Architecting ternary heteronanocomposites Bi2S3/BiOCl@In2S3 and Bi2S3/BiOBr@In2S3 for photocatalytic detoxification of organoarsenic compound

IF 11.4 1区 工程技术 Q1 ENGINEERING, CHEMICAL
Namasivayam Dhenadhayalan
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Abstract

Ternary heteronanocomposites Bi2S3/BiOCl@In2S3 and Bi2S3/BiOBr@In2S3 were designed as potent and sustainable photocatalysts and demonstrated their visible light-driven detoxification of the organoarsenic pollutant (carbarsone). A facile wet chemical-based synthesis method was applied to fabricate ternary nanocomposites, and their structural properties were analyzed using several analytical techniques (FETEM, XRD, XPS, etc.). In both nanocomposites, the monodispersed nanorod-structured Bi2S3 and nanosheet-structured In2S3, BiOCl, and BiOBr materials were combined to form multi-structured nanocomposites. Both nanocomposites exhibited good photocurrent responses and lower band gap energies that led to their use as photocatalysts for the degradation of carbarsone. As expected, Bi2S3/BiOCl@In2S3 and Bi2S3/BiOBr@In2S3 displayed excellent catalytic performance, achieving carbarsone degradation within 34 and 20 min, with corresponding higher rate constants of 0.1022 and 0.1572 min1, respectively. This enhanced photocatalytic activity arose due to synergistic double Z-scheme heterojunctions originating based on the band energies within nanocomposites, which can increase the inhibition of the photogenerated electrons and holes pair’s recombination and relatively maintain the strong catalytic redox properties. Bi2S3 acts as an interfacial mediator for effective charge separation, whereas In2S3 and BiOCl/BiOBr feasibly generate hydroxyl radical reactive species. Mass spectral analysis was employed to prove the oxidative pathway mechanism wherein hydroxyl radicals effectively degrade carbarsone. Furthermore, these nanocomposites displayed strong structural stability along with sustaining catalytic performance, and insignificant loss during the recycling processes. The integration of visible-light sensitivity with strong oxidative capabilities establishes Bi2S3, In2S3, BiOCl, and BiOBr as excellent candidates for photocatalytic detoxification of pollutants.

Abstract Image

构建三元杂烷复合材料Bi2S3/BiOCl@In2S3和Bi2S3/BiOBr@In2S3光催化解毒有机砷化合物
Bi2S3/BiOCl@In2S3和Bi2S3/BiOBr@In2S3三元杂烷复合材料被设计为有效的、可持续的光催化剂,并证明了它们在可见光下对有机砷污染物(碳巴松)的解毒作用。采用简易湿法化学合成法制备了三元复合纳米材料,并利用FETEM、XRD、XPS等多种分析技术对其结构性能进行了分析。在这两种纳米复合材料中,单分散纳米棒结构的Bi2S3和纳米片结构的In2S3、BiOCl和BiOBr材料被组合成多结构的纳米复合材料。这两种纳米复合材料都表现出良好的光电流响应和较低的带隙能,这使得它们可以作为降解碳巴酮的光催化剂。正如预期的那样,Bi2S3/BiOCl@In2S3和Bi2S3/BiOBr@In2S3表现出优异的催化性能,在34分钟和20分钟内实现了对碳巴松的降解,相应的速率常数分别为0.1022和0.1572 min−1。这种增强的光催化活性是由于纳米复合材料内部基于能带产生的协同双Z-scheme异质结,它可以增加对光生电子和空穴对重组的抑制,并相对保持强的催化氧化还原性能。Bi2S3作为有效电荷分离的界面介质,而In2S3和BiOCl/BiOBr可产生羟基自由基反应物质。质谱分析证实了羟基自由基有效降解碳巴酮的氧化途径机制。此外,这些纳米复合材料具有较强的结构稳定性和持续的催化性能,并且在回收过程中损失较小。可见光敏感性与强氧化能力的结合使Bi2S3、In2S3、BiOCl和BiOBr成为光催化解毒污染物的优秀候选者。
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来源期刊
npj Clean Water
npj Clean Water Environmental Science-Water Science and Technology
CiteScore
15.30
自引率
2.60%
发文量
61
审稿时长
5 weeks
期刊介绍: npj Clean Water publishes high-quality papers that report cutting-edge science, technology, applications, policies, and societal issues contributing to a more sustainable supply of clean water. The journal's publications may also support and accelerate the achievement of Sustainable Development Goal 6, which focuses on clean water and sanitation.
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