4.8 Article

Photoexcited Small Polaron Formation in Goethite (α-FeOOH) Nanorods Probed by Transient Extreme Ultraviolet Spectroscopy

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JOURNAL OF PHYSICAL CHEMISTRY LETTERS
卷 9, 期 14, 页码 4120-4124

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acs.jpclett.8b01525

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资金

  1. U.S. Department of Energy, Office of Science, Office of Basic Energy Sciences, Materials Sciences and Engineering Division within the Physical Chemistry of Inorganic Nanostructures Program [DEAC02-05-CH11231, KC3103]
  2. Department of Energy, Office of Energy Efficiency and Renewable Energy (EERE) Postdoctoral Research Award under the EERE Solar Energy Technologies Office
  3. Air Force Office of Scientific Research (AFOSR) [FA9550-15-1-0037]
  4. National Science Foundation [DGE 1752814]
  5. Directorate For Engineering
  6. Div Of Engineering Education and Centers [1461231] Funding Source: National Science Foundation

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Small polaron formation limits the mobility and lifetimes of photoexcited carriers in metal oxides. As the ligand field strength increases, the carrier mobility decreases, but the effect on the photoexcited small polaron formation is still unknown. Extreme ultraviolet transient absorption spectroscopy is employed to measure small polaron formation rates and probabilities in goethite (alpha-FeOOH) crystalline nanorods at pump photon energies from 2.2 to 3.1 eV. The measured polaron formation time increases with excitation photon energy from 70 +/- 10 fs at 2.2 eV to 350 +/- 30 fs at 2.6 eV, whereas the polaron formation probability (85 +/- 10%) remains constant. By comparison to hematite (alpha-Fe2O3), an oxide analogue, the role of ligand composition and metal center density in small polaron formation time is discussed. This work suggests that incorporating small changes in ligands and crystal structure could enable the control of photoexcited small polaron formation in metal oxides.

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