High dopant activation in arsenic doped single-crystal CdTe thin films: Insights from MBE growth and rapid thermal processing
Source abstract
Abstract
Single-crystal model systems are valuable tools to investigate fundamental material properties. In this work, we use molecular beam epitaxy to deposit in situ arsenic (As) doped single-crystal CdTe films on large area Si substrates to better understand As doping for photovoltaic applications. We found that As incorporation is highly temperature dependent: a substrate temperature difference of 50 °C can lead to several orders of magnitude difference in As concentration. Cd overpressure during in situ doping may limit out-diffusion of As but decrease As incorporation, especially at lower growth temperatures. Carrier concentrations greater than 1016 cm−3 can be achieved with or without Cd overpressure when annealed at temperatures above 500 °C. However, unlike the low (∼1% to 5%) dopant activation commonly observed in polycrystalline CdTe, our films achieve significantly higher activation ratios—exceeding 50%, and in some cases approaching 80%. These values are consistent with or exceed prior reports in single-crystal CdTe systems. In addition to as-deposited arsenic concentrations, we also consider arsenic distribution after different rapid thermal processing temperatures. We propose a detailed definition and description of how arsenic incorporation is considered and calculated. Due to carrier concentration saturation, As incorporation also needs to be controlled to average levels of 1017 cm−3 to achieve high activation. These findings suggest that higher annealing temperature regimes may be beneficial to polycrystalline CdTe based PV devices.
Source: crossref · Quality: baseline
Research context
OpenAlex topics: Chalcogenide Semiconductor Thin Films · Quantum Dots Synthesis And Properties · Advanced Semiconductor Detectors and Materials
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
National Renewable Energy Laboratory 1 , Golden, Colorado 80401,
Colorado School of Mines 2 , Golden, Colorado 80401,
Sivananthan Laboratories 3 , Bolingbrook, Illinois 60440,
Funding
U.S. Department of Energy
References (45)
Show source-provided references
1. Arsenic-doped CdSeTe solar cells achieve world record 22.3% efficiency10.1109/JPHOTOV.2023.3282581 ↗
2. Exceeding 20% efficiency with in situ group V doping in polycrystalline CdTe solar cells10.1038/s41560-019-0446-7 ↗
3. Effects of absorber near-interface compensation on Cd(Se,Te) solar cell performance10.1016/j.solmat.2022.111928 ↗
4. CdTe-based thin film photovoltaics: Recent advances, current challenges and future prospects10.1016/j.solmat.2023.112289 ↗
5. Why increased CdSeTe charge carrier lifetimes and radiative Efficiencies did not result in voltage boost for CdTe solar cells10.1002/aenm.202301784 ↗
6. Impact of dopant-induced optoelectronic tails on open-circuit voltage in arsenic-doped Cd(Se)Te solar cells10.1063/5.0018955 ↗
7. The roles of carrier concentration and interface, bulk, and grain-boundary recombination for 25% efficient CdTe solar cells10.1063/1.4984320 ↗
8. Enhanced p-type dopability of P and As in CdTe using non-equilibrium thermal processing10.1063/1.4926748 ↗
9. Dependence of the minority-carrier lifetime on the stoichiometry of CdTe using time-resolved photoluminescence and first-principles calculations10.1103/PhysRevLett.111.067402 ↗
10. Shallow and deep acceptor states in CdTe10.1016/0031-9163(63)90423-2 ↗
11. p-doping limit and donor compensation in CdTe polycrystalline thin film solar cells10.1016/j.solmat.2010.05.006 ↗
12. Self-compensation in arsenic doping of CdTe10.1038/s41598-017-04719-0 ↗
13. Arsenic doping and diffusion in CdTe: A DFT study of bulk and grain boundaries10.1088/1361-648X/aca8e5 ↗
14. Understanding arsenic incorporation in CdTe with atom probe tomography10.1016/j.solmat.2018.02.023 ↗
15. Grain boundaries in CdTe thin film solar cells: A review10.1088/0268-1242/31/9/093001 ↗
16. Doping levels, trap density of states and the performance of co-doped CdTe(As,Cl) photovoltaic devices10.1016/j.solmat.2009.04.010 ↗
17. Impurity doping and compensation mechanisms in CdTe10.1016/S0040-6090(00)01717-X ↗
18. Sources of carrier compensation in arsenic-doped HgCdTe10.1016/j.jpcs.2012.07.019 ↗
19. Highly arsenic doped CdTe layers for the back contacts of CdTe solar cells10.1557/PROC-1012-Y12-08 ↗
20. Comparison of Sb, As, and P doping in Cd-rich CdTe single crystals: Doping properties, persistent photoconductivity, and long-term stability10.1063/5.0004883 ↗
21. In situ arsenic doping of CdTe/Si by molecular beam epitaxy10.1007/s11664-015-3913-3 ↗
22. Arsenic activation and compensation in single crystal CdTe bilayers10.1063/5.0246994 ↗
23. Dislocation reduction in CdTe/Si by molecular beam epitaxy through in-situ annealing10.1016/j.jcrysgro.2008.09.023 ↗
24. High quality large-area CdTe(211)B on Si(211) grown by molecular beam epitaxy10.1063/1.119406 ↗
25. 1995
26. 1989
27. First-principles multiple-barrier diffusion theory: The case study of interstitial diffusion in CdTe10.1103/PhysRevB.91.075202 ↗
28. Doping limits of phosphorus, arsenic, and antimony in CdTe10.1021/acs.jpclett.2c03233 ↗
29. Chemical diffusion in CdTe:Cl10.1088/0268-1242/25/4/045019 ↗
30. Diffusion of Cd vacancy and interstitials of Cd, Cu, Ag, Au and Mo in CdTe: A first principles investigation10.1016/j.solener.2013.12.017 ↗
31. Empirical correlations between the Arrhenius’ parameters of impurities’ diffusion coefficients in CdTe crystals10.1007/s11669-015-0364-8 ↗
32. Precise arsenic doping of HgCdTe by MBE and effects on compositional interdiffusion10.1007/s11664-006-0266-y ↗
33. Heavy arsenic doping of silicon by molecular beam epitaxy10.1016/S0022-0248(02)02197-8 ↗
34. Beyond thermodynamic defect models: A kinetic simulation of arsenic activation in CdTe10.1103/PhysRevMaterials.2.103803 ↗
35. Experimental and theoretical comparison of Sb, As, and P diffusion mechanisms and doping in CdTe10.1088/1361-6463/aaa67e ↗
36. Overcoming carrier concentration limits in polycrystalline CdTe thin films with in situ doping10.1038/s41598-018-32746-y ↗
37. Study of thin film poly-crystalline CdTe solar cells presenting high acceptor concentrations achieved by in-situ arsenic doping10.1016/j.solmat.2019.02.025 ↗
38. Incorporation and activation of arsenic dopant in single-crystal CdTe grown on Si by molecular beam epitaxy10.1007/s11664-014-3173-7 ↗
39. Nonstoichiometric composition shift in physical vapor deposition of CdTe thin films10.1016/j.jcrysgro.2015.02.018 ↗
40. Multiscale modeling and optimization of group V doping and compensation in CdSexTe1−x10.1021/acsaem.4c02744 ↗
41. Direct observation of group-V dopant substitutional defects in CdTe single crystals10.1021/jacs.3c01248 ↗
42. Optimization of doping Cd Te with group-V elements: A first-principles study10.1103/PhysRevApplied.15.054045 ↗
43. Tailoring MgZnO/CdSeTe interfaces for photovoltaics10.1109/JPHOTOV.2018.2877982 ↗
44. Obtaining large columnar CdTe grains and long lifetime on nanocrystalline CdSe, MgZnO, or CdS layers10.1002/aenm.201702666 ↗
45. Data for `High dopant activation in arsenic doped single-crystal CdTe thin films: Insights from MBE growth and rapid thermal processing10.7799/2572306 ↗