Zhu Shihu, Yang Yingxing, Zhao Mengyao, Zhao Hui, Liu Siyuan, Zheng Jinyou
State Key Laboratory of Coking Coal Resources Green Exploitation, Engineering Research Center of Advanced Functional Material Manufacturing of Ministry of Education, School of Chemical Engineering, Zhengzhou University, Zhengzhou 450001, China.
School of Mechanical and Power Engineering, Zhengzhou University, Zhengzhou 450001, China.
Nanomaterials (Basel). 2025 Jun 7;15(12):883. doi: 10.3390/nano15120883.
Hydrogen energy holds great promise for alleviating energy and environmental issues, with alkaline electrochemical water splitting being a key approach for hydrogen production. However, the high cost and limited availability of noble-metal catalysts hinder its widespread application. This study presents a novel method to fabricate a NiFeP-CoP/CF electrode. By growing CoOOH nanosheets on Co foam at low temperatures and filling the gaps between nanosheets with Ni and Fe phosphides, the prepared electrode exhibits outstanding electrocatalytic performance. For the oxygen evolution reaction (OER) in alkaline media, it requires overpotentials of only 235 mV and 290 mV to reach current densities of 10 mA cm and 100 mA cm, respectively. In the case of the hydrogen evolution reaction (HER), overpotentials of 89 mV and 172 mV are needed to achieve current densities of -10 mA cm and -100 mA cm. The NiFeP-CoP/CF-based electrolytic cell requires a cell voltage of only 1.70 V to achieve a current density of 100 mA cm for overall water splitting. Moreover, during long-term continuous operation at 100 mA cm, the overpotential for OER remains constant while that for HER decreases. The low-temperature growth of CoOOH nanosheets on Co foam provides a new strategy for large-scale electrode production applicable in electrochemical processes and pollutant degradation. Significantly, filling the nanosheet gaps with phosphides effectively enhances the electrocatalytic performance of the system. This work offers a facile and cost-effective technique for the large-scale production of metallic (oxyhydr)hydroxides for electrocatalytic water splitting, showing great potential for industrial applications.
氢能在缓解能源和环境问题方面具有巨大潜力,碱性电化学水分解是制氢的关键方法。然而,贵金属催化剂的高成本和有限可用性阻碍了其广泛应用。本研究提出了一种制备NiFeP-CoP/CF电极的新方法。通过在低温下在泡沫钴上生长CoOOH纳米片并用镍和铁磷化物填充纳米片之间的间隙,制备的电极表现出出色的电催化性能。对于碱性介质中的析氧反应(OER),分别达到10 mA cm²和100 mA cm²的电流密度仅需要235 mV和290 mV的过电位。在析氢反应(HER)的情况下,达到-10 mA cm²和-100 mA cm²的电流密度需要89 mV和172 mV的过电位。基于NiFeP-CoP/CF的电解槽在全水解中仅需1.70 V的电池电压即可达到100 mA cm²的电流密度。此外,在100 mA cm²的长期连续运行期间,OER的过电位保持恒定,而HER的过电位降低。在泡沫钴上低温生长CoOOH纳米片为适用于电化学过程和污染物降解的大规模电极生产提供了一种新策略。值得注意的是,用磷化物填充纳米片间隙有效地提高了系统的电催化性能。这项工作为电催化水分解的金属(羟基)氢氧化物的大规模生产提供了一种简便且经济高效的技术,显示出巨大的工业应用潜力。