Qin Shili, Lei Jinlong, Xiong Yun, Xu Xiaohu, Geng Xinhua, Wang Jiahai
Department of Chemistry and Chemical Engineering, Guangzhou Key Laboratory for Environmentally Functional Materials and Technology, Guangzhou University Guangzhou 510006 P. R. China
Wuhan Economic and Technological Development Zone, Wuhan HydraV Fuel Cell Tech. Co., Ltd Wuhan 430056 P. R. China.
RSC Adv. 2019 Apr 2;9(18):10231-10236. doi: 10.1039/c9ra00724e. eCollection 2019 Mar 28.
Directly synthesizing bicomponent electrocatalysts in the nanostructured form from bulk alloy foam has many potential advantages: robust stability, synergistic effects and fast electron transfer. Here, NiFeS/NiS film with micrometer thickness on bulk substrate was synthesized by a simple one-step hydrothermally assisted sulfurization of NiFe alloy foam for the oxygen evolution reaction (OER) in basic media. Benefiting from the synergetic effect of the bicomponent, reduced interfacial resistance between electrocatalyst and metal substrate, and more exposed catalytic sites on the microstructured film, the as-prepared electrocatalyst (NiFeS/NiS‖NiFe) behaves as a highly efficient and robust oxygen evolution electrode with felicitous current density in alkaline electrolytes (1 M KOH). It requires an overpotential of only 264 mV to drive 100 mA cm with its catalytic activity being maintained for at least 20 h in 1 M KOH. In the near future, this kind of synthesis strategy can be easily extended to investigate many electrocatalysts derived from 3D alloyed foam with various ratios of the different components, opening new avenue for understanding the relationship between material properties and electrochemical performance.
稳定性强、协同效应以及电子转移快速。在此,通过对块状基底上的镍铁合金泡沫进行简单的一步水热辅助硫化反应,合成了用于碱性介质中析氧反应(OER)的、厚度为微米级的NiFeS/NiS薄膜。得益于双组分的协同效应、电催化剂与金属基底之间降低的界面电阻以及微结构薄膜上更多暴露的催化位点,所制备的电催化剂(NiFeS/NiS‖NiFe)在碱性电解质(1 M KOH)中表现为高效且稳定的析氧电极,具有合适的电流密度。在1 M KOH中驱动100 mA cm²电流仅需264 mV的过电位,其催化活性至少可维持20小时。在不久的将来,这种合成策略能够轻易扩展,用于研究源自具有不同组分比例的三维合金泡沫的许多电催化剂,为理解材料性能与电化学性能之间的关系开辟新途径。