Wang Hui, Zhao Wei, Xu Cong-Hui, Chen Hong-Yuan, Xu Jing-Juan
State Key Laboratory of Analytical Chemistry for Life Science , Collaborative Innovation Center of Chemistry for Life Sciences , School of Chemistry and Chemical Engineering , Nanjing University , Nanjing 210023 , China . Email:
Chem Sci. 2019 Aug 13;10(40):9308-9314. doi: 10.1039/c9sc02804h. eCollection 2019 Oct 28.
Plasmonic photocatalysts have opened up a new direction in utilization of visible light and promoting photocatalytic efficiency. An electrochemical deposition method is reported to synthesise metal@semiconductor (M@SC) core-shell nanocrystals. Due to the strong affinity of Au atoms to S and Se reduced at negative potential, CdS, CdSe and ZnS were selectively deposited on the surface of the Au core to form a uniform shell with a clear metal/semiconductor interface, which conquered the barrier caused by the large lattice mismatch between the two components. Plasmonic effects increased the photocatalytic performance, as well as provided a chance to monitor the surface nucleation and growth. The structure formation process could be observed under dark-field microscopy (DFM) in real-time and precisely controlled the scattering color, intensity and wavelength. The proof-of-concept strategy combines the electrochemical deposition and plasmonic imaging, which provides a universal approach in controllable synthesis of core-shell heterostructures, and leads to the improvement of plasmonic photocatalysts.
等离子体光催化剂为可见光的利用和光催化效率的提升开辟了新方向。据报道,一种电化学沉积方法可用于合成金属@半导体(M@SC)核壳纳米晶体。由于金原子对在负电位下还原的硫和硒具有很强的亲和力,硫化镉、硒化镉和硫化锌被选择性地沉积在金核表面,形成具有清晰金属/半导体界面的均匀壳层,克服了两种组分之间大晶格失配所造成的障碍。等离子体效应提高了光催化性能,同时也为监测表面成核和生长提供了机会。结构形成过程可在暗场显微镜(DFM)下实时观察,并能精确控制散射颜色、强度和波长。这种概念验证策略将电化学沉积和等离子体成像相结合,为核壳异质结构的可控合成提供了一种通用方法,并有助于提升等离子体光催化剂的性能。