TY - JOUR
T1 - One-step low-temperature synthesis of 0D CeO2 quantum dots/2D BiOX (X = Cl, Br) nanoplates heterojunctions for highly boosting photo-oxidation and reduction ability
AU - Yang, Jian
AU - Liang, Yujun
AU - Li, Kai
AU - Yang, Gui
AU - Yin, Shu
N1 - Funding Information:
This work was supported by the National Natural Science Foundation of China (Grant Nos. 21571162 ), also partly supported by the JSPS KAKENHI Grant Number JP16H06439 (Grant-in-Aid for Scientific Research on Innovative Areas), the Dynamic Alliance for Open Innovation Bridging Human, Environment and Materials, the Cooperative Research Program of “Network Joint Research Center for Materials and Devices”.
Publisher Copyright:
© 2019 Elsevier B.V.
Copyright:
Copyright 2020 Elsevier B.V., All rights reserved.
PY - 2019/8/5
Y1 - 2019/8/5
N2 - 0D/2D heterojunctions, especially quantum dots (QDs)/nanoplates have attracted noteworthy attention for use of the high charge mobility of photoinduced electrons and holes. Herein, we report a novel one-step low-temperature route for the controlled synthesis of CeO2 QDs/BiOX (X = Cl, Br) nanoplates heterojunctions with the self-created in-built Ce4+/Ce3+ redox centers. The as-prepared heterojunctions exhibited outstanding photocatalytic abilities not only for the oxidation of tetracycline (TC) but also for the reduction of hexavalent chromium (Cr6+) although under 5 W white LED light irradiation. The considerably enhanced capabilities were attributed to the improvement of light absorption and the highly effective transfer and separation of photoexcited carriers, which encouraged by the strong synergistic effects of inner Ce4+/Ce3+ redox centers and the formation of intimately contacted interface between CeO2 QDs and BiOX nanoplates. Meanwhile, the likely degradation pathway of TC was proposed on the basis of the intermediate products detected by GC–MS, and the appearance photocatalytic mechanisms were also discussed in detail. This work could open new possibilities to provide some insight into a facile, energy saving and environmental friendly pathway for synthesizing versatile 0D/2D Bi-based heterojunction materials with high photocatalytic performance.
AB - 0D/2D heterojunctions, especially quantum dots (QDs)/nanoplates have attracted noteworthy attention for use of the high charge mobility of photoinduced electrons and holes. Herein, we report a novel one-step low-temperature route for the controlled synthesis of CeO2 QDs/BiOX (X = Cl, Br) nanoplates heterojunctions with the self-created in-built Ce4+/Ce3+ redox centers. The as-prepared heterojunctions exhibited outstanding photocatalytic abilities not only for the oxidation of tetracycline (TC) but also for the reduction of hexavalent chromium (Cr6+) although under 5 W white LED light irradiation. The considerably enhanced capabilities were attributed to the improvement of light absorption and the highly effective transfer and separation of photoexcited carriers, which encouraged by the strong synergistic effects of inner Ce4+/Ce3+ redox centers and the formation of intimately contacted interface between CeO2 QDs and BiOX nanoplates. Meanwhile, the likely degradation pathway of TC was proposed on the basis of the intermediate products detected by GC–MS, and the appearance photocatalytic mechanisms were also discussed in detail. This work could open new possibilities to provide some insight into a facile, energy saving and environmental friendly pathway for synthesizing versatile 0D/2D Bi-based heterojunction materials with high photocatalytic performance.
KW - Ce/Ce redox centers
KW - CeO QDs/BiOX nanoplates
KW - Photo-oxidation
KW - Photo-reduction
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U2 - 10.1016/j.apcatb.2019.03.017
DO - 10.1016/j.apcatb.2019.03.017
M3 - Article
AN - SCOPUS:85062732233
VL - 250
SP - 17
EP - 30
JO - Applied Catalysis B: Environmental
JF - Applied Catalysis B: Environmental
SN - 0926-3373
ER -