Tian Xiangyun, Yi Peng, Sun Junwei, Li Caiyun, Liu Rongzhan, Sun Jian-Kun
College of Textiles and Clothing, Qingdao University, Qingdao 266071, China.
College of Chemistry and Chemical Engineering, Qingdao University, Qingdao 266071, China.
Nanomaterials (Basel). 2022 May 28;12(11):1848. doi: 10.3390/nano12111848.
The exploration of high-performance and low-cost electrocatalysts towards the oxygen evolution reaction (OER) is essential for large-scale water/seawater splitting. Herein, we develop a strategy involving the in situ generation of a template and pore-former to encapsulate a NiP/NiP heterojunction and dispersive FeNi alloy hybrid particles into a three-dimensional hierarchical porous graphitic carbon framework (labeled as NiP/NiP-FeNi@C) via a room-temperature solid-state grinding and sodium-carbonate-assisted pyrolysis method. The synergistic effect of the components and the architecture provides a large surface area with a sufficient number of active sites and a hierarchical porous pathway for efficient electron transfer and mass diffusion. Furthermore, a graphitic carbon coating layer restrains the corrosion of alloy particles to boost the long-term durability of the catalyst. Consequently, the NiP/NiP-FeNi@C catalyst exhibits extraordinary OER activity with a low overpotential of 242 mV (10 mA cm), outperforming the commercial RuO catalyst in 1 M KOH. Meanwhile, a scale-up of the NiP/NiP-FeNi@C catalyst created by a ball-milling method displays a similar level of activity to the above grinding method. In 1 M KOH + seawater electrolyte, NiP/NiP-FeNi@C also displays excellent stability; it can continuously operate for 160 h with a negligible potential increase of 2 mV. This work may provide a new avenue for facile mass production of an efficient electrocatalyst for water/seawater splitting and diverse other applications.
开发高性能、低成本的析氧反应(OER)电催化剂对于大规模水/海水分解至关重要。在此,我们开发了一种策略,通过室温固态研磨和碳酸钠辅助热解方法,原位生成模板和成孔剂,将NiP/NiP异质结和分散的FeNi合金杂化颗粒封装到三维分级多孔石墨碳框架中(标记为NiP/NiP-FeNi@C)。各组分与结构的协同效应提供了大表面积、足够数量的活性位点以及用于高效电子转移和质量扩散的分级多孔通道。此外,石墨碳涂层抑制了合金颗粒的腐蚀,提高了催化剂的长期耐久性。因此,NiP/NiP-FeNi@C催化剂表现出卓越的OER活性,在1 M KOH中过电位低至242 mV(10 mA cm),优于商业RuO催化剂。同时,通过球磨法制备的NiP/NiP-FeNi@C催化剂放大规模后显示出与上述研磨法相似的活性水平。在1 M KOH + 海水电解液中,NiP/NiP-FeNi@C也表现出优异的稳定性;它可以连续运行160 h,电位仅增加2 mV,几乎可以忽略不计。这项工作可能为水/海水分解及其他多种应用的高效电催化剂的简便大规模生产提供一条新途径。