Dynamics of Bound Exciton Complexes in CdS Nanobelts

• Published in: ACS nano Vol. 5; no. 5; pp. 3660 - 3669
• Main Authors: Xu, Xinlong, Zhao, Yanyuan, Sie, Edbert Jarvis, Lu, Yunhao, Liu, Bo, Ekahana, Sandy Adhitia, Ju, Xiao, Jiang, Qike, Wang, Jianbo, Sun, Handong, Sum, Tze Chien, Huan, Cheng Hon Alfred, Feng, Yuan Ping, Xiong, Qihua
• Format: Journal Article
• Language: English
• Published: United States American Chemical Society 24.05.2011
• Subjects: Cadmium Compounds - chemistry; Electron Transport; Nanostructures - chemistry; Nanostructures - ultrastructure; Particle Size; Selenium Compounds - chemistry; defect level; CdS nanobelt; bound exciton complex; ultrafast dynamics; exciton interaction
• ISSN: 1936-0851; 1936-086X
• DOI: 10.1021/nn2008832

Intrinsic defects such as vacancies, interstitials, and anti-sites often introduce rich luminescent properties in II−VI semiconductor nanomaterials. A clear understanding of the dynamics of the defect-related excitons is particularly important for the design and optimization of nanoscale optoelectronic devices. In this paper, low-temperature steady-state and time-resolved photoluminescence (PL) spectroscopies have been carried out to investigate the emission of cadmium sulfide (CdS) nanobelts that originates from the radiative recombination of excitons bound to neutral donors (I2) and the spatially localized donor−acceptor pairs (DAP), in which the assignment is supported by first principle calculations. Our results verify that the shallow donors in CdS are contributed by sulfur vacancies while the acceptors are contributed by cadmium vacancies. At high excitation intensities, the DAP emission saturates and the PL is dominated by I2 emission. Beyond a threshold power of approximately 5 μW, amplified spontaneous emission (ASE) of I2 occurs. Further analysis shows that these intrinsic defects created long-lived (spin triplet) DAP trap states due to spin-polarized Cd vacancies which become saturated at intense carrier excitations.