Pang Wei, Fan Ailing, Guo Yaqi, Xie Dengkui, Gao Dianchao
Key Laboratory of Advanced Functional Materials, Education Ministry of China, Beijing University of Technology, Beijing 100124, China.
ACS Omega. 2021 Oct 11;6(41):26822-26828. doi: 10.1021/acsomega.1c01650. eCollection 2021 Oct 19.
Although transition-metal-based phosphides as cost-effective catalysts have great potential for transforming water to hydrogen, their electrocatalytic property for industrial application is still limited. Herein, we focus on developing amorphous NiCoP with dandelion-like arrays anchored on nanowires through a universal strategy of hydrothermal and phosphorization. The hierarchical structure features in larger catalytic surface areas expedited reaction kinetics and improved structural stability. Benefiting from these merits, the NiCoP reaches 10 mA cm at an overpotential of mere 57 mV for a hydrogen evolution reaction in standard solution. Also, a profound activity for the generation of oxygen is along with it, which requires 276 mV to attain 10 mA cm. Moreover, it demonstrates satisfying durability for both processes.
尽管过渡金属基磷化物作为具有成本效益的催化剂在将水转化为氢气方面具有巨大潜力,但其在工业应用中的电催化性能仍然有限。在此,我们专注于通过水热和磷化的通用策略开发一种锚定在纳米线上的具有蒲公英状阵列的非晶态NiCoP。这种分级结构具有更大的催化表面积,加快了反应动力学并提高了结构稳定性。受益于这些优点,在标准溶液中进行析氢反应时,NiCoP在仅57 mV的过电位下即可达到10 mA cm 。此外,它还具有很强的析氧活性,达到10 mA cm 需要276 mV。而且,它在这两个过程中都表现出令人满意的耐久性。