Nonlinear optical absorption and ultrafast carrier dynamics of copper antimony sulfide semiconductor nanocrystals

Ternary copper antimony sulfide nanocrystals (CAS NCs), a promising solar cell candidate, have been proposed and investigated from the perspective of synthesis method, linear optical response, and size and band structure tunability. Herein, we present the intensity related nonlinear absorption using...

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Veröffentlicht in:Journal of materials chemistry. C, Materials for optical and electronic devices Materials for optical and electronic devices, 2018, Vol.6 (33), p.8977-8983
Hauptverfasser: Zhang, Feng, Chen, Keqiang, Jiang, Xiantao, Wang, Yunzheng, Ge, Yanqi, Wu, Leimin, Xu, Shixiang, Bao, Qiaoliang, Zhang, Han
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Sprache:eng
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Zusammenfassung:Ternary copper antimony sulfide nanocrystals (CAS NCs), a promising solar cell candidate, have been proposed and investigated from the perspective of synthesis method, linear optical response, and size and band structure tunability. Herein, we present the intensity related nonlinear absorption using the Z-scan technique. Electron and hole relaxation dynamics for the as-prepared three phases, CuSbS 2 , Cu 3 SbS 4 and Cu 12 Sb4S 13 NCs, are studied at the visible spectrum band. With the assistance of fs-resolved transient absorption spectrum technology, photon induced charge carrier dynamics within the valence/conduction band and trap states are analyzed and attributed to three relaxation processes, the corresponding lifetimes of which are ∼400 fs, ∼5 ps and ∼60 ps, respectively. This analysis on electron and hole spatial separation and recombination is significant for the improvement of CAS NC based devices, and paves the way for the application of semiconductor NCs in photovoltaic devices, optical detection and other optoelectronic devices. Ternary copper antimony sulfide nanocrystals (CAS NCs), a promising solar cell candidate, have been proposed and investigated from the perspective of nonlinear optical response and ultrafast photoinduced carrier dynamics.
ISSN:2050-7526
2050-7534
DOI:10.1039/c8tc01606b