Abstract
Direct electrochemical two-electron oxygen reduction (2eORR) into H 2O 2 provides a promising alternative for on-site green H 2O 2 production to the predominant anthraquinone oxidation technology. Oxidized carbon materials have demonstrated their impressive 2eORR activity due to oxygenated functional groups beneficial to the H 2O 2 formation pathways. However, the 2eORR capability of O-doped carbon catalysts is hindered by the density of O-induced active sites due to the rather low O content (<15%). Herein, we reported a carbon quantum dot (CQD) catalyst with an ultrahigh O content (30.4 at%) fabricated by using glucose (C 6H 12O 6) as the carbon source due to its high atomic ratio of oxygen-to-carbon. The O-rich CQD catalyst exhibits an excellent catalytic capability of H 2O 2 production with nearly 100% selectivity, exceeding all reported O-doped carbon catalysts. Besides, the CQD catalyst exhibits great potential in practical H 2O 2 production with a high yield of 10.06 mg cm −2 h −1 and Faraday efficiency of 97.7%, as well as good stability over 10 hours. Experimental and theoretical investigations confirm that the great majority of the C-O bonds are from the etheric groups in the CQD catalyst, and the carbon atoms of the C-O bonds are the most active sites for the 2eORR.
Original language | English |
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Pages (from-to) | 4167-4174 |
Number of pages | 8 |
Journal | Energy and Environmental Science |
Volume | 15 |
Issue number | 10 |
Early online date | 15 Aug 2022 |
DOIs | |
Publication status | Published - 1 Oct 2022 |
Externally published | Yes |
Bibliographical note
Publisher Copyright:© 2022 The Royal Society of Chemistry.
Funding
This work was supported by the National Key R&D Program of China under Project 2019YFA0705104 and General Research Fund (GRF) under Project CityU11212920.