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能带结构匹配的构筑策略用于制备高效光催化剂,以应用于太阳能燃料生成和环境修复领域。

Band structure alignment transitioning strategy for the fabrication of efficient photocatalysts for solar fuel generation and environmental remediation applications.

机构信息

Department of Chemistry, College of Natural Sciences, Yeungnam University, 280 Daehak-Ro, Gyeongsan, Gyeongbuk 38541, Republic of Korea..

Department of Chemistry, College of Natural Sciences, Yeungnam University, 280 Daehak-Ro, Gyeongsan, Gyeongbuk 38541, Republic of Korea.

出版信息

J Colloid Interface Sci. 2022 Dec;627:247-260. doi: 10.1016/j.jcis.2022.07.031. Epub 2022 Jul 8.

Abstract

Indium hydroxide (In(OH)) and indium oxide (InO) have proven to be efficient catalysts for photocatalytic water-splitting reactions to produce hydrogen (H) and for organic pollutant degradation applications. However, the limited optical absorption features of indium-based nanostructures have restricted their practical applications. In this study, we have successfully designed indium hydroxide- and indium oxide-loaded metal sulfide (cadmium sulfide, CdS) heterostructures as excellent photocatalytic systems for photocatalytic hydrogen evolution and tetracycline hydrochloride pollutant degradation reactions. In this system, In(OH) and InO established Type-I and S-scheme heterojunctions, respectively, with CdS, resulting in superior charge separation properties and outstanding photocatalytic activity. Specifically, the rational and appropriate design of the aforementioned indium-based heterostructures promoted the separation of photoexcited charge carriers via Type-I and S-scheme paths. Accordingly, enhanced photocatalytic H evolution activities of 9.58 and 14.98 mmol·g·h were achieved for CdS-In(OH) and CdS-InO, respectively. Furthermore, the highest degradation efficiency of CdS-InO was ∼ 90%, which was higher than those of CdS-In(OH) (72%) and bare CdS nanorods (51%). Therefore, the results of this study provide an opportunity to enhance the catalytic activities of heterostructured photocatalytic systems by utilizing the strategy of transitioning band structure alignment from the Type-I to the S-scheme.

摘要

氢氧化铟(In(OH))和氧化铟(InO)已被证明是用于光催化水分解反应以产生氢气和用于有机污染物降解应用的有效催化剂。然而,基于铟的纳米结构的有限光吸收特性限制了它们的实际应用。在这项研究中,我们成功设计了负载有氢氧化铟和氧化铟的金属硫化物(硫化镉,CdS)异质结构,作为用于光催化产氢和盐酸四环素污染物降解反应的优异光催化系统。在该系统中,In(OH)和 InO 分别与 CdS 建立了 Type-I 和 S 型异质结,从而具有优异的电荷分离性能和出色的光催化活性。具体而言,上述基于铟的异质结构的合理和适当设计通过 Type-I 和 S 型途径促进了光激发载流子的分离。因此,CdS-In(OH) 和 CdS-InO 的光催化 H 演化活性分别达到了 9.58 和 14.98 mmol·g·h。此外,CdS-InO 的最高降解效率约为 90%,高于 CdS-In(OH)(72%)和 bare CdS 纳米棒(51%)。因此,本研究的结果为通过从 Type-I 到 S 型的能带结构排列转变策略来提高异质结构光催化系统的催化活性提供了机会。

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