2022
DOI: 10.1039/d1cy01850g
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Construction of a Z-scheme g-C3N4/NBGO/BiVO4 heterostructure with visible-light driven photocatalytic degradation of tetracycline: efficiency, reaction pathway and mechanism

Abstract: In this study, an aminated graphene-like biochar (NGBO) was used as a solid-state electron mediator at a g-C3N4/BiVO4 interface to construct a hybrid Z-scheme system (g-C3N4/NBGO/BiVO4) for the photocatalytic degradation of tetracycline (TC) from aqueous solutions.

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Cited by 29 publications
(13 citation statements)
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References 80 publications
(77 reference statements)
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“…In general, the increased current response demonstrates the accelerated photogenerated charge carrier transport kinetics under light illumination. 83,84 The consequence illustrates that the hetero-structure, B doping, RP, and CoP can increase the charge separation efficiency. As shown in Fig.…”
Section: Resultsmentioning
confidence: 97%
“…In general, the increased current response demonstrates the accelerated photogenerated charge carrier transport kinetics under light illumination. 83,84 The consequence illustrates that the hetero-structure, B doping, RP, and CoP can increase the charge separation efficiency. As shown in Fig.…”
Section: Resultsmentioning
confidence: 97%
“…In general, the higher the relative amount of pyridinic N, the better the catalytic performance of the photocatalyst. 46 This is perhaps because the electron-withdrawing pyridinic N sites can accept electrons from the adjacent C atoms, promoting the adsorption of intermediates necessary for the generation of ROS (e.g., OH − , OOH − ). 58 From Figure 6, the ratios of pyridinic N to pyrrolic N in WNGA-1, WNGA-2, WNGA-3, and WNGA-4 are 0.14, 0.31, 0.34, and 0.28, respectively.…”
Section: ■ Results and Discussionmentioning
confidence: 99%
“…This indicates that such an interfacial charge transfer facilitates the separation of photogenerated electron–hole pairs. Moreover, the conduction band (CB) position of TiO 2 (−0.43 eV) is more negative than the standard reduction potentials of O 2 /·O 2 – (−0.33 eV), indicating that the CB potential of TiO 2 is sufficient to reduce O 2 to ·O 2 – . The E VB of TiO 2 (2.75 eV) is more positive than the standard oxidation potential of ·OH/H 2 O (2.68 eV), so part of TiO 2 can oxidize H 2 O to form ·OH.…”
Section: Resultsmentioning
confidence: 99%