Dual roles of the electronic effect on selectivity: pincer nickel-electrocatalyzed CO2 reduction
- 18 November 2020
- journal article
- research article
- Published by Royal Society of Chemistry (RSC) in Catalysis Science & Technology
- Vol. 11 (3) , 874-885
Abstract
The electronic effect is crucial for the electrocatalytic reduction of CO2. In contrast to the previous understanding of the monotonic influence of the electronic effect on the selectivity of CO2 reduction, the dual roles of the electronic effect on the selectivity are revealed in the present study, i.e., (1) the electronic effect on redox originating from σ-donation and (2) the electronic effect on π-back-donation, via comprehensive DFT studies on four representative classes of pincer NHC NiII catalysts. On the one hand, the electron-rich C, B-coordinating (CCC and CBC) ligands guarantee that the catalysts possess the driving force to reduce CO2 in a lower-electron reduction state (NiI), leading to lower free energy barriers for the formation of HCOOH, which results from the lower ligand-field deformation energies for the hydride transfer and the stronger p–σ* interactions in the metal–hydride intermediates. In contrast, the less electron-rich N-coordinating (CNC and C(B)NC) ligands require an Ni0 electron reduction state to reduce CO2, preferring kinetic-controlled CO formation due to the higher free energy barriers for the generation of HCOOH. This redox effect well explains the unprecedented experimentally observed selectivity of HCOOH in the stronger electron donor CCC-Ni system, which is different from the traditional understanding of the electronic effect. On the other hand, at an identical reduction state, the electronic effect plays an important role in tuning the back-donation ability of the metal center, benefiting the π-back-donation in the metal–carbonyl intermediates, and thus favors the formation of CO. This back-donation effect is consistent with the traditional understanding of selectivity. This work provides comprehensive insights into the dual role of the electronic effect on the selectivity for CO2 reduction, which can be instructive for the future design and development of catalysts.Keywords
Funding Information
- National Natural Science Foundation of China (21673301, 21773312, 21973113)
- Natural Science Foundation of Guangdong Province (2015A030306027, 2015A030313677)
- Tip-top Scientific and Technical Innovative Youth Talents of Guangdong Special Support Program (20153100042090537)
- China Postdoctoral Science Foundation (2018M643289)
- Fundamental Research Funds for the Central Universities
This publication has 32 references indexed in Scilit:
- Catalysis for the Valorization of Exhaust Carbon: from CO2to Chemicals, Materials, and Fuels. Technological Use of CO2Chemical Reviews, 2013
- Turnover Numbers, Turnover Frequencies, and Overpotential in Molecular Catalysis of Electrochemical Reactions. Cyclic Voltammetry and Preparative-Scale ElectrolysisJournal of the American Chemical Society, 2012
- Selective Electrocatalytic Reduction of CO2 to Formate by Water-Stable Iridium Dihydride Pincer ComplexesJournal of the American Chemical Society, 2012
- Thermodynamics and kinetics of CO2, CO, and H+ binding to the metal centre of CO2reductioncatalystsChemical Society Reviews, 2011
- Multiwfn: A multifunctional wavefunction analyzerJournal of Computational Chemistry, 2011
- The M06 suite of density functionals for main group thermochemistry, thermochemical kinetics, noncovalent interactions, excited states, and transition elements: two new functionals and systematic testing of four M06-class functionals and 12 other functionalsTheoretical Chemistry Accounts, 2007
- Single-Ion Solvation Free Energies and the Normal Hydrogen Electrode Potential in Methanol, Acetonitrile, and Dimethyl SulfoxideThe Journal of Physical Chemistry B, 2006
- Calculation of the aqueous solvation free energy of the protonThe Journal of Chemical Physics, 1998
- Electroreduction of CO2 catalyzed by polymeric [Ru(bpy)(CO)2]n films in aqueous media: Parameters influencing the reaction selectivityJournal of Electroanalytical Chemistry, 1998
- Ab initio effective core potentials for molecular calculations. Potentials for the transition metal atoms Sc to HgThe Journal of Chemical Physics, 1985