School of Materials Engineering, Shanghai University of Engineering Science, Shanghai 201620, P.R. China.
Dalton Trans. 2023 May 22;52(20):6860-6869. doi: 10.1039/d3dt00583f.
The design and synthesis of cost-effective and stable bifunctional electrocatalysts for water splitting a green and sustainable fabrication way remain a challenging problem. Herein, a bio-inspired method was used to synthesize NiFeP nanoparticles embedded in (N,P) co-doped carbon with the added carbon nanotubes. The obtained NiFeP-C catalyst displayed excellent hydrogen evolution reaction (HER) and oxygen evolution reaction (OER) performances in both alkaline and alkaline simulated seawater solutions. The optimal NiFeP-C/NF only needs overpotentials of 45 and 242 mV to reach the current density of 10 mA cm under HER and OER working conditions in 1.0 M KOH solution, respectively. First-principles calculations revealed the presence of a strong interaction between the carbon layer and metal phosphide nanoparticles. Benefiting from this and carbon nanotubes modification, the fabricated NiFeP-C presents impressive stability, working continuously for 100 h without collapse. A low alkaline cell voltage of 1.56 V for the assembled NiFeP-C/NF//NiFeP-C/NF electrocatalyzer could afford a current density of 10 mA cm. Moreover, when integrated with a photovoltaic device, the bifunctional NiFeP-C electrocatalyst demonstrates application potential for sustainable solar-driven water electrolysis.
用于水分解的具有成本效益和稳定的双功能电催化剂的设计和合成 - 一种绿色和可持续的制造方法仍然是一个具有挑战性的问题。本文采用仿生方法合成了嵌入(N,P)共掺杂碳中的 NiFeP 纳米粒子,并添加了碳纳米管。所获得的 NiFeP-C 催化剂在碱性和碱性模拟海水中均显示出优异的析氢反应(HER)和析氧反应(OER)性能。在 1.0 M KOH 溶液中,最优的 NiFeP-C/NF 在 HER 和 OER 工作条件下仅需要 45 和 242 mV 的过电势即可达到 10 mA cm 的电流密度。第一性原理计算揭示了碳层和金属磷化物纳米颗粒之间存在强烈的相互作用。得益于这一点和碳纳米管的修饰,所制备的 NiFeP-C 表现出令人印象深刻的稳定性,连续工作 100 小时而不会崩溃。组装的 NiFeP-C/NF//NiFeP-C/NF 电催化剂的碱性电池电压低至 1.56 V,可提供 10 mA cm 的电流密度。此外,当与光伏器件集成时,双功能 NiFeP-C 电催化剂表现出用于可持续太阳能驱动水分解的应用潜力。