Abstract

Cation substitution is a promising approach to reduce the antisite defects and further improve the efficiency of Cu2ZnSn(S,Se)4 (CZTSSe) cells. In this paper, silver (Ag) has been introduced into Cu2ZnSn(S,Se)4 (CZTSSe) thin film to replace Cu partially and form (Cu1-xAgx)2ZnSn(S,Se)4 (0 ≤ x ≤ 1) (CAZTSSe) alloy films by combination of solution method and a rapid annealing technique. The fundamental properties of the mixed Ag-Cu kesterite compound are systematically reported as a function of the Ag/(Ag+Cu) ratio. The results show that band gap of kesterite CAZTSSe is incessantly increased by adjusting the Ag doping content, indicating that the CAZTSSe alloy film is a potentially applicable bandgap grading absorption layers material to obtain higher CZTSSe device. Furthermore, CAZTSSe alloy films with better electrical performance were also obtained by adjusting the Ag content during film fabrication. Finally, we also observed an increment in open circuit voltage (Voc) by 160 mV and an accompanying rise in device efficiency from 4.24 to 5.95%. The improvement is correlated to the improved grain size and decreased antisite defects of Cu instead of Zn site (CuZn) in the lattice. The Voc enhancement evidences that the solution method is facile and viable to achieve proper cation substitution toward higher efficiency kesterite solar cells. In addition, the CAZTSSe cell also displays better charge collection performance because of the higher fill factor (FF) and power conversion efficiency (PCE). Therefore, it can be concluded that the doping of Ag is a potentially appropriate method to reduce the Cuzn antisite defects of CZTSSe and improve efficiency of CZTSSe device.

Highlights

  • Cu2ZnSn(S,Se)4 (CZTSSe) film has been regarded as a promising film because of the earth abundant elements and favorable optoelectronic properties, which may substitute Cu(In,Ga)Se2 (CIGS) thin film and other inorganic films [1,2,3,4,5,6,7]

  • Some literatures have indicated that the occupation of Cu atoms in the Zn lattice sites producing the antisite defects of the occupation of Cu atoms in the Zn lattice sites (CuZn) should be avoided because they can generate band tailing, deep surface or bulk defects, which limited the Voc of devices [12,13]

  • In addition to inhibiting the formation energy of CuZn antisite defects, the replacement of cations can adjust band gap of the CZTSSe film and make it better match to CdS layer [15,16]

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Summary

Introduction

Cu2ZnSn(S,Se)4 (CZTSSe) film has been regarded as a promising film because of the earth abundant elements and favorable optoelectronic properties, which may substitute Cu(In,Ga)Se2 (CIGS) thin film and other inorganic films [1,2,3,4,5,6,7]. The CZTSSe film exists a high concentration of CuZn antisite defects [12]. In addition to inhibiting the formation energy of CuZn antisite defects, the replacement of cations can adjust band gap of the CZTSSe film and make it better match to CdS layer [15,16].

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