As alternative energy sources are essential to reach a climate-neutral economy, hydrogen peroxide (HO) as futuristic energy carrier gains enormous awareness. However, seeking for stable and electrochemically selective HO ORR electrocatalyst is yet a challenge, making the design of-ideally-bifunctional catalysts extremely important and outmost of interest. In this study, we explore the application of a trimetallic cobalt(II) triazole pyridine bis-[cobalt(III) corrole] complex CoTP[CoC] in OER and ORR catalysis due to its remarkable physicochemical properties, fast charge transfer kinetics, electrochemical reversibility, and durability. With nearly 100 % selective catalytic activity towards the two-electron transfer generated HO, an ORR onset potential of 0.8 V vs RHE and a cycling stability of 50 000 cycles are detected. Similarly, promising results are obtained when applied in OER catalysis. A relatively low overpotential at 10 mA cm of 412 mV, Faraday efficiency 98 % for oxygen, an outstanding Tafel slope of 64 mV dec combined with superior stability.
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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10952570 | PMC |
http://dx.doi.org/10.1002/ange.202302208 | DOI Listing |
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