surface, which potentially facilitates a synergistic rectifying interface to enhance the asymmetric adsorption of intermediates. The theoretical electrostatic potential energies of the samples are plotted in Fig. 2G, where the surface potentials of the models are calibrated based on the corresponding Fermi levels (EFermi). Noteworthy, the charge transfer at the interface of CuL/Cu2O results in the formation of interface dipole, thereby decreasing the WF of CuL/Cu2O in the vacuum region. The distribution of electron density differences of the internal electric field inside CuL/Cu2O were explored to estimate the potential adsorption of electrically charged intermediates. As shown in Fig. 2H, the electron clouds around the side of Cu+ at the rectifying interface of CuL/Cu2O are much more enriched due to the stronger electronegativity of O than Cl and a low-coordination number than that of CuP/Cu2O (Supplementary Fig. 14 and Supplementary Table 4), indicating the preferred nucleophilic addition reaction process on CuL/Cu2O. Due to the difference in electron density, the Cu+ region becomes nucleophilic, while the Cu0 region prefers an electrophilic addition reaction process (Fig. 2I). In conclusion, the faster electron exchange at enhanced rectifying interface regions, resulting from the asymmetric electron aggregation, will boost the nucleophilic or electrophilic addition reaction process for C–C or C2–C coupling. Generally, the enhanced adsorption of negatively charged *CO may focus on the electrophilic Cu sites, while the C2 end of *C2H2O, with a high positive charge, prefers bonding with nucleophilic Cu2O.
To analyze the origins of enhanced rectifying interfaces, electro paramagnetic resonance (EPR), XPS, and X-ray absorption spectroscopy were utilized to characterize the refined structure of CuL/Cu2O. As shown in Fig. 3A, the O 1s XPS spectrum is deconvoluted into four peaks situated at 529.7, 530.3, 530.8, and 531.7 eV, corresponding to the lattice oxygen (Cu–O), oxygen vacancies (Vo), C–O bond and adsorbed oxygen on CuL/Cu2O samples, respectively38. The ratio of Vo/Cu–O demonstrates a descendant trend with Ar+ etching, implying surface and subsurface oxygen deficiency in the oxide-derived Cu. The shift of bonding energy of Cu–O toward a higher level also indicates the disappearance of Vo within the depth of CuL/Cu2O. A characteristic sign of Vo is observed at g = 2.004 (Fig. 3B)39, which supports the electron-rich status of oxygen-deficient Cu+. However, the CuP/Cu2O exhibits a perfect Mott−Schottky structure without any signs of deficient oxygen (Fig. 3B and Supplementary Fig. 15). From the Cl 2p spectrums in Fig. 3C, the bonding energy of Cu–Cl also shifts to a higher state with deeper Ar+ etching due to the presence of sufficient Cl and O atoms in the depth of CuL/Cu2O. The clean rectifying interface regions of CuL/Cu2O ensure smooth absorption and desorption, as well as the coupling behavior of oxyhydrocarbon intermediates. In contrast with Cu 2p spectra of the CuP/Cu2O species, the Cu 2p 3/2 peak of CuL/Cu2O shows a strong characteristic signal for Cu0/Cu+ at 932.3 eV, accompanied by weak satellite peaks (Fig. 3D). The AES of CuP/Cu2O and CuL/Cu2O were analyzed by Cu LMM Auger spectra to prove the clearer evidence of the valence states of Cu (Fig. 3E). The kinetic energy of the Auger electron transitions of CuL/Cu2O corresponding to Cu+, Cu2+, and Cu0 are measured at 916.4, 917.2, and 918.3 eV, respectively, further confirming the coexistence of Cu+ and Cu0 (Supplementary Fig. 16)40. Synchrotron-based X-ray absorption fine spectroscopy was employed to analyze the coordination environment of Cu. The adsorption edge position of CuL/Cu2O (8980 eV) is closer to that of Cu2O (8983.5 eV) and Cu foil, while it is further away from that of CuO, indicating the presence of integral valence Cuδ+ (0 <δ <1) in the CuL/Cu2O catalyst (Fig. 3F and Supplementary Fig. 17)41. Figure 3G shows the Fourier transform (FT) extended X-ray absorption fine structure spectra of CuL/Cu2O. A strong signal of the Cu–O bond at 1.5 Å can be detected in CuL/Cu2O, accompanied by the Cu–Cu bond at 2.32 Å, which also proves the coexistence of Cu0 and oxidized Cu+. Furthermore, the Cu–O bong length of CuL/Cu2O is slightly longer than that of Cu–O in pure Cu2O (1.44 Å), implying the presence of Cu–Cl because of the longer Cu–Cl bond compared to Cu–O42. Unfortunately, the Cu–Cl sign has fallen out due to the low content of chlorine elements and the shading impact of the strong Cu–O sign. In addition, the Cu+ in CuL/Cu2O may have a low-coordination number due to the deficiency of oxygen and chlorine. To better quantify the coordination number of Cu, EXAFS fitting was carried out (Fig. 3H and Supplementary Table 4). The experimental k3–weight Cu K-edge EXAFS fits perfectly with the calculated R-space fitting model of CuL/Cu2O. According to the fitting results, the coordination number of Cu atom of CuL/Cu2O (10.3) is smaller than that of Cu2O (12.3) and Cu (12), which correspond to the fitting of Cu2O and Cu, respectively (Supplementary Fig. 18). The structure of the Mott–Schottky catalyst was further analyzed by wavelet transform of the EXAFS. As shown in Fig. 3I, both Cu2O and CuL/Cu2O have the K values centered around 6.3 Å−1, while the value from CuL/Cu2O is located at 7.1, closer to 7.9 Å−1 observed from the Cu foil. These analyses confirm that the low-coordinated CuL/Cu2O possesses an electron-rich region and abundant defect sites, which receive nucleophilic addition reaction of C–C or C2–C coupling in the mixed-valence boundary region to generate ethanol and n-propanol.
Performance of CER in the flow cell
The cathodic electrochemical experiments of CO2 reduction reaction were implemented in flow cells using 1 M KOH as electrolyte under ambient conditions (Supplementary Fig. 19). All working potentials are converted into the reversible hydrogen electrode (RHE) scale with iR correction of 85%. The linear sweep voltammetry (LSV) curves in Fig. 4A show that the CuL/Cu2O catalyst provides higher conductivity and activity for CER, with a total current density (jtotal) of −200 at the applied potential of −0.66 V. The splendid kinetic property of CuL/Cu2O reveals a smaller charge-transfer resistance and higher catalytic activity (tafel slope of 232 mV dec−1 and electrochemically active surface area of 6.1 mF cm−2) for CER (Supplementary Figs. 20 and 21). Remarkably, CuL/Cu2O shows excellent selectivity of C2+ alcohols with a maximum faradic efficiency (FE) of 64.15 ± 1.92% (ethanol of ~56% and n-propanol of ~8%), whereas CuP/Cu2O only reaches a maximum FEethylene and FEalcohols of ~38.4% and 11.4%, respectively (Fig. 4B, C and Supplementary Fig. 22). As shown in Fig. 4D, at a jtotal of −200 mA cm−2, the partial current density of alcohols (jalcohols) rapidly rises to 128.3 mA cm−2 on the CuL/Cu2O catalyst (the applied potential is −0.66 V), which is 13-fold higher than that of CuP/Cu2O (9.9 mA cm−2 at −0.81 V). Meanwhile, the half-cell cathodic energy efficiency (EE) and production rate of alcohols on CuL/Cu2O also reach optimal values of 39.32% and 379.78 μmol cm−2 h−1, respectively (Fig. 4E, F). Our results feature one of the most excellent efficiencies for alcohol compared with the reported literature to date (Supplementary Table 5). To further investigate the positive effect of halogen anion on CER, comparative experiments with introducing Cl were conducted. The acid-aqueous solution of NH4Cl resulted in the oxidized Cu2+ and physically adsorbed Cl on the surface of NH4Cl–Cu2O (Supplementary Fig. 23). In addition, the distribution of Cl was estimated by XPS after undergoing Ar+ etching, confirming the superficial adsorption of Cl (Supplementary Fig. 24 and Supplementary Table 2). The peak values of FEalcohols and jalcohols on NH4Cl–Cu2O are 17.7% and −50.6 mA cm−2, respectively, indicating a slight increase limited by the negligible Cl concentration. However, a significantly enhanced selectivity of alcohols (a maximum FEalcohols of 23.5%) is achieved on CuP/Cu2O in 1 M KOH electrolyte with 3 M KCl, suggesting that the specific adsorption of surface-bound Cl, located on the inner Helmholtz planes of Cu electrode, contributes to the C–C or C2–C coupling owing to the strong chemical affinity of the anion for meal (Supplementary Fig. 25)43. Notably, the CuL/Cu2O catalyst still retains its original profile with a mott−schottky interface and unspoiled nanoparticles, as well as an unaltered presence of Cl after CER (Supplementary Figs. 26 and 27). Furthermore, the electrochemical stability of CuL/Cu2O for CER was evaluated through chronopotentiometry electrolysis at 200 mA cm−2 (Fig. 4G). Despite a steady decline over the course of 50 h electrochemical process, CuL/Cu2O achieves a sustained FEalcohols of > 50% and an alcohols yield of 17.1 mmol. However, the mention of pulse electrolysis is necessary for long-term industrial production, which may still be an essential strategy for the CO2 electrolysis community, especially due to its unique advantage in electrolysis stability (>1000 h)44,45. The structure of CuL/Cu2O maintains a classic architecture of Mott–Schottky catalyst, while slight morphological changes occur (Supplementary Fig. 28). Cl–Cu2O powders of different particle sizes were prepared and tested under the same electrochemical conditions (Supplementary Figs. 29 and 30). The selectivity of C2+ alcohols gradually increases on a gas diffusion electrode loaded with larger-sized particles, which is attributed to the stability of low-coordinated Cu/Cu2O. The appropriate particle size contributes to the stabilization of the enhanced rectifying interface of the low-coordinated CuL/Cu2O Mott–Schottky catalyst. To explore the effect of electrolytes on the selectivity of C2+ alcohols, various electrolytes were used to offer a different pH environment (Supplementary Fig. 31). It undergoes electrochemical reduction reaction of CO2 with synergistic effect of CO2 coverage and catalyst in pH-compatible electrolyte and thermodynamics-mediated competitive reaction in a strong alkaline electrolyte. The Cl element shows a positive effect on improving the selectivity of C2+ products, but the sensitivity of ethylene is stronger than that of C2+ alcohols.
Structure–property correlation and oxidation state of CuL/Cu2O
Operando FTIR and Raman spectroscopy were employed for investigating the reconstruction of catalysts and adsorbates on both CuL/Cu2O and CuP/Cu2O. The electrochemical reactions were executed in CO2-saturated 0.1 M KHCO3 electrolyte. The reference spectrum was taken at open-circuit potential, and additional spectra were provided in the range of −0.2 ~ −1.1 V vs. RHE. Two bands emerge at 1663 and 1280 cm−1 during CO2 bubbling, which corresponds to the C = O and C−OH stretching vibrations of COOH. These peaks indicate the presence of the COOH* intermediate during the reduction of CO2 on CuL/Cu2O. Furthermore, the C≡O stretch band in the 2000–2100 cm–1 range can be attributable to the linear bonding mode of CO molecules (COL)46. In contrast to the behavior of the COL band, the band in the ≈1800–1900 cm–1 range, caused by the bridging bonding mode of CO molecules (COB), exhibits a significant degree of hysteresis. The redshift of the COB band at more negative potentials is a result of the stark tuning effect47. Simultaneously with the CO-related band, a band at 1305 cm−1 associated with *COH stretching grows, and *COOH disappears in the spectra. which indicates the performance of CO2 reduction. The absence of the bands at 1589 cm−1 in the transmission spectra points out the possibility of the *OCCOH coupling reaction during the reduction of CO2 on CuL/Cu2O (Fig. 5A). However, in contrast to CuL/Cu2O catalyst, some new signals at 1706, 1543, and 1399 cm−1 corresponding to the stretch of *CHO, *OCCO, and *OCHO intermediates emerged in spectra of CuP/Cu2O, certifying the coupling mode of OC–CO and possible formate product (Supplementary Fig. 32)48. Combining with time-independent spectral analysis (Supplementary Fig. 33A, B), apparent peaks are determined at 1064 and 1558 cm−1, which correspond well to the symmetric and asymmetric vibrations of the *OCCOH intermediate, respectively49,50. In addition, the stretching vibration at 1335 and 1716 cm−1 are in close proximity to the stretching of *OCH2CH3 and *CHO, respectively, which serve as the important intermediates for the subsequent C–C coupling in the production of C2+ alcohols51,52. These conclusions are consistent with the results obtained from the product analysis of CuP/Cu2O and CuL/Cu2O. In the Raman spectra (Fig. 5B and Supplementary Fig. 33D), the CuL/Cu2O powder loaded on carbon paper substrate exhibits typical characteristic peaks of adsorbed *CO intermediates, which are deconvoluted into a low-frequency band (LFB) at ∼2045 cm−1 and a high-frequency band (HFB) at ∼2097 cm−1, which verifies the bonding styles on terrace and step sites, respectively53,54. A redshift of the υ(CO) band indicates the enhanced interaction between the catalyst surface and *CO, resulting in a higher *CO coverage55. In addition, the frequencies of υ(CO) bands are correlated with the coordination states of Cu sites. Therefore, the low-coordination states of Cu sites in CuL/Cu2O will induce a positive shift of the d-band center of Cu and boost the hybridization of the d-band with the 2π* orbital of CO. The HFB modes derived from the low-coordinated Cu sites will favor the breeding of the υ(C–C) band (~1960 cm−1), where a blueshift may predict the protonation process C–C bonds29,30. On the contrary, the weak signs of the υ(CO) and υ(C–C) bands on CuP/Cu2O catalyst also verify the poor *CO coverage and C–C coupling (Supplementary Fig. 34B). To verify the origin of the oxidation state of CuL/Cu2O, Raman spectroscopy was conducted in the shift range of 200–1600 cm−1, and the results are presented in Supplementary Figs. 33A and 34A. In the case of Cl–Cu2O samples, characteristic signals were observed at 224, 425, 522, and 626 cm−1, which were attributed to the 2Γ−12, 4Γ−12, Γ+25, and Γ−12 + Γ+25 phonon modes, respectively56,57. These Raman signals gradually disappear within the potential range from −0.2 to −0.7 V vs RHE, indicating the complete reduction of Cu2O to metallic Cu. In contrast, the Cl–Cu2O samples retain the characteristic Raman modes (2Γ−12 and Γ−12 + Γ+25) even at potentials greater than −0.7 V, suggesting that the low-coordinated CuL/Cu2O can protect Cu+ species against reduction due to a combination of environmental and structural factors. Overall, CuL/Cu2O catalyst exhibits a stronger adsorption capacity for *CO due to the restricted rotation and stretching vibration peaks of adsorbed *CO and the Cu–CO bond at around 274 and 358 cm−1, respectively58. Specifically, the coverage of *CO is closely correlated with the intensity ratio of ν(Cu−CO) to ν(*CO)59. Importantly, the intensity ratio of ν(Cu−CO) to ν(*CO) of CuL/Cu2O is higher in the case of CuL/Cu2O compared to CuP/Cu2O, implying a greater CO coverage, which is favorable for the oxidation state of Cu+. The peaks observed at 1015, 1024, and 1069 cm−1 can be assigned to the vibrations of ν1(C–O) of HCO3−, OCO antisymmetric stretching from *COOH, and ν2(C–O) of CO32−, respectively60. Furthermore, as the potential increases, CO32− accumulates and disappears on the catalyst surface, indicating the dissolution and reduction of CO2. Briefly, the origin of the oxidation state of CuL/Cu2O can be summarized as follows: (1) the lattice shrinkage resulting from fast electron transfer from Cu to Cu+ at the enhanced rectifying interface inhibits the loss of oxygen atoms and stabilizes the chemical valence of the cation Cu+ species working with residual Cl atoms61,62. (2) The presence of coordination defects and oxygen vacancies increases the adsorption of intermediates rather than forming proton bonds with O atoms of Cu–O to avoid the reduction of Cu+ species63,64. (3) Strong electronic interactions occur between carbon intermediates and Cu+ species65,66. When CO forms a hybridization orbital with the Cu d-states, the 5σ and 2π* orbitals of *CO split into bonding and anti-bonding orbitals. In this process, electrons from the Cu d-band are transferred to the 2π orbitals of *CO through d-2π back donation, while electrons from the 5σ orbital of *CO donate to the Cu d-band through 5σ-d donation30. These effects stabilize the oxidation state of Cu+ species during CO2 electroreduction, allowing for the synergistic effect of Cu and Cu+ species.
The reaction barriers for the hydrogenation process of C2+ intermediates on the models of Cu/Cu2O with and without Cl, respectively, were calculated by DFT. Firstly, by analyzing the Bader charge and bond length of CuL/Cu2O (Fig. 5C, D), it is observed that the lower Bader charge value (0.477 |e|) compared to CuP/Cu2O (1.01 |e|) indicates that the populated electronic orbitals of low-coordinated Cu sites will easily bind to intermediates and reduce the rate-determining energy barrier67. CuL/Cu2O with additionally formed empty orbitals can facilitate electron transfer from hydrogen to nucleophilic intermediates, suggesting the Cu 3d orbitals overlap with the π orbitals of C and further reduced activation energy for CO2 hydrogenation on Cu/Cu2O68. As a result, the nucleophilic addition reaction process of *CH2CO–*CO coupling may effectively react on the mixed-valence boundary region33, which reduces the formation energy of *CH2COCO on CuL/Cu2O (−0.148 eV) toward n-propanol (Fig. 5E, Supplementary Fig. 35, and Supplementary Table 6). For the C–C coupling on CuL/Cu2O model (Fig. 5F, Supplementary Fig. 36 and Supplementary Table 7), the *CO–COH coupling is the rate-determining step for CuL/Cu2O catalyst (1.46 eV), indicating the vital rule of *CO coverage in the post-coupled proton-electron transfer (CPET) reaction. The energy barriers of intermediates gradually decrease until *C2H3O is reached, which can be further reduced to *C2H4O or *O for ethanol or C2H4, respectively. The CuL/Cu2O model exhibits a more stable adsorption for C2H4O* (−0.293 eV) than CuP/Cu2O (−0.154 eV), implying facilitated thermodynamics for increasing the adsorption of key intermediate.
Discussion
The mentioned theoretical and experimental studies provide tangible proof that the enhanced rectifying interface of low-coordinated Cu/Cu2O Mott–Schottky catalyst plays an essential role in the selective production of C2+ alcohols. We emphasize several elements of the low-coordinated CuL/Cu2O catalyst for the upgraded CER performance. Firstly, the fast electron exchange and enhanced intermediate adsorption at synergistic rectifying interface regions are due to the low coordination and asymmetric electron aggregation inside the CuL/Cu2O catalyst. In addition, the excellent conductivity and charge difference of Cu+/Cu0 boost the nucleophilic or electrophilic addition reaction process for C–C or C2–C coupling. Secondly, the fast electron transfer from Cu to Cu+ at the enhanced rectifying interface can induce lattice shrinkage, inhibiting the loss of residual oxygen atoms responsible for stabilizing the chemical valence of Cu+ when working with residual Cl atoms. The clean Cu/Cu2O regions ensure smooth absorption and desorption, as well as the coupling behavior of the oxyhydrocarbon intermediates. Thirdly, abundant defects originated from oxygen vacancies and residual Cl, as a result of electrochemically reconstructing Cl–Cu2O, supply rich free electrons and landing sites for adsorbed intermediates. These results work together on low-coordinated CuL/Cu2O Mott–Schottky catalyst to improve the selectivity of C2+ alcohols. The faradic efficiency and energy efficiency of C2+ alcohols are up to 64.15% and 39.32%, respectively, where the stability of over 50 h (FEC2+ alcohols>50% at jtotal = 200 mA cm−2) explains the positive effects of the above results.
Methods
Synthesis of CuP/Cu2O, CuL/Cu2O, and NH4Cl–Cu2O nanoparticles
In the synthesis of the Cu2O nanocrystals, glucose served as a reductant, contributing to the reduction process69. Detail: a mixed solution containing 2 mL of OA and 5 mL of ethanol was added under magnetic stirring for 30 min after dissolving 1 mmol CuSO4·5H2O in 15 mL of deionized water and placed in a water bath at 80 °C. Then, 5 mL of 1 M NaOH aqueous solution was added and kept for 10 min. Next, 5 mL of 2 M glucose aqueous solution was added as a reductant to maintain chlorine-free environment for 3 h at 80 °C. The brick red products were obtained by centrifugation and thoroughly cleaned with cyclohexane and ethanol multiple times to eliminate any remaining OA. They were then dried and stored under vacuum at room temperature for future use. As-prepared Cu2O nanocrystals (2 mg) were mixed with 20 µL of 5 wt% Nafion in a solution composed of ethanol (190 µL) and water (190 µL). The mixture was deposited onto a gas diffusion layer (2 cm × 2 cm) using an airbrush. It was subsequently electrochemically reduced at –50 mA cm−2 for 10 min with flowing CO2 in 1 M KOH electrolyte. The obtained catalyst was named as CuP/Cu2O, which provided a chlorine-free environment. Using the impregnation approach, a specific quantity of NH4Cl was loaded onto the Cu2O. In this case, Cu2O particles were fully immersed in an NH4Cl solution. To reduce acidity and prevent surface etching, a mixed solution of 80% ethanol and 20% water was used as the solvent. The residuals were then promptly dried and stored for later use in a vacuum at room temperature. After electrochemical reconstruction, the obtained catalyst was named NH4Cl–Cu2O, which exhibited a surface Cl-modified environment.
In addition, 20 mL of water was used to dissolve 2 mmol of Cu(CH3COO)2·H2O. Then, 7 mL of 1 M NaOH aqueous solution was added and kept there while being stirred magnetically for 10 min. After that, 3.5 mL of 2 M NH2OH·HCl aqueous solution was added as a reductant and kept there for 1 h. The orange products (Cl–Cu2O) were obtained by centrifugation and repeatedly cleaned with methanol and deionized water before being dried and stored for later use under vacuum at room temperature. The Cl–Cu2O powders with different particle sizes were prepared by modulating the inputs of reactants and reaction time (15 min–5 h). Similar to the electrochemical reconstruction method described above, the only difference is that Cl–Cu2O nanocrystal as the precursor loaded on carbon paper instead of Cu2O nanocrystal. The obtained catalyst was named as CuL/Cu2O, which showed a chlorine-rich environment.
Catalyst characterization
X-ray diffraction patterns (XRD) of samples were carried out by TTR-III operating at 40 KV voltage and 15 mA current with Cu Kα radiation (λ = 0.15406 nm). Transmission electron microscopy (TEM), high-resolution TEM, high-angle annular darkfield scanning transmission electron microscopy (HAADF-STEM) and energy disperse spectroscopy (EDS) are recorded on a JEM-2100 (JOEL). Scanning electron microscope (SEM) was performed on FESEM SU8200. Raman data were collected on a Renishaw in Via using 785-nm laser. X-ray photoelectron spectroscopy (XPS) data were collected on Kratos Axis supra + . An Ar+ beam was employed to detect the quantity of Cl and oxygen vacancy with a electron energy of 12.5 V, filament current of 3 mA, emission current of 7.5 A and energy of 2 KV. UPS excitation source: He light source (hv = 21.22 eV), beam spot 2mm. Room temperature UV–Vis absorption was recorded using a Solid 3700 DUV spectrophotometer in the wavelength range of 300–2500 nm. Kelvin probe force microscopy (KPFM) was performed on Atomic force microscopy (AFM) with a Veeco DI Nanoscope MultiMode V system. Electron Paramagnetic Resonance (EPR) was performed on JES-FA200. Fourier transform infrared (FTIR) spectroscopy was performed with a Thermo-Fisher Nicolet iS10. X-ray absorption near edge structure (XANES) and extended X-ray absorption fine structure (EXAFS) data were collected on beamline 14 W at the Shanghai Synchrotron Radiation Facility. The electro-catalysis actions were tested by CorrTest workstations. The gas chromatographs (GC 7900) equipped with a TCD and FID detector is used to detect the generated gas. Liquid NMR were quantified by the Bruker AVANCE III 400MHZ using dimethyl sulfoxide as an internal standard.
Operando FTIR and Raman tests
Raman experiments were performed using a Renishaw in Via Raman microscope in a commercial flow cell at the excitation laser source of 785 nm, the electrolyte was 0.1 M KHCO3 aqueous solution. The Cl-doped Cu2O and Cu2O precursors were monitored at different potentials and time under the same configuration condition. Then, the intermediates-adsorption measurements were collected signals at different potentials after the precursors were reduced to obtain the CuP/Cu2O and CuL/Cu2O. The Raman spectra were collected every 0.1 V at a range of −0.2 ~ −1.1 V (vs. RHE) and 150s with bubbling CO2 into the electrolyte. FTIR were measured using a Thermo Scientific Nicolet iS50 FTIR Spectrometer with a Pike VeeMAX III attachment. In total, 2 mg of the catalyst was dispersed in a mixture of 0.38 mL ethanol, and 20 μL 5 wt.% Nafion solution (Sigma-Aldrich) and sonicated, then dropped on carbon paper. Spectra were recorded at different potentials and time in a CO2–saturated 0.1 M KHCO3-D2O electrolyte. During the Operando FTIR tests, spectra were collected every 0.1 V and 120s with bubbling CO2 into the electrolyte. The spectrum collected at open circuit potential (OCP) in CO2-saturated 0.1 M KHCO3-D2O electrolyte was used as a background.
Electrochemical measurements for CER
The experiments were performed in a custom-designed flow-cell system. The carbon paper electrode (the commercial Sigracet 29BC gas diffusion layers with the standard microporous layer based on 77% carbon black and 23% PTFE) was sprayed by airbrush with a loading catalyst of 1 mg/cm2. The geometric area of the electrode was set to 1 cm2. and Ni foam or IrO2/Ti mesh with IrO2 loading of 1 mg/cm2 (for studying the stability of cathode) were acted as working and counter electrode, respectively, which was separated by an anion exchange membrane (Fumasep, FAB-PK-130). The FAB-PK-130 is an anion exchange membrane with a thickness of 130 μm, which is cut to 1.5 cm * 1.5 cm size for practical use. The purchased FAB-PK-130 membrane was placed in 1 M KOH solution for 72 h to activate the anion exchange and subsequently used directly in electrochemical tests. The Hg/HgO electrode was used as a reference electrode. The relevant electrochemical tests were performed in 1 M KOH (or 0.1, 0.5, 1 M KHCO3, 2 M KOH, 3 M KCl) with using a Corrtest Workstation. During the measurements, CO2 was directly fed to the back of cathode GDE at a rate of 20 sccm. The electrolyte was forced to continuously circulate through the chamber at a rate of 10 sccm. All the applied cathode potentials after iR cell compensation were converted to the RHE reference scale using \({E}_{R{HE}}={E}_{{Ag}/{AgCl}}+0.204V+0.0591\times {pH}-0.85\times i\times R\) (i: applied current; R: cell resistance). The electrochemical impedance spectroscopy (EIS) measurement for measuring the ohmic loss between the working and reference electrodes was performed with frequency ranges from 100,000 to 0.1 Hz and an amplitude of 5 mV at open-circuit voltage in three-electrode system. The linear sweep voltammetry (LSV) curves were carried with a scan rate of 5 mV s−1. Controlled potential electrolysis was performed at each potential for 10 min.
CER product analysis
The collected products were analyzed via gas chromatography (GC) and 1H NMR on a 400 MHz NMR spectrometer. The gaseous products of CO2 reduction, including carbon monoxide, methane, ethylene, ethane, and propylene, are detected and quantified using GC with an FID detector equipped with a nickel conversion furnace. Hydrogen is quantitatively detected using a TCD detector. The liquid products, including methanol, ethanol, n-propanol, formic acid, and acetic acid, are quantitatively detected using NMR with dimethyl sulfoxide serving as the internal standard. Typically, 0.5 mL KOH electrolyte after electrolysis was mixed with 100 μL of D2O and 67 μL of DMSO, including 5 mM as an internal standard. The 1H NMR spectrum was measured with water suppression via a pre-saturation method. The faradaic efficiency is calculated based on the calibration curve as follows:
where \({N}_{{products}}\) is total number of product transfer electron, \({C}_{{products}}\) is the concentration of product, V is the volume of electrolyte or gases, NA : avogadro constant, 6.022 × 1023 mol−1, n is the number of electron transferred for product formation, e is electron, Q is the number of transfer charge, \({N}_{{total}}\) is total number of transfer electron.
The energy efficiency (EE) was defined as the ratio of fuel energy to applied energy, which was calculated for the half-cell of CRR with the following equation:
Where \({E}_{{ethanol}}^{0}\) = 0.07 V, \({E}_{n-{propanol}}^{0}\)= 0.1 V is the thermodynamic potential of CRR to ethanol and n-propanol, \({{FE}}_{{products}}\) are the faradaic efficiencies of ethanol and n-propanol productions at an applied potential. \({E}_{{products}}^{{applied}}\) is the applied potential for alcohols production.
The production rate for formate was calculated using the following equation:
where Q is the total charge passed, t is the time (1 h) and S is the geometric area of the electrode (1 cm2).
The partial current densities (\({j}_{a{lcohols}}\)) of products were calculated as below, where S is the geometric area (1 cm2) of the cathode, i is the current of the electrode:
Density functional theory (DFT) calculations
All calculations in this study were performed using the Vienna ab initio simulation package (VASP) based on density functional theory (DFT)70. We employed projector augmented wave (PAW) pseudopotentials and the Perdew–Burke–Ernzerhof (PBE) exchange-correlation functional within the semi-local generalized gradient approximation (GGA)71. To adequately capture weak long-range van der Waals (vdW) interactions, we employed an empirical dispersion-corrected DFT method (DFT-D3)72. The kinetic energy cutoff for the plane wave expansion was set to 500 eV. The self-consistent field (SCF) iteration was considered to converge when the threshold reached 10−5 eV. Geometry optimization was performed using the conjugate gradient method, with forces on each atom constrained below 0.03 eV Å−1.
The Cu/Cu2O model was obtained by selectively removing specific oxygen atoms from the Cu2O(111) surface unit cell, adopting a p(4*2) Cu2O(111) unit cell. Subsequently, we optimized the lattice parameters and atomic positions. The optimized Cu/Cu2O composite exhibited lattice parameters of a = 21.48 Å, b = 10.29 Å, c = 23.62 Å, α = 90°, β = 90°, γ = 118.63°. To incorporate chlorine (Cl), an O atom on the surface was replaced with a Cl atom, yielding the Cl-Cu/Cu2O model. For the Cu/Cu2O composite slab models, we employed a 1 × 2 × 1 k-point mesh. The Cu2O(111) model was based on a p(2*2) unit cell, while the Cu(111) model also utilized a p(2*2) unit cell. The atomic coordinates of the optimized computational models are provided in Supplementary Dataset 1, which are defined as Cu-POSCAR, Cu2O-POSCAR, CuP/Cu2O-POSCAR, CuL/Cu2O-POSCAR. To take into account the on-site Coulomb interaction between 3d electrons of Cu, the GGA+U approach was also employed with a U–J value of 4 eV73,74. Note that Cu(111) does not use GGA+U. The reaction free energy change and adsorption energy can be obtained with the equation below:
Where \(\Delta E\) represents the total energy difference before and after the intermediate is adsorbed, \(\Delta {ZPE}\) and \(\Delta S\) denote the differences in zero-point energy and entropy, respectively. The zero-point energy and entropy of the free molecules and adsorbents were derived from vibrational frequency calculations. \({E}_{*X}\) corresponds to the total energy of the system when molecule X is adsorbed on the surface of the slab, \({E}_{*}\) represents the energy of the slab system, and \({E}_{X}\) signifies the energy of the adsorbed intermediate X.
Data availability
The raw data of the figures in the main manuscript are available in figshare with the identifier(s) https://doi.org/10.6084/m9.figshare.25124129. All other data needed to evaluate the conclusions in the paper are present in the paper and the Supplementary Information or can be obtained from the corresponding authors upon request. All data are available in the manuscript, the supplementary materials, and from the authors on request. Source data are provided with this paper.
Code availability
The code used in this work can be obtained from the corresponding authors on request.
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Acknowledgements
G.Z. acknowledges the financial support from the National Natural Science Foundation of China (Grant No. 52072359), the Recruitment Program of Global Experts, and the Fundamental Research Funds for the Central Universities (WK2060000016). The numerical calculations in this paper have been done in the Supercomputing Center of the University of Science and Technology of China and TianHe-2 at LvLiang Cloud Computing Center of China. The authors are grateful to infrared beamline (BL01B) at National Synchrotron Radiation Laboratory for the experimental beamtime support. This work was partially carried out at the Instruments Center for Physical Science, University of Science and Technology of China.
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G.Z. conceived and supervised the study. Y.Z. conducted experiments and analyzed data. Y.C. performed and prepared the DFT calculations section. X.W. and Y.F. conducted some experiments. Z.D. and M.C. assisted the electrochemical in situ Fourier Transform Infrared (FTIR) spectroscopy and Raman analysis. G.Z. contributed significantly to the analysis and manuscript preparation. All authors participated in the analysis with constructive discussions.
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Zhang, Y., Chen, Y., Wang, X. et al. Low-coordinated copper facilitates the *CH2CO affinity at enhanced rectifying interface of Cu/Cu2O for efficient CO2-to-multicarbon alcohols conversion. Nat Commun 15, 5172 (2024). https://doi.org/10.1038/s41467-024-49247-4
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DOI: https://doi.org/10.1038/s41467-024-49247-4
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