Matched Redox Kinetics on Triazine‐Based Carbon Nitride/Ni(OH)2 for Stoichiometric Overall Photocatalytic CO2 Conversion

Author:

Wang Jing1,Sheng Ren1,Xiao Juanxiu2,Lu Li3,Peng Yuhao1,Gu Dong4,Xiao Wei1ORCID

Affiliation:

1. College of Chemistry and Molecular Sciences Hubei Key Laboratory of Electrochemical Power Sources Wuhan University Wuhan 430072 P. R. China

2. State Key Laboratory of Marine Resources Utilization in South China Sea Collaborative Innovation Center of Marine Science and Technology School of Marine Science and Engineering Hainan University Haikou 570228 P. R. China

3. National University of Singapore (Chongqing) Research Institute Chongqing 401123 P. R. China

4. The Institute for Advanced Studies Wuhan University Wuhan 430072 P. R. China

Abstract

AbstractMismatched reaction kinetics of CO2 reduction and H2O oxidation is the main obstacle limiting the overall photocatalytic CO2 conversion. Here, a molten salt strategy is used to construct tubular triazine‐based carbon nitride (TCN) with more adsorption sites and stronger activation capability. Ni(OH)2 nanosheets are then grown over the TCN to trigger a proton‐coupled electron transfer for a stoichiometric overall photocatalytic CO2 conversion via “3CO2 + 2H2O = CH4 + 2CO + 3O2.” TCN reduces the energy barrier of H2O dissociation to promote H2O oxidation to O2 and supply sufficient protons to Ni(OH)2, whereby the CO2 conversion is accelerated due to the enhanced proton‐coupled electron transfer process enabled by the sufficient proton supply from TCN. This work highlights the importance of matching the reaction kinetics of CO2 reduction and H2O oxidation by proton‐coupled electron transfer on stoichiometric overall photocatalytic CO2 conversion.

Funder

National Natural Science Foundation of China

Fundamental Research Funds for the Central Universities

Publisher

Wiley

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