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局域表面等离激元共振诱导的双金属纳米链组装。

Localized surface plasmon resonance induced assembly of bimetal nanochains.

机构信息

School of Materials Science and Engineering, Shanghai University, Shanghai 200444, PR China; Research Center of Nano Science and Technology, College of Sciences, Shanghai University, Shanghai 200444, PR China.

Research Center of Nano Science and Technology, College of Sciences, Shanghai University, Shanghai 200444, PR China.

出版信息

J Colloid Interface Sci. 2022 Feb;607(Pt 2):1888-1897. doi: 10.1016/j.jcis.2021.10.001. Epub 2021 Oct 6.

Abstract

Bimetal nanochains (NCs) are attracting increasing attention in the fields of catalysis and electrocatalysis due to the synergistic effects in electronic and optical properties, but the fabrication of bimetal NCs remains challenging. Here, we report a general strategy named "nucleation in the irradiation then growth in the dark" for the preparation of Au/M (second metal) NCs. In the irradiation stage, the localized surface plasmon resonance (LSPR) effect of Au NPs is excited to overcome the nucleation energy barrier for the deposition of second metals (Pt, Ag and Pd). In the followed dark process, the preferential growth of second metals on the existed nucleus leads to the formation of nanochain rather than the core/shell nanostructure. In the model reaction of electrocatalytic hydrogen evolution, the optimized Au/Pt NCs showed much better performance compared with the commercial Pt/C.

摘要

双金属纳米链(NCs)由于其电子和光学性能的协同效应,在催化和电催化领域引起了越来越多的关注,但双金属 NCs 的制备仍然具有挑战性。在这里,我们报道了一种通用策略,称为“光照下成核,黑暗中生长”,用于制备 Au/M(第二种金属)NCs。在光照阶段,通过激发 Au NPs 的局域表面等离子体共振(LSPR)效应来克服沉积第二种金属(Pt、Ag 和 Pd)的成核能垒。在随后的黑暗过程中,第二种金属优先在已有的核上生长,导致形成纳米链而不是核/壳纳米结构。在电催化析氢的模型反应中,优化后的 Au/Pt NCs 表现出比商业 Pt/C 更好的性能。

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