A Single Cu-Center Containing Enzyme-Mimic Enabling Full Photosynthesis under CO2 Reduction

被引:222
作者
Wang, Jiu [1 ]
Heil, Tobias [3 ]
Zhu, Bicheng [1 ]
Tung, Ching-Wei [2 ]
Yu, Jiaguo [1 ]
Hao Ming Chen [2 ]
Antonietti, Markus [3 ]
Cao, Shaowen [1 ,3 ]
机构
[1] Wuhan Univ Technol, State Key Lab Adv Technol Mat Synth & Proc, Wuhan 430070, Peoples R China
[2] Natl Taiwan Univ, Dept Chem, Taipei 10617, Taiwan
[3] Max Planck Inst Colloids & Interfaces, Dept Colloid Chem, D-14476 Potsdam, Germany
基金
中国国家自然科学基金;
关键词
single-atom catalysis; photocatalysis; carbon nitride; CO2; reduction; artificial enzyme; CARBON NITRIDE G-C3N4; IN-SITU EPR; OXYGEN REDUCTION; HYDROGEN-PRODUCTION; CATALYTIC-ACTIVITY; MOLECULAR-CLONING; H-2; EVOLUTION; QUANTUM YIELD; ATOM; NANOPARTICLES;
D O I
10.1021/acsnano.0c02940
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Polymeric carbon nitride (CN) is one of the most promising metal-free photocatalysts to alleviate the energy crisis and environmental pollution. Loading cocatalysts is regarded as an effective way to improve the photocatalytic efficiency of CNs. However, commonly used noble metal cocatalysts limit their applications due to their rarity and high cost. Herein, we present the effective synthesis of single-atom copper-modified CN via supramolecular preorganization with subsequent condensation, which provides effective charge transfer pathways by an "infused" delocalized state with variable-valence catalysis at the same time. The C-Cu-N-2 single-atom catalytic site can activate CO2 molecules and reduces the energy barrier toward photocatalytic CO2 reduction. Excellent performance for photocatalytic CO2 reduction was found. This work thereby provides a general protocol of designing a noble-metal-free photocatalyst with infused metal centers toward a wide range of applications.
引用
收藏
页码:8584 / 8593
页数:10
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