具有双通道电荷转移路径的Bi2MoO6/CoOx/Au体系的构建及其对四环素的降解

IF 4.2 3区 化学 Q2 CHEMISTRY, PHYSICAL
Tongyu Han , Yigang Chen , Haifeng Shi
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引用次数: 0

摘要

在环境友好型光催化技术的发展中,提高光生电子-空穴对的分离效率是一项艰巨的挑战。本文通过光沉积的方法,将不同类型的助催化剂Au和CoOx成功地负载在Bi2MoO6 (BMO)纳米片的表面。BMO/CoOx/1.5Au三元复合材料对四环素(TC)的降解率比纯BMO提高2.75倍。光催化性能的显著提高可归因于两种助催化剂的协同作用。在Au和CoOx的辅助下,光催化体系增强了可见光吸收能力,并构建了双通道来加速电子和空穴的转移,从而抑制了光生载流子的重组。值得注意的是,该光催化剂具有优异的稳定性,在5个循环后仍能保持较高的活性。同时,光致发光分析(PL)和时间分辨光致发光光谱(TRPL)表明,该体系促进了载流子的电荷转移,延长了载流子的寿命。该研究为设计实用高效的光催化剂去除有机污染物提供了新的思路,并为构建电荷转移双通道促进电荷分离提供了新的思路。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Construction of a Bi2MoO6/CoOx/Au system with a dual-channel charge transfer path for enhanced tetracycline degradation†

Construction of a Bi2MoO6/CoOx/Au system with a dual-channel charge transfer path for enhanced tetracycline degradation†

In the development of environment-friendly photocatalytic technology, improving the separation efficiency of photogenerated electron–hole pairs is an arduous challenge. Herein, different types of cocatalysts Au and CoOx were successfully loaded on the surface of Bi2MoO6 (BMO) nanosheets through the photodeposition method. The ternary BMO/CoOx/1.5Au composite displayed an enhanced degradation rate of tetracycline (TC), which was 2.75 times higher than that of pure BMO. The significantly improved photocatalytic performance could be attributed to the synergistic effect of the two cocatalysts. With the assistance of Au and CoOx, the photocatalytic system enhanced the visible light absorption capacity and constructed dual channels to accelerate the transfer of electrons and holes, thus suppressing the recombination of photogenerated carriers. Noticeably, the photocatalyst possessed excellent stability, and could still maintain a high activity after five cycles. Meanwhile, photoluminescence analysis (PL) and time-resolved photoluminescence spectroscopy (TRPL) demonstrated that the system promoted charge transfer and prolonged the lifetime of carriers. This research provides insights into designing practical and efficient photocatalysts to remove organic pollutants and sheds new light on constructing charge transfer dual-channel for boosting charge separation.

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来源期刊
Catalysis Science & Technology
Catalysis Science & Technology CHEMISTRY, PHYSICAL-
CiteScore
8.70
自引率
6.00%
发文量
587
审稿时长
1.5 months
期刊介绍: A multidisciplinary journal focusing on cutting edge research across all fundamental science and technological aspects of catalysis. Editor-in-chief: Bert Weckhuysen Impact factor: 5.0 Time to first decision (peer reviewed only): 31 days
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