You Ziyi, Yue Xiaoyang, Zhang Dainan, Fan Jiajie, Xiang Quanjun
State Key Laboratory of Electronic Thin Film and Integrated Devices, School of Electronic Science and Engineering, University of Electronic Science and Technology of China, Chengdu 610054, PR China; Yangtze Delta Region Institute (Huzhou), University of Electronic Science and Technology of China, Huzhou 313001, PR China.
State Key Laboratory of Electronic Thin Film and Integrated Devices, School of Electronic Science and Engineering, University of Electronic Science and Technology of China, Chengdu 610054, PR China.
J Colloid Interface Sci. 2022 Feb;607(Pt 1):662-675. doi: 10.1016/j.jcis.2021.09.001. Epub 2021 Sep 3.
In recent years, the use of quantum dots (QDs) cocatalysts to improve the hydrogen evolution activity from the water splitting of photocatalysts has become a popular research topic. Herein, we successfully prepared a novel 0 dimension/2 dimension (0D/2D) heterojunction nanocomposite (denoted AgS quantum dots (QDs)/g-CN) with excellent photocatalytic performance by anchoring the AgS QDs cocatalyst on the surface of g-CN through a self-assembly strategy. AgS QDs with an average particle size of approximately 5.8 nm were uniformly and tightly modified on g-CN. The AgS QDs/g-CN composite with 0.5 wt% AgS QDs loading achieved the highest hydrogen evolution rate of 471.1 μmol·g·h with an apparent quantum efficiency (AQE) of 1.48% at 405 nm. Such remarkable hydrogen evolution activity far exceeded that of undoped g-CN and AgS nanoparticles (NPs)/g-CN. Moreover, it was 2.04 times the activity of Pt/g-CN with Pt as the cocatalyst. The enhanced photocatalytic performance was attributed to the energy band broadening of AgS QDs caused by the quantum size effect and the convenient and effective charge transfer between g-CN and AgS QDs cocatalysts. The mechanism underlying the enhanced photocatalytic H evolution activity was further proposed. This study demonstrates that semiconductor-based quantum dots are strong candidates for excellent cocatalysts in photocatalysis.
近年来,使用量子点(QDs)助催化剂来提高光催化剂水分解产氢活性已成为一个热门研究课题。在此,我们通过自组装策略将AgS量子点助催化剂锚定在g-CN表面,成功制备了一种具有优异光催化性能的新型零维/二维(0D/2D)异质结纳米复合材料(表示为AgS量子点(QDs)/g-CN)。平均粒径约为5.8 nm的AgS量子点均匀且紧密地修饰在g-CN上。负载量为0.5 wt% AgS量子点的AgS QDs/g-CN复合材料在405 nm处实现了最高产氢速率471.1 μmol·g·h,表观量子效率(AQE)为1.48%。如此显著的产氢活性远远超过了未掺杂的g-CN和AgS纳米颗粒(NPs)/g-CN。此外,它是以Pt作为助催化剂的Pt/g-CN活性的2.04倍。光催化性能的增强归因于量子尺寸效应导致的AgS量子点能带展宽以及g-CN与AgS量子点助催化剂之间便捷有效的电荷转移。进一步提出了光催化析氢活性增强的机理。本研究表明,基于半导体的量子点是光催化中优异助催化剂的有力候选者。