Abstract Cs2NaInCl6 have become a hot research topic in perovskite optoelectronic materials. However, there is no research on the vacancy properties of Cs2NaInCl6 at present. Herein,using density functional theory-based first-principles calculations, the impact of Cs, Na, In, and Cl single vacancies on the microstructure, electronic, optical, and mechanical properties of the double perovskite Cs2NaInCl6 were investigated. The research shows that the presence of vacancy defects leads to distortion of the Cs2NaInCl6 double perovskite structure and an increase in the unit cell volume. Cs vacancy (VCs) and Na vacancy (VNa) cause an increased band gap for Cs2NaInCl6, by 2.92eV and 3.1eV respectively, without changing the characteristics of the initial direct band gap; VIn and VCl cause the intrinsic semiconductor Cs2NaInCl6 to transform into p-type and n-type semiconductors, respectively, altering the conductivity of Cs2NaInCl6. In terms of optical properties, different vacancy defect systems exhibit different absorption abilities in the visible and ultraviolet light ranges. The defect system overall improves light absorption in the low energy region, and as the incident photon energy increases, the material exhibits the best optical performance at around 15eV. In addition, it is found that VCs, VNa, and VIn caused blue shift in the absorption edge of Cs2NaInCl6, while VCl caused red shift in the absorption edge. In terms of mechanical properties, defects cause varying degrees of reduction in Young's modulus (E), shear modulus (G), and bulk modulus (B) of Cs2NaInCl6, which to some extent alters the mechanical properties of Cs2NaInCl6. These research results provide theoretical guidance for understanding the influence of vacancies on the properties of Cs2NaInCl6 double perovskite and optimizing the performance of perovskite optoelectronic devices, and they also enhance its applications in photovoltaic cells, optoelectronic sensors, and other optoelectronic coupling devices.
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