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Title: Self-compensation in arsenic doping of CdTe

Journal Article · · Scientific Reports
ORCiD logo [1];  [2];  [3];  [4];  [4];  [4];  [4];  [5]; ORCiD logo [2]
  1. National Renewable Energy Lab. (NREL), Golden, CO (United States); Washington State Univ., Pullman, WA (United States)
  2. Washington State Univ., Pullman, WA (United States)
  3. Soochow Univ., Suzhou (China)
  4. National Renewable Energy Lab. (NREL), Golden, CO (United States)
  5. Beijing Computational Science Research Center, Beijing (China)

Efficient p-type doping in CdTe has remained a critical challenge for decades, limiting the performance of CdTe-based semiconductor devices. Arsenic is a promising p-type dopant; however, reproducible doping with high concentration is difficult and carrier lifetime is low. We systematically studied defect structures in As-doped CdTe using high-purity single crystal wafers to investigate the mechanisms that limit p-type doping. Two As-doped CdTe with varying acceptor density and two undoped CdTe were grown in Cd-rich and Te-rich environments. The defect structures were investigated by thermoelectric-effect spectroscopy (TEES), and first-principles calculations were used for identifying and assigning the experimentally observed defects. Measurements revealed activation of As is very low in both As-doped samples with very short lifetimes indicating strong compensation and the presence of significant carrier trapping defects. Defect studies suggest two acceptors and one donor level were introduced by As doping with activation energies at ~88 meV, ~293 meV and ~377 meV. In particular, the peak shown at ~162 K in the TEES spectra is very prominent in both As-doped samples, indicating a signature of AX-center donors. The AX-centers are believed to be responsible for most of the compensation because of their low formation energy and very prominent peak intensity in TEES spectra.

Research Organization:
National Renewable Energy Laboratory (NREL), Golden, CO (United States); Washington State Univ., Pullman, WA (United States)
Sponsoring Organization:
USDOE Office of Energy Efficiency and Renewable Energy (EERE), Renewable Power Office. Solar Energy Technologies Office
Grant/Contract Number:
AC36-08GO28308; EE0007537
OSTI ID:
1372626
Alternate ID(s):
OSTI ID: 1836064
Report Number(s):
NREL/JA-5K00-68633
Journal Information:
Scientific Reports, Vol. 7, Issue 1; ISSN 2045-2322
Publisher:
Nature Publishing GroupCopyright Statement
Country of Publication:
United States
Language:
English
Citation Metrics:
Cited by: 49 works
Citation information provided by
Web of Science

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Cited By (8)

Machine-learned impurity level prediction for semiconductors: the example of Cd-based chalcogenides journal April 2020
Exceeding 20% efficiency with in situ group V doping in polycrystalline CdTe solar cells journal August 2019
Rigid-band electronic structure of scandium nitride across the n -type to p -type carrier transition regime journal April 2019
Excitation-dependent carrier lifetime and diffusion length in bulk CdTe determined by time-resolved optical pump-probe techniques journal January 2018
Beyond thermodynamic defect models: A kinetic simulation of arsenic activation in CdTe journal October 2018
Optical and electrical design guidelines for ZnO/CdS nanorod-based CdTe solar cells journal January 2019
Self-compensation in chlorine-doped CdTe journal June 2019
High p-type doping, mobility, and photocarrier lifetime in arsenic-doped CdTe single crystals journal May 2018

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