Intrinsic point defects and complexes in the quaternary kesterite semiconductor Cu2ZnSnS4.
PHYS REV B
Current knowledge of the intrinsic defect properties of Cu2ZnSnS4 (CZTS) is limited, which is hindering further improvement of the performance of CZTS-based solar cells. Here, we have performed first-principles calculations for a series of intrinsic defects and defect complexes in CZTS, from which we have the following observations. (i) It is important to control the elemental chemical potentials during crystal growth to avoid the formation of secondary phases such as ZnS, CuS, and Cu2SnS3. (ii) The intrinsic p-type conductivity is attributed to the Cu-Zn antisite which has a lower formation energy and relatively deeper acceptor level compared to the Cu vacancy. (iii) The low formation energy of many of the acceptor defects will lead to the intrinsic p-type character, i.e., n-type doping is very difficult in this system. (iv) The role of electrically neutral defect complexes is predicted to be important, because they have remarkably low formation energies and electronically passivate deep levels in the band gap. For example, [Cu-Zn(-) + Zn-Cu(+)], [V-Cu(-) + Zn-Cu(+)], and [Zn-Sn(2-) + 2Zn(Cu)(+)] may form easily in nonstoichiometric samples. The band alignment between Cu2ZnSnS4, CuInSe2 and the solar-cell window layer CdS has also been calculated, revealing that a type-II band alignment exists for the CdS/Cu2ZnSnS4 heterojunction. The fundamental differences between CZTS and CuInSe2 for use in thin-film photovoltaics are discussed. The results are expected to be relevant to other I-2-II-IV-VI4 semiconductors.
|Title:||Intrinsic point defects and complexes in the quaternary kesterite semiconductor Cu2ZnSnS4|
|Keywords:||FILM SOLAR-CELLS, THIN-FILMS, BAND OFFSETS, II-VI, CUINSE2, RECOMBINATION, PHOTOVOLTAICS, NANOCRYSTALS, EVAPORATION, GROWTH|
|UCL classification:||UCL > School of BEAMS > Faculty of Maths and Physical Sciences
UCL > School of BEAMS > Faculty of Maths and Physical Sciences > Chemistry
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