研究目的
Investigating recombination in polytype gallium arsenide (GaAs) nanowires (NWs) for photovoltaic applications through photoluminescence studies coupled with rate equation analysis.
研究成果
The study provides insight into the recombination mechanisms in polytype GaAs NWs, showing that carriers quickly thermalize to the spatially closest, lowest energy level, where they radiatively recombine across a sub-bandgap energy gap at a slower radiative rate than band-to-band. The rate equation model developed in this paper compares well with experimental data, suggesting spatially indirect recombination between different polytypes and defect-related recombination due to twin planes and other defects.
研究不足
The large laser spot relative to the density of twin defects and polytype heterointerfaces prevents analyzing each type of transition in isolation. The study is limited to the specific conditions and materials used in the experiments.
1:Experimental Design and Method Selection:
Photoluminescence studies coupled with rate equation analysis were used to investigate recombination in polytype GaAs NWs. Time-resolved photoluminescence (TRPL) at liquid helium temperature and time-integrated photoluminescence (TIPL) at various temperatures were conducted.
2:Sample Selection and Data Sources:
GaAs NWs grown by molecular beam epitaxy (MBE) system via the gold-free gallium-assisted vapor-liquid-solid (VLS) mechanism on GaAs (1(cid:22)11)B substrates coated with thin SiO
3:List of Experimental Equipment and Materials:
He-Ne red laser, picosecond diode laser, closed-loop helium cryostat, silicon photo-avalanche diodes (SPAD) for time-correlated single photon counting (TCSPC).
4:Experimental Procedures and Operational Workflow:
NWs were transferred onto polished silicon substrates for PL measurements. TIPL measurements were performed using a continuous wave He-Ne red laser, and TRPL measurements were performed using a picosecond diode laser.
5:Data Analysis Methods:
Rate equation model was used to analyze the recombination mechanisms.
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