Park Joon Ho, Jin Seon-Mi, Lee Eunji, Ahn Hyun S
Department of Chemistry, Yonsei University 50 Yonsei-ro, Seodaemun-gu Seoul 03722 Republic of Korea
School of Materials Science and Engineering, Gwangju Institute of Science and Technology (GIST) 123 Cheomdangwagiro, Bukgu Gwangju Republic of Korea
Chem Sci. 2021 Sep 8;12(40):13557-13563. doi: 10.1039/d1sc03625d. eCollection 2021 Oct 20.
Conventional solvothermal synthesis of core-shell nanoparticles results in them being covered with surfactant molecules for size control and stabilization, undermining their practicality as electrocatalysts. Here, we report an electrochemical method for the synthesis of core-shell nanoparticles directly on electrodes, free of surfactants. By implementation of selective electrodeposition on gold cores, 1-row transition metal shells were constructed with facile and precise thickness control. This type of metal-on-metal core-shell synthesis by purely electrochemical means is the first of its kind. The applicability of the nanoparticle decorated electrodes was demonstrated by alkaline oxygen evolution catalysis, during which the Au-Ni example displayed stable catalysis with low overpotential.
传统的核壳纳米颗粒溶剂热合成法会使其表面覆盖有用于尺寸控制和稳定化的表面活性剂分子,这削弱了它们作为电催化剂的实用性。在此,我们报告了一种直接在电极上合成核壳纳米颗粒的电化学方法,该方法无需表面活性剂。通过在金核上进行选择性电沉积,构建了具有易于控制且精确厚度的单排过渡金属壳层。这种通过纯电化学手段进行的金属对金属核壳合成是首例。通过碱性析氧催化证明了纳米颗粒修饰电极的适用性,在此过程中,金 - 镍示例表现出稳定的催化作用且过电位较低。