Published July 19, 2019 | Version v1

Increasing N content in GaNAsP nanowires suppresses the impact of polytypism on luminescence

  • 1. Department of Physics, Chemistry and Biology, Linköping University, SE-58183 Linköping, Sweden
  • 2. Laboratoire des Matériaux Semiconducteurs, Institut des Matériaux, Ecole Polytechnique Fédérale de Lausanne, 1015 Lausanne, Switzerland
  • 3. Department of Electrical and Computer Engineering, University of California, San Diego, La Jolla, CA 92093, United States of America

Description

Cathodoluminescence (CL) and micro-photoluminescence spectroscopies are employed to investigate effects of structural defects on carrier recombination in GaNAsP nanowires (NWs) grown by molecular beam epitaxy on Si substrates. In the NWs with a low N content of 0.08%, these defects are found to promote non-radiative (NR) recombination, which causes spatial variation of the CL peak position and its intensity. Unexpectedly, these detrimental effects can be suppressed even by a small increase in the nitrogen composition from 0.08% to 0.12%. This is attributed to more efficient trapping of excited carriers/excitons to the localized states promoted by N-induced localization and also the presence of other NR channels. At room temperature, the structural defects no longer dominate in carrier recombination even in the NWs with the lower nitrogen content, likely due to increasing importance of other recombination channels. Our work underlines the need in eliminating important thermally activated NR defects, other than the structural defects, for future optoelectronic applications of these NWs.

Notes

Financial support by Linköping University through the Professor Contracts, the Swedish Research Council (Grant No. 2016-05091), the Swedish Energy Agency (Grant No. P40119-1) and the Swedish Government Strategic Research Area in Materials Science on Functional Materials at Linköping University (Faculty Grant SFO-Mat-LiU No 2009 00971) is greatly appreciated. AFiM and LF thank funding from the Swiss National Foundation through the NCCR QSIT.

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Is supplement to
Journal article: 10.1088/1361-6528/ab2cdb (DOI)