Controllable synthesis of a self-assembled ultralow Ru, Ni-doped Fe2O3 lily as a bifunctional electrocatalyst for large-current-density alkaline seawater electrolysis

电催化剂 过电位 双功能 析氧 电解 分解水 催化作用 材料科学 化学工程 无机化学 电解质 碱性水电解 电解水 双功能催化剂 电极 电化学 化学 有机化学 物理化学 工程类 光催化
作者
Tong Cui,Xuejun Zhai,Lili Guo,Jingqi Chi,Yu Zhang,Jiawei Zhu,Xuemei Sun,Lei Wang
出处
期刊:Chinese Journal of Catalysis [China Science Publishing & Media Ltd.]
卷期号:43 (8): 2202-2211 被引量:80
标识
DOI:10.1016/s1872-2067(22)64093-2
摘要

Highly efficient and stable bifunctional electrocatalysts that can be used for large-current-density electrolysis of alkaline seawater are highly desirable for carbon-neutral economies, but their facile and controllable synthesis remains a challenge. Here, self-assembled ultralow Ru, Ni-doped Fe2O3 with a lily shaped morphology was synthesized on iron foam (RuNi-Fe2O3/IF) via a facile one-step hydrothermal process, in which the intact lily shaped RuNi-Fe2O3/IF was obtained by adjusting the ratio of Ru/Ni. Benefitting from the Ru/Ni chemical substitution, the as-synthesized RuNi-Fe2O3/IF can act as free-standing dual-function electrodes that are applied to electrocatalysis for the hydrogen evolution (HER) and oxygen evolution reactions (OER) in 1.0 mol L−1 KOH, requiring an overpotential of 75.0 mV to drive 100 mA cm−2 for HER and 329.0 mV for OER. Moreover, the overall water splitting catalyzed by RuNi-Fe2O3/IF only demands ultralow cell voltages of 1.66 and 1.73 V to drive 100 mA cm−2 in 1.0 mol L−1 KOH and 1.0 mol L−1 KOH seawater electrolytes, respectively. The electrodes show remarkable long-term durability, maintaining current densities exceeding 100 mA cm−2 for more than 100 h and thus outperforming the two-electrode system composed of noble catalysts. This work provides an efficient, economical method to synthesize self-standing bifunctional electrodes for large-current-density alkaline seawater electrolysis, which is of significant importance for ecological protection and energy exploitation.
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