4.7 Article

Probing ultrafast hot charge carrier migration in MoS2 embedded CdS nanorods

Journal

JOURNAL OF CHEMICAL PHYSICS
Volume 156, Issue 3, Pages -

Publisher

AIP Publishing
DOI: 10.1063/5.0074155

Keywords

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Funding

  1. CSIR , India [09/1129(0009)/2017-EMR-I]
  2. Institute of Nano Science and Technology (INST), Mohali, India
  3. NPDF, India [PDF/2019/000549]
  4. DST, Govt. of India [JCB/2018/000047]
  5. SERB/DST project [CRG/2019/000938]
  6. INST, Mohali, India

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Efficient utilization of hot charge carriers is essential for semiconductor-based optoelectronic devices. In this study, a one-dimensional/two-dimensional heterojunction of CdS/MoS2 nanorod/nanosheet composite was fabricated to investigate the migration behavior of hot charge carriers. The results showed that hot carriers in the high energy states of CdS preferentially migrated into the higher energy states of MoS2, rather than being cooled to the band edge. Additionally, higher energy pump photons were found to be more efficient in the hot carrier transfer process, leading to an extended charge carrier separation.
Efficient utilization of hot charge carriers is of utmost benefit for a semiconductor-based optoelectronic device. Herein, a one-dimensional (1D)/two-dimensional (2D) heterojunction was fabricated in the form of CdS/MoS2 nanorod/nanosheet composite and migration of hot charge carriers was being investigated with the help of transient absorption (TA) spectroscopy. The band alignment was such that both the electrons and holes in the CdS region tend to migrate into the MoS2 region following photoexcitation. The composite system is composed of optical signatures of both CdS and MoS2, with the dominance of CdS nanorods. In addition, the TA signal of MoS2 is substantially enhanced in the heterosystem at the cost of the diminished CdS signal, confirming the migration of charge carrier population from CdS to MoS2. This migration phenomenon was dominated by the hot carrier transfer. The hot carriers in the high energy states of CdS are preferentially migrated into the MoS2 states rather than being cooled to the band edge. The hot carrier transfer time for a 400 nm pump excitation was calculated to be 0.21 ps. This is much faster than the band edge electron transfer process, occurring at 2.0 ps time scale. We found that these migration processes are very much dependent on the applied pump photon energy. Higher energy pump photons are more efficient in the hot carrier transfer process and place these hot carriers in the higher energy states of MoS2, further extending charge carrier separation. This detailed spectroscopic investigation would help in the fabrication of better 1D/2D heterojunctions and advance the optoelectronic field.

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