Cs3Bi2Br9 Nanodots Stabilized on Defective BiOBr Nanosheets by Interfacial Chemical Bonding: Modulated Charge Transfer for Photocatalytic C(sp3)-H Bond Activation

被引:49
作者
Bai, Zhang-Jun [1 ]
Tian, Sheng [1 ]
Zeng, Tian-Qin [1 ]
Chen, Lang [1 ]
Wang, Bing-Hao [1 ]
Hu, Biao [1 ]
Wang, Xiong [1 ]
Zhou, Wei [1 ]
Pan, Jin-Bo [1 ]
Shen, Sheng [1 ]
Guo, Jun-Kang [1 ]
Xie, Ting-Liang [1 ]
Li, You-Ji [2 ]
Au, Chak-Tong [3 ]
Yin, Shuang-Feng [1 ]
机构
[1] Hunan Univ, Coll Chem & Chem Engn, Adv Catalyt Engn Res Ctr, State Key Lab Chemo Biosensing & Chemometr,Minist, R China, Changsha 410082, Peoples R China
[2] Jishou Univ, Coll Chem & Chem Engn, Jishou 416000, Hunan, Peoples R China
[3] Fuzhou Univ, Coll Chem Engn, Fuzhou 350002, Peoples R China
基金
中国国家自然科学基金;
关键词
Cs3Bi2Br9; nanodots; defective BiOBr; interfacial chemical bond-modulated Z-scheme structure; photocatalysis; C(sp3)-H bond activation; C-H BONDS; SELECTIVE OXIDATION; PEROVSKITE; TOLUENE; BENZALDEHYDE; PHASE;
D O I
10.1021/acscatal.2c04652
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
In the design of photocatalysts for C(sp3)-H selective oxidation, photogenerated holes have been regarded as critical for C(sp3)-H dissociation. However, poor charge-transfer efficiency restricts the localization of holes on the surface of the catalyst. Herein, a Z-scheme structure modulated by interfacial chemical bonding is constructed via the in situ growth of Cs3Bi2Br9 nanodots (CBB) on defective BiOBr nanosheets (d-BiOBr) for photocatalytic toluene selective oxidation. Benefited from the interfacial internal electric field, the Bi-Br bond becomes a direct channel to accelerate electron transfer from the conduction band of d-BiOBr to the valence band of CBB, resulting in a higher localization of charges on the surface of CBB/d-BiOBr. By in situ diffuse reflectance infrared Fourier transform spectroscopy, electron paramagnetic resonance, and density functional theory calculations, the surface localization of holes is proved to be essential for toluene adsorption and the dissociation of C(sp3)-H bond. The optimized CBB/d-BiOBr performs well in the selective oxidation of toluene to benzaldehyde and benzyl alcohol, giving a conversion rate of up to 72.3 mu mol h-1 and a selectivity of nearly 100%. The activity of CBB/d-BiOBr is 26.6-fold and 6.8-fold that of pristine d-BiOBr and CBB, respectively.
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页码:15157 / 15167
页数:11
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