摘要： Photocatalyst performance largely depends on the arrangement of surface atoms, especially nanomaterials. Herein, we proposed a novel defect-filled strategy by filling Bi defects on BiOCl surface with Pt4+ to achieve the controlled arrangement of BiOCl-surface atoms. The resulting PtO/Pt4+-BiOCl photocatalyst showed higher sulfamethoxazole (SMZ) degradation and photocatalytic nitrogen-fixation efficiency than PtO/BiOCl. The first-order kinetic constant of SMZ degradation over PtO/Pt4+-BiOCl (0.1312 min?1) was nearly twofold higher than that of PtO/BiOCl (0.0776 min?1). The photocatalytic nitrogen fixation activities of PtO/BiOCl and PtO/Pt4+-BiOCl were 244.2 mol·L?1·h?1 and 375.6 mol·L?1·h?1, respectively. The enhanced photocatalytic activity mainly attributed to the increased light absorption ability and separation efficiency of electron-hole pairs by Pt4+ doping. The defect-filled mechanism was confirmed by X-ray diffraction(XRD), X-ray photoelectron spectroscopy(XPS), Electron spin resonance(ESR), and Positron annihilation spectrometry. All these results indicated that the electrostatic interaction between Pt4+ in the precursor and Bi defects on the BiOCl surface was the key step in the defect-filled process. This work provides a new strategy for controlling the surface atom arrangement of nanomaterials.