Photocatalytic Degradation of Methyl Orange Dyes Using Green Synthesized MoS2/Co3O4 Nanohybrids

In this work, a new binary MoS2/Co3O4 nanohybrids was successfully fabricated and the chemical structures, morphologies, electrochemical and optical characterizations were carried out. In addition, heterojunction nanoparticles present in S-scheme structures act as electron traps and promote light absorption capacity for the degradation of Methyl orange (MO) with visible-light activity. MoS2/Co3O4 nanohybrids suggested excellent photocatalytic performance compared to bare MoS2 and Co3O4, where 95.6% of MO was degraded within 170 min, respectively. The results also showed excellent stability and recyclability over five consecutive cycles, without noticeable changes in the nanocomposite structure. The boosted photocatalytic degradation and redox activities of MoS2/Co3O4 can be attributed to the created S-scheme heterostructure to facilitate the separation of and to delay recombination of photoinduced charge carriers. We believe that this strategy of exploiting nanohybrid photocatalysts has great potential in the field of environmental catalysis and diverse applications.

Automated summary

In this work, a new binary MoS2/Co3O4 nanohybrids with excellent photocatalytic performance and stability was successfully fabricated. The enhanced photocatalytic degradation and redox activities can be attributed to the created S-scheme heterostructure to facilitate the separation of and to delay recombination of photoinduced charge carriers. This strategy of exploiting nanohybrid photocatalysts has great potential in the field of environmental catalysis and diverse applications.