Angstrom‐Scale Electrochemistry at Electrodes with Dimensions Commensurable and Smaller than Individual Reacting Species

Author:

Zhou Lijun1,Yang Chongyang1,Yang Xiaohui1,Zhang Jie2,Wang Cong1,Wang Wei1,Li Mengyan1,Lu Xiangchao1,Li Ke1,Yang Huiping1,Zhou Han1,Chen Jiajia1,Zhan Dongping1,Fal'ko Vladimir I.34,Cheng Jun1,Tian Zhongqun1,Geim Andre K.34,Cao Yang156ORCID,Hu Sheng156

Affiliation:

1. State Key Laboratory of Physical Chemistry of Solid Surfaces Collaborative Innovation Center of Chemistry for Energy Materials (iChEM) College of Chemistry and Chemical Engineering Xiamen University Xiamen 361005 P. R. China

2. School of Chemistry and Chemical Engineering Hunan University of Science and Technology Xiangtan 411201 P. R. China

3. Department of Physics and Astronomy the University of Manchester Manchester M13 9PL UK

4. National Graphene Institute the University of Manchester Manchester M13 9PL UK

5. Innovation Laboratory for Sciences and Technologies of Energy Materials of Fujian Province (IKKEM) Xiamen 361005 P. R. China

6. Pen-Tung Sah Institute of Micro-Nano Science and Technology Xiamen University Xiamen 361005 P. R. China

Abstract

AbstractIn nature and technologies, many chemical reactions occur at interfaces with dimensions approaching that of a single reacting species in nano‐ and angstrom‐scale. Mechanisms governing reactions at this ultimately small spatial regime remain poorly explored because of challenges to controllably fabricate required devices and assess their performance in experiment. Here we report how efficiency of electrochemical reactions evolves for electrodes that range from just one atom in thickness to sizes comparable with and exceeding hydration diameters of reactant species. The electrodes are made by encapsulating graphene and its multilayers within insulating crystals so that only graphene edges remain exposed and partake in reactions. We find that limiting current densities characterizing electrochemical reactions exhibit a pronounced size effect if reactant's hydration diameter becomes commensurable with electrodes’ thickness. An unexpected blockade effect is further revealed from electrodes smaller than reactants, where incoming reactants are blocked by those adsorbed temporarily at the atomically narrow interfaces. The demonstrated angstrom‐scale electrochemistry offers a venue for studies of interfacial behaviors at the true molecular scale.

Publisher

Wiley

Subject

General Medicine

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