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将 CdS 量子点和树枝状 Pt 纳米晶体固定在巯基化石墨烯纳米片上,实现高效光催化 H2 演化。

Immobilizing CdS quantum dots and dendritic Pt nanocrystals on thiolated graphene nanosheets toward highly efficient photocatalytic H2 evolution.

机构信息

School of Chemical and Biomedical Engineering, Nanyang Technological University, 70 Nanyang Dr., Singapore 637457.

出版信息

Nanoscale. 2013 Oct 21;5(20):9830-8. doi: 10.1039/c3nr03043a.

Abstract

We report the development of a highly efficient photocatalytic system by immobilizing high-quality CdS quantum dots and dendritic Pt nanocrystals on thiol-functionalized graphene substrates. We have demonstrated that the use of QDs with compact sizes leads to a dramatically enhanced performance in comparison with their bulk counterparts. Our design allows for systematic examination of the impact of QD sizes and the loading, morphology, and surface coating of the Pt nanocrystal cocatalyst on the H2 evolution activity. It was found that the CdS-Pt binary system has a high photocatalytic efficiency of 1.37 mmol h(-1) for visible light driven H2 evolution, and there was a 30% improvement by introducing the thiolated reduced graphene oxide to form the three-component CdS-Pt-Gcys nanocomposites. The highest H2 evolution rate of 2.15 mmol h(-1) (λ ≥ 420 nm) with a QE of 50.7% was achieved by further photo-annealing of the CdS-Pt-Gcys nanocomposites prior to the photocatalytic reaction.

摘要

我们报告了一种高效的光催化系统的开发,该系统通过将高质量的 CdS 量子点和树枝状 Pt 纳米晶体固定在巯基功能化的石墨烯基底上。我们已经证明,与体相比,使用具有紧凑尺寸的 QD 可以显著提高性能。我们的设计允许系统地研究 QD 尺寸以及 Pt 纳米晶助催化剂的负载量、形态和表面涂层对 H2 演化活性的影响。结果发现,CdS-Pt 二元体系在可见光驱动的 H2 演化中具有 1.37 mmol h(-1) 的高光催化效率,通过引入硫醇化还原氧化石墨烯形成三元 CdS-Pt-Gcys 纳米复合材料,可以提高 30%的效率。通过在光催化反应之前对 CdS-Pt-Gcys 纳米复合材料进行进一步的光退火,实现了最高的 H2 演化速率 2.15 mmol h(-1)(λ≥420nm),QE 为 50.7%。

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