构建Bi4Ti3O12与g-C3N4偶联的无机/有机s型异质结用于光催化纯水制H2O2

IF 10.8 2区 化学 Q1 CHEMISTRY, PHYSICAL
Ke Li , Chuang Liu , Jingping Li , Guohong Wang , Kai Wang
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引用次数: 0

摘要

过氧化氢(H2O2)作为工业化学和势能载体发挥着重要作用。然而,常见的H2O2光合作用催化剂存在太阳光谱吸收受限、团聚严重、再利用困难等问题,阻碍了其广泛应用。本研究采用静电纺丝辅助自组装的方法合成了一种由g-C3N4纳米片和Bi4Ti3O12纳米纤维组成的无机/有机异质结光催化剂。Bi4Ti3O12/g- c3n4异质结能显著提高H2O2产率(1650 μmol∙g−1∙h−1),并能直接从纯水中进行有效的H2O2光合作用。性能的提高是由于S-scheme异质结中光诱导载流子的可见光吸收、电荷分离效率和氧化还原性能的增强。此外,利用原位x射线光电子能谱(ISXPS)可以研究无机/有机Bi4Ti3O12/g-C3N4异质结的S-scheme机制和动力学。本研究提出了一种设计用于太阳能驱动H2O2生产的无机/有机异质结光催化剂的新方法。下载:下载高清图片(98KB)下载:下载全尺寸图片
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Architecting Inorganic/Organic S-Scheme Heterojunction of Bi4Ti3O12 Coupling with g-C3N4 for Photocatalytic H2O2 Production from Pure Water
Hydrogen peroxide (H2O2) plays a significant role as an industrial chemical and potential energy carrier. However, common H2O2 photosynthesis catalysts face challenges such as limited solar spectrum absorption, severe agglomeration, and difficulty in reuse, hindering their widespread application. In this study, an inorganic/organic heterojunction photocatalyst comprising g-C3N4 nanosheets and Bi4Ti3O12 nanofibers is synthesized using electrospinning assisted self-assembly methods. The Bi4Ti3O12/g-C3N4 heterojunction exhibits significantly enhanced H2O2 yield of 1650 μmol∙g−1∙h−1 and efficient H2O2 photosynthesis directly from pure water. The improved performance is attributed to enhanced visible light absorption, charge separation efficiency, and boosting redox properties of photoinduced carriers in S-scheme heterojunctions. Additionally, the utilization of in situ X-ray photoelectron spectroscopy (ISXPS) enables the investigation of the S-scheme mechanism and dynamics of inorganic/organic Bi4Ti3O12/g-C3N4 heterojunctions. This research presents a novel approach for designing inorganic/organic heterojunction photocatalysts for solar-driven H2O2 production.
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来源期刊
物理化学学报
物理化学学报 化学-物理化学
CiteScore
16.60
自引率
5.50%
发文量
9754
审稿时长
1.2 months
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