Enhanced performance and stability of sulfite/sulfide-assisted photocatalytic fuel cell with CdS@TNTs/Ti mesh photoanode

IF 13.2 1区 工程技术 Q1 ENGINEERING, CHEMICAL Chemical Engineering Journal Pub Date : 2025-01-28 DOI:10.1016/j.cej.2025.160038
Yuxin Liu, Youxu Yu, Jinwang Li, Xun Zhu, Dingding Ye, Yang Yang, Zhefei Pan, Rong Chen, Qiang Liao
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Abstract

In this work, a Z-scheme heterojunction CdS@TNTs/Ti mesh photoanode is developed and incorporated into a photocatalytic fuel cell (PFC) with the addition of sulfite/sulfide, forming a sulfite/sulfide-assisted PFC with the CdS@TNTs/Ti mesh photoanode. Such a photoanode enhances not only the light absorption range but also the charge separation with maintaining redox potentials. The addition of sulfite/sulfide greatly improves the photoanode stability and the solution conductivity. More importantly, strong synergistic effect between the activation of sulfite/sulfide and Z-scheme heterojunction having a high intrinsic activity allows for more reactive radicals to be generated, spreads the reaction region from the photoanode interface to the entire system and suppresses the charge recombination. Thus, the CdS@TNTs/Ti mesh photoanode exhibits superior photocatalytic/photoelectrochemical performances in the presence of sulfite/sulfide. The sulfite/sulfide-assisted PFC with the Z-scheme heterojunction CdS@TNTs/Ti mesh photoanode yields the degradation efficiency, maximal power density and short current density as high as 80.25 %, 0.90 mW/cm2, and 2.58 mA/cm2, respectively, substantially exceeding the PFC without sulfite/sulfide. This work not only enhances the comprehension of the synergistic enhancement mechanism by inducing sulfite/sulfide, but also provides a promising and green choice for the development of the PFC system to efficiently remove pollutants in sewage and generate electricity concurrently.
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利用 CdS@TNTs/Ti 网状光阳极提高亚硫酸盐/硫化物辅助光催化燃料电池的性能和稳定性
在这项工作中,开发了Z-scheme异质结CdS@TNTs/Ti网状光阳极,并通过添加亚硫酸盐/硫化物将其整合到光催化燃料电池(PFC)中,形成了具有CdS@TNTs/Ti网状光阳极的亚硫酸盐/硫化物辅助PFC。这种光阳极不仅提高了光吸收范围,而且在保持氧化还原电位的情况下提高了电荷分离。亚硫酸盐/硫化物的加入大大提高了光阳极的稳定性和溶液的电导率。更重要的是,亚硫酸盐/硫化物的活化与具有高本征活性的z -图式异质结之间具有很强的协同效应,可以产生更多的活性自由基,将反应区域从光阳极界面扩展到整个体系,抑制电荷复合。因此,CdS@TNTs/Ti网状光阳极在亚硫酸盐/硫化物存在下表现出优异的光催化/光电化学性能。采用Z-scheme异质结CdS@TNTs/Ti网状光阳极的亚硫酸盐/硫化物辅助PFC的降解效率、最大功率密度和短电流密度分别高达80.25 %、0.90 mW/cm2和2.58 mA/cm2,大大超过无亚硫酸盐/硫化物的PFC。本研究不仅加深了对亚硫酸盐/硫化物诱导的协同增强机理的理解,而且为PFC系统的发展提供了一种有前景的绿色选择,以高效去除污水中的污染物并同时发电。
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来源期刊
Chemical Engineering Journal
Chemical Engineering Journal 工程技术-工程:化工
CiteScore
21.70
自引率
9.30%
发文量
6781
审稿时长
2.4 months
期刊介绍: The Chemical Engineering Journal is an international research journal that invites contributions of original and novel fundamental research. It aims to provide an international platform for presenting original fundamental research, interpretative reviews, and discussions on new developments in chemical engineering. The journal welcomes papers that describe novel theory and its practical application, as well as those that demonstrate the transfer of techniques from other disciplines. It also welcomes reports on carefully conducted experimental work that is soundly interpreted. The main focus of the journal is on original and rigorous research results that have broad significance. The Catalysis section within the Chemical Engineering Journal focuses specifically on Experimental and Theoretical studies in the fields of heterogeneous catalysis, molecular catalysis, and biocatalysis. These studies have industrial impact on various sectors such as chemicals, energy, materials, foods, healthcare, and environmental protection.
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