Sheng Minhao, Yang Yawei, Bin Xiaoqing, Que Wenxiu
Electronic Materials Research Laboratory, International Center for Dielectric Research, Shaanxi Engineering Research Center of Advanced Energy Materials and Devices, School of Electronic Science and Engineering, Xi'an Jiaotong University, Xi'an 710049, China.
Materials (Basel). 2023 Feb 11;16(4):1529. doi: 10.3390/ma16041529.
We adopted a simple one-step electrochemical deposition to acquire an efficient nickel cobalt phosphorus (NiCoP) catalyst, which avoided the high temperature phosphatization engineering involved in the traditional synthesis method. The effects of electrolyte composition and deposition time on electrocatalytic performance were studied systematically. The as-prepared NiCoP achieved the lowest overpotential (η = 111 mV in the acidic condition and η = 120 mV in the alkaline condition) for the hydrogen evolution reaction (HER). Under 1 M KOH conditions, optimal oxygen evolution reaction (OER) activity (η = 276 mV) was also observed. Furthermore, the bifunctional NiCoP catalyst enabled a high-efficiency overall water-splitting by applying an external potential of 1.69 V. The surface valence and structural evolution of NiCoP samples with slowly decaying stability under alkaline conditions are revealed by XPS. The NiCoP is reconstructed into the Ni(Co)(OH) (for HER) and Ni(Co)OOH (for OER) on the surface with P element loss, acting as real "active sites".
我们采用了一种简单的一步电化学沉积法来制备高效的镍钴磷(NiCoP)催化剂,该方法避免了传统合成方法中涉及的高温磷化工程。系统研究了电解液组成和沉积时间对电催化性能的影响。所制备的NiCoP在析氢反应(HER)中实现了最低过电位(酸性条件下η = 111 mV,碱性条件下η = 120 mV)。在1 M KOH条件下,还观察到了最佳析氧反应(OER)活性(η = 276 mV)。此外,双功能NiCoP催化剂通过施加1.69 V的外部电位实现了高效的全水解。XPS揭示了在碱性条件下稳定性缓慢衰减的NiCoP样品的表面价态和结构演变。NiCoP在表面重构为Ni(Co)(OH)(用于HER)和Ni(Co)OOH(用于OER),同时伴随着P元素的损失,这些重构产物充当真正的“活性位点”。