4.6 Article

Electron-phonon coupling mechanisms of broadband near-infrared emissions from Cr3+ in the Ca3Sc2Si3O12 garnet

期刊

PHYSICAL CHEMISTRY CHEMICAL PHYSICS
卷 22, 期 18, 页码 10343-10350

出版社

ROYAL SOC CHEMISTRY
DOI: 10.1039/d0cp00240b

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资金

  1. National Key Research and Development Program of China [2016YFC0104502, 2017YFC0111602]
  2. Fujian Institute of Innovation, Chinese Academy of Sciences [FJCXY18040203]
  3. Public Projects of Zhejiang Province [LGG18E020007]
  4. Science and Technology Major Project of Ningbo Municipality [2017C110028]
  5. Natural Science Foundation of Shanxi Province [201801D121020, 201801D221132]

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Cr3+ in the Ca3Sc2Si3O12 garnet (CSSG) has the ability to convert blue light to broadband near-infrared (NIR) emissions, which is a promising strategy for next-generation smart NIR light sources based on blue LEDs. The Cr3+ luminescence strongly depends on temperature due to electron-phonon coupling (EPC). We reveal the EPC mechanism of Cr3+ in CSSG for the first time by temperature-dependent photoluminescence measurement from 77 to 573 K and cathodoluminescence using a scanning electron microscope. Cr3+ occupies the Sc3+ site and experiences a weak crystal field in CSSG, manifesting a broad NIR emission in the 700-900 nm range that originates from the T-4(2g) -> (4)A(2g) transition. The zero phonon line (ZPL) of the T-4(2) state is observed at similar to 713 nm with a vibrational energy of similar to 310 cm(-1). A strong EPC leads to a large Stokes shift (similar to 2900 cm(-1)). The Huang-Rhys parameter (S = 4), crystal field strength (D-q/B), and Racah parameters (B and C) are estimated.

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