CoNiP(S)@WC as a Bifunctional Electrocatalyst for Efficient Alkaline Water Splitting

ACS Sustainable Resource Management Pub Date : 2026-09-24 Epub Date: 2026-09-02 DOI:10.1021/acssusresmgt.6c00392
Samikannu Prabu, Madhan Vinu, B. Sudharsan Bangaru, Suresh Babu S K, Kung-Yuh Chiang, Ashutosh Tiwari, George Rajendra Kumar
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Abstract

Developing low-cost and high-performance electrocatalysts for overall water splitting is essential for advancing sustainable hydrogen (H2) production and renewable energy technologies. In this work, a bifunctional CoNiP(S)@WC electrocatalyst was successfully synthesized through a facile multi-step strategy involving hydrothermal treatment, followed by phosphorization and sulfurization. The integration of a Co-Ni phosphosulfide heterostructure with waste-wood-derived carbon provides abundant active sites, enhanced electrical conductivity, and improved structural stability, resulting in efficient catalytic activity toward both the hydrogen evolution reaction (HER) and oxygen evolution reaction (OER) in alkaline media. The optimized catalyst exhibits low overpotentials of 38 mV for HER and 185 mV for OER at 10 mA cm–2, along with favorable Tafel slopes, indicating fast reaction kinetics. Moreover, the synergistic electronic interactions among Co, Ni, P, and S species further enhance the intrinsic electrocatalytic performance. In a two-electrode alkaline electrolyzer, CoNiP(S)@WC achieves a low cell voltage of 1.45 V at 10 mA cm–2 and demonstrates excellent long-term stability over 120 h of continuous operation. The results highlight the effectiveness of combining transition metal phosphosulfides with biomass-derived conductive carbon for the development of efficient, durable, and scalable electrocatalysts for practical alkaline water splitting and sustainable H2 production.

CoNiP(S)@WC作为高效碱水分解双功能电催化剂
开发低成本、高性能的整体水分解电催化剂对于推进可持续氢生产和可再生能源技术至关重要。在这项工作中,通过水热处理、磷酸化和硫化等简单的多步骤策略,成功合成了双功能CoNiP(S)@WC电催化剂。Co-Ni磷硫化物异质结构与废木衍生碳的集成提供了丰富的活性位点,增强了导电性,提高了结构稳定性,从而在碱性介质中对析氢反应(HER)和析氧反应(OER)都具有高效的催化活性。优化后的催化剂在10 mA cm-2下,HER的过电位为38 mV, OER的过电位为185 mV,并且具有良好的塔菲尔斜率,表明反应动力学快速。此外,Co、Ni、P和S之间的协同电子相互作用进一步提高了本征电催化性能。在双电极碱性电解槽中,CoNiP(S)@WC在10 mA cm-2下实现了1.45 V的低电池电压,并在连续运行120小时以上表现出出色的长期稳定性。研究结果表明,将过渡金属磷硫化物与生物质衍生的导电碳结合,可以开发高效、耐用、可扩展的电催化剂,用于实际的碱性水裂解和可持续的氢气生产。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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