4.8 Article

Fabrication of Nanoporous Nickel-Iron Hydroxylphosphate Composite as Bifunctional and Reversible Catalyst for Highly Efficient Intermittent Water Splitting

期刊

ACS APPLIED MATERIALS & INTERFACES
卷 9, 期 41, 页码 35837-35846

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acsami.7b10385

关键词

NiFe hydroxylphosphate composite; water reduction and water oxidation; electrocatalysis; intermittent electrolysis; bifunctional catalyst

资金

  1. National Natural Science Foundation of China [21273144]
  2. 111 Project [B14041]
  3. Program for Chang Jiang Scholars and Innovative Research Team in University [IRT-14R33]
  4. Australian Research Council [DP160103107]

向作者/读者索取更多资源

Global-scale application of water-splitting technology for hydrogen fuel production and storage of intermittent renewable energy sources has called for the development of oxygen- and hydrogen-evolution catalysts that are inexpensive, efficient, robust, and can withstand frequent power interruptions and shutdowns. Here, we report the controlled electrodeposition of porous nickel iron hydrox-ylphosphate (NiFe-OH-PO4) nanobelts onto the surface of macroporous nickel foams (NF) as a bifunctional electrocatalyst for efficient whole-cell water electrolysis. The NiFeOH-PO4/NF electrode shows both high water oxidation and water reduction catalytic activity in alkaline solutions and is able to deliver current densities of 20 and 800 mA cm(-2) at overpotentials of merely 249 and 326 mV for oxygen-evolution reaction, current densities of 20 and 300 mA cm(-2) at overpotentials of only 135 and 208 mV for hydrogen-evolution reaction. Further, in a two-electrode water electrolytic cell, the bifunctional NiFe-OH-PO4/NF electrodes can obtain the current densities of 20 and 100 mA cm(-2) at an overall cell potential of only 1.68 and 1.91 V, respectively. Remarkably, the NiFe-OH-PO4(/)NF catalyst also represents prolonged stability under both continuous and intermittent electrolysis and can be used for oxygen evolution and hydrogen evolution reversibly without degradation.

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

4.8
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