Plasma-Wind-Assisted In2S3 Preparation with an Amorphous Surface Structure for Enhanced Photocatalytic Hydrogen Production

被引:6
|
作者
Guo, Shaohui [1 ]
Luo, Hui [2 ]
Duan, Xiaochuan [1 ]
Wei, Bingqing [3 ]
Zhang, Xianming [4 ]
机构
[1] Taiyuan Univ Technol, Coll Chem, Taiyuan 030024, Peoples R China
[2] Imperial Coll London, Dept Chem Engn, South Kensington Campus, London SW7 2AZ, England
[3] Univ Delaware, Dept Mech Engn, Newark, DE 19716 USA
[4] Taiyuan Univ Technol, Key Lab Interface Sci & Engn Adv Mat, Minist Educ, Taiyuan 030024, Peoples R China
基金
中国国家自然科学基金;
关键词
photocatalytic hydrogen evolution; crystal-amorphous interface; plasma-wind treatment; indium sulfide; H-2; EVOLUTION; HETEROJUNCTION; CRYSTALLINE; JUNCTION;
D O I
10.3390/nano12101761
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Photocatalytic production from water is considered an effective solution to fossil fuel-related environmental concerns, and photocatalyst surface science holds a significant interest in balancing photocatalysts' stability and activity. We propose a plasma-wind method to tune the surface properties of a photocatalyst with an amorphous structure. Theoretical calculation shows that the amorphous surface structure can cause an unsaturated coordination environment to adjust the electron distribution, forming more adsorption sites. Thus, the photocatalyst with a crystal-amorphous (C-A) interface can strengthen light absorption, harvest photo-induced electrons, and enrich the active sites, which help improve hydrogen yield. As a proof of concept, with indium sulfide (In2S3) nanosheets used as the catalyst, an impressive hydrogen production rate up to 457.35 mu mol cm(-2) h(-1) has been achieved. Moreover, after plasma-assisted treatment, In2S3 with a C-A interface can produce hydrogen from water under natural outdoor conditions. Following a six-hour test, the rate of photocatalytic hydrogen evolution is found to be 400.50 mu mol cm(-2) g(-1), which demonstrates that a catalyst prepared through plasma treatment is both effective and highly practical.
引用
收藏
页数:12
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