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Compositional Control as the Key for Achieving Highly Efficient OER Electrocatalysis with Cobalt Phosphates Decorated Nanocarbon Florets
Author(s) -
Saha Jayeeta,
Verma Sonam,
Ball Ranadeb,
Subramaniam Chandramouli,
Murugavel Ramaswamy
Publication year - 2020
Publication title -
small
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.785
H-Index - 236
eISSN - 1613-6829
pISSN - 1613-6810
DOI - 10.1002/smll.201903334
Subject(s) - overpotential , electrocatalyst , cobalt , oxygen evolution , materials science , catalysis , chemical engineering , electrochemistry , chemistry , inorganic chemistry , electrode , organic chemistry , engineering
Compositional interplay of two different cobalt phosphates (Co(H 2 PO 4 ) 2 ; Co‐DP and Co(PO 3 ) 2 ; Co‐MP) loaded on morphologically engineered high surface area nanocarbon leads to an increased electrocatalytic efficiency for oxygen evolution reaction (OER) in near neutral conditions. This is reflected as significant reduction in the onset overpotential (301 mV) and enhanced current density (30 mA cm −2 @ 577 mV). In order to achieve uniform surface loading, organic‐soluble thermolabile cobalt‐bis(di‐ tert ‐butylphosphate) is synthesized in situ inside the nanocarbon matrix and subsequently pyrolyzed at 150 °C to produce Co(H 2 PO 4 ) 2 /Co(PO 3 ) 2 (80:20 wt%). Annealing this sample at 200 or 250 °C results in the redistribution of the two phosphate systems to 55:45 or 20:80 (wt%), respectively. Detailed electrochemical measurements clearly establish that the 55:45 (wt%) sample prepared at 200 °C performs the best as a catalyst, owing to a relay mechanism that enhances the kinetics of the 4e − transfer OER process, which is substantiated by micro‐Raman spectroscopic studies. It is also unraveled that the engineered nanocarbon support simultaneously enhances the interfacial charge‐transfer pathway, resulting in the reduction of onset overpotential, compared to earlier investigated cobalt phosphate systems.