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Porous dehydroxyl cobalt phytate as electrocatalyst for high-efficiency water oxidation.
- Source :
-
Applied Surface Science . Jan2023, Vol. 609, pN.PAG-N.PAG. 1p. - Publication Year :
- 2023
-
Abstract
- [Display omitted] • Porous dehydroxyl cobalt phytate displays superior OER stability with a V- t test for 80 h. • The role of dehydroxyl temperature in improving the OER performance is critical. • The OER activity and stability of cobalt phytate are even comparable to commercial RuO 2. Phytic acid (PA) is a six-fold dihydrogenphosphate ester of inositol with cost-effective, environmentally friendly, and safe properties. Here, we successfully synthesize the dehydroxyl cobalt phytate (PA-Co-400) using PA as phosphorus sources by a one-pot wet-chemistry strategy to prepare the precursor PA-Co and then heat treatment at 400 °C under an N 2 atmosphere for dehydroxylation. The average diameter, specific surface area, surface element distribution, and catalytic activity of the catalyst are significantly affected by dehydroxylation temperature. The specific surface area increases first and then decreases with the treatment temperature from 200 °C to 600 °C. The SEM results indicate that the average diameter of PA-Co-400 particle is 68.90 nm. The as-prepared samples are used as an anode catalyst for electrocatalytic oxygen evolution reaction (OER). The PA-Co-400 exhibits splendid OER performances with an overpotential of 310.31 mV at j 10 (η 50 = 349.35 mV, η 100 = 367.20 mV), which are even comparable to commercial RuO 2 (η 10 = 310.54 mV, η 50 = 389.80 mV, η 100 = 450.60 mV). Moreover, the PA-Co-400 has a small Tafel slope of 53.27 mV dec−1, which is lower than commercial RuO 2 (81.71 mV dec−1). The ultra-long durability of PA-Co-400 was tested for over 80 h at current densities of 10 mA cm−2 without a significant reduction in 1 M KOH. [ABSTRACT FROM AUTHOR]
Details
- Language :
- English
- ISSN :
- 01694332
- Volume :
- 609
- Database :
- Academic Search Index
- Journal :
- Applied Surface Science
- Publication Type :
- Academic Journal
- Accession number :
- 160209370
- Full Text :
- https://doi.org/10.1016/j.apsusc.2022.155405