Details
| Original language | English |
|---|---|
| Pages (from-to) | 6379-6387 |
| Number of pages | 9 |
| Journal | Journal of Physical Chemistry C |
| Volume | 122 |
| Issue number | 11 |
| Early online date | 24 Feb 2018 |
| Publication status | Published - 22 Mar 2018 |
Abstract
Growing a wide band gap shell on bare core and/or core@shell materials is a fascinating idea for improving the photoluminescence (PL) efficiency and stability. An epitaxially grown shell adds another degree of complexity to the system and modulates the excited-state relaxation dynamics, which remain poorly understood. Employing time-resolved PL and femtosecond transient absorption (TA) spectroscopy, we present a thorough study on charge carrier dynamics of CdSe@CdS and CdSe@CdS/ZnS quantum rods (QRs). Various excitation wavelengths were used to identify the contribution of individual segment toward the optical properties of the QRs. Our femtosecond TA measurements provide a clear evidence of excitation migration from CdS as well as ZnS to CdSe core within few picoseconds of photoexcitation. The excitons recombine faster in the CdSe moiety of the CdSe@CdS/ZnS than that of the CdSe@CdS QRs via an extra decay path. The interband trap states that are created via the formation of extended defects because of lattice strain relaxation (or ion exchange during the formation of ZnS segment) in CdSe@CdS/ZnS QRs could provide the additional decay channel leading to low PL intensity and quantum yield. We believe that our study will help to develop a strategy for enhancing the PL efficiency through energy funneling across semiconductor heterojunctions and to understand the charge carrier dynamics in nanoheterostructures.
ASJC Scopus subject areas
- Materials Science(all)
- Electronic, Optical and Magnetic Materials
- Energy(all)
- General Energy
- Chemistry(all)
- Physical and Theoretical Chemistry
- Materials Science(all)
- Surfaces, Coatings and Films
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In: Journal of Physical Chemistry C, Vol. 122, No. 11, 22.03.2018, p. 6379-6387.
Research output: Contribution to journal › Article › Research › peer review
}
TY - JOUR
T1 - Role of ZnS Segment on Charge Carrier Dynamics and Photoluminescence Property of CdSe@CdS/ZnS Quantum Rods
AU - Kumar, Pushpendra
AU - Ray, Rajeev
AU - Adel, Patrick
AU - Luebkemann, Franziska
AU - Dorfs, Dirk
AU - Pal, Suman Kalyan
N1 - Funding information: Financial support from the Council of Scientific and Industrial Research (CSIR), Government of India, under grant no. 03(1325)/14/EMR-II is gratefully acknowledged. Authors are thankful to the Advanced Materials Research Centre (AMRC), IIT Mandi, for the experimental facilities. Thanks to Juergen Caro and Armin Feldhoff for providing access to HR-TEM facilities.
PY - 2018/3/22
Y1 - 2018/3/22
N2 - Growing a wide band gap shell on bare core and/or core@shell materials is a fascinating idea for improving the photoluminescence (PL) efficiency and stability. An epitaxially grown shell adds another degree of complexity to the system and modulates the excited-state relaxation dynamics, which remain poorly understood. Employing time-resolved PL and femtosecond transient absorption (TA) spectroscopy, we present a thorough study on charge carrier dynamics of CdSe@CdS and CdSe@CdS/ZnS quantum rods (QRs). Various excitation wavelengths were used to identify the contribution of individual segment toward the optical properties of the QRs. Our femtosecond TA measurements provide a clear evidence of excitation migration from CdS as well as ZnS to CdSe core within few picoseconds of photoexcitation. The excitons recombine faster in the CdSe moiety of the CdSe@CdS/ZnS than that of the CdSe@CdS QRs via an extra decay path. The interband trap states that are created via the formation of extended defects because of lattice strain relaxation (or ion exchange during the formation of ZnS segment) in CdSe@CdS/ZnS QRs could provide the additional decay channel leading to low PL intensity and quantum yield. We believe that our study will help to develop a strategy for enhancing the PL efficiency through energy funneling across semiconductor heterojunctions and to understand the charge carrier dynamics in nanoheterostructures.
AB - Growing a wide band gap shell on bare core and/or core@shell materials is a fascinating idea for improving the photoluminescence (PL) efficiency and stability. An epitaxially grown shell adds another degree of complexity to the system and modulates the excited-state relaxation dynamics, which remain poorly understood. Employing time-resolved PL and femtosecond transient absorption (TA) spectroscopy, we present a thorough study on charge carrier dynamics of CdSe@CdS and CdSe@CdS/ZnS quantum rods (QRs). Various excitation wavelengths were used to identify the contribution of individual segment toward the optical properties of the QRs. Our femtosecond TA measurements provide a clear evidence of excitation migration from CdS as well as ZnS to CdSe core within few picoseconds of photoexcitation. The excitons recombine faster in the CdSe moiety of the CdSe@CdS/ZnS than that of the CdSe@CdS QRs via an extra decay path. The interband trap states that are created via the formation of extended defects because of lattice strain relaxation (or ion exchange during the formation of ZnS segment) in CdSe@CdS/ZnS QRs could provide the additional decay channel leading to low PL intensity and quantum yield. We believe that our study will help to develop a strategy for enhancing the PL efficiency through energy funneling across semiconductor heterojunctions and to understand the charge carrier dynamics in nanoheterostructures.
UR - http://www.scopus.com/inward/record.url?scp=85044345715&partnerID=8YFLogxK
U2 - 10.1021/acs.jpcc.7b12223
DO - 10.1021/acs.jpcc.7b12223
M3 - Article
AN - SCOPUS:85044345715
VL - 122
SP - 6379
EP - 6387
JO - Journal of Physical Chemistry C
JF - Journal of Physical Chemistry C
SN - 1932-7447
IS - 11
ER -