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In situ synthesis of Z-scheme BiPO4/BiOCl0.9I0.1 heterostructure with multiple vacancies and valence for efficient photocatalytic degradation of organic pollutant
摘要： Design and construction of Z-scheme photocatalyst has been attracted much attention, which is a great challenge to develop highly efficient photocatalyst without the external redox mediators. Herein, a novel efficient redox-mediator-free Z-scheme BiPO4/BiOCl0.9I0.1 heterojunction is synthesized in situ via a mild 90℃ water bath reaction. The as-synthesized BiPO4/BiOCl0.9I0.1 heterostructure exhibits outstanding photocatalytic performance for degradation of phenol and Rhodamine B, approximately 2.6 and 4.3 times higher than that of BiOCl0.9I0.1, respectively. The BiPO4/BiOCl0.9I0.1 heterostructure have multiple vacancies and valence, such as Bi5+, Bi3+, Bi(3-x)+, I-, I3-, and IO3-, which could facilitate the charge separation and transfer in the photocatalytic process. The higher photocatalytic activity of redox-mediator-free Z-scheme BiPO4/BiOCl0.9I0.1 heterostructure could be attributed to the strong redox ability, multiple charge transfer channels via the various defects, and tight contact due to in situ synthesis. The finding provides some new insights for the design of effective direct Z-scheme photocatalyst with multiple defects.
关键词： direct Z-scheme heterojunction,photocatalysis,BiOCl0.9I0.1/BiPO4,redox-mediator-free,multiple defects
更新于2025-09-04 15:30:14
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<i>In situ</i> topotactic fabrication of direct Z-scheme 2D/2D ZnO/Zn <sub/>x</sub> Cd <sub/>1?x</sub> S single crystal nanosheet heterojunction for efficient photocatalytic water splitting
摘要： Direct Z-scheme heterojunction can effectively enhance the photocatalytic activity due to its low carrier recombination rate and high redox ability. In this study, a 2D/2D ZnO/ZnxCd1?xS single crystal nanosheet heterojunction is synthesized in situ by topotactic sulfurization/oxidization pyrolysis of Zn/Cd/Al layer double hydroxides (LDHs). Its unique structure provides not only numerous intimate interfaces but also a direct Z-scheme junction. The in situ topotactic fabrication of ZnO by the oxidation process causes some Zn ions to dissolve out from the Zn0.67Cd0.33S solid solution nanosheets with increase in annealing temperature and time. The longer the time for oxidation, the more ZnO is obtained. The formation of ZnO yields 2D/2D ZnO/ZnxCd1?xS single crystal nanosheet heterojunction, which increases the visible light absorption and boosts the separation of photogenerated carriers. The ZnO/ZnxCd1?xS-4 single crystal nanosheet heterojunction presents the highest photocatalytic activity under visible light irradiation (38.93 mmol h?1 g?1), which is nearly 16.93 times higher than that of Zn0.67Cd0.33S-300, and an external quantum efficiency of 40.97% at λ = 420 nm. The proposed synthetic route for the construction of 2D/2D ZnO/ZnxCd1?xS single crystal nanosheet provides a direct Z-scheme structure with highly efficient photocatalytic hydrogen evolution activity.
关键词： 2D/2D ZnO/ZnxCd1?xS,photocatalytic water splitting,Zn/Cd/Al layer double hydroxides,Direct Z-scheme heterojunction,topotactic sulfurization/oxidization pyrolysis
更新于2025-09-04 15:30:14