纳米棒
光催化
异质结
材料科学
量子点
光电流
光致发光
纳米复合材料
纳米技术
化学工程
光电子学
可见光谱
量子产额
催化作用
化学
光学
物理
工程类
荧光
生物化学
作者
Yongjin Ma,Yuan Bian,Yi Liu,Anquan Zhu,Hong Wu,Hao Cui,Dewei Chu,Jun Pan
出处
期刊:ACS Sustainable Chemistry & Engineering
[American Chemical Society]
日期:2017-12-21
卷期号:6 (2): 2552-2562
被引量:113
标识
DOI:10.1021/acssuschemeng.7b04049
摘要
Photocatalytic hydrogen evolution from water splitting is a promising approach in energy conversion and storage. Here, the 0D/1D CdS quantum dots (QDs)/CeO2 nanorods heterojunction was designed and fabricated by a facile two-step method. The optimum photocatalytic H2 evolution activity for CeO2-based composites with 3 at. % CdS QDs (101.12 μ mol h–1 g–1) was 45 times as high as that of pure CeO2 nanorods (2.25 μ mol h–1 g–1) under light irradiation. Meanwhile, the photocurrent response intensity increased 17.75 times higher than pure CeO2 nanorods. Furthermore, the 0D/1D CdS QDs/CeO2 heterojunctions exhibited enhanced photocatalytic stability for long lifetime (60 h). The reasons that dramatically enhanced photocatalytic performance could be the improved light harvesting, enhanced photoresponse and stronger electronic conductivity while the CdS QDs was loaded in CeO2 nanorods to form the 0D/1D heterojunctions CdS QDs/CeO2 nanocomposites. What's more, the remarkably increased photocatalytic performance of CdS QDs/CeO2 composites was mainly attributed to the Z-scheme between CdS QDs and CeO2 nanorods, which was confirmed by the PL (photoluminescence) method. Therefore, the proposed system is highly promising for large scale photocatalytic hydrogen evolution.
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