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Journal article

Unique hole-accepting carbon-dots promoting selective carbon dioxide reduction nearly 100% to methanol by pure water

Abstract:
X.L., M.K.B., J.T. acknowledge EPSRC (EP/S018204/2/1), Leverhulme Trust (Grant No: RPG-2017-122) and Newton Advanced Fellowship grant ((NA170422 and NAF\R1\191163).). X.H., Z.X.G. and S.A.S. acknowledge UCL Grace High-Performance Computing Facility (Grace@UCL) and EPSRC (EP/K021192/1, EP/L018330/1). R.G. thanks the FRQNT for postdoctoral funding and NSERC for operational funding. Y.W., J.C. and C.J., acknowledge CSC Scholarship. R.G., J.F.T. and J.R.D. acknowledge ERC AdG Intersolar grant (291482). J.F.T. acknowledges EPSRC CDT (EP/L015277/1). W.Z. thanks EPSRC for Titan Themis S/TEM microscope (EP/L017008/01). We also thank Dr. Jijia Xie for constructive comments on experimental design.Solar-driven CO2 reduction by abundant water to alcohols can supply sustainable liquid fuels and alleviate global warming. However, the sluggish water oxidation reaction has been hardly reported to be efficient and selective in CO2 conversion due to fast charge recombination. Here, using transient absorption spectroscopy, we demonstrate that microwave-synthesised carbon-dots (mCD) possess unique hole-accepting nature, prolonging the electron lifetime (t50%) of carbon nitride (CN) by six folds, favouring a six-electron product. mCD-decorated CN stably produces stoichiometric oxygen and methanol from water and CO2 with nearly 100% selectivity to methanol and internal quantum efficiency of 2.1% in the visible region, further confirmed by isotopic labelling. Such mCD rapidly extracts holes from CN and prevents the surface adsorption of methanol, favourably oxidising water over methanol and enhancing the selective CO2 reduction to alcohols. This work provides a unique strategy for efficient and highly selective CO2 reduction by water to high-value chemicals.Publisher PDFPeer reviewe
Publication status:
Published
Peer review status:
Peer reviewed

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Publisher copy:
10.1038/s41467-020-16227-3

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ORCID:
0000-0001-8395-726X
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ORCID:
0000-0001-5042-5769
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ORCID:
0000-0001-7545-4259
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ORCID:
0000-0001-7945-8548
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ORCID:
0000-0001-8453-3979


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Funder identifier:
https://ror.org/012mzw131
Grant:
RPG-2017-122
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Funder identifier:
https://ror.org/0439y7842
Grant:
EP/S018204/2/1


Publisher:
Nature Research
Journal:
Nature Communications More from this journal
Volume:
11
Issue:
1
Pages:
2531-2531
Publication date:
2020-05-21
DOI:
EISSN:
2041-1723
ISSN:
2041-1723


Language:
English
Keywords:
Pubs id:
1106326
Local pid:
pubs:1106326
Source identifiers:
W3027479287
Deposit date:
2025-12-04
ARK identifier:
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