光催化
铟
异质结
材料科学
氢氧化物
氧化物
硫化镉
催化作用
纳米棒
化学工程
硫化物
降级(电信)
制氢
氧化铟锡
无机化学
纳米技术
化学
光电子学
薄膜
计算机科学
冶金
电信
工程类
生物化学
作者
Rama Krishna Chava,Namgyu Son,Misook Kang
标识
DOI:10.1016/j.jcis.2022.07.031
摘要
Indium hydroxide (In(OH)3) and indium oxide (In2O3) have proven to be efficient catalysts for photocatalytic water-splitting reactions to produce hydrogen (H2) 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)3 and In2O3 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 H2 evolution activities of 9.58 and 14.98 mmol·g-1·h-1 were achieved for CdS-In(OH)3 and CdS-In2O3, respectively. Furthermore, the highest degradation efficiency of CdS-In2O3 was ∼ 90%, which was higher than those of CdS-In(OH)3 (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.
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