用于光催化氢₂进化的有机-无机杂化材料:光致伸缩纳米复合材料与 Co(II) 氧化还原介质之间的电子穿梭

IF 3 4区 化学 Q3 CHEMISTRY, PHYSICAL
Ashil Augustin, Manova Santhosh Yesupatham, Sulakshana Shenoy, M.D. Dhileepan, Bernaurdshaw Neppolian, KARTHIKEYAN SEKAR
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引用次数: 0

摘要

在本报告中,通过一种简单的原位合成方法,开发出了一种导电聚合物封装金属氧化物光催化剂,其中聚噻吩与二氧化钛纳米颗粒结合,增强了样品对可见光的吸收,并由于空位缺陷和高导电性显著提高了电荷转移效率,最终实现了优异的 H2 生成性能。值得注意的是,通过沉积简单的氧化还原介质,H2 的产生率得到了进一步提高。Co2+ 的引入促进了价带中光生成空穴的转移,使其从 +2 氧化态转变为 +3 氧化态,从而进一步实现了氧化机制。由于光生空穴的有效转移,激子的重组率大大降低,光催化产生 H2 的速率也得到提高。有趣的是,通过利用 Ti K-edge XANES 和 EXAFS 分析,确定了合成样品中 Ti 物种的价态和局部原子结构,验证了能量位置。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Organic-Inorganic Hybrid Material for Photocatalytic H₂ Evolution: Electron Shuttling between Photoresponsive Nanocomposite and Co(II) Redox Mediator
In this report, a conductive polymer encapsulated metal oxide photocatalyst is developed through a straightforward insitu synthesis method wherein, polythiophene is incorporated with TiO2 nanoparticles which imparts enhanced visible-light absorption to the samples and significantly improves the efficiency of charge transfer resulting due to the vacancy defects and high conductivity, ultimately leading to exceptional performance in H2 production. Significantly, the rate of H2 production was enhanced even further through the deposition of simple redox mediator. The introduction of Co2+ facilitates the transfer of photogenerated holes from the valence band by its conversion from +2 to +3 oxidation state which further enables the oxidation mechanism. The recombination rate of excitons has been significantly reduced due to the efficient transfer of photogenerated holes and the rate of photocatalytic H2 production is improved. Interestingly, the valence states and local atomic structure of the Ti species in the synthesized sample were ascertained through the utilization of Ti K-edge XANES and EXAFS analysis, which validated the energy position.
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来源期刊
ChemPhotoChem
ChemPhotoChem Chemistry-Physical and Theoretical Chemistry
CiteScore
5.80
自引率
5.40%
发文量
165
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