Precursor-driven defect engineering in CdS photocatalyst: Influence of sulfur sources on structure, charge dynamics, and solar-light-driven photocatalytic performance

IF 5.9 3区 化学 Q1 CHEMISTRY, INORGANIC & NUCLEAR
Inorganic Chemistry Communications Pub Date : 2026-04-01 Epub Date: 2026-02-08 DOI:10.1016/j.inoche.2026.116323
Teeredech Senasu , Suwat Nanan
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引用次数: 0

Abstract

The application of cadmium sulfide (CdS) photocatalyst for practical wastewater treatment in the photocatalysis field is strictly limited by the main disadvantages of ultrafast charge-carrier recombination rate and extensive photo-corrosion under solar exposure, making the CdS less than ideal for large-scale lifetime potentials and translatability. Although recent literature attempts to remedy such concerns with complicated heterojunction construction or elemental doping, such methods increase synthetic intricacies making real-world implementation impossible. On the other hand, limited focus has been placed on the precursor sulfur source to create the desired defects, crystallite formations, and charge transfer mechanisms despite its fundamental research toward tuning photocatalyst performance. Thus, in the present paper, we explore the precursory sulfur source during the synthetic step to demonstrate a structure-function relationship across two distinct precursors of surfer (S) namely sodium sulfide (CdS-SS) and thiourea (CdS-TU). The finding shows that the CdS-TU photocatalyst boasts superior long-range crystallinity while the CdS-SS photocatalyst provides a mesoporous structure abundant in advantageous sulfur-vacancy defects. Interestingly, the CdS-SS exhibits greatly quenched photoluminescence emission which corelates well with the exceptional solar-driven photocatalytic performance of 99% degradation of azo dyes, Reactive Red 141 (RR141) dye and Congo Red (CR) dye, together with 90% detoxification of ofloxacin (OFL) antibiotic. The prepared CdS-SS photocatalyst provides the enhanced first-order rate constant, about three times higher than that detected from the CdS-TU photocatalyst. Trapping experiment demonstrates that photogenerated holes (h+) are the dominant reactive species involved in removal of the pollutant. The prepared CdS-SS retains its promising photoactivity with the original morphology after five cycles of use. This paper demonstrates the precursor-based defect engineering strategy to fabricate a promising solar-driven CdS photocatalyst for environmental application.

Abstract Image

CdS光催化剂前驱体驱动缺陷工程:硫源对结构、电荷动力学和太阳能光驱动光催化性能的影响
硫化镉(cd)光催化剂在实际废水处理中的应用受到了光催化领域的严格限制,其主要缺点是电荷-载流子复合速率超快和在太阳照射下广泛的光腐蚀,使得CdS不太理想的大规模寿命电位和可译性。尽管最近的文献试图用复杂的异质结结构或元素掺杂来解决这些问题,但这些方法增加了合成的复杂性,使现实世界的实现变得不可能。另一方面,尽管前驱体硫源在调整光催化剂性能方面进行了基础研究,但人们对其产生所需缺陷、晶体形成和电荷转移机制的关注有限。因此,在本文中,我们在合成步骤中探索了前体硫源,以证明两种不同的冲浪剂(S)前体即硫化钠(CdS-SS)和硫脲(CdS-TU)之间的结构-功能关系。结果表明,CdS-TU光催化剂具有优异的远端结晶度,而CdS-SS光催化剂具有丰富的中孔结构,具有有利的硫空位缺陷。有趣的是,CdS-SS表现出极大的猝灭光致发光,这与优异的太阳能驱动光催化性能密切相关,该性能可降解偶氮染料、活性红141 (RR141)染料和果果红(CR)染料99%,并可解毒氧氟沙星(OFL)抗生素90%。制备的CdS-SS光催化剂提供了提高的一级速率常数,比CdS-TU光催化剂高约3倍。捕集实验表明,光生空穴(h+)是参与污染物去除的主要反应物质。经5次循环使用后,所制备的CdS-SS仍具有良好的光活性。本文展示了基于前驱体的缺陷工程策略,以制造一种有前途的环境应用太阳能驱动CdS光催化剂。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Inorganic Chemistry Communications
Inorganic Chemistry Communications 化学-无机化学与核化学
CiteScore
5.50
自引率
7.90%
发文量
1013
审稿时长
53 days
期刊介绍: Launched in January 1998, Inorganic Chemistry Communications is an international journal dedicated to the rapid publication of short communications in the major areas of inorganic, organometallic and supramolecular chemistry. Topics include synthetic and reaction chemistry, kinetics and mechanisms of reactions, bioinorganic chemistry, photochemistry and the use of metal and organometallic compounds in stoichiometric and catalytic synthesis or organic compounds.
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