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Title: Combinatorial Insights into Doping Control and Transport Properties of Zinc Tin Nitride

Journal Article · · Journal of Materials Chemistry. C
DOI:https://doi.org/10.1039/C5TC02663F· OSTI ID:1227680
 [1];  [2];  [2];  [3];  [2];  [2];  [2];  [1];  [1]
  1. National Renewable Energy Lab. (NREL), Golden, CO (United States); Colorado School of Mines, Golden, CO (United States)
  2. National Renewable Energy Lab. (NREL), Golden, CO (United States)
  3. Harvey Mudd College, Claremont, CA (United States)

ZnSnN2 is an Earth-abundant semiconductor analogous to the III–nitrides with potential as a solar absorber due to its direct bandgap, steep absorption onset, and disorder-driven bandgap tunability. Despite these desirable properties, discrepancies in the fundamental bandgap and degenerate n-type carrier density have been prevalent issues in the limited amount of literature available on this material. We we use a combinatorial RF co-sputtering approach, we explored a growth-temperature-composition space for Zn1+xSn1-xN2 over the ranges 35–340 °C and 0.30–0.75 Zn/(Zn + Sn). In this way, we identified an optimal set of deposition parameters for obtaining as-deposited films with wurtzite crystal structure and carrier density as low as 1.8 × 1018 cm-3. Films grown at 230 °C with Zn/(Zn + Sn) = 0.60 were found to have the largest grain size overall (70 nm diameter on average) while also exhibiting low carrier density (3 × 1018 cm-3) and high mobility (8.3 cm2 V-1 s-1). Using this approach, we establish the direct bandgap of cation-disordered ZnSnN2 at 1.0 eV. Moreover, we report tunable carrier density as a function of cation composition, in which lower carrier density is observed for higher Zn content. Consequently, this relationship manifests as a Burstein–Moss shift widening the apparent bandgap as cation composition moves away from Zn-rich. Collectively, these findings provide important insight into the fundamental properties of the Zn–Sn–N material system and highlight the potential to utilize ZnSnN2 for photovoltaics.

Research Organization:
National Renewable Energy Lab. (NREL), Golden, CO (United States)
Sponsoring Organization:
USDOE Office of Energy Efficiency and Renewable Energy (EERE), Renewable Power Office. Solar Energy Technologies Office
DOE Contract Number:
AC36-08GO28308
OSTI ID:
1227680
Report Number(s):
NREL/JA-5J00-64356
Journal Information:
Journal of Materials Chemistry. C, Vol. 3, Issue 42; Related Information: Journal of Materials Chemistry C; ISSN 2050-7526
Publisher:
Royal Society of Chemistry
Country of Publication:
United States
Language:
English