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Ru nanoparticles supported on alginate-derived graphene as hybrid electrodes for the hydrogen evolution reaction
The development of organic-inorganic hybrid materials for redox catalysis is key to access new energy conversion schemes and the sustainable production of dihydrogen. Here, bare and P-doped graphene arising from the pyrolysis of biomass (alginate from marine algae) has been used as a support for the...
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Published in: | New journal of chemistry 2021-12, Vol.46 (1), p.49-56 |
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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: | The development of organic-inorganic hybrid materials for redox catalysis is key to access new energy conversion schemes and the sustainable production of dihydrogen. Here, bare and P-doped graphene arising from the pyrolysis of biomass (alginate from marine algae) has been used as a support for the growth and stabilization of ultra-small Ru/RuO
2
NPs through organometallic synthesis. P-doped graphene allows obtaining smaller and better dispersed NPs in hybrid electrodes of lower roughness and electroactive surface area. Electrochemical activation of the as-synthesised supported nanoparticles by reduction of the passivating RuO
2
layer generates excellent HER electrocatalysts under acidic conditions (
η
10
of 29 mV and 15 mV for the bare and P-doped electrodes, respectively). P doping, identified as surface phosphates by
31
P solid state NMR, induces improvement of all HER benchmarking parameters studied, including overpotential and exchange and specific current densities. All studied materials show excellent long-term stability and selectivity for hydrogen generation with no sign of deactivation after 12 h under turnover conditions and almost quantitative faradaic efficiencies.
Ultra-small Ru NPs grown on biomass-derived bare/P-doped graphene supports yield efficient and durable electrocatalytic H
2
production from water. |
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ISSN: | 1144-0546 1369-9261 |
DOI: | 10.1039/d1nj05215b |