Thundiyil Shibin, Vinod C P, Kurungot Sreekumar, Devi R Nandini
Catalysis and Inorganic Chemistry Division, CSIR-National Chemical Laboratory, Pune-411008, India.
Phys Chem Chem Phys. 2020 Jul 21;22(27):15520-15527. doi: 10.1039/d0cp02391d. Epub 2020 Jul 1.
The role of B site doping with transition metals in brownmillerites, a perovskite related family of compounds, in bifunctional oxygen electrocatalysis, viz., simultaneous reduction and evolution reactions, is analysed. CaFeMO (M = Mn, Co, Ni, and Cu) is synthesised and structurally characterised by powder XRD and Rietveld refinement. Valence states of the surface B site ions are identified by X-ray photoelectron spectroscopy. Bifunctional oxygen electrochemistry is studied with the RDE and RRDE techniques and correlated with the structural and electronic parameters like oxygen non-stoichiometry and B site catalytic activity. Since the widely accepted electronic descriptors like e filling may not be sufficient for explaining the bifunctional activity, B site electron donating capability as well as the extent of oxygen vacancies enhancing O adsorption is also considered. Such structural parameters are also found to influence both the ORR and OER and based on this, Ni doping is proposed as advantageous for the bifunctional activity.
分析了在钙钛矿相关化合物家族——褐锰矿中,用过渡金属进行B位掺杂在双功能氧电催化(即同时进行还原和析出反应)中的作用。合成了CaFeMO(M = Mn、Co、Ni和Cu),并通过粉末XRD和Rietveld精修对其结构进行了表征。通过X射线光电子能谱确定了表面B位离子的价态。用旋转圆盘电极(RDE)和旋转环盘电极(RRDE)技术研究了双功能氧电化学,并将其与诸如氧非化学计量比和B位催化活性等结构和电子参数相关联。由于诸如电子填充等广泛接受的电子描述符可能不足以解释双功能活性,因此还考虑了B位给电子能力以及氧空位增强O吸附的程度。还发现这些结构参数会影响氧还原反应(ORR)和析氧反应(OER),基于此,提出Ni掺杂对双功能活性有利。