纳米棒
光催化
制氢
材料科学
催化作用
化学工程
贵金属
吸附
离子键合
分解水
电化学
比表面积
可见光谱
纳米颗粒
氢
电子转移
纳米技术
复合数
光化学
辐照
反应机理
硫化镉
吸收(声学)
扫描电子显微镜
无机化学
作者
Guorong Wang,Zhiliang Jin
标识
DOI:10.1016/j.apsusc.2018.10.239
摘要
Abstract Noble metal-free NiSe2 nanoparticles as co-catalyst to modify CdS nanorods for enhancement hydrogen evolution was successfully synthesized by semi-solid reaction method and heterogenous NiSe2/CdS nanorods arrays were fabricated by using a facile successive ionic adsorption under phase-change environment. With the introduction of NiSe2, the H2 production of 30% NiSe2/CdS photocatalyst reached the peak value about 61522 μmol/g under continuous visible light irradiation for 5 h, which was 2.6 times higher than that of the pure CdS photocatalyst. Moreover, cyclic experiments exhibited that the composite catalyst has excellent stability. The possible detail enhancement mechanism was speculated and discussed by morphological, optical and electrochemical characterization such as SEM, TEM, XRD, EDS, BET, XPS, UV–vis DRS, PL spectrum, LSV, EIS and etc. All results showed good consistency. Based on it, we speculated the heterojuction formed with special VB and CB of CdS and NiSe2 caused efficient charge separation and lowed the over potential of H+ reduction. NiSe2 co-catalyst loaded on the surface of CdS nanorods, which not only blocked the CdS from photocorrosion, but also provided an electron transfer medium which transfers photogenerated electrons from CdS to NiSe2 surface rapidly, enhancing the photocatalytic hydrogen evolution.
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