4.7 Article

Self-supported Al-doped cobalt phosphide nanosheets grown on three-dimensional Ni foam for highly efficient water reduction and oxidation

期刊

INORGANIC CHEMISTRY FRONTIERS
卷 6, 期 1, 页码 74-81

出版社

ROYAL SOC CHEMISTRY
DOI: 10.1039/c8qi01026a

关键词

-

资金

  1. National Natural Science Foundation of China [21421001, 21573115, 21766026]
  2. Natural Science Foundation of Tianjin [17JCYBJC17100]
  3. 111 project [B12015]
  4. Fundamental Research Funds for the Central Universities [63185015]
  5. Foundation of State Key Laboratory of High-efficiency Utilization of Coal and Green Chemical Engineering [2017-K13]

向作者/读者索取更多资源

Developing efficient non-noble-metal electrocatalysts for overall water-splitting is still a great challenge for future renewable energy conversion and storage systems. Herein, cross-linked Al-doped CoP nanosheets on three-dimensional (3D) nickel foam (Al-CoP/NF) are synthesized by a simple low-temperature phosphidation method using a CoAl layer double hydroxide precursor and exhibit high activity and good stability towards the hydrogen evolution reaction (HER) at all pH values, with low overpotentials of 51 mV (0.5 M H2SO4, pH = 0), 66 mV (1.0 M KOH, pH = 14) and 83 mV (1.0 M PBS, pH = 7) to achieve a current density of 10 mA cm(-2). In addition, this self-supported electrode shows excellent activity towards the oxygen evolution reaction (OER) in alkaline media, affording an anodic current density of 10 mA cm(-2) at an overpotential of 330 mV. As a result, Al-CoP/NF as a bifunctional electrocatalyst can afford a current density of 10 mA cm(-2) at a cell voltage of 1.63 V over a long-term overall water splitting operation in 1.0 M KOH. The remarkable catalytic performance of the self-supported Al-CoP/NF is closely associated with its outstanding structural advantages such as a 3D conductive framework, fascinating porous characteristics and Al doping. This study might open up a new route to improve the activity and durability of self-supported electrocatalysts by heteroatom doping.

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

4.7
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