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Atomically Dispersed Mo Supported on Metallic Co 9 S 8 Nanoflakes as an Advanced Noble‐Metal‐Free Bifunctional Water Splitting Catalyst Working in Universal pH Conditions
Author(s) -
Wang Ligang,
Duan Xinxuan,
Liu Xijun,
Gu Jing,
Si Rui,
Qiu Yi,
Qiu Yaming,
Shi Dier,
Chen Fanhong,
Sun Xiaoming,
Lin Jianhua,
Sun Junliang
Publication year - 2020
Publication title -
advanced energy materials
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 10.08
H-Index - 220
eISSN - 1614-6840
pISSN - 1614-6832
DOI - 10.1002/aenm.201903137
Subject(s) - bifunctional , catalysis , water splitting , noble metal , oxygen evolution , materials science , metal , density functional theory , adsorption , inorganic chemistry , alkali metal , chemical engineering , nanotechnology , chemistry , computational chemistry , electrochemistry , metallurgy , organic chemistry , electrode , photocatalysis , engineering
Water splitting requires development of cost‐effective multifunctional materials that can catalyze both the hydrogen evolution reaction (HER) and the oxygen evolution reaction (OER) efficiently. Currently, the OER relies on the noble‐metal catalysts; since with other catalysts, its operation environment is greatly limited in alkaline conditions. Herein, an advanced water oxidation catalyst based on metallic Co 9 S 8 decorated with single‐atomic Mo (0.99 wt%) is synthesized (Mo‐Co 9 S 8 @C). It exhibits pronounced water oxidization activity in acid, alkali, and neutral media by showing positive onset potentials of 200, 90, and 290 mV, respectively, which manifests the best Co 9 S 8 ‐based single‐atom Mo catalyst till now. Moreover, it also demonstrates excellent HER performance over a wide pH range. Consequently, the catalyst even outperforms noble metal Pt/IrO 2 ‐based catalysts for overall water splitting (only requiring 1.68 V in acid, and 1.56 V in alkaline). Impressively, it works under a current density of 10 mA cm −2 with no obvious decay during a 24 h (0.5 m H 2 SO 4 ) and 72 h (1.0 m KOH) durability experiment. Density functional theory (DFT) simulations reveal that the synergistic effects of atomically dispersed Mo with Co‐containing substrates can efficiently alter the binding energies of adsorbed intermediate species and decrease the overpotentials of the water splitting.