The synergistic effect of Ni–NiMo4N5 heterointerface construction and Fe-doping enables active and durable alkaline water splitting at industrial current density†

IF 9.5 2区 材料科学 Q1 CHEMISTRY, PHYSICAL Journal of Materials Chemistry A Pub Date : 2025-02-28 DOI:10.1039/D5TA00038F
Yaling Zhao, Jinsheng Li, Kai Li, Liang Liang, Jianbing Zhu, Meiling Xiao, Changpeng Liu and Wei Xing
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Abstract

Alkaline anion-exchange membrane water electrolysis (AEMWE) is hailed as a promising approach to green hydrogen production due to its cost-effectiveness and high compatibility with intermittent renewable electricity, yet its practical implementation is hindered by the lack of active and durable bifunctional water-splitting electrocatalysts. Here, we developed a heterogeneous NiFeMo-based catalyst with abundant metal–metal nitride heterostructures towards efficient and durable water electrolysis. The heterostructure not only leads to a smaller work function (Φ) for accelerating the electron transfer process, but also tailors the adsorption–desorption behavior of intermediates due to the modified electronic states. As a result, the optimal NiFeMo-based catalyst significantly improves the water-splitting performance with an ultra-low overpotential of 68 and 228 mV at 100 mA cm−2 for alkaline hydrogen evolution reaction (HER) and oxygen evolution reaction (OER), respectively. When assembled in an AEM water electrolyzer, the catalyst achieves a current density of 500 and 1000 mA cm−2 at a low voltage of 1.620 and 1.753 V, respectively. More importantly, it can stably operate over 1630 hours at 500 mA cm−2, demonstrating its superior long-term stability. This work not only affords a high-performance bifunctional electrocatalyst for AEMWE, but also provides a multi-faceted structural regulation strategy to tailor the catalytic properties of heterogeneous electrocatalysts.

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Ni-NiMo4N5异质界面的构建和fe掺杂的协同效应使得在工业电流密度下碱性水的活性和持久性得以实现
碱性阴离子交换膜电解(AEMWE)因其成本效益和与间歇性可再生电力的高兼容性而被誉为一种有前途的绿色制氢方法,但其实际实施受到缺乏活性和耐用的双功能水分解电催化剂的阻碍。在这里,我们开发了一种基于nifemo的多相催化剂,具有丰富的金属-金属氮化物异质结构,用于高效耐用的水电解。异质结构不仅导致了更小的功函数(Φ),加速了电子转移过程,而且由于电子态的改变,中间体的吸附-解吸行为也有所改变。结果表明,优化后的nifemo基催化剂在100 mA cm−2下的过电位分别为68 mV和228 mV,显著提高了碱性析氢反应(HER)和析氧反应(OER)的裂解性能。当在AEM水电解槽中组装时,催化剂在1.620和1.753 V的低电压下分别达到500和1000 mA cm - 2的电流密度。更重要的是,它可以在500毫安厘米−2下稳定运行超过1630小时,显示出其优越的长期稳定性。这项工作不仅为AEMWE提供了一种高性能的双功能电催化剂,而且为多相电催化剂的催化性能提供了多方位的结构调控策略。
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来源期刊
Journal of Materials Chemistry A
Journal of Materials Chemistry A CHEMISTRY, PHYSICAL-ENERGY & FUELS
CiteScore
19.50
自引率
5.00%
发文量
1892
审稿时长
1.5 months
期刊介绍: The Journal of Materials Chemistry A, B & C covers a wide range of high-quality studies in the field of materials chemistry, with each section focusing on specific applications of the materials studied. Journal of Materials Chemistry A emphasizes applications in energy and sustainability, including topics such as artificial photosynthesis, batteries, and fuel cells. Journal of Materials Chemistry B focuses on applications in biology and medicine, while Journal of Materials Chemistry C covers applications in optical, magnetic, and electronic devices. Example topic areas within the scope of Journal of Materials Chemistry A include catalysis, green/sustainable materials, sensors, and water treatment, among others.
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