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Hydrothermal Cation Exchange Enabled Gradual Evolution of Au@ZnS–AgAuS Yolk–Shell Nanocrystals and Their Visible Light Photocatalytic Applications

机译:水热阳离子交换使Au @ ZnS–AgAuS卵黄壳纳米晶体逐步演化及其可见光的光催化应用

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摘要

Yolk–shell hybrid nanoparticles with noble metal core and programmed semiconductor shell composition may exhibit synergistic effects and tunable catalytic properties. In this work, the hydrothermal cation exchange synthesis of Au@ZnS–AgAuS yolk–shell nanocrystals (Y–S NCs) with well‐fabricated void size, grain‐boundary‐architectured ZnS–AgAuS shell and in situ generated Au cocatalyst are demonstrated. Starting from the novel cavity‐free Au@AgAuS core‐shell NCs, via aqueous cation exchange reaction with Zn2+, the gradual evolution with produced Au@ZnS–AgAuS Y–S NCs can be achieved successfully. This unprecedented evolution can be reasonably explained by cation exchange initialized chemical etching of Au core, followed by the diffusion through the shell to be AgAuS and then ZnS. By hydrothermal treatment provided optimal redox environment, Au ions in shell were partially reduced to be Au NCs on the surface. The UV–vis absorption spectra evolution and visible light photocatalytic performances, including improved photodegradation behavior and photocatalytic hydrogen evolution activity, have demonstrated their potential applications. This new one‐pot way to get diverse heterointerfaces for better photoinduced electron/hole separation synergistically can be anticipated for more kinds of photocatalytic organic synthesis.
机译:具有贵金属核和程序化的半导体壳组成的卵黄壳杂化纳米颗粒可能表现出协同效应和可调的催化性能。在这项工作中,展示了具有精心制作的空隙尺寸,晶界结构的ZnS-AgAuS壳和原位生成的Au助催化剂的Au @ ZnS–AgAuS卵黄壳纳米晶体(Y–S NCs)的水热阳离子交换合成。从新颖的无腔Au @ AgAuS核壳型NCs开始,通过与Zn 2 + 的水阳离子交换反应,可以成功实现随着生产的Au @ ZnS–AgAuS Y–S NCs的逐步发展。可以通过阳离子交换初始化的Au核化学刻蚀,然后通过壳层扩散成AgAuS,然后扩散到ZnS,来合理地解释这种空前的演化。通过水热处理提供了最佳的氧化还原环境,壳中的Au离子在表面被部分还原为Au NCs。紫外可见吸收光谱的演化和可见光的光催化性能,包括改善的光降解行为和光催化的氢析出活性,都证明了它们的潜在应用。这种新型的一锅法获得多种异质界面,以协同方式更好地实现光致电子/空穴的分离,有望用于更多种类的光催化有机合成。

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