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Cobalt Colloid-derived Efficient and Durable Nanoscale Electrocatalytic Films for High-Activity Water Oxidation
Author(s) -
NoorUlAin Babar,
Khurram Saleem Joya
Publication year - 2020
Publication title -
acs omega
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.779
H-Index - 40
ISSN - 2470-1343
DOI - 10.1021/acsomega.9b03576
Subject(s) - tafel equation , noble metal , catalysis , electrolysis , cobalt , materials science , oxygen evolution , chemical engineering , electrochemistry , nanotechnology , electrocatalyst , nanoparticle , electrolysis of water , colloid , nanoscopic scale , chemistry , electrode , metallurgy , organic chemistry , electrolyte , engineering
Oxygen evolution reaction is of immense importance and is vitally necessary for devices such as electrolyzers, fuel cells, and other solar and chemical energy conversion devices. The major challenges that remain in this quest are due to the lack of effective catalytic assemblages operating with optimum efficiency and obtainable following much simpler setups and easily accessible methods. Here, we demonstrate that the robust electrocatalytic activity toward water oxidation can be achieved employing straightforwardly obtainable nanoscale electrocatalysts derived from easily made colloidal-cobalt nanoparticles (Co-CNPs) prepared in clean carbonate systems. Thin-film non-noble metal nanoscale electrocatalysts such as simple Co-CNPs/FTO and annealed Co-CNPs/FTO 250 and Co-CNPs/FTO 500 obtained by depositing Co-CNPs on the FTO substrate are shown to initiate water oxidation at much lower overpotentials such as just 240 mV for Co-CNPs/FTO 250 under mildly alkaline conditions while demonstrating an impressive Tafel slope of just 40 mV dec -1 . Furthermore, the robust catalyst demonstrated a high electrochemical surface area of 91 cm 2 and high turnover frequency and mass activity of 0.26 s -1 and 18.84 mA mg -1 , respectively, just at 0.35 V, and superior durability during long-term electrolysis. These outstanding catalytic outcomes using easily prepared Co-CNPs/FTO 250 -type catalytic systems are comparable and even better than other noble and non-noble metal-based nanoscale catalytic assemblages obtained by much difficult methods. Most advantageously, the colloidal route also offers the easiest approach of incorporating carbon contents in the catalytic layer, which can ultimately increase mechanical stability and mass transfer capability of the system.

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