Coupled internal electric field with hydrogen release kinetics for promoted photocatalytic hydrogen production through employing carbon coated transition metal as co-catalyst

被引:60
作者
Shi, Yuxing [1 ]
Li, Lingling [1 ]
Xu, Zheng [1 ]
Qin, Xiuling [1 ]
Cai, Yi [4 ]
Zhang, Wenlei [3 ]
Shi, Weilong [2 ,3 ]
Du, Xin [2 ,3 ]
Guo, Feng [1 ,2 ]
机构
[1] Jiangsu Univ Sci & Technol, Sch Energy & Power, Zhenjiang 212003, Jiangsu, Peoples R China
[2] Jiangsu Univ Sci & Technol, Sch Mat Sci & Engn, Zhenjiang 212003, Peoples R China
[3] Zhengzhou Univ, Coll Chem, Zhengzhou 450001, Peoples R China
[4] Southwest Minzu Univ, Sch Chem & Environm, Key Lab Pollut Control Chem, Environm Funct Mat Qinghai Tibet Plateau Natl Ethn, Chengdu 610041, Peoples R China
基金
中国国家自然科学基金;
关键词
Photocatalysis; Internal electric field; H2; evolution; Co@C; Co-catalyst; CHARGE-TRANSFER; POROUS G-C3N4; WATER; NANOPARTICLES; SHELL; NANOCOMPOSITES; DEGRADATION; MICRORODS; STRATEGY; NITRIDE;
D O I
10.1016/j.jcis.2022.10.022
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 ideal solution to the energy shortage problem is to split water into hydrogen (H2) utilizing solar -driven semiconductor photocatalytic technology. Nevertheless, severe carrier recombination is the major cause of decreased activity over photocatalysts. Construction of internal electric field (IEF) by coupling semiconductor with metal co-catalyst can effectively promote carrier separation. Herein, Co@C with the Co encapsulated in the C layer as a co-catalyst anchored on the surface of ZnIn2S4 nanosheets via a facile electrostatic self-assembly strategy, achieving outstanding photocatalytic water splitting into H2 under simulated solar irradiation (AM 1.5G) with the production rate of 18.1 mmol h-1 g-1, which is 109.7 times higher than that of bare ZIS without assisted of Pt. Enhancement of photocatalytic H2 evolu-tion activity of Co@C/ZIS is mainly attributed to the construction of giant IEF (4.6-fold higher than ZIS) and suitable environment for hydrogen adsorption and desorption (DGH* ti 0), which endows the follow-ing several advantages: (i) accelerating the migration and separation of photo-generated charges; (ii) improving the hydrogen release kinetics. Our work not only provides a design idea for facile preparation of a high-efficient composite photocatalyst, but also expands the application range of transition metal@ -carbon as a co-catalyst in energy photocatalysis.(c) 2022 Elsevier Inc. All rights reserved.
引用
收藏
页码:274 / 285
页数:12
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