Abstract

In this study, the unique 1D/2D CdS nanorod@Ti3C2 MXene (CdS@Ti3C2) composites photocatalysts are prepared by a hydrothermal strategy. The suitable band structure and superior electronic reduction capability of CdS in CdS@Ti3C2 composites are achieved, efficiently prolong the light absorption range and enhance photocatalytic performance of CdS. Moreover, Ti3C2 MXene NSs with good electronic transfer capability can prevent photoinduced carrier recombination, and the accordion-like multilayer can provide more reactive sites. The best sample of CdS@Ti3C2 with 15 mg Ti3C2 MXene adding amount exhibits super good photocatalytic H2 evolution rate (63.53 μmol h−1), and photocatalytic nitrogen fixation rate of 293.06 μmol L−1 h−1. The corresponding apparent quantum efficiencies (AQE) are 2.28% and 7.88%, respectively, higher than those of pure CdS NRs and CdS@Pt (0.1 wt%). Besides, CdS@Ti3C2-15 composite shows good long-term stability under simulated sunlight irradiation.

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