Novel dual Z-scheme Bi/BiOI-Bi2O3-C3N4 heterojunctions with synergistic boosted photocatalytic degradation of phenol
Photocatalysis is an emerging technique for the remediation of refractory organic contaminants. Herein, a novel dual Z-scheme Bi/BiOI-Bi 2 O 3 -C 3 N 4 heterojunctions were constructed through a calcining process following with I − etching and UV-reduction processes. Various analytical technologies were adopted to characterize the materials. As a result, the Bi 0 decorated composite presented improved visible-light-response and rapid charge transfer. Due to the synergy of Bi 0 and dual Z-scheme heterostructures, a remarkable photocatalytic performance toward phenol degradation was achieved with the highest degradation efficiency of 93.2% and rate constant of 0.0161 min −1 over the optimal composite within 75 min of visible light irradiation. Interestingly, the concentration of the yielded benzoquinone considerably decreased with the introduction of C 3 N 4 . Trapping experiments and electron spin resonance (ESR) tests indicated that h + , O 2 − , OH and e − contributed to phenol remediation, and h + and O 2 − were the crucial species toward phenol degradation. Furthermore, outstanding stability was obtained only with a decline of 3.8% after 4 cycles. A reasonable charge transfer mechanism was also proposed. This work provides a new route for in situ construction of Bi 0 decorated dual Z-scheme heterojunction for phenolic compounds degradation.
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