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

被引:6
|
作者
Wang, Jing [1 ]
Sheng, Ren [1 ]
Xiao, Juanxiu [2 ]
Lu, Li [3 ]
Peng, Yuhao [1 ]
Gu, Dong [4 ]
Xiao, Wei [1 ]
机构
[1] Wuhan Univ, Coll Chem & Mol Sci, Hubei Key Lab Electrochem Power Sources, Wuhan 430072, Peoples R China
[2] Hainan Univ, Collaborat Innovat Ctr Marine Sci & Technol, State Key Lab Marine Resource Utilizat South China, Haikou 570228, Peoples R China
[3] Natl Univ Singapore, Chongqing Res Inst, Chongqing 401123, Peoples R China
[4] Wuhan Univ, Inst Adv Studies, Wuhan 430072, Peoples R China
基金
中国国家自然科学基金;
关键词
carbon dioxide fixation; overall photocatalytic CO2 conversion; photocatalysis; proton-coupled electron transfer; triazine-based carbon nitride; CHARGE-TRANSFER; HYDROGEN; REDUCTION; WATER; FRAMEWORK; ARRAYS;
D O I
10.1002/smll.202309707
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Mismatched 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 "3CO(2) + 2H(2)O = CH4 + 2CO + 3O(2)." TCN reduces the energy barrier of H2O dissociation to promote H2O oxidation to O-2 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.
引用
收藏
页数:10
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