Observing atomic layer electrodeposition on single nanocrystals surface by dark field spectroscopy

• Published in: Nature communications Vol. 11; no. 1; p. 2518
• Main Authors: 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
• Format: Journal Article
• Language: English
• Published: London Nature Publishing Group UK 20.05.2020; Nature Publishing Group; Nature Portfolio
• Subjects: 140/125; 639/638/161; 639/638/298; 639/638/440; 639/638/440/527; 639/638/542; Catalysis; Crystals; Electrochemistry; Electronic structure; Gold; Humanities and Social Sciences; Monolayers; multidisciplinary; Nanocrystals; Nanomaterials; Nanoparticles; Nanotechnology; Science; Science (multidisciplinary); Silver; Spectroscopy; Spectrum analysis; Surface properties; Underpotential deposition
• ISSN: 2041-1723; 2041-1723
• 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. Underpotential deposition (UPD) is important to modify the surface properties of nanocrystals. Here, the authors show the application of in situ electrochemical dark field spectroscopy in identifying the UPD processes of silver on different facets of gold nanocrystals at the single nanoparticle level.