Duan Ran, Li Yejun, Wang Shu, Gong Jun, Tong Yonggang, Qi Weihong
Hunan Key Laboratory of Nanophotonics and Devices, School of Physics and Electronics, Central South University, 410083 Changsha, P. R. China.
School of Materials Science and Engineering, Central South University, 410083 Changsha, P. R. China.
J Phys Chem Lett. 2022 Feb 17;13(6):1446-1452. doi: 10.1021/acs.jpclett.1c04136. Epub 2022 Feb 7.
Although there is a general consensus that the electrocatalysts will undergo reconstruction to generate (oxy)hydroxides as real active sites during the electrochemical oxygen evolution reaction (OER), the understanding of this process is still far from satisfactory. In particular, the reconstruction process of most of these electrocatalysts is either slow or occurs only on the surface, which thus restrains the OER performance of the electrocatalysts. Herein, we reveal a fast and deep reconstruction of the coprecipitated Fe phosphates on nickel foam, via in situ Raman spectroscopy together with electron microscopy, X-ray photoelectron spectroscopy, and electrochemical tests. The generated NiFe (oxy)hydroxide nanosheets after reconstruction behave as the real active sites for the OER in the alkaline condition, with a low overpotential and excellent durability. The present work provides deep insights on the reconstruction dynamics of OER electrocatalysts.
尽管人们普遍认为,在电化学析氧反应(OER)过程中,电催化剂会发生重构以生成(氧)氢氧化物作为真正的活性位点,但对这一过程的理解仍远不能令人满意。特别是,大多数这些电催化剂的重构过程要么缓慢,要么仅发生在表面,因此限制了电催化剂的OER性能。在此,我们通过原位拉曼光谱结合电子显微镜、X射线光电子能谱和电化学测试,揭示了泡沫镍上共沉淀磷酸铁的快速且深度的重构。重构后生成的NiFe(氧)氢氧化物纳米片在碱性条件下作为OER的真正活性位点,具有低过电位和优异的耐久性。本工作为OER电催化剂的重构动力学提供了深入见解。