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Origin of Activity and Stability Enhancement for Ag3PO4 Photocatalyst after Calcination

机译:焙烧后Ag3PO4光催化剂的活性起源和稳定性增强

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摘要

Pristine Ag3PO4 microspheres were synthesized by a co-precipitation method, followed by being calcined at different temperatures to obtain a series of calcined Ag3PO4 photocatalysts. This work aims to investigate the origin of activity and stability enhancement for Ag3PO4 photocatalyst after calcination based on the systematical analyses of the structures, morphologies, chemical states of elements, oxygen defects, optical absorption properties, separation and transfer of photogenerated electron-hole pairs, and active species. The results indicate that oxygen vacancies (VO˙˙) are created and metallic silver nanoparticles (Ag NPs) are formed by the reaction of partial Ag+ in Ag3PO4 semiconductor with the thermally excited electrons from Ag3PO4 and then deposited on the surface of Ag3PO4 microspheres during the calcination process. Among the calcined Ag3PO4 samples, the Ag3PO4-200 sample exhibits the best photocatalytic activity and greatly enhanced photocatalytic stability for photodegradation of methylene blue (MB) solution under visible light irradiation. Oxygen vacancies play a significantly positive role in the enhancement of photocatalytic activity, while metallic Ag has a very important effect on improving the photocatalytic stability. Overall, the present work provides some powerful evidences and a deep understanding on the origin of activity and stability enhancement for the Ag3PO4 photocatalyst after calcination.
机译:通过共沉淀法合成了原始的Ag3PO4微球,然后在不同的温度下煅烧以获得一系列煅烧的Ag3PO4光催化剂。这项工作旨在基于对结构,形态,元素化学状态,氧缺陷,光吸收特性,光生电子-空穴对的转移和转移的系统分析,来研究煅烧后Ag3PO4光催化剂的活性和稳定性增强的起源,和活跃的物种。结果表明,通过使Ag3PO4半导体中的部分Ag + 与来自Ag3PO4的热激发电子反应,产生了氧空位(VO˙˙),并形成了金属银纳米颗粒(Ag NPs)在煅烧过程中在Ag3PO4微球的表面上沉积。在煅烧的Ag3PO4样品中,Ag3PO 4 -200样品在可见光照射下表现出最好的光催化活性,并大大增强了亚甲基蓝(MB)溶液的光降解稳定性。氧空位在增强光催化活性方面起着明显的积极作用,而金属银对提高光催化稳定性具有非常重要的作用。总体而言,目前的工作为煅烧后Ag 3 PO 4 光催化剂的活性起源和增强稳定性提供了深刻的理解。

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