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Design and Development of Efficient Bifunctional Catalysts by Tuning the Electronic Properties of Cobalt–Manganese Tungstate for Oxygen Reduction and Evolution Reactions
Author(s) -
Karkera Guruprakash,
Sarkar Tanmay,
Bharadwaj Mridula Dixit,
Prakash Annigere. S.
Publication year - 2017
Publication title -
chemcatchem
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.497
H-Index - 106
eISSN - 1867-3899
pISSN - 1867-3880
DOI - 10.1002/cctc.201700540
Subject(s) - overpotential , oxygen evolution , bifunctional , tungstate , catalysis , water splitting , manganese , cobalt , chemistry , electrocatalyst , electrochemistry , electrochemical energy conversion , redox , density functional theory , electron transfer , bifunctional catalyst , materials science , inorganic chemistry , chemical engineering , electrode , computational chemistry , photocatalysis , organic chemistry , biochemistry , engineering
Solid‐state electrochemistry is drawing considerable interest as the interconversion of O 2 and water playing an important role in energy conversion and storage technologies. With the aim of developing an efficient bifunctional catalyst by tuning the electronic properties and local structure around the 3d metal in CoWO 4 , solid solutions of Co 1− x Mn x WO 4 are investigated. Nanocrystalline Co 1− x Mn x WO 4 ( x= 0 to 1) phases with a unique exposure of low surface energy planes are synthesized by hydrothermal methods. Replacing an optimum amount of Co with Mn to enhance the catalytic activity leads a observation of a negative shift in the Co 2+/3+ redox wave and onset of the oxygen evolution reaction (OER), indicating a strong electronic interaction between the two elements. The composition corresponding to Co 0.5 Mn 0.5 WO 4 has demonstrated great ability to catalyze both the OER and oxygen reduction reaction (ORR) with a combined overpotential of 0.89 V. It exhibited an OER current density of 10 mA cm −2 at an overpotential of 400 mV. Whereas ORR current density of 3 mA cm −2 is reached at a potential of 0.74 V versus reversible hydrogen electrode (RHE). The density functional theory revealed that the substitution of Mn in CoWO 4 elevate the 3d metal d band center closer to the Fermi energy and hence ease the electron transfer to facilitate ORR and OER.