光催化
材料科学
纳米复合材料
复合数
化学工程
分解水
纳米颗粒
纳米技术
光化学
电子转移
催化作用
复合材料
化学
有机化学
工程类
作者
Tianjun Chen,Chengjie Song,Mingshan Fan,Yuanzhi Hong,Bo Hu,Longbao Yu,Weidong Shi
标识
DOI:10.1016/j.ijhydene.2017.03.188
摘要
Abstract In this work, novel CuS/g-C3N4 composite photocatalysts were successfully prepared via a simple in-situ growth method. CuS nanoparticles, with an average diameter of ca.10 nm, were well dispersed on the surface of g-C3N4, revealing that g-C3N4 nanosheets were promising support for in-situ growth of nanosize materials. The CuS/g-C3N4 composites exhibited highly enhanced visible light photocatalytic H2 evolution from water-splitting compared to pure g-C3N4. The optimum photocatalytic activity of 2 wt% CuS/g-C3N4 composite photocatalytic H2 evolution was about 13.76 times higher than pure g-C3N4. The enhanced photocatalytic activity is attributed to the interfacial charge transfer (IFCT). In this system, electrons in the valence band (VB) of g-C3N4 can transfer directly to CuS clusters, causing the reduction of partial CuS to Cu2S, which can act as an electron sink and co-catalyst to promote the separation and transfer of photo-generated electrons. The accumulated photoinduced electrons in CuS/Cu2S clusters could effectively reduce H+ to produce H2. This work provides a possibility for constructing low-cost CuS as a substitute for noble metals in the photocatalytic production of H2 via a facile method based on g-C3N4.
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