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In-situ “encapsulation” of Mo:Mo2C with nano-mosaic structure on wood-derived carbon for hydrogen evolution reaction
Coupling metallic and Mo2C phases uniformly on conductive matrix at nanoscale is a promising route to solve the poor electrical conductivity and aggregation problems of nano-Mo2C. In this work, a 3D self-supporting carbonized wood (CW) electrode encapsulation with mosaic structure Mo:Mo2C for hydrog...
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Published in: | International journal of hydrogen energy 2023-03, Vol.48 (24), p.8819-8829 |
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Main Authors: | , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | Coupling metallic and Mo2C phases uniformly on conductive matrix at nanoscale is a promising route to solve the poor electrical conductivity and aggregation problems of nano-Mo2C. In this work, a 3D self-supporting carbonized wood (CW) electrode encapsulation with mosaic structure Mo:Mo2C for hydrogen evolution reaction was fabricated successfully by a facile annealing treatment and a gas-solid reaction. The presence of Mo phase accelerated the transfer rate of electrons and provided heterogeneous interface. The obtained electrode shows abundant catalytic active sites and low electrochemical impedance, thus improving the catalytic process of splitting water for HER. The Mo:Mo2C-775 electrode requires an overpotential of 73.5 mV and 117 mV to achieve the current density of 10 mA cm−2 in 0.5 M H2SO4 and 1.0 M KOH, respectively. Moreover, Mo:Mo2C-775 electrode displayed excellent stability performance, which almost maintained a constant current density for 12 h (at −100 mV vs RHE) in 0.5 M H2SO4 and 1.0 M KOH, respectively. This study provides a new idea for preparation of efficient 3D self-supporting electro-catalyst for HER.
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•3D high electronic conductivities wood-based matrix was constructed.•In-situ “coating” of Mo:Mo2C with nano-mosaic structure on wood-based porous carbon.•The Mo phase speeds up the electron shift rate showed pretty catalytic activity. |
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ISSN: | 0360-3199 1879-3487 |
DOI: | 10.1016/j.ijhydene.2022.11.330 |