Hu Shu, Yi Jun, Zhang Yue-Jiao, Lin Kai-Qiang, Liu Bi-Ju, Chen Liang, Zhan Chao, Lei Zhi-Chao, Sun Juan-Juan, Zong Cheng, Li Jian-Feng, Ren Bin
State Key Laboratory of Physical Chemistry of Solid Surfaces, Collaborative Innovation Center of Chemistry for Energy Materials (i-ChEM), Department of Chemistry, College of Chemistry and Chemical Engineering, Xiamen University, 361005, Xiamen, China.
Nat Commun. 2020 May 20;11(1):2518. doi: 10.1038/s41467-020-16405-3.
Underpotential deposition offers a predominant way to tailor the electronic structure of the catalytic surface at the atomic level, which is key to engineering materials with a high activity for (electro)catalysis. However, it remains challenging to precisely control and directly probe the underpotential deposition of a (sub)monolayer of atoms on nanoparticle surfaces. In this work, we in situ observe silver electrodeposited on gold nanocrystals surface from sub-monolayer to one monolayer by designing a highly sensitive electrochemical dark field scattering setup. The spectral variation is used to reconstruct the optical "cyclic voltammogram" of every single nanocrystal for understanding the underpotential deposition process on nanocrystals, which cannot be achieved by any other methods but are essential for creating novel nanomaterials.
欠电位沉积提供了一种在原子水平上定制催化表面电子结构的主要方法,这是设计具有高(电)催化活性材料的关键。然而,精确控制并直接探测纳米颗粒表面上(亚)单层原子的欠电位沉积仍然具有挑战性。在这项工作中,我们通过设计一种高度灵敏的电化学暗场散射装置,原位观察了银在金纳米晶体表面从亚单层到单层的电沉积过程。利用光谱变化来重建每个单个纳米晶体的光学“循环伏安图”,以了解纳米晶体上的欠电位沉积过程,这是其他任何方法都无法实现的,但对于创造新型纳米材料至关重要。