Enhanced photocatalytic Cr(VI) reduction and H2 production of CdSe quantum dots supported on Co-encapsulated N-doped carbon
•Co@N-doped carbon was prepared by pyrolysis of ZIF-8@ZIF-67 to modify CdSe QDs.•The k of Cr(VI) reduction over 2%Co@C/CdSe is 33.9 times higher than that of CdSe.•The best H2 evolution rate of 2%Co@C/CdSe is 139 times larger than that of CdSe.•Enhanced charge separation and light absorption is resp...
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Veröffentlicht in: | Journal of the Taiwan Institute of Chemical Engineers 2023-05, Vol.146, p.104798, Article 104798 |
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Sprache: | eng |
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Zusammenfassung: | •Co@N-doped carbon was prepared by pyrolysis of ZIF-8@ZIF-67 to modify CdSe QDs.•The k of Cr(VI) reduction over 2%Co@C/CdSe is 33.9 times higher than that of CdSe.•The best H2 evolution rate of 2%Co@C/CdSe is 139 times larger than that of CdSe.•Enhanced charge separation and light absorption is responsible for high activity.
Solar-driven water splitting is regarded as one promising green way to produce H2. Photo-reduction of hexavalent chromium (Cr(Ⅵ)) to hypotoxic Cr(III) can control the Cr(VI)-induced pollution. A key in these processes is to develop a photocatalyst with high specific surface area, good light absorption and efficient charge carrier separation.
A Co-encapsulated N-doped carbon (Co@NC) was prepared by pyrolysis ZIF-8@ZIF-67 precursor to modify CdSe quantum dots (QDs). The obtained catalyst was used to reduce Cr(Ⅵ) and split water under visible light irradiation.
Modification CdSe with Co@NC made obtained Co@NC/CdSe possessing enhanced visible-light absorption and photoexcited charge separation. The optimal 2%Co@NC/CdSe exhibited the excellent Cr(Ⅵ) reduction performance with a rate constant of 0.28 min–1 in the absence of sacrificial agent, as well as high H2 evolution rate of 6.48 mmol g–1 h–1 in 10% lactic acid solution. The H2O2 and electrons were the active species to reduce Cr(VI). This work gives a beneficial insight for improving the photocatalytic activity of QDs.
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ISSN: | 1876-1070 1876-1089 |
DOI: | 10.1016/j.jtice.2023.104798 |