4.6 Article

Phosphorus-driven mesoporous Co3O4 nanosheets with tunable oxygen vacancies for the enhanced oxygen evolution reaction

期刊

ELECTROCHIMICA ACTA
卷 259, 期 -, 页码 962-967

出版社

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.electacta.2017.11.028

关键词

Oxygen vacancy; Cobalt oxide; Phosphorus doping; Oxygen evolution reaction

资金

  1. National Natural Science Foundation of China [21522602, 51672082, 91534202]
  2. Social Development Program of Shanghai [17DZ1200900]
  3. Program for Shanghai Youth Top-notch Talent
  4. Fundamental Research Funds for the Central Universities [222201718002]

向作者/读者索取更多资源

Uniformly and controllably introducing oxygen vacancy (Ov) into spinel electrocatalysts is still a great challenge for the oxygen evolution reaction (OER). Herein, we demonstrate the synthesis of spinel Co3O4 mesoporous nanosheets aggregation with tunable Ov by a simple phosphorus (P) doping strategy. It is found that a trade-off between Ov and electronic conductivity plays an important role in improving OER electrocatalytic activity. The optimized Co3O4-xP0.15 electrocatalyst delivers a current density of 20 mA cm(-2) in alkaline media within a small overpotential of only 338 mV, which is much lower than the corresponding Co3O4 (395 mV) and the commercial RuO2 (368 mV) catalysts. The Tafel slope is 52 mV dec(-1) and the overpotential gives negligible increase even through 8 h OER at 10 mA cm(-2). The superior OER catalytic activity is mainly attributed to the 2D mesoporous nanosheets (rich active sites) and appropriate Ov (fast electrons transfer). This work provides a simple and effective strategy to control Ov concentration in spinel electrocatalysts for enhancing water oxidation capability. (C) 2017 Elsevier Ltd. All rights reserved.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.6
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据