Enhanced photocatalytic nitrogen fixation on Cu2O clusters/MIL-100 (Fe) heterojunction

被引:9
|
作者
Huang, Xingxing [1 ]
Shi, Yingzhang [1 ]
Liu, Cheng [1 ]
Wang, Zhiwen [2 ]
Bi, Jinhong [3 ]
Yu, Jimmy C. [4 ]
Wu, Ling [1 ]
机构
[1] Fuzhou Univ, Coll Chem, State Key Lab Photocatalysis Energy & Environm, Fuzhou 350116, Peoples R China
[2] Hainan Univ, Hainan Prov Key Lab Fine Chem, Haikou 570228, Peoples R China
[3] Fuzhou Univ, Dept Environm Sci & Engn, Minhou 350108, Fujian, Peoples R China
[4] Chinese Univ Hong Kong, Dept Chem, Shatin, Hong Kong, Peoples R China
基金
中国国家自然科学基金;
关键词
MIL-100(Fe); Cu2O clusters; Photocatalytic nitrogen fixation; Surface interaction; Type-II heterojunction; METAL-ORGANIC FRAMEWORK; BENZYL ALCOHOL; NANOSHEETS; REDUCTION; NANOPARTICLES; OXIDATION;
D O I
10.1016/j.apsusc.2023.158443
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
A series of Cu2O clusters/MIL-100(Fe) heterojunctions with different Cu2O mass ratios were constructed as the photocatalysts for N2 fixation. An optimal nitrogen fixation performance of 51.22 mu mol center dot g- 1 center dot h- 1 is achieved when the mass fraction of Cu2O is 20 %. Isotope analysis experiments confirmed that the nitrogen source is N2. Possible intermediate signals during photocatalytic reactions were detected by in situ DRIFTS. XPS results further confirm the formation of Cu2O/MIL-100(Fe) heterojunctions, and that the existence of Cu-O surface interactions is the key to efficient electron transfer. It is revealed that the improvement of the catalytic performance is derived from the formation of heterojunction which regulates the energy band structure as well as promotes the separation of photogenerated electron-hole pairs. This study proposes a possible mechanism of photocatalytic nitrogen fixation and emphasizes the role of surface interaction and electron transfer in type-II heterojunction in improving ni-trogen fixation performance.
引用
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页数:9
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