共 67 条
Acoustically-Induced Water Frustration for Enhanced Hydrogen Evolution Reaction in Neutral Electrolytes
被引:39
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Sherrell, Peter C.
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Univ Melbourne, Dept Chem Engn, Parkville, Vic 3010, Australia RMIT Univ, Sch Engn, Micro Nanophys Res Lab, Melbourne, Vic 3001, Australia

Rezk, Amgad R.
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RMIT Univ, Sch Engn, Micro Nanophys Res Lab, Melbourne, Vic 3001, Australia RMIT Univ, Sch Engn, Micro Nanophys Res Lab, Melbourne, Vic 3001, Australia

Yeo, Leslie Y.
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RMIT Univ, Sch Engn, Micro Nanophys Res Lab, Melbourne, Vic 3001, Australia RMIT Univ, Sch Engn, Micro Nanophys Res Lab, Melbourne, Vic 3001, Australia
机构:
[1] RMIT Univ, Sch Engn, Micro Nanophys Res Lab, Melbourne, Vic 3001, Australia
[2] Univ Melbourne, Dept Chem Engn, Parkville, Vic 3010, Australia
关键词:
acoustics;
frustrated water;
hydrogen bonds;
hydrogen;
neutral electrolytes;
water splitting;
PLATINUM;
OXIDATION;
ELECTROCATALYSTS;
DISSOCIATION;
SPECTROSCOPY;
ENERGY;
D O I:
10.1002/aenm.202203164
中图分类号:
O64 [物理化学(理论化学)、化学物理学];
学科分类号:
070304 ;
081704 ;
摘要:
A novel strategy utilizing high-frequency (10 MHz) hybrid sound waves to dramatically enhance hydrogen evolution reactions (HER) in notoriously difficult neutral electrolytes by modifying their network coordination state is presented. Herein, the practical limitations associated with existing electrolyzer technology is addressed, including the need for highly corrosive electrolytes and expensive electrocatalysts, by redefining conceptually-poor hydrogen electrocatalysts in neutral electrolytes. The improvement in HER performance is attributed to the unique capability of the intense local electromechanical coupling arising from the acoustic-forcing to 'frustrate' the tetrahedrally-coordinated hydrogen bond network of water molecules at the electrode-electrolyte interface, resulting in the generation of a high concentration of "free" water molecules that are more readily able to access catalytic sites on the unmodified polycrystalline electrode. Together with the other synergistic effects that accompany the acoustic excitation (e.g., hydronium ion generation, convective relaxation of diffusion mass transfer limitations, and prevention of bubble build-up and their removal from the electrode), the resultant overpotential reduction of 1.4 V at -100 mA cm(-2) and corresponding 14-fold increase in current density, together with a net-positive energy saving of 27.3%, showcases the potential of the technology as a scalable platform for effectively enhancing the efficiency of green hydrogen production.
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Aalborg Univ, Dept Energy Technol, Niels Bohrs Vej 8, DK-6700 Esbjerg, Denmark Univ Oslo, Dept Technol Syst, Gunnar Randers Vei 19, N-2007 Kjeller, Norway

Sartori, Sabrina
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机构:
Univ Oslo, Dept Technol Syst, Gunnar Randers Vei 19, N-2007 Kjeller, Norway Univ Oslo, Dept Technol Syst, Gunnar Randers Vei 19, N-2007 Kjeller, Norway