Silver Nanowires‐Based Flexible Gold Electrode Overcoming Interior Impedance of Nanomaterial Electrodes

Author:

Xue Hongsheng1,Shi Yacheng2,Tian Wenshuai34,Cao Meng5,Cao Houyong3,Na Zhaolin3,Jiang Ge6,Jin Zhengmu7,Lang Ming‐Fei8ORCID,Liu Yang2,Sun Jing3

Affiliation:

1. Affiliated Zhongshan Hospital of Dalian University Dalian Liaoning 116001 China

2. Department of Chemistry Beijing Key Laboratory for Analytical Methods and Instrumentation Key Lab of Bioorganic Phosphorus Chemistry and Chemical Biology of Ministry of Education Tsinghua University Beijing 100084 China

3. College of Chemical and Environmental Engineering Dalian Key Laboratory of Oligosaccharide Recombination and Recombinant Protein Modification Dalian University Dalian Liaoning 116622 China

4. College of Marine Engineering Dalian Maritime University Dalian Liaoning 116026 China

5. School of Science and Engineering The Chinese University of Hong Kong (Shenzhen) Shenzhen 518172 China

6. College of Life and Health Dalian University Dalian Liaoning 116622 China

7. Dalian Ofei Electronics CO.,LTD. Dalian Liaoning 116021 China

8. Medical College Dalian Key Laboratory of Oligosaccharide Recombination and Recombinant Protein Modification Dalian University Dalian Liaoning 116622 China

Abstract

AbstractIn the development of nanomaterial electrodes for improved electrocatalytic activity, much attention is paid to the compositions, lattice, and surface morphologies. In this study, a new concept to enhance electrocatalytic activity is proposed by reducing impedance inside nanomaterial electrodes. Gold nanodendrites (AuNDs) are grown along silver nanowires (AgNWs) on flexible polydimethylsiloxane (PDMS) support. The AuNDs/AgNWs/PDMS electrode affords an oxidative peak current density of 50 mA cm−2 for ethanol electrooxidation, a value ≈20 times higher than those in the literature do. Electrochemical impedance spectroscopy (EIS) demonstrates the significant contribution of the AgNWs to reduce impedance. The peak current densities for ethanol electrooxidation are decreased 7.5‐fold when the AgNWs are electrolytically corroded. By in situ surface‐enhanced Raman spectroscopy (SERS) and density functional theory (DFT) simulation, it is validated that the ethanol electrooxidation favors the production of acetic acid with undetectable CO, resulting in a more complete oxidation and long‐term stability, while the AgNWs corrosion greatly decreases acetic acid production. This novel strategy for fabricating nanomaterial electrodes using AgNWs as a charge transfer conduit may stimulate insights into the design of nanomaterial electrodes.

Funder

Natural Science Foundation of Liaoning Province

National Natural Science Foundation of China

Dalian Science and Technology Bureau

Publisher

Wiley

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