Jijil Chamundi P, Patil Indrajit M, Kakade Bhalchandra, Devi R Nandini
Catalysis and Inorganic Chemistry Division, CSIR-National Chemical Laboratory, Pune 411008, India.
Academy of Scientific and Innovative Research, Ghaziabad 201002, India.
ACS Omega. 2018 Feb 9;3(2):1710-1717. doi: 10.1021/acsomega.7b01655. eCollection 2018 Feb 28.
A series of compounds with cobalt doping in the indium site of BaInO brownmillerites exhibited excellent oxygen reduction activity under alkaline conditions. Doping (25%) retains the brownmillerite structure with disorder in the O3 site in the two-dimensional alternate layer along the plane. Further substitution of cobalt in the indium site leads to the loss of a brownmillerite structure, and the compound attains a perovskite structure. Cobalt-doped samples exhibited far better oxygen reduction reaction (ORR) activity when compared to the parent BaInO brownmillerite. Among the series of compounds, BaInCoO with the highest Co doping and oxygen vacancies randomly distributed in the lattice exhibited the best ORR activity. BaInCoO showed a 40 mV positive shift in the onset potential with better limiting current density and a nearly four-electron-transfer reduction pathway when compared to the parent BaInO brownmillerite.
一系列在褐锰矿型BaInO的铟位点进行钴掺杂的化合物在碱性条件下表现出优异的氧还原活性。25%的掺杂在沿 平面的二维交替层的O3位点保持了具有无序性的褐锰矿结构。铟位点进一步用钴替代会导致褐锰矿结构的丧失,该化合物会形成钙钛矿结构。与母体BaInO褐锰矿相比,钴掺杂样品表现出远更好的氧还原反应(ORR)活性。在该系列化合物中,具有最高钴掺杂且氧空位随机分布在晶格中的BaInCoO表现出最佳的ORR活性。与母体BaInO褐锰矿相比,BaInCoO的起始电位正移40 mV,具有更好的极限电流密度和近乎四电子转移的还原途径。