| Literature DB >> 30536845 |
Guihua Liu1, Jingde Li1, Jing Fu1, Gaopeng Jiang1, Gregory Lui1, Dan Luo1, Ya-Ping Deng1, Jing Zhang1, Zachary P Cano1, Aiping Yu1, Dong Su2, Zhengyu Bai3, Lin Yang3, Zhongwei Chen1.
Abstract
The highly oxidative operating conditions of rechargeable zinc-air batteries causes significant carbon-support corrosion of bifunctional oxygen electrocatalysts. Here, a new strategy for the catalyst support design focusing on oxygen vacancy (OV)-rich, low-bandgap semiconductor is proposed. The OVs promote the electrical conductivity of the oxide support, and at the same time offer a strong metal-support interaction (SMSI), which enables the catalysts to have small metal size, high catalytic activity, and high stability. The strategy is demonstrated by successfully synthesizing ultrafine Co-metal-decorated 3D ordered macroporous titanium oxynitride (3DOM-Co@TiOx Ny ). The 3DOM-Co@TiOx Ny catalyst exhibits comparable activities for oxygen reduction and evolution reactions, but much higher cycling stability than noble metals in alkaline conditions. The zinc-air battery using this catalyst delivers an excellent stability with less than 1% energy efficiency loss over 900 charge-discharge cycles at 20 mA cm-2 . The high stability is attributed to the strong SMSI between Co and 3DOM-TiOx Ny which is verified by density functional theory calculations. This work sheds light on using OV-rich semiconductors as a promising support to design efficient and durable nonprecious electrocatalysts.Entities:
Keywords: bifunctional catalysts; metal-support interactions; oxygen evolution reaction; oxygen vacancies; zinc-air batteries
Year: 2018 PMID: 30536845 DOI: 10.1002/adma.201806761
Source DB: PubMed Journal: Adv Mater ISSN: 0935-9648 Impact factor: 30.849