Abstract
Adatom engineering represents a highly promising opportunity for enhancing electrochemical CO reduction reaction (CORR). However, the aggregation of adatoms under typical reaction conditions often leads to a decline in catalyst activity. Recent studies have revealed that N-heterocyclic carbene (NHC) can stabilize surface adatoms. Herein, based on density functional theory calculations, we reveal a significant enhancement in the catalytic activity of Cu adatoms decorated with NHC molecules for CORR. The NHC decoration strengthens the interaction between the dxy orbital of the Cu adatom and the px orbital of the C atom, reducing the energy barriers in both CO hydrogenation and C-C coupling steps. Moreover, the CORR catalytic activity of the NHC decorated adatom can be further improved by tuning the side groups of NHC molecules. These results provide insights for the design of efficient CORR catalysts and offer a theoretical framework that can be extended to other hydrogenation reactions.
Similar content being viewed by others
Introduction
Efficient strategies for CO2 recycling play a crucial role in maintaining the carbon cycle and preventing the negative impact of CO2 emissions on global warming1,2,3,4,5. In the industry, various pathways can be utilized for CO2 recycling, including thermal hydrogenation, photocatalytic CO2 reduction, and electrochemical CO2 reduction. Among them, the electrochemical CO2 reduction reaction (CO2RR) is promising for converting CO2 into value chemicals and fuels on a practical scale1,6,7,8,9. Significant progress has been achieved in the two-electron reductions of CO2 to CO10. However, further reduction of CO to multiple-carbon products still suffers from poor energy efficiency and selectivity11. The electrocatalysts can reduce the overpotential of CO reduction reaction (CORR), accelerate the reaction rate, and improve the selectivity of value-added multiple-carbon products. Therefore, developing highly efficient electrocatalysts to produce economically valuable C2 products is essential for CORR12,13,14.
Several strategies have been developed to enhance the performance of electrocatalyst, including selective facet exposure15,16, interface engineering17, and surface adatom modification18,19,20. Among these strategies, the adatoms show advantages of unique electronic structures, low coordination metal atoms, strong metal-carrier interactions, and maximum atomic utilization efficiency21,22, which can enhance the catalytic activity and reaction selectivity20,21,23. For instance, surface adatom modification has demonstrated its ability to activate the catalytically inert surface of MoS2 for CO2RR, resulting in a significant improvement in its catalytic activity24. However, the aggregation of surface adatoms due to the large surface energy leads to the degradation of catalyst activity25. The key challenge is to stabilize the isolated surface adatom during CORR reaction process26,27. In recent years, it has been reported that N-heterocyclic carbene (NHC) molecules can stabilize surface adatoms when combined with transition metal atoms28,29,30,31. The NHC-decorated adatoms demonstrate stability at the temperature of 70 °C28, indicating that the catalysts based on the NHC-decorated adatoms are thermodynamically stable under the reaction condition32. Moreover, NHC molecules also possess tunable side groups that facilitate various functionalities in the fields of catalysis and materials chemistry on material surfaces and nanoparticles33,34,35,36.
In this paper, we propose a strategy to improve the catalytic activity of the Cu adatoms on Cu(100) surface for CORR through NHC molecules decoration. Employing density functional theory (DFT) calculations, we found that the decoration of NHC molecules enhances the interaction between the dxy orbital of Cu adatoms and the px orbital of C atom in CO. As a result, the energy barriers for CO hydrogenation and C-C coupling reaction are significantly reduced. The energy barrier for CO reduction to CHO decreases from 0.970 eV to 0.440 eV, while the CO-CHO coupling reaction changes from an endothermic reaction to an exothermic one with an energy barrier of 0.452 eV. The calculation results demonstrate that the NHC decorated Cu adatoms serve as new CO adsorption sites, resulting in the pre-activating of CO molecules. By tuning the side groups of NHC molecules, the CORR catalytic activity of the adatoms on Cu(100) surface can be further improved. As the electron-donating ability of the side groups increases, the adsorption interaction between CO and the adatom decreases, reducing the change in the standard Gibbs free energy for C-C coupling. These results indicate that the effectiveness of NHC decorated Cu adatoms in reducing the energy barrier for CORR, thereby providing a promising strategy for the design of efficient CORR catalysts.
Results and discussions
NHC molecules have strong σ-donating and moderately π-accepting properties, making them particularly suitable as ligands for the transition metals, including Au, Ag and Cu37. Recent scanning tunneling microscopy observations and DFT calculations have uncovered various binding modes of NHCs on metallic surfaces30,38,39. To determine the most stable adsorption configuration, four binding modes of the NHC molecule on the Cu(100) surface were investigated, including NHC adsorption on an adatom, NHC dimers adsorption on an adatom and NHC adsorption on surface atoms in both the top and bridge sites. It is found that the NHC-adatom mode exhibits the lowest adsorption energy, suggesting that binding NHC to an adatom is favorable.
Based on the NHC decoration, the reaction pathways of CO reduction to ethanol on Cu(100) surface with Cu adatom were investigated, as shown in Fig. 1. The black dashes represent the relative Gibbs free energies of the intermediates of each proton-electron transfer step on Cu(100) surface with NHC decorated adatom. The free energy of *CO adsorption is used as the reference. The gray dashes represent the relative Gibbs free energies of same CORR pathway on the pristine Cu(100) surface reported by previous work15. The results indicate that the reaction pathway for *CO reduction to ethanol on Cu(100) surface with NHC decorated adatom is similar with that on pristine Cu(100) surface, except for the first protonation of *CO and C-C coupling steps. The reaction energy for *CO hydrogenation to *CHO is 0.189 eV on the Cu(100) surface with NHC decorated adatom, much lower than that of previously reported pristine Cu(100) surface (0.62 eV), demonstrating the enhanced catalytic activity of Cu(100) surface promoted by NHC decoration. Furthermore, the reaction energy of *CO hydrogenation to *COH is 0.842 eV, 4 times that of *CHO, indicating the high selectivity for *CO hydrogenation products on Cu(100) surface with NHC decorated adatom. In contrast, the reaction energy for *COH formation on the pristine Cu(100) surface is only about 0.12 eV higher than that of *CHO. Thus, the NHC decoration improves both the reaction activity and selectivity for *CO hydrogenation to *CHO on Cu(100) surface.
The C-C coupling is essential for generating economically desirable C2 products. However, the coupling of *CO is impractical due to its reaction energy of 1.00 eV, while the *OCCO dimer is unstable on the Cu(100) surface15,40. In contrast, the coupling of *CHO and *CO is more energy-favorable on the pristine Cu(100) surface with a reaction energy of 0.26 eV15. After the decoration of NHC, the endothermic *CO-*CHO coupling reaction on the Cu(100) surface changes to exothermic with a reaction energy of −0.129 eV, which significantly promotes the formation of C2 products. Then, the *COCHO is further reduced to *OCHCHO with a reaction energy of −0.684 eV. The third protonation step at *OCHCHO favors the formation of *OCHCHOH with an uphill reaction energy of 0.318 eV. Among the subsequent steps, the reaction pathway is generally downhill towards ethanol in most cases, except for a slightly free energy increase of about 0.162 eV at the sixth protonation step.
To explore the origin of reaction activity improvement by NHC decoration in *CO hydrogenation reaction, the activation barriers for *CO hydrogenation are calculated on pristine Cu(100) surface, Cu(100) surface with adatom, and Cu(100) surface with NHC decorated adatom. As shown in Fig. 2a, the activation barriers for *CO hydrogenation are 0.970 eV, 0.648 eV, and 0.440 eV on the pristine Cu(100) surface, Cu(100) surface with adatom, and Cu(100) surface with NHC decorated adatom, respectively. Figure 2b shows the atomic structures of the initial state (IS), transition state (TS), and final state (FS) of the *CO hydrogenation on three surfaces according to Fig. 2a. The NHC-adatom decoration significantly reduces the activation barrier of *CO hydrogenation on the Cu(100) surface by 55%, meanwhile the adatom decoration reduces the activation barrier by 33%. This suggests that the adatom decoration makes an important contribution to the improvement of the reaction activity of Cu(100) surface. On the other hand, the configurations in Fig. 2b indicate that the adsorption configuration of *CO in IS changes after the decoration of adatoms on the surface. On the pristine Cu(100) surface, *CO is only bound to one surface atom. While on the surface with an adatom, *CO is bound to the adatom and an adjacent surface atom. The bond length of the C-O bond in IS is 1.162 Å on the pristine Cu(100) surface, while they are 1.175 Å on the Cu(100) surface with adatom and NHC-decorated adatom. The elongation of the C-O bond indicates the weakening of bond strength, which may contribute to the activation of the *CO.
To investigate the role of surface adatoms in the *CO activation, we conduct a crystal orbital Hamilton population (COHP) analysis. The projected crystal orbital Hamilton population (pCOHP) for CO adsorption on the pristine and adatom-decorated Cu(100) surfaces are presented in Fig. 2c, d, respectively. The atomic coordinates of optimized models are in Supplementary Data 1. Compared to the case of *CO adsorption on the pristine Cu(100) surface, the anti-bonding state of *CO adsorbed on the adatom-decorated Cu(100) surface is more-occupied and is at a lower energy level. The integrated overlap populations (ICOHP) up to the Fermi level of C-O bond are −16.256 and −14.675 for *CO adsorbed on the pristine and adatom-decorated Cu(100) surfaces, respectively. A higher ICOHP of *CO adsorbed on the adatom indicates a weaker C-O bond, demonstrating that the *CO is more active on the adatom site. The changes in the C-O bond suggest that the surface adatoms serve as new *CO adsorption sites, optimizing the adsorption configuration of *CO and activating it, therefore, reducing the reaction barrier of *CO hydrogenation at the first protonation step of CORR.
In addition, we further investigate the influence of NHC on the electronic structure of Cu adatom. Figure 2e presents the projected density of states (PDOS) of the dxy orbital of the Cu adatom (Cuad) and the px orbital of the C atom of TS during *CO hydrogenation on the Cu(100) surface with adatom and Cu(100) surface with NHC decorated adatom. The atomic coordinates of optimized models are in Supplementary Data 1. The dxy orbital of the Cu adatom interacts with the px orbital of the C atom. Notably, the NHC decoration strengthens the overlap between the dxy orbital of the Cu adatom and the px orbital of the C atom, leading to a much stronger interaction between the Cu adatom and *CO, resulting in an enhanced catalytic performance.
Furthermore, the charge density difference of a NHC decorated adatom is presented in Fig. 2f, revealing a significant charge transfer between the Cu adatom and the NHC molecule. The electrons accumulate between the carbene C atom and the Cu adatom, indicating the formation of a strong metal-carbene bond, while the electron depletion around the Cu adatom reveals a clear charge transfer from Cu adatom to the NHC molecule. This is also confirmed by our Bader charge analysis that the presence of NHC molecule leads to the partially oxidization of Cu adatom in a positive charge of +0.179 e. In contrast, the undecorated Cu surface adatom is uncharged. Previous studies have shown that surface Cuδ+ sites in Cu-based catalysts exhibit higher catalytic activity for C2 products compared to pure Cu, which is attributed to their enhanced adsorption strength for key reaction intermediates such as CO41,42,43. Therefore, the oxidation of Cu adatom induced by NHC decoration may contribute to a lower activation barrier, thus promoting the catalytic performance.
The C-C coupling reaction is well-known to be the rate-determining step in the process of *CO reduction to C2 products. Thus, reducing the activation barrier of the C-C coupling is crucial for increasing the yield of C2 products44. Fig. 3a presents the activation barriers of *CO-*CHO coupling on pristine Cu(100) surface, Cu(100) surface with adatom, and Cu(100) surface with NHC decorated adatom. The activation barriers of C-C coupling are 0.590 eV, 0.499 eV and 0.452 eV on pristine Cu(100) surface, Cu(100) surface with adatom, and Cu(100) surface with NHC decorated adatom, respectively. Similar to the *CO hydrogenation process, the activation barrier of C-C coupling is reduced in the presence of surface Cu adatom and further decreases through NHC decoration.
The atomic structures of the IS, TS and FS of C-C coupling on three surfaces are shown in Fig. 3b, which reveals that the adsorption configuration of *COCHO undergoes significantly changes after the introduction of Cu adatom. On the pristine Cu(100) surface, the bond order of C-O in *O-CCHO is 1.34, which is close to that of a C-O single bond. The bond order of the C-C is 1.31, which is close to that of a C-C single bond. While on the Cu(100) with adatom and NHC decorated adatom, the bond orders of C-O in *O-CCHO are 1.91 and 1.86, resembling C = O double bonds. The bond orders of C-C are 1.16 and 1.15, resembling C-C single bonds. These changes in bond order indicate the enhanced stability of *COCHO on the surface adatom compared to the pristine Cu(100) surface. This result shows that the presence of surface adatom stabilizes *COCHO, which reduces the Gibbs free energy of the FS. Thus, similar to the step of *CO hydrogenation, the atom formed by NHC adsorption on Cu(100) surface stabilize the crucial intermediate (*COCHO) and driving the C-C coupling from endothermic to exothermic.
To investigate the influence of molecular electronic properties of NHC on the Cu(100) surface with NHC decorated adatom and further improve its catalytic activity, the σ-donation and π-acceptor ability of NHC molecules is adjusted by tuning the side groups. Therefore, 8 kinds of side groups are considered, including methyl, ethyl, propyl, isopropyl, acetyl, formyl, methoxy and phenyl, in a range of electronic properties from electron-donating to electron-withdrawing, as shown in Fig. 4a. Among them, methyl, ethyl, propyl and isopropyl are weak electron-donating groups, acetyl and carboxyl are strong electron-withdrawing groups, while methoxy and phenyl are strong electron-donating groups.
To assess the effect of side group substitution on the activation barriers, the Bader charge of the carbene C atom and the change in standard Gibbs free energy (ΔG) of C-C coupling are calculated to provide insights into the NHC-decorated system. According to the Brønsted-Evans-Polanyi relationship, there is a linear correspondence between the activation barrier and the ΔG in surface reactions45,46. As shown in Fig. 4b, the ΔG of C-C coupling decreases with the increase of the Bader charge of the carbene C atom. It indicates that the catalytic activity of Cu adatoms decorated by NHC molecules is enhanced by the strong electron-donating side group. Furthermore, the adsorption energies of the reactant *CO on the Cu adatoms decorated by NHC with different side groups are calculated. Figure 4c illustrates that the adsorption energies of *CO (Eads) increase as the Bader charges on the carbene C atoms increase, indicating that the stronger the electron-donating ability of the side groups results in weaker adsorption of *CO on the NHC-decorated Cu adatoms. A scaling relation between reaction energies and *CO adsorption energies is in Fig. 4d, similar to the previous works47. Thus, the reduction of reaction energy can be attributed to the increase in *CO adsorption energy, which is highly correlated to the electronic structure of Cu adatom adjusted by side group substitution.
Conclusions
In conclusion, our DFT calculations predict that NHC decoration is a promising strategy to improve the catalytic activity of Cu adatoms on Cu(100) surfaces for CORR. The relative Gibbs free energy diagrams indicate that the decoration of NHC molecules significantly reduces both the standard Gibbs free energy change and the activation barrier of CO hydrogenation and the C-C coupling on the Cu(100) surface with Cu adatom. The reduction in reaction barrier for CORR is mainly attributed to the enhanced interaction between the dxy orbital of Cu adatoms and the px orbital of C atom in CO, facilitated by the NHC decoration. Furthermore, the catalytic activity of Cu adatom can be tailored by varying the side group of NHC molecules. Our DFT calculations reveal that the side groups with strong electron-donating ability result in weak *CO adsorption, leading to the low reaction energies of C-C coupling. This finding provides a considerably practical strategy for the design active catalysts for CORR.
Methods
First-principle calculations based on DFT were performed by using the Vienna ab initio simulation package48,49. The projector augmented wave50 method was applied with Perdew-Burke-Ernzerhof51 type exchange-correlation functional. Dispersion correction was included using the DFT-D3 method of Grimme52. A kinetic energy cutoff of 400 eV was applied for all calculations. The k-points sampling was 2 × 2 × 1, generated by Monkhorst–Pack grids with the origin at the Γ-point53. The convergence criterion of electronic relaxation was 10−6 eV.
The Cu(100) slab model was constructed with four atomic layers and a 6 × 6 supercell containing a total of 144 Cu atoms. A vacuum layer of 20 Å was placed above the slabs to avoid interactions between the periodic images. All atoms were fully relaxed except the two bottom layers of Cu. The structures were relaxed until the residual force on each atom was smaller than 0.01 eVÅ-1.
Free energies, G, were computed with the energetic correction terms according to the following equation:
where the \({E}_{{electronic}}\) was obtained by DFT calculations, the entropy (\(S\)), the zero-point energies (\({ZPE}\)) of adsorbates and the heat capacity (\({C}_{p}\)) were derived from the vibrational frequency calculations10,54. The temperature (\(T\)) were set to be at 300 K. The anharmonic terms were not included. In the case of adsorbed molecules, the contributions from translation and rotation to entropy are significantly reduced and turn into vibrational modes55. For the vibrational frequency calculations, the convergence criterion of electronic relaxation was 10−7 eV. The computational hydrogen electrode (CHE) approach was used for proton−electron transfer steps56. Transition states were calculated using the climbing image nudged elastic band57,58 and dimer methods59 for CO hydrogenation and C-C coupling.
Data availability
The authors declare that data supporting the findings of this study are available within the paper. The atomic coordinates of the optimized computational models for electronic structure calculations are in Supplementary Data 1. Additional data are available from the corresponding author on reasonable request.
References
Chu, S. & Majumdar, A. Opportunities and challenges for a sustainable energy future. Nature 488, 294–303 (2012).
Vergara, J., McKesson, C. & Walczak, M. Sustainable energy for the marine sector. Energy Policy 49, 333–345 (2012).
Wang, S. & Wang, X. Imidazolium ionic liquids, imidazolylidene heterocyclic carbenes, and zeolitic imidazolate frameworks for CO2 capture and photochemical reduction. Angew. Chem. Int. Ed. 55, 2308–2320 (2016).
Alper, E. & Yuksel Orhan, O. CO2 utilization:developments in conversion processes. Petroleum 3, 109–126 (2017).
Ma, J. et al. A short review of catalysis for CO2 conversion. Catal. Today 148, 221–231 (2009).
Han, N., Ding, P., He, L., Li, Y. & Li, Y. Promises of main group metal–based nanostructured materials for electrochemical CO2 reduction to formate. Adv. Energy Mater. 10, 1902338 (2020).
Wu, J., Huang, Y., Ye, W. & Li, Y. CO2 reduction: from the electrochemical to photochemical approach. Adv. Sci. 4, 1700194 (2017).
Appel, A. M. et al. Frontiers, opportunities, and challenges in biochemical and chemical catalysis of CO2 fixation. Chem. Rev. 113, 6621–6658 (2013).
Nielsen, D. U., Hu, X.-M., Daasbjerg, K. & Skrydstrup, T. Chemically and electrochemically catalysed conversion of CO2 to CO with follow-up utilization to value-added chemicals. Nat. Catal. 1, 244–254 (2018).
Wang, V., Xu, N., Liu, J.-C., Tang, G. & Geng, W.-T. VASPKIT: a user-friendly interface facilitating high-throughput computing and analysis using VASP code. Comput. Phys. Commun. 267, 108033 (2021).
Bagger, A., Arnarson, L., Hansen, M. H., Spohr, E. & Rossmeisl, J. Electrochemical CO reduction: a property of the electrochemical interface. J. Am. Chem. Soc. 141, 1506–1514 (2019).
Whipple, D. T. & Kenis, P. J. A. Prospects of CO2 utilization via direct heterogeneous electrochemical reduction. J. Phys. Chem. Lett. 1, 3451–3458 (2010).
Hori, Y., Takahashi, I., Koga, O. & Hoshi, N. Electrochemical reduction of carbon dioxide at various series of copper single crystal electrodes. J. Mol. Catal. A: Chem. 199, 39–47 (2003).
Hori, Y. Electrochemical CO2 reduction on metal electrodes. 89-189 (Springer New York, 2008).
Luo, W., Nie, X., Janik, M. J. & Asthagiri, A. Facet dependence of CO2 reduction paths on Cu electrodes. Acs Catal. 6, 219–229 (2016).
Hahn, C. et al. Engineering Cu surfaces for the electrocatalytic conversion of CO2: Controlling selectivity toward oxygenates and hydrocarbons. Proc. Natl. Acad. Sci. 114, 5918–5923 (2017).
Li, J., Abbas, S. U., Wang, H., Zhang, Z. & Hu, W. Recent advances in interface engineering for electrocatalytic CO2 reduction reaction. Nano-Micro Lett. 13, 216 (2021).
Hua, Y., Wang, J., Min, T. & Gao, Z. Electrochemical CO2 conversion towards syngas: recent catalysts and improving strategies for ratio-tunable syngas. J. Power Sour. 535, 231453 (2022).
Yang, H. et al. Scalable production of efficient single-atom copper decorated carbon membranes for CO2 electroreduction to methanol. J. Am. Chem. Soc. 141, 12717–12723 (2019).
Jia, M., Fan, Q., Liu, S., Qiu, J. & Sun, Z. Single-atom catalysis for electrochemical CO2 reduction. Curr. Opin. Green. Sustain. Chem. 16, 1–6 (2019).
Li, M. et al. Heterogeneous single-atom catalysts for electrochemical CO2 reduction reaction. Adv. Mater. 32, 2001848 (2020).
Wang, A., Li, J. & Zhang, T. Heterogeneous single-atom catalysis. Nat. Rev. Chem. 2, 65–81 (2018).
Vidal-Iglesias, F. J., Solla-Gullón, J., Herrero, E., Aldaz, A. & Feliu, J. M. Pd adatom decorated (100) preferentially oriented Pt nanoparticles for formic acid electrooxidation. Angew. Chem. Int. Ed. 49, 6998–7001 (2010).
Li, H. et al. Synergetic interaction between neighbouring platinum monomers in CO2 hydrogenation. Nat. Nanotechnol. 13, 411–417 (2018).
Mu, Y. et al. Single-atom catalysts: advances and challenges in metal-support interactions for enhanced electrocatalysis. Electrochem. Energy Rev. 5, 145–186 (2022).
Wang, L., Wang, L., Meng, X. & Xiao, F.-S. New strategies for the preparation of sinter-resistant metal-nanoparticle-based catalysts. Adv. Mater. 31, 1901905 (2019).
Lu, J. et al. Coking- and sintering-resistant palladium catalysts achieved through atomic layer deposition. Science 335, 1205–1208 (2012).
Bakker, A. et al. Elucidating the binding modes of N-heterocyclic carbenes on a gold surface. J. Am. Chem. Soc. 140, 11889–11892 (2018).
Deng, C., Chen, J. & Tang, Q. Theoretical investigation on the adsorption and interface bonding between N-heterocyclic carbenes and metal surfaces. J. Phys. Chem. C. 125, 4489–4497 (2021).
Wang, G. et al. Ballbot-type motion of N-heterocyclic carbenes on gold surfaces. Nat. Chem. 9, 152–156 (2017).
Navarro, J. J. et al. Covalent adsorption of N-heterocyclic carbenes on a copper oxide surface. J. Am. Chem. Soc. 144, 16267–16271 (2022).
Vos, R. E. et al. How temperature affects the selectivity of the electrochemical CO2 reduction on copper. ACS Catal. 13, 8080–8091 (2023).
Danopoulos, A. A., Simler, T. & Braunstein, P. N-heterocyclic carbene complexes of copper, nickel, and cobalt. Chem. Rev. 119, 3730–3961 (2019).
Ghosh, M. & Khan, S. N-heterocyclic carbenes capped metal nanoparticles: An overview of their catalytic scope. ACS Catal. 13, 9313–9325 (2023).
Kaeffer, N., Liu, H.-J., Lo, H.-K., Fedorov, A. & Copéret, C. An N-heterocyclic carbene ligand promotes highly selective alkyne semihydrogenation with copper nanoparticles supported on passivated silica. Chem. Sci. 9, 5366–5371 (2018).
Kaeffer, N., Mance, D. & Copéret, C. N-heterocyclic carbene coordination to surface copper sites in selective semihydrogenation catalysts from solid-state NMR spectroscopy. Angew. Chem. Int. Ed. 59, 19999–20007 (2020).
Nemcsok, D., Wichmann, K. & Frenking, G. The significance of π interactions in group 11 complexes with N-heterocyclic carbenes. Organometallics 23, 3640–3646 (2004).
Jain, M., Gerstmann, U., Schmidt, W. G. & Aldahhak, H. Adatom mediated adsorption of N-heterocyclic carbenes on Cu(111) and Au(111). J. Comput. Chem. 43, 413–420 (2022).
Navarro, J. J. et al. Growth of N-heterocyclic carbene assemblies on Cu(100) and Cu(111): From single molecules to magic-number islands. Angew. Chem. Int. Ed. 61, e202202127 (2022).
Santatiwongchai, J., Faungnawakij, K. & Hirunsit, P. Comprehensive mechanism of CO2 electroreduction toward ethylene and ethanol: The solvent effect from explicit water–Cu(100) interface models. ACS Catal. 11, 9688–9701 (2021).
Zhou, Y. et al. Dopant-induced electron localization drives CO2 reduction to C2 hydrocarbons. Nat. Chem. 10, 974–980 (2018).
Yang, P.-P. et al. Protecting copper oxidation state via intermediate confinement for selective CO2 electroreduction to C2+ fuels. J. Am. Chem. Soc. 142, 6400–6408 (2020).
Jung, H. et al. Electrochemical fragmentation of Cu2O nanoparticles enhancing selective C–C coupling from CO2 reduction reaction. J. Am. Chem. Soc. 141, 4624–4633 (2019).
Calle-Vallejo, F. & Koper, M. T. M. Theoretical considerations on the electroreduction of CO to C2 species on Cu(100) electrodes. Angew. Chem. Int. Ed. 52, 7282–7285 (2013).
Bligaard, T. et al. The Brønsted-Evans-Polanyi relation and the volcano curve in heterogeneous catalysis. J. Catal. 224, 206–217 (2004).
Montoya, J. H., Peterson, A. A. & Nørskov, J. K. Insights into C-C coupling in CO2 electroreduction on copper electrodes. ChemCatChem 5, 737–742 (2013).
Liu, X. et al. Understanding trends in electrochemical carbon dioxide reduction rates. Nat. Commun. 8, 15438 (2017).
Kresse, G. & Furthmüller, J. Efficiency of ab-initio total energy calculations for metals and semiconductors using a plane-wave basis set. Comput. Mater. Sci. 6, 15–50 (1996).
Kresse, G. & Furthmüller, J. Efficient iterative schemes for ab initio total-energy calculations using a plane-wave basis set. Phys. Rev. B 54, 11169–11186 (1996).
Blöchl, P. E. Projector augmented-wave method. Phys. Rev. B 50, 17953–17979 (1994).
Perdew, J. P., Burke, K. & Ernzerhof, M. Generalized gradient approximation made simple. Phys. Rev. Lett. 77, 3865–3868 (1996).
Grimme, S., Antony, J., Ehrlich, S. & Krieg, H. A consistent and accurate ab initio parametrization of density functional dispersion correction (DFT-D) for the 94 elements H-Pu. J. Chem. Phys. 132, 154104 (2010).
Monkhorst, H. J. & Pack, J. D. Special points for Brillouin-zone integrations. Phys. Rev. B 13, 5188–5192 (1976).
McQuarrie, D. A. & Simon, J. D. Molecular thermodynamics. (Sterling Publishing Company, 1999).
Nørskov, J. K., Studt, F., Abild-Pedersen, F. & Bligaard, T. Fundamental concepts in heterogeneous catalysis. (John Wiley & Sons, 2014).
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).
Henkelman, G., Uberuaga, B. P. & Jónsson, H. A climbing image nudged elastic band method for finding saddle points and minimum energy paths. J. Chem. Phys. 113, 9901–9904 (2000).
Henkelman, G. & Jónsson, H. Improved tangent estimate in the nudged elastic band method for finding minimum energy paths and saddle points. J. Chem. Phys. 113, 9978–9985 (2000).
Henkelman, G. & Jónsson, H. A dimer method for finding saddle points on high dimensional potential surfaces using only first derivatives. J. Chem. Phys. 111, 7010–7022 (1999).
Acknowledgements
This work was supported by the National Key Research and Development Program of China (Grant No. 2022YFA1204100 and 2019YFA0308500), CAS Project for Young Scientists in Basic Research (YSBR-003), and the Fundamental Research Funds for the Central Universities.
Author information
Authors and Affiliations
Contributions
The manuscript was written through contributions of all authors. All authors have given approval to the final version of the manuscript. Y.G. performed the simulations and analyzed the results under the guidance of S.D., L.T. and Y.-Y.Z. contributed to the discussion of the project. S.D. conceived the idea of this work and supervised the research.
Corresponding author
Ethics declarations
Competing interests
The authors declare no competing interests.
Peer review
Peer review information
Communications Chemistry thanks the anonymous reviewers for their contribution to the peer review of this work.
Additional information
Publisher’s note Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
Supplementary information
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
Gao, Y., Tao, L., Zhang, YY. et al. Enhanced catalytic activity of N-heterocyclic carbene stabilized surface adatoms for CO reduction reaction. Commun Chem 6, 270 (2023). https://doi.org/10.1038/s42004-023-01066-2
Received:
Accepted:
Published:
DOI: https://doi.org/10.1038/s42004-023-01066-2
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.