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Superior ultra-thin nanoporous g-C3N4 photocatalyst embedded with S quantum dots: a non-metal Z-scheme visible-light composite

机译:嵌入S量子点的超薄纳米多孔g-C3N4光催化剂:一种非金属Z型可见光复合材料

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摘要

The replacing and surpassing of some functions of traditional metal-based photocatalysts by low-cost and high-efficiency non-metal semiconductor materials have become a research hotspot in functional materials. In this paper, the ultra-thin nanoporous g-C3N4 nanosheets were successfully embedded with highly dispersed S quantum dots (S QDs) by ultrasonic-assisted in-situ growth method, which originates from the disproportionation reaction of sodium thiosulfate. The formation of the composite was proved by XRD, XPS, AFM, TEM and HRTEM and proved that S QDs with a size of 1-3.5 nm were uniformly embedded in the surface of ultra-thin nanoporous g-C3N4, in which a tight and uniform 0D/2D heterojunction structure was designed and built. Meanwhile, the photocatalytic mechanism was investigated. It showed that the tight Z-Scheme heterojunction structure formed between S QDs and g-C3N4 improved the redox activity as well as the transfer ability of photogenerated electron holes. The system exhibited excellent photocatalytic efficiency that the complete degradation of RhB was achieved within 90 min under visible-light irradiation and revealed high stability. We believe that this research is important for the development of low-cost and efficient non-metal photocatalysts.
机译:低成本、高效率的非金属半导体材料取代和超越传统金属基光催化剂的某些功能,已成为功能材料领域的研究热点。本文采用超声辅助原位生长方法,成功包埋了超薄纳米多孔g-C3N4纳米片,该方法源于硫代硫酸钠的歧化反应,成功包埋了高度分散的S量子点(S QDs)。通过XRD、XPS、AFM、TEM和HRTEM等手段证明了复合材料的形成,并证明了尺寸为1-3.5 nm的S量子点均匀地嵌入超薄纳米多孔g-C3N4表面,设计并构建了紧密均匀的0D/2D异质结结构。同时,研究了光催化机理。结果表明,S QDs与g-C3N4之间形成的紧密Z-Scheme异质结结构提高了光生电子空穴的氧化还原活性和转移能力。该系统在可见光照射下90 min内实现了RhB的完全降解,表现出优异的光催化效率,并表现出较高的稳定性。我们认为,这项研究对于开发低成本、高效率的非金属光催化剂具有重要意义。

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