设计串联s -方案光催化系统:机理见解,表征技术和应用

IF 13.5 2区 化学 Q1 CHEMISTRY, PHYSICAL
Rohit Kumar , Anita Sudhaik , Aftab Asalam Pawaz Khan , Van-Huy Nguyen , Archana Singh , Pardeep Singh , Sourbh Thakur , Pankaj Raizada
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引用次数: 0

摘要

串联s型异质结已成为光催化领域一个极具前景的创新,为环境修复提供了有效的解决方案。与传统的Z-scheme或ii型光催化剂不同,S-scheme结构选择性地保留了积极参与氧化还原反应的高能光载流子。这种独特的机制增强了电荷分离,增强了内部电场,增强了光吸收。但是,s格式的单结存在量子效率低的问题。因此,利用s -方案设计多组分体系可以有效地提高光催化性能。串联s方案系统由多个具有交错能带位置的半导体/材料组成,以创建逐步或定向电荷转移机制。这种阶梯式电位梯度负责更强的电荷分离,光吸收,氧化还原能力,稳定性和整体光催化活性。本文对串联s方案异质结的原理进行了深入的概述,讨论了通过半导体配对、共催化剂的添加和介质的包含来设计串联s方案异质结,以实现最大的电荷迁移率和最小的重组。探讨了串联s型异质结的各种合成途径以及动力学和热力学。讨论了一系列先进的表征工具,包括密度泛函理论(DFT)模拟,原位x射线光电子能谱(XPS),瞬态吸收光谱(TAS),光致发光(PL)和电化学阻抗谱(EIS)研究,这些研究共同提供了对电子行为和界面动力学的有价值的见解。讨论了这些异质结在二氧化碳还原、H2演化和有机污染物降解等主要领域的应用。虽然潜力是显而易见的,但复杂的合成过程、材料稳定性和可扩展性等挑战仍然需要解决。为了克服这些局限性,本文提出了未来的研究路径。总的来说,串联S-scheme异质结是构建高效和可持续光催化技术的绝佳途径。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Designing tandem S-scheme photo-catalytic systems: Mechanistic insights, characterization techniques, and applications

Designing tandem S-scheme photo-catalytic systems: Mechanistic insights, characterization techniques, and applications
Tandem S-scheme heterojunctions have emerged as a highly promising innovation in photocatalysis, offering an effective solution for environmental remediation. Unlike traditional Z-scheme or type-II photocatalysts, the S-scheme architecture selectively retains high-energy photocarriers that actively participate in redox reactions. This unique mechanism enhances charge separation, strengthens internal electric fields, and enhance light absorption. However, the single junction of S-scheme suffers from low quantum efficiency. Therefore, engineering a multicomponent system with S-scheme effectively improve the photocatalytic properties. Tandem S-scheme systems consist of multiple semiconductors/materials with staggered energy band positions to create a stepwise or directional charge transferal mechanism. This stepwise potential gradient is responsible for more enhanced charge separation, light absorption, redox ability, stability, and overall photocatalytic activity. This article provides an in-depth overview of the principles governing tandem S-scheme heterojunctions, discussing the design of tandem S-scheme heterojunctions through semiconductor pairing, co-catalyst addition, and mediator inclusion for maximum charge mobility and minimum recombination. The various synthesis pathways are explored along with the kinetics and thermodynamics of tandem S-scheme heterojunction. A range of advanced characterization tools, including density functional theory (DFT) simulations, in-situ X-ray photoelectron spectroscopy (XPS), transient absorption spectroscopy (TAS), photoluminescence (PL), and electrochemical impedance spectroscopy (EIS) studies are discussed, which together offer valuable insight into electronic behaviours and interfacial dynamics. Applications of these heterojunctions are discussed across major domains such as carbon dioxide reduction, H2 evolution, and degradation of organic pollutants. While the potential is clear, challenges such as complex synthesis procedures, material stability, and scalability still need to be addressed. To overcome the limitations, the article suggests future research paths. Overall, tandem S-scheme heterojunctions stand out as an excellent approach for building efficient and sustainable photocatalytic technologies.
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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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