4.8 Article

Rich atomic interfaces between sub-1 nm RuOx clusters and porous Co3O4 nanosheets boost oxygen electrocatalysis bifunctionality for advanced Zn-air batteries

期刊

ENERGY STORAGE MATERIALS
卷 32, 期 -, 页码 20-29

出版社

ELSEVIER
DOI: 10.1016/j.ensm.2020.06.015

关键词

Zn-air battery; Bifunctional electrocatalyst; RuOx cluster; Ru-O-Co bond; Atomic interface

资金

  1. National Natural Science Foundation of China [51802152]
  2. National Key R&D Program of China [2018YFB0905400]
  3. Natural Science Foundation of Jiangsu Province of China [BK20170974]
  4. Priority Academic Program Development of Jiangsu Higher Education Institutions

向作者/读者索取更多资源

The practical use of Zn-air batteries (ZABs) is strongly dependent on the availability of bifunctional oxygen electrocatalysts that should have high activity and durability for both oxygen evolution/reduction reactions (OER/ORR) in alkaline solution. Herein, we report the design of a new Ru-based bifunctional catalyst characterized with rich atomic interfaces through the in-situ growth of sub-lam RuOx clusters on the surface of porous Co3O4 nanosheets with 4.1 wt% Ru loaded. Such unique architecture ensures the creation of high-energy interfacial Ru-O-Co bond that allows fine tuning of the electronic structure of both Ru and Co. The as-prepared catalyst exhibits superior oxygen electrocatalysis bifunctionality, indicated by an ultralow potential gap of 0.71 V between the potential of OER at 10 mA cm(-2) (1.51 V) and the half-wave potential for ORR (0.80 V). Remarkably, rechargeable ZAB with such electrocatalyst demonstrates not only high rate performance (50 mA cm(-2)) and power density (150 mW cm(-2)), but also superior round-trip efficiency (68.4%, after 250 h). X-ray photoelectron and Raman spectroscopy reveal that the active sites for ORR/OER are mainly the unsaturated trivalence Ru in RuOx clusters, and the formed interfacial Ru-O-Co bond can avoid the dissolution of RuOx in alkaline electrolyte, holding great potential in implementation of long-life rechargeable ZABs.

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