A high-efficiency mediator-free Z-scheme Bi2MoO6/AgI heterojunction with enhanced photocatalytic performance

A high-efficiency Z-scheme Bi2MoO6/AgI heterojunction was designed and fabricated via in situ growth of AgI on Bi2MoO6. Its photocatalytic activity was investigated with the degradation of malachite green (MG). After 40 min of visible light irradiation, near complete degradation of MG (20 mg/L) occurred when BA11 (Bi2MoO6:AgI = 1:1, 2.0 g/L) was present, while only 29.0% and 49.7% of the MG could be degraded in the presence of Bi2MoO6 and AgI, respectively. The excellent photocatalytic activity of BA11 results from strong visible light absorption and the low recombination efficiency of photogenerated electron-hole pairs induced by the formation of heterojunction. Density function theory (DFT) calculations revealed that the formation of built-in electric field at the interface between Bi2MoO6 and AgI facilitates the effective separation and transfer of photogenerated charge carriers. Results of reuse experiments indicated that the heterostructured photocatalyst has excellent stability. Radical scavenging experiments and electron spin resonance spectra showed that superoxide radicals (center dot O-2(-)) and hydroxyl radicals (center dot OH) were the major reactive oxygen species in the photocatalytic system. The photocatalytic degradation pathway of MG was proposed based on the organic degradation intermediates detected. These findings demonstrate that the mediator-free Z-scheme Bi2MoO6/AgI heterojunction could serve as a promising photocatalyst in photocatalytic treatment of organic pollutants. (C) 2021 Elsevier B.V. All rights reserved.

Automated summary

A high-efficiency Z-scheme Bi2MoO6/AgI heterojunction was designed and fabricated, showing excellent photocatalytic activity in the degradation of malachite green. The Ba11 sample exhibited strong visible light absorption and low recombination efficiency of photogenerated electron-hole pairs, with DFT calculations revealing the role of the built-in electric field at the interface. The heterostructured photocatalyst demonstrated great stability and the presence of superoxide radicals and hydroxyl radicals as the major reactive oxygen species in the photocatalytic system.