期刊
JOURNAL OF MATERIALS CHEMISTRY A
卷 4, 期 38, 页码 14614-14624出版社
ROYAL SOC CHEMISTRY
DOI: 10.1039/c6ta04737h
关键词
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资金
- Department of Science and Technology (DST), Government of India [SR/S1/PC-28/2011]
- University Grants Commission (UGC)
- Council of Scientific and Industrial Research (CSIR), New Delhi, India
- IISER Kolkata
The challenging water oxidation reaction to generate molecular oxygen requires low-cost efficient catalysts for its application in renewable energy technologies. Carbon dot (C-dot) catalysts synthesized by microwave irradiation can trap an anti-oxidant, 5-hydroxymethyl-2-furaldehyde (5-HMF) inside the carbon framework. The C-dot with the highest concentration of 5-HMF acts as a stable metal-free oxygen evolution reaction (OER) catalyst which operates at a decently low 0.21(+/- 0.03) V overpotential and can generate current density up to 33.6(+/- 2.3) mA cm(-2). With increased microwave reaction time, the concentration of 5-HMF inside the C-dots decreases at the cost of different furan derivatives which decreases the OER activity. The 5-HMF molecules in close vicinity to the catalytically active sites containing C=O groups can extract the (OH)-O-center dot/(OOH)-O-center dot radicals and can increase the in situ H2O concentration to facilitate the forward reaction of O-2 evolution. During continuous electrolysis beyond 10 min, 5-HMF gets converted to 2,5-diformylfuran entities, which increases the catalytically active sites and thereby maintains the OER activity of the C-dots for at least 4 h. The ability of microwave irradiated sucrose derived C-dots to electro-oxidize water is generalized with C-dots and graphene dots (G-dots) prepared from different precursors.
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