Carbon Nitride Photocatalysts with Integrated Oxidation and Reduction Atomic Active Centers for Improved CO2 Conversion

被引:183
作者
Ou, Honghui [1 ]
Ning, Shangbo [2 ,3 ]
Zhu, Peng [1 ]
Chen, Shenghua [1 ]
Han, Ali [1 ]
Kang, Qing [3 ]
Hu, Zhuofeng [4 ]
Ye, Jinhua [2 ,5 ]
Wang, Dingsheng [1 ]
Li, Yadong [1 ]
机构
[1] Tsinghua Univ, Dept Chem, Beijing 100084, Peoples R China
[2] Tianjin Univ, Sch Mat Sci & Engn, TJU NIMS Int Collaborat Lab, Tianjin 300072, Peoples R China
[3] Jinan Univ, Dept Inst Surface Anal & Chem Biol, Jinan 250022, Shandong, Peoples R China
[4] Sun Yat sen Univ, Sch Environm Sci & Engn, Guangdong Prov Key Lab Environm Pollut Control &, Guangzhou, Peoples R China
[5] Natl Inst Mat Sci NIMS, Int Ctr Mat Nanoarchitecton WPI MANA, Tsukuba, Ibaraki 3050047, Japan
基金
中国国家自然科学基金; 国家重点研发计划; 中国博士后科学基金;
关键词
Bimetallic; CO2; Conversion; Photocatalysis; Redox Site; Single-Atom Catalysts; PHOTOSYSTEM-II; PHOTOREDUCTION; SITES;
D O I
10.1002/anie.202206579
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Single-atom active-site catalysts have attracted significant attention in the field of photocatalytic CO2 conversion. However, designing active sites for CO2 reduction and H2O oxidation simultaneously on a photocatalyst and combining the corresponding half-reaction in a photocatalytic system is still difficult. Here, we synthesized a bimetallic single-atom active-site photocatalyst with two compatible active centers of Mn and Co on carbon nitride (Mn1Co1/CN). Our experimental results and density functional theory calculations showed that the active center of Mn promotes H2O oxidation by accumulating photogenerated holes. In addition, the active center of Co promotes CO2 activation by increasing the bond length and bond angle of CO2 molecules. Benefiting from the synergistic effect of the atomic active centers, the synthesized Mn1Co1/CN exhibited a CO production rate of 47 mu mol g(-1) h(-1), which is significantly higher than that of the corresponding single-metal active-site photocatalyst.
引用
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页数:8
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