Cyclic Voltammetric Investigation on the Catalysis of Electrodeposited Manganese Oxide on the Electrochemical Reduction of Oxygen (ORR) in Room Temperature Ionic Liquids (RTILs) of 1-Ethyl-3-Methylimidazolium Tetrafluorobroate (EMIBF4) on Glass Carbon (GC) Electrode
Author(s) -
Kunlun Ding,
Q. Wang,
Minru Zhao
Publication year - 2007
Publication title -
portugaliae electrochimica acta
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.252
H-Index - 27
eISSN - 1647-1571
pISSN - 0872-1904
DOI - 10.4152/pea.200703335
Subject(s) - ionic liquid , electrochemistry , manganese , catalysis , manganese oxide , materials science , inorganic chemistry , oxide , chemistry , electrode , organic chemistry , metallurgy
In this preliminary work, for the first time, the electrochemical oxygen reduction reaction (ORR) was investigated using cyclic voltammetry (CV) on the electrodeposited manganese oxide (MnO x)-modified glass carbon electrode (MnO x-GC) at room temperature ionic liquids (RTILs) of EMIBF 4, i.e., 1-ethyl-3-methylimidazolium tetrafluorobroate (EMIBF 4). The results demonstrated that, after being modified by MnO x on GC, the reduction peak current of oxygen was increased to some extent, while the oxidation peak current, corresponding to the oxidation of superoxide anion, O 2 - , was attenuated in some degree, suggesting that MnO x catalyzed ORR in RTILs of EMIBF 4, which is consistent with the results obtained in aqueous solution. To accelerate the electron transfer rate, multi-walled carbon nanotubes (MWCNTs) were modified on GC, and then MnO x was electrodeposited onto the MWCNTs-modified GC electrode to give rise to the MnO x /MWCNTs–modified GC electrode; consequently, the improved standard rate constant, 9s, originated from the modified MWCNTs, along with the modification of electrodeposited MnO x, showed us a satisfactory electrocatalysis for ORR in RTILs of EMIBF 4. In addition, not only for the MnO x-modified GC but also for the MnO x/ MWCNTs-modified GC, there is a novel small oxidation peak appearing at – 0.2 V vs . solid Ag/AgCl, implying that the catalysis of MnOx for ORR in EMIBF 4 is somewhat different from that observed in aqueous solution, though the exact interpretation is not achieved in this preliminary work. Initiating the catalysis of MnO x on ORR in RTILs is the main contribution of this work. Further discussions are in progress.
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