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Title: Role of Atomic Structure on Exciton Dynamics and Photoluminescence in NIR Emissive InAs/InP/ZnSe Quantum Dots

Journal Article · · Journal of Physical Chemistry. C
ORCiD logo [1]; ORCiD logo [2];  [3];  [4]; ORCiD logo [4]; ORCiD logo [5];  [3];  [6]; ORCiD logo [4];  [3]; ORCiD logo [7]; ORCiD logo [4]; ORCiD logo [6]; ORCiD logo [4]; ORCiD logo [8];  [9]
  1. Department of Chemistry, University of Illinois at Urbana Champaign, Urbana, Illinois 61801, United States, Department of Chemistry, Western Washington University, Bellingham, Washington 98225, United States
  2. Department of Chemistry, University of California, Berkeley, California 94720, United States
  3. Department of Chemistry, University of Illinois at Urbana Champaign, Urbana, Illinois 61801, United States
  4. Department of Applied Physics and Materials Science, California Institute of Technology, Pasadena, California 91125, United States
  5. Department of Chemistry, University of California, Berkeley, California 94720, United States, Materials Sciences Division, Lawrence Berkeley National Laboratory, Berkeley, California 94720, United States
  6. Department of Materials Science and Engineering, University of Illinois at Urbana-Champaign, Urbana, Illinois 61801, United States
  7. Department of Chemical and Biomolecular Engineering, University of Illinois at Urbana Champaign, Urbana, Illinois 61801, United States
  8. Department of Chemistry, University of California, Berkeley, California 94720, United States, Materials Sciences Division, Lawrence Berkeley National Laboratory, Berkeley, California 94720, United States, The Sackler Center for Computational Molecular and Materials Science, Tel Aviv University, Tel Aviv 69978, Israel
  9. Department of Chemistry, University of Illinois at Urbana Champaign, Urbana, Illinois 61801, United States, Surface and Corrosion Science, School of Engineering Sciences in Chemistry, Biotechnology and Health, KTH Royal Institute of Technology, Stockholm 10044, Sweden

The development of bright, near-infrared-emissive quantum dots (QDs) is a necessary requirement for the realization of important new classes of technology. Specifically, there exist significant needs for brighter, heavy metal-free, near-infrared (NIR) QDs for applications with high radiative efficiency that span diverse applications, including down-conversion emitters for high-performance luminescent solar concentrators. In this work, we use a combination of theoretical and experimental approaches to synthesize bright, NIR luminescent InAs/InP/ZnSe QDs and elucidate fundamental material attributes that remain obstacles for development of near-unity NIR QD luminophores. First, using Monte Carlo ray tracing, we identify the atomic and electronic structural attributes of InAs core/shell, NIR emitters, whose luminescence properties can be tailored by synthetic design to match most beneficially those of high-performance, single-band-gap photovoltaic devices based on important semiconductor materials, such Si or GaAs. Second, we synthesize InAs/InP/ZnSe QDs based on the optical attributes found to maximize LSC performance and develop methods to improve the emissive qualities of NIR emitters with large, tunable Stokes ratios, narrow emission linewidths, and high luminescence quantum yields (here reaching 60 ± 2%). Third, we employ atomistic electronic structure calculations to explore charge carrier behavior at the nanoscale affected by interfacial atomic structures and find that significant exciton occupation of the InP shell occurs in most cases despite the InAs/InP type I bulk band alignment. Furthermore, the density of the valence band maximum state extends anisotropically through the (111) crystal planes to the terminal InP surfaces/interfaces, indicating that surface defects, such as unpassivated phosphorus dangling bonds, located on the (111) facets play an outsized role in disrupting the valence band maximum and quenching photoluminescence.

Research Organization:
Univ. of Illinois at Urbana-Champaign, IL (United States); Energy Frontier Research Centers (EFRC) (United States). Photonics at Thermodynamic Limits; Lawrence Berkeley National Laboratory (LBNL), Berkeley, CA (United States)
Sponsoring Organization:
USDOE Office of Science (SC), Basic Energy Sciences (BES)
Grant/Contract Number:
SC0019140; SC0019323; AC02-05CH11231
OSTI ID:
1865203
Alternate ID(s):
OSTI ID: 1866743; OSTI ID: 1925194
Journal Information:
Journal of Physical Chemistry. C, Journal Name: Journal of Physical Chemistry. C Vol. 126 Journal Issue: 17; ISSN 1932-7447
Publisher:
American Chemical SocietyCopyright Statement
Country of Publication:
United States
Language:
English

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