Shape - dependent exciton spin polarization studied by time - resolved magneto - optical spectroscopy
نویسندگان
چکیده
Submitted for the MAR10 Meeting of The American Physical Society Shape-dependent exciton spin polarization studied by timeresolved magneto-optical spectroscopy KENNETH KNAPPENBERGER, DANIEL BLUMLING, Florida State University — Shape-dependent exciton spin polarization of semiconducting nanoparticles will be presented. Timeand polarization-resolved magneto-photoluminescence spectroscopy is carried out at low temperature in magnetic fields up to 17.5 Tesla to investigate the extent of spin polarization in CdSe quantum dots and nanorods. One-dimensional CdSe nanorods exhibit a large degree of circular polarization when even small magnetic fields are applied. The large spin polarization achieved in 1-D nanostructures is not observed in 0-D quantum dots. The experimentally measured polarization is attributed to strong mixing of “dark” and “bright” exciton fine-structure states in 1-D nanostructures, which leads to the formation of spin-polarized excitons. The polarized emission is also confirmed by wavelength-resolved intensity-integrated and timecorrelated single-photon counting measurements. The findings may have significant impacts on devices based on the nanocrystals platform, including; solar-to-electric energy conversion, spintronics and chemical lasers. Kenneth Knappenberger Florida State University Date submitted: 12 Nov 2009 Electronic form version 1.4
منابع مشابه
Time- and polarization-resolved optical spectroscopy of colloidal CdSe nanocrystal quantum dots in high magnetic fields.
In an effort to elucidate the spin (rather than charge) degrees of freedom in colloidal semiconductor nanocrystal quantum dots, we report on a series of static and time-resolved photoluminescence measurements of colloidal CdSe quantum dots in ultrahigh magnetic fields up to 45 T. At low temperatures (1.5-40 K), the steady-state photoluminescence (PL) develops a high degree of circular polarizat...
متن کاملThe influence of applied magnetic fields on the optical properties of zero- and one-dimensional CdSe nanocrystals.
Shape-dependent exciton relaxation dynamics of CdSe 0-D nanocrystals and 1-D nanorods were studied using low-temperature (4.2 K), time-resolved and intensity-integrated magneto-photoluminscence (MPL) spectroscopy. Analysis of the average MPL rate constants from several different nanocrystal quantum dots and rods excited by 400 nm light in applied magnetic fields up to 17.5 T revealed size-depen...
متن کاملUltrafast Multi-Level Logic Gates with Spin-Valley Coupled Polarization Anisotropy in Monolayer MoS2
The inherent valley-contrasting optical selection rules for interband transitions at the K and K' valleys in monolayer MoS2 have attracted extensive interest. Carriers in these two valleys can be selectively excited by circularly polarized optical fields. The comprehensive dynamics of spin valley coupled polarization and polarized exciton are completely resolved in this work. Here, we present a...
متن کاملOptical Properties of All-inorganic Metal-halide Perovskites and Metal Chalcogenides Colloidal Nano-crystals
Colloidal nanocrystals (NCs) are of considerable interest due to their size-dependent optical and electronic properties, which allow their implementation in photovoltaic cells, light-emitting diodes, photo-detectors and more. Along with the development of the synthesis procedures, numerous investigations have explored the optical and electronic properties of different NCs, involving the study o...
متن کاملValley and spin dynamics in MoSe2 two-dimensional crystals.
We study valley and spin dynamics in monolayer molybdenum diselenide by polarization-resolved femtosecond transient absorption spectroscopy. Valley- and spin-polarized excitons are injected by a circularly polarized laser pulse, with an excess energy of 120 meV. Relaxation of the valley polarization is time-resolved by measuring dynamical circular dichroism of a linearly polarized probe pulse t...
متن کاملذخیره در منابع من
با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید
عنوان ژورنال:
دوره شماره
صفحات -
تاریخ انتشار 2012