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Morphology Regulated Hierarchical Rods-, Buds-, and Sheets-like CoMoO4 for Electrocatalytic Oxygen Evolution Reaction
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Mahato, Neelima
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Chungnam Natl Univ, Dept Elect Engn, Energy Storage & Convers Lab, Daejeon 34134, South Korea Chungnam Natl Univ, Dept Elect Engn, Energy Storage & Convers Lab, Daejeon 34134, South Korea

Yoo, Kisoo
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Yeungnam Univ, Sch Mech Engn, Gyongsan 38541, South Korea Chungnam Natl Univ, Dept Elect Engn, Energy Storage & Convers Lab, Daejeon 34134, South Korea

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[1] Chungnam Natl Univ, Dept Elect Engn, Energy Storage & Convers Lab, Daejeon 34134, South Korea
[2] Yeungnam Univ, Sch Mech Engn, Gyongsan 38541, South Korea
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关键词:
CoMoO4;
nanoparticles;
morphology evolution;
electrocatalyst;
oxygen evolution reaction;
EFFICIENT ELECTROCATALYST;
BIFUNCTIONAL ELECTROCATALYSTS;
CONTROLLABLE SYNTHESIS;
HIGHLY EFFICIENT;
NANOPLATE ARRAY;
COBALT OXIDE;
MIXED-OXIDE;
NANOPARTICLES;
HYDROGEN;
ALKALINE;
D O I:
10.3390/en16052441
中图分类号:
TE [石油、天然气工业];
TK [能源与动力工程];
学科分类号:
0807 ;
0820 ;
摘要:
One of the hugely focused areas of research for addressing the world's energy and environmental challenges is electrochemical water oxidation. Morphological modulation of nanomaterials is essential for producing efficient electrocatalysts to achieve the required results. The purpose can be achieved by controlling synthesis parameters, and this is a key factor which greatly influences the oxygen evolution reaction (OER) performance during electrochemical water splitting. In this study, synthesis of cobalt molybdate (CoMoO4) through a simple and low-cost hydrothermal/solvothermal strategy with tunable morphology is demonstrated. Different morphologies, namely rods-like, buds-like, and sheets-like, referred to as R-CMO, B-CMO, and S-CMO, respectively, have been obtained by systematically varying the solvent media. Their catalytic activity towards OER was investigated in 1.0 M aqueous KOH medium. R-CMO nanoparticles synthesized in an aqueous medium demonstrated the lowest overpotential value of 349 mV to achieve a current density of 10 mA cm(-2) compared with other as-prepared catalysts. In contrast, the B-CMO and S-CMO exhibited overpotential values of 369 mV and 384 mV, respectively. Furthermore, R-CMO demonstrated an exceptional electrochemical stability for up to 12 h.
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