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硅烷和叔胺键合的等离子体金纳米棱镜的近红外驱动光催化产氢

NIR-Driven Photocatalytic Hydrogen Production by Silane- and Tertiary Amine-Bound Plasmonic Gold Nanoprisms.

作者信息

Joshi Gayatri, Saha Avishek, Dutta Arnab, Khatua Saumyakanti

机构信息

Chemistry Discipline, Indian Institute of Technology Gandhinagar, Palaj, Gujarat 382355, India.

CSIR-Central Scientific Instruments Organization (CSIR-CSIO), Chandigarh 160030, India.

出版信息

ACS Appl Mater Interfaces. 2022 Aug 31;14(34):38815-38823. doi: 10.1021/acsami.2c10152. Epub 2022 Aug 18.

DOI:10.1021/acsami.2c10152
PMID:35980736
Abstract

Near-infrared (NIR) photon-driven H production from water is regarded as one of the best routes for establishing a sustainable hydrogen-based energy economy. Here, we have developed a gold nanoprism-based photocatalytic assembly, rationally capped with an amine and a silane ligand pair, which exhibited an excellent H production rate (146 μL mg h) in neutral water while achieving an absolute incident photon-to-hydrogen conversion efficiency of 0.53%. An array of spectroscopic and microscopic experiments unravel that the amine ligand scavenges the hot hole while the silane aids the H production via hydrolysis during the photocatalysis on the plasmon surface. This photocatalytic H production reactivity can be retained for multiple cycles following the replenishment of amine and silane. Hence, this photocatalytic assembly can set up the template for a large-scale NIR-driven H production unit.

摘要

近红外(NIR)光子驱动水制氢被认为是建立可持续氢基能源经济的最佳途径之一。在此,我们开发了一种基于金纳米棱镜的光催化组件,通过合理地用胺和硅烷配体对进行封端,该组件在中性水中表现出优异的产氢速率(146 μL mg⁻¹ h⁻¹),同时实现了0.53%的绝对入射光子到氢的转换效率。一系列光谱和显微镜实验表明,在等离子体表面的光催化过程中,胺配体捕获热空穴,而硅烷通过水解辅助产氢。在补充胺和硅烷后,这种光催化产氢反应性可以保留多个循环。因此,这种光催化组件可为大规模近红外驱动的制氢装置建立模板。

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