Construction of 3D hollow NiCo-layered double hydroxide nanostructures for high-performance industrial overall seawater electrolysis

氢氧化物 海水 电解 纳米结构 材料科学 化学工程 纳米技术 化学 地质学 电极 工程类 海洋学 物理化学 电解质
作者
Lili Wang,Di Wang,Linlin Zheng,Xiaorong Song,Ya Yan,Jiahui Li,Shuheng Tian,Maolin Wang,Mi Peng,Zhaohui Yin,Hong Wang,Junqing Xu,Bowen Cheng,Zhen Yin,Ding Ma
出处
期刊:Nano Research [Springer Science+Business Media]
卷期号:17 (11): 9472-9482 被引量:24
标识
DOI:10.1007/s12274-024-6850-8
摘要

Green hydrogen production via seawater electrolysis holds a great promise for carbon-neutral energy production. However, the development of efficient and low-cost bifunctional electrocatalysts for seawater electrolysis at an industrial level remains a significant challenge. Herein, we report a facile approach based on one-dimensional (1D) cobalt carbonate hydroxide (CCH) nanoneedles (NNs) as skeleton and zeolitic imidazolate framework-67 (ZIF-67) as a sacrificial template to construct a self-supported NiCo layered double hydroxide (NiCo LDH) heterostructure nanocage (CCH@NiCo LDH) anchoring on the carbon felt (CF). The NiCo LDHs have hollow features, consisting of ultrathin layered hydroxide nanosheets. Benefiting from the structural advantages, unique carbon substrate and desirable composition, three-dimensional (3D) NiCo LDH nanocages exhibit superior performance as a bifunctional catalyst for overall seawater splitting at an industrial level and good corrosion resistance in alkaline media. In the alkaline seawater (1 M KOH + 0.5 M NaCl), it exhibits low overpotentials of 356 mV for hydrogen evolution reaction (HER) and 433 mV for oxygen evolution reaction (OER) at 400 mA·cm−2, much better than most of reported non-noble metal catalysts. Consequently, the obtained CF electrode loading of CCH@NiCo LDH exhibits outstanding performance as anodes and cathodes for overall alkaline seawater splitting, with remarkably low cell voltages of 1.56 and 1.89 V at current densities of 10 and 400 mA·cm−2, respectively. Moreover, the robust stability of 100 h is also demonstrated at above 200 mA·cm−2 in alkaline seawater. Our present work demonstrates significant potential for constructing effective cost-efficient and non-noble-metal bifunctional electrocatalyst and electrode for industrial seawater splitting.
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