Engineered charge transfer and reactive site over hierarchical Ti3C2T x MXene@In2S3-NiS toward enhanced photocatalytic H2 evolution

被引:4
作者
Xie, Guanshun [1 ]
Zhu, Yisong [1 ]
Yu, Changqiang [1 ]
Xie, Xiuqiang [1 ]
Zhang, Nan [1 ]
机构
[1] Hunan Univ, Coll Mat Sci & Engn, Changsha, Peoples R China
基金
中国国家自然科学基金;
关键词
MXene; NiS; H-2 evolution site; multichannel charge transfer; photocatalysis; HYDROGEN EVOLUTION; COCATALYST; REDUCTION;
D O I
10.1088/2053-1583/ac97a6
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
Steering photogenerated electron flow to the effective reactive sites is ideal for photocatalytic H-2 evolution. Herein, as a proof-of-concept, NiS is coupled with a typical Schottky heterojunction of Ti3C2T (x) MXene@In2S3 through the photodepotition method towards improving the photocatalytic H-2 evolution performance. In addition to the Schottky effect-mediated electron transfer in Ti3C2T (x) MXene@In2S3 heterojunctions, p-n junctions form between In2S3 and NiS to extract photoinduced electrons, which is found to cooperate with the role of effective H-2 evolution reactive sites. The synergistic dual functions of NiS cooperate with Ti3C2T (x) MXene promote multichannel electron transfer in Ti3C2T (x) MXene@In2S3-NiS hybrids to improve the photocatalytic hydrogen evolution reaction (HER) efficiency by 41 times compared to the bare In2S3. These results enlighten the engineering of the spatial transfer of photoinduced electrons to the reactive sites toward boosting the efficiency of photocatalytic HER.
引用
收藏
页数:11
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