In situ growth of bismuth oxybromide/bismuth molybdate 2D/2D Z-scheme heterojunctions with rich interfacial oxygen vacancies for photocatalytic benzylic C(sp3)-H bond activation

被引:2
作者
Gu, Songting [1 ]
Li, Chenyu [1 ]
Lin, Xinyan [1 ]
Lin, Xiaotong [1 ]
Xiao, Yingxi [1 ]
Zhao, Xiaoyang [2 ]
Nan, Junmin [1 ]
Xiao, Xin [1 ]
机构
[1] South China Normal Univ, Sch Chem, MOE Key Lab Theoret Chem Environm, Guangzhou 510006, Peoples R China
[2] Henan Polytech Inst, Dept Environm Engn, Nanyang 473009, Peoples R China
基金
中国国家自然科学基金;
关键词
Selective oxidation of toluene; Photocatalytic C(sp 3 )-H bond activation; Direct Z -scheme heterojunction; Interface-induced oxygen vacancies; 2D/2D BiOBr/Bi 2 MoO 6; HIGHLY-SELECTIVE OXIDATION; CATALYTIC-OXIDATION; TOLUENE; BENZALDEHYDE; EFFICIENT; CONSTRUCTION; HYDROCARBONS; COMPOSITE; BI4O5BR2; GREEN;
D O I
10.1016/j.jcis.2024.11.233
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
The selective oxidation of toluene into valuable chemicals via photocatalytic C(sp3)-H bond activation represents a significant, yet challenging process. Here, the in situ construction of bismuth oxybromide/bismuth molybdate (BiOBr/Bi2MoO6) 2D/2D Z-scheme heterojunctions featuring interface-induced oxygen vacancies (OVs) is introduced. The optimized BiOBr/Bi2MoO6 sample has a remarkable yield rate of benzaldehyde at 2134.28 mu mol g- 1 h- 1 under blue LED irradiation, surpassing the performance of BiOBr and Bi2MoO6 by 8.1 and 2.9 times, respectively. Insights from density functional theory (DFT) calculations, electron paramagnetic resonance (EPR), and in situ diffuse reflectance infrared Fourier transform spectroscopy (DRIFTS) studies highlight the critical role of the Z-scheme electronic configuration and OVs in attaining the superior photocatalytic toluene conversion efficiency. This study advances the photocatalytic conversion of benzaldehyde within an OV-enhanced direct Zscheme system, facilitating the activation of inert C(sp3)-H bonds, and contributes to the development of highperformance catalysts for sustainable chemical processes.
引用
收藏
页码:467 / 477
页数:11
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