Influence of Particle Size on Mass Transport during the Oxygen Reduction Reaction at Single Silver Particles Using Scanning Electrochemical Cell Microscopy

被引:1
作者
Salek, Samaneh [1 ]
Byers, Joshua C. [1 ]
机构
[1] Univ Quebec Montreal, Dept Chim, Montreal, PQ H3C 3P8, Canada
来源
JOURNAL OF PHYSICAL CHEMISTRY LETTERS | 2024年 / 15卷 / 33期
基金
加拿大自然科学与工程研究理事会;
关键词
ROTATING-DISK ELECTRODES; CO2; ELECTROREDUCTION; ELECTROCATALYSIS; EVOLUTION; ENTITY; NOBLE;
D O I
10.1021/acs.jpclett.4c01832
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Single entity electrochemical measurements enable insight into the electrocatalytic activity of individual particles based on composition, shape, and crystallographic orientation. In addition to structural effects, particle size can further influence electrocatalytic activity and reaction mechanisms through mass transport effects. In this work, electrodeposition was used to grow well-separated silver particles of varying sizes from 100 to 500 nm in radius. Using a multimicroscopy approach of scanning electrochemical cell microscopy combined with scanning electron microscopy, the electrocatalytic current of individual silver particles toward the oxygen reduction reaction was evaluated as a function of their size. It was found that the current density increased with decreasing particle radius, which was correlated to the mass transport of oxygen to the silver particle, demonstrating the importance of size dependent mass transport effects that can occur at the single particle level using scanning electrochemical cell microscopy and opening new opportunities for quantitative electrocatalysis measurements.
引用
收藏
页码:8494 / 8500
页数:7
相关论文
共 53 条
[1]   Evaluating Analytical Expressions for Scanning Electrochemical Cell Microscopy (SECCM) [J].
Anderson, Kamsy Lerae ;
Edwards, Martin Andrew .
ANALYTICAL CHEMISTRY, 2023, 95 (21) :8258-8266
[2]   Scanning electrochemical cell microscopy for the study of (nano)particle electrochemistry: From the sub-particle to ensemble level [J].
Bentley, Cameron L. .
ELECTROCHEMICAL SCIENCE ADVANCES, 2022, 2 (03)
[3]   Nanoscale electrochemical movies and synchronous topographical mapping of electrocatalytic materials [J].
Bentley, Cameron L. ;
Unwin, Patrick R. .
FARADAY DISCUSSIONS, 2018, 210 :365-379
[4]   Nanoscale Electrocatalysis: Visualizing Oxygen Reduction at Pristine, Kinked, and Oxidized Sites on Individual Carbon Nanotubes [J].
Byers, Joshua C. ;
Gueell, Aleix G. ;
Unwin, Patrick R. .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2014, 136 (32) :11252-11255
[5]   Voltammetric Scanning Electrochemical Cell Microscopy: Dynamic Imaging of Hydrazine Electro-oxidation on Platinum Electrodes [J].
Chen, Chang-Hui ;
Jacobse, Leon ;
McKelvey, Kim ;
Lai, Stanley C. S. ;
Koper, Marc T. M. ;
Unwin, Patrick R. .
ANALYTICAL CHEMISTRY, 2015, 87 (11) :5782-5789
[6]   High resolution mapping of oxygen reduction reaction kinetics at polycrystalline platinum electrodes [J].
Chen, Chang-Hui ;
Meadows, Katherine E. ;
Cuharuc, Anatolii ;
Lai, Stanley C. S. ;
Unwin, Patrick R. .
PHYSICAL CHEMISTRY CHEMICAL PHYSICS, 2014, 16 (34) :18545-18552
[7]   Electrocatalysis under conditions of high mass transport rate: Oxygen reduction on single submicrometer-sized Pt particles supported on carbon [J].
Chen, SL ;
Kucernak, A .
JOURNAL OF PHYSICAL CHEMISTRY B, 2004, 108 (10) :3262-3276
[8]   Probing Single-Particle Electrocatalytic Activity at Facet-Controlled Gold Nanocrystals [J].
Choi, Myunghoon ;
Siepser, Natasha P. ;
Jeong, Soojin ;
Wang, Yi ;
Jagdale, Gargi ;
Ye, Xingchen ;
Baker, Lane A. .
NANO LETTERS, 2020, 20 (02) :1233-1239
[9]   Visualization of Hydrogen Evolution at Individual Platinum Nanoparticles at a Buried Interface [J].
Gao, Rui ;
Edwards, Martin A. ;
Qiu, Yinghua ;
Barman, Koushik ;
White, Henry S. .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2020, 142 (19) :8890-8896
[10]   Drop-cast gold nanoparticles are not always electrocatalytically active for the borohydride oxidation reaction [J].
Gaudin, Lachlan F. ;
Funston, Alison M. ;
Bentley, Cameron L. .
CHEMICAL SCIENCE, 2024, 15 (19) :7243-7258