Efficient and stable H2O2 production from H2O and O2 on BiPO4 photocatalyst

被引:81
|
作者
Pan, Chengsi [1 ,2 ]
Bian, Gaoming [1 ,2 ]
Zhang, Yaning [1 ,2 ]
Lou, Yang [1 ,2 ]
Zhang, Ying [1 ,2 ]
Dong, Yuming [1 ,2 ]
Xu, Jing [3 ]
Zhu, Yongfa [1 ,2 ,4 ]
机构
[1] Jiangnan Univ, Sch Chem & Mat Engn, Key Lab Synthet & Biol Colloids, Minist Educ, Wuxi 214122, Jiangsu, Peoples R China
[2] Jiangnan Univ, Int Joint Res Ctr Photorespons Mol & Mat, Wuxi 214122, Jiangsu, Peoples R China
[3] Jiangnan Univ, Sch Food Sci & Technol, Wuxi 214122, Peoples R China
[4] Tsinghua Univ, Dept Chem, Beijing 100084, Peoples R China
基金
国家重点研发计划; 中国国家自然科学基金;
关键词
Photocatalysis; Sustainable chemistry; Peroxides; Nanostructures; Bismuth phosphate; HYDROGEN-PEROXIDE SYNTHESIS; CARBON NITRIDE; OXYGEN REDUCTION; WATER OXIDATION; NANOPARTICLES; DEGRADATION; SEPARATION;
D O I
10.1016/j.apcatb.2022.121675
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
Photocatalytic H2O2 production from H2O and O-2 is a sustainable alternative to the present anthraquinone process, but most available systems need sacrificial reagents to maintain continuous activity. In this work, BiPO4 photocatalyst is reported to produce H2O2 efficiently from non-sacrificial systems. The photocatalyst exhibits H2O2 production activity as high as 12.0 mM/h/g and negligible decay for 40 cycles (ca. 200 h) with only H2O and O-2. The photocatalyst is demonstrated to show a core-shell structure. The monoclinic BiPO4 core exhibits a wide bandgap of 3.85 eV, supplying sufficient driven force for photogenerated e(-) and h(+) to produce H2O2. More importantly, instinct hydrate voids in coated hexagonal BiPO(4 )cause strong adsorption with H2O and O-2 rather than H2O2 via the steric hindrance effect, which facilitates the diffusion of H2O2 away from the active photo -catalyst surface, avoiding its overreaction. The findings may help to design more efficient and stable photo -catalysts for H2O2 production in the future.
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页数:8
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