光催化
量子点
材料科学
光化学
辐照
纳米复合材料
原位
可见光谱
氢
纳米颗粒
化学工程
制氢
复合数
催化作用
纳米技术
化学
光电子学
复合材料
有机化学
物理
核物理学
工程类
作者
Shaowen Cao,Yupeng Yuan,Jun Fang,Mohammad Mehdi Shahjamali,Freddy Boey,James Barber,Say Chye Joachim Loo,Can Xue
标识
DOI:10.1016/j.ijhydene.2012.10.116
摘要
Abstract Well dispersed CdS quantum dots were successfully grown in-situ on g-C3N4 nanosheets through a solvothermal method involving dimethyl sulfoxide. The resultant CdS–C3N4 nanocomposites exhibit remarkably higher efficiency for photocatalytic hydrogen evolution under visible light irradiation as compared to pure g-C3N4. The optimal composite with 12 wt% CdS showed a hydrogen evolution rate of 4.494 mmol h−1 g−1, which is more than 115 times higher than that of pure g-C3N4. The enhanced photocatalytic activity induced by the in-situ grown CdS quantum dots is attributed to the interfacial transfer of photogenerated electrons and holes between g-C3N4 and CdS, which leads to effective charge separation on both parts.
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