4.7 Article

Nanoscale visualization of hot carrier generation and transfer at non-noble metal and oxide interface

期刊

JOURNAL OF MATERIALS SCIENCE & TECHNOLOGY
卷 98, 期 -, 页码 151-159

出版社

JOURNAL MATER SCI TECHNOL
DOI: 10.1016/j.jmst.2021.04.064

关键词

Non -noble metal; Hot carrier; Real-space photocurrent mapping; Local -probe force microscopy

资金

  1. National Research Foundation of Korea (NRF) - Ministry of Science and ICT [NRF-2019H1D3A1A01102524, NRF-2019M3F3A1A03079739, NRF-2019R1A2C2003804]
  2. Ajou University
  3. National Research Foundation of Korea [2019H1D3A1A01102524] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)

向作者/读者索取更多资源

The study effectively utilized hot-carriers at the nanoscale and their transfer dynamics from a non-noble metal to a metal oxide interface through real-space photocurrent mapping using local probe techniques and femtosecond transient absorption measurements. The results showed that hot carriers were injected into the metal oxide layer from the TiN layer, indicating efficient electron transfer between the layers and achieving high conversion efficiency for optoelectronic devices.
The conversion efficiency of energy-harvesting devices can be increased by utilizing hot-carriers (HCs). However, due to ultrafast carrier-carrier scattering and the lack of carrier injection dynamics, HC-based devices have low efficiencies. In the present work, we report the effective utilization of HCs at the nanoscale and their transfer dynamics from a non-noble metal to a metal oxide interface by means of real-space photocurrent mapping by using local probe techniques and conducting femtosecond transient absorption (TA) measurements. The photocurrent maps obtained under white light unambiguously show that the HCs are injected into the metal oxide layer from the TiN layer, as also confirmed by conductive atomic force microscopy. In addition, the increased photocurrent in the bilayer structure indicates the injection of HCs from both layers due to the broadband absorption efficiency of TiN layer, passivation of the surface states by the top TiN layer, and smaller barrier height of the interfaces. Furthermore, electrostatic force microscopy and Kelvin probe force microscopy provide direct evidence of charge injection from TiN to the MoO x film at the nanoscale. The TA absorption spectra show a strong photo-bleaching signal over wide spectral range and ultrafast decaying behavior at the picosecond time scale, which indicate efficient electron transfer from TiN to MoO x . Thus, our simple and effective approach can facilitate HC collection under white light, thereby achieving high conversion efficiency for optoelectronic devices. (c) 2022 Published by Elsevier Ltd on behalf of The editorial office of Journal of Materials Science & Technology.

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