Acta Phys. -Chim. Sin.

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S-scheme 0.5Co-BiOCl/Co3O4: synergistic regulation of charge separation by heterojunction and spin polarization for enhanced photodegradation performance

Ying Li1, Zhiling Huang2, Tianhui Yu1, Yue Meng2, Zheming Ni1, Shengjie Xia1   

  1. 1 Department of Chemistry, College of Chemical Engineering, Zhejiang University of Technology, Hangzhou 310014, Zhejiang Province, China;
    2 Department of Pharmaceutical Engineering, School of Life and Health Sciences, Huzhou College, Huzhou 313000, Zhejiang Province, China
  • Received:2026-07-01 Revised:2026-08-12 Accepted:2026-08-13
  • Contact: Shengjie Xia, Yue Meng E-mail:xiasj@zjut.edu.cn;mengyue@zjhzu.edu.cn

Abstract: Spin polarization control can suppress the recombination of photogenerated carriers at the intrinsic electron spin level, significantly enhancing charge separation efficiency. This study proposes a synergistic strategy combining spin polarization with an S-scheme heterojunction. Specifically, Co doping is introduced into BiOCl (BOC) nanosheets via a coupled hydrothermal-calcination method to induce spin polarization. Meanwhile, the material is coupled with cubic Co3O4 to construct a 0.5Co-BOC/Co3O4 Sscheme heterojunction. Characterization results from density functional theory (DFT) calculations, vibrating sample magnetometer (VSM), and Kelvin probe force microscopy (KPFM) collectively confirm that Co doping induces asymmetric occupation of spin-polarized electronic states near the Fermi level of BOC. This narrows the bandgap and promotes charge transfer. The work function difference drives interfacial electrons to transfer directionally from Co3O4 to 0.5Co-BOC, forming a built-in electric field. This built-in electric field drives the spatial directional separation of photogenerated carriers. Meanwhile, spin polarization regulates the spin states of carriers and suppresses spinmatched recombination. Their synergy achieves dual regulation of “spatial separation + spin-forbidden effect”, significantly enhancing carrier separation efficiency and interfacial transport kinetics. Under optimal conditions, the degradation rate of ciprofloxacin (CIP) reaches 95.4% within 80 min. This is 1.50 times that of pristine BOC and 4.79 times that of pristine Co3O4. Liquid chromatography-mass spectrometry (LC-MS) and toxicity estimation software tool (T.E.S.T.) assessments indicate that CIP is degraded stepwise via multiple pathways, with significantly reduced toxicity of the intermediate products. This study elucidates the mechanism of synergistic enhancement of carrier separation by spin polarization and the built-in electric field, providing new insights for designing efficient photocatalytic systems.

Key words: Spin polarization, Co-doping, S-scheme heterojunction, Photodegradation, Built-in electric field