Effect of nitrogen atom positioning on the trade-off between emissive and photocatalytic properties of carbon dots
Santanu Bhattacharyya (),
Florian Ehrat,
Patrick Urban,
Roland Teves,
Regina Wyrwich,
Markus Döblinger,
Jochen Feldmann,
Alexander S. Urban () and
Jacek K. Stolarczyk ()
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Santanu Bhattacharyya: Ludwig-Maximilians-Universität München
Florian Ehrat: Ludwig-Maximilians-Universität München
Patrick Urban: Ludwig-Maximilians-Universität München
Roland Teves: Ludwig-Maximilians-Universität München
Regina Wyrwich: Ludwig-Maximilians-Universität München
Markus Döblinger: Ludwig-Maximilians-Universität München
Jochen Feldmann: Ludwig-Maximilians-Universität München
Alexander S. Urban: Ludwig-Maximilians-Universität München
Jacek K. Stolarczyk: Ludwig-Maximilians-Universität München
Nature Communications, 2017, vol. 8, issue 1, 1-9
Abstract:
Abstract Carbon dots (CDs) are a versatile nanomaterial with attractive photoluminescent and photocatalytic properties. Here we show that these two functionalities can be easily tuned through a simple synthetic means, using a microwave irradiation, with citric acid and varying concentrations of nitrogen-containing branched polyethyleneimine (BPEI) as precursors. The amount of BPEI determines the degree of nitrogen incorporation and the different inclusion modes within the CDs. At intermediate levels of BPEI, domains grow containing mainly graphitic nitrogen, producing a high photoluminescence yield. For very high (and very low) BPEI content, the nitrogen atoms are located primarily at the edge sites of the aromatic domains. Accordingly, they attract photogenerated electrons, enabling efficient charge separation and enhanced photocatalytic hydrogen generation from water. The ensuing ability to switch between emissive and photocatalytic behavior of CDs is expected to bring substantial improvements on their efficiency for on-demand light emission or energy conversion applications.
Date: 2017
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Persistent link: https://EconPapers.repec.org/RePEc:nat:natcom:v:8:y:2017:i:1:d:10.1038_s41467-017-01463-x
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DOI: 10.1038/s41467-017-01463-x
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