Cations promoting synthesis of self-supported nanoporous silver electrode and its catalytic activity for oxygen reduction reaction
- 1. College of Material Science & Engineering, Qingdao University of Science & Technology, Qingdao, 266042, PR (China)
Description
Self-supported nanoporous metals are promising catalysts and battery materials due to their continuous channels, excellent conductivity and high surface area. In this work, we found that Cu2+ cations could promote the spontaneous formation of AgCl on Ag surface via microcell reactions. Applying a potential to the silver electrode promotes the surface enrichment of Cu2+ cations, and further speeds the formation of AgCl. After electro-reduced, AgCl was transformed to self-supported silver electrode with nanoporous structures, which shows good catalytic activity for the oxygen reduction reaction and electrochemical stability together with superior methanol tolerance property, compared to the pristine silver electrode. The approach used in this work provides an alternative way to prepare self-supported nanoporous metals.
Additional details
Identifiers
- DOI
- 10.1016/j.apsusc.2018.09.078;
- PII
- S0169433218324954;
Publishing Information
- Journal Title
- Applied Surface Science
- Journal Volume
- 464
- Journal Page Range
- p. 21-29
- ISSN
- 0169-4332
- CODEN
- ASUSEE
INIS
- Country of Publication
- Netherlands
- Country of Input or Organization
- International Atomic Energy Agency (IAEA)
- INIS RN
- 55041871
- Subject category
- S75: CONDENSED MATTER PHYSICS, SUPERCONDUCTIVITY AND SUPERFLUIDITY;
- Descriptors DEI
- CATALYSTS; CATIONS; COPPER IONS; ELECTROCHEMISTRY; ELECTRODES; METHANOL; REDOX REACTIONS; SILVER; SILVER CHLORIDES; SURFACE AREA; SURFACES; TOLERANCE
- Descriptors DEC
- ALCOHOLS; CHARGED PARTICLES; CHEMICAL REACTIONS; CHEMISTRY; CHLORIDES; CHLORINE COMPOUNDS; ELEMENTS; HALIDES; HALOGEN COMPOUNDS; HYDROXY COMPOUNDS; IONS; METALS; ORGANIC COMPOUNDS; SILVER COMPOUNDS; SILVER HALIDES; SURFACE PROPERTIES; TRANSITION ELEMENT COMPOUNDS; TRANSITION ELEMENTS
Optional Information
- Copyright
- Copyright (c) 2018 Elsevier B.V. All rights reserved.