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Polycrystalline thin films of AgSbS2 of thickness 140 nm and crystalline structure matching that of the mineral cuboargyrite (a = 0.5652 nm) are obtained by heating chemically deposited thin films at 150–320 °C. These films are deposited at 40 °C from a solution mixture containing antimony‐thiosulfate complex and Ag‐nitrate at a mole‐fraction Ag/(Ag+Sb) of 0.31. The as‐deposited films are progressively transformed to cubic‐AgSbS2, with the fraction of crystalline matter at 3.7% after heating at 150 °C and 98% at 280 °C. The crystalline grain diameter is limited to 8–11 nm. The amorphous film has an optical band gap (Eg) of 2.03 eV and the film heated at 320 °C has an Eg of 1.79 eV. The crystalline films are photoconductive; with electrical conductivity of 10−5 Ω−1 cm−1 under an intensity of illumination, 1000 W m−2 (tungsten‐halogen). The mobility–lifetime product of the material is 7.5 × 10−7 cm2 V−1. A solar cell, SnO2:F/CdS/AgSbS2(420 nm)/C, has open circuit voltage, 0.615 V; short‐circuit current density, 1.67 mA cm−2; and conversion efficiency, 0.57% for air‐mass 1.5 global solar radiation. Estimate for the maximum photo‐generated current density for cubic‐AgSbS2 is 16 mA cm−2; hence a supplementary absorber is recommended for future development of the solar cell.
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Capistrán‐Martínez et al. (2015) studied this question.
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