Carbon Materials Containing Single-Atom Co-N4 Sites Enable Near-Infrared Photooxidation

被引:4
|
作者
Li, Longjian [1 ]
Wang, Junhui [1 ]
Zhang, Qinhua [1 ]
Wang, Shuai [1 ]
Zhang, Hangkai [1 ]
Xing, Tao [2 ]
Wang, Mingqing [2 ]
Wu, Mingbo [1 ]
Wang, Zhenxing [3 ]
Wu, Wenting [1 ]
机构
[1] China Univ Petr East China, Coll Chem Engn, State Key Lab Heavy Oil Proc, Qingdao 266580, Peoples R China
[2] ShanDong Energy Grp CO LTD, Natl Engn Res Ctr Coal Gasificat & Coal Based Adv, Jinan 250101, Peoples R China
[3] Huazhong Univ Sci & Technol, Natl Pulsed High Magnet Field Sci Ctr, Wuhan 430074, Peoples R China
来源
ACS CATALYSIS | 2024年 / 14卷 / 05期
基金
美国国家科学基金会;
关键词
Co-N site; IR driven; triplet energy transfer; calcination temperatures; photooxidation; OXYGEN; PERFORMANCE;
D O I
10.1021/acscatal.3c05441
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
Near-infrared light occupies 54.3% of the solar spectrum and has greater penetration depth, and its effective utilization is of great significance in the practical application of photocatalysis on a larger scale. However, the development of catalysts that can directly utilize near-infrared light is still a huge challenge. This paper proposes a strategy to directly utilize near-infrared light (excitation wavelength extending to 850 nm) by creating carbon material doped with a high-spin-state Co(II)-N x single-atom site. In the near-infrared-light-irradiated photooxidation of 1,5-dihydroxynaphthalene, the yield of juglone can reach 45% without a significant decrease, even when the catalytic volume is increased by 20 times, which was much higher than that irradiated by 460 nm wavelength (reduced by about 23%). Our study sets the stage for fabricating stable NIR photocatalysts and provides a solution to directly enhance NIR photooxidation in a large-scale manner.
引用
收藏
页码:3041 / 3048
页数:8
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