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Femtosecond Charge Density Modulations in Photoexcited CuWO4.
Uemura, Yohei; Ismail, Ahmed S M; Park, Sang Han; Kwon, Soonnam; Kim, Minseok; Niwa, Yasuhiro; Wadati, Hiroki; Elnaggar, Hebatalla; Frati, Federica; Haarman, Ties; Höppel, Niko; Huse, Nils; Hirata, Yasuyuki; Zhang, Yujun; Yamagami, Kohei; Yamamoto, Susumu; Matsuda, Iwao; Katayama, Tetsuo; Togashi, Tadashi; Owada, Shigeki; Yabashi, Makina; Halisdemir, Uufuk; Koster, Gertjan; Yokoyama, Toshihiko; Weckhuysen, Bert M; de Groot, Frank M F.
Affiliation
  • Uemura Y; Inorganic Chemistry and Catalysis, Debye Institute for Nanomaterials Science, Utrecht University, Universiteitslaan 99, 3584 CG Utrecht, The Netherlands.
  • Ismail ASM; Institute for Catalysis, Hokkaido University, Kita 21 Nishi 10, Kita-ku, Sapporo, Hokkaido 001-0021, Japan.
  • Park SH; Inorganic Chemistry and Catalysis, Debye Institute for Nanomaterials Science, Utrecht University, Universiteitslaan 99, 3584 CG Utrecht, The Netherlands.
  • Kwon S; PAL-XFEL, Pohang Accelerator Laboratory, 77 Cheongam-Ro, Nam-Gu, Pohang, Gyeongbuk 37673, South Korea.
  • Kim M; PAL-XFEL, Pohang Accelerator Laboratory, 77 Cheongam-Ro, Nam-Gu, Pohang, Gyeongbuk 37673, South Korea.
  • Niwa Y; PAL-XFEL, Pohang Accelerator Laboratory, 77 Cheongam-Ro, Nam-Gu, Pohang, Gyeongbuk 37673, South Korea.
  • Wadati H; Photon Factory, Institute for Materials Structure Science, KEK, Tsukuba 305-0801, Japan.
  • Elnaggar H; Institute for Solid State Physics, University of Tokyo, Kashiwa, Chiba 277-8581, Japan.
  • Frati F; Graduate School of Material Science, University of Hyogo, Kamigori, Hyogo 678-1297, Japan.
  • Haarman T; Inorganic Chemistry and Catalysis, Debye Institute for Nanomaterials Science, Utrecht University, Universiteitslaan 99, 3584 CG Utrecht, The Netherlands.
  • Höppel N; Inorganic Chemistry and Catalysis, Debye Institute for Nanomaterials Science, Utrecht University, Universiteitslaan 99, 3584 CG Utrecht, The Netherlands.
  • Huse N; Inorganic Chemistry and Catalysis, Debye Institute for Nanomaterials Science, Utrecht University, Universiteitslaan 99, 3584 CG Utrecht, The Netherlands.
  • Hirata Y; Department of Physics and Center for Free-Electron Laser Science, University of Hamburg, Luruper Chaussee 149, 22761 Hamburg, Germany.
  • Zhang Y; Department of Physics and Center for Free-Electron Laser Science, University of Hamburg, Luruper Chaussee 149, 22761 Hamburg, Germany.
  • Yamagami K; Institute for Solid State Physics, University of Tokyo, Kashiwa, Chiba 277-8581, Japan.
  • Yamamoto S; Institute for Solid State Physics, University of Tokyo, Kashiwa, Chiba 277-8581, Japan.
  • Matsuda I; Institute for Solid State Physics, University of Tokyo, Kashiwa, Chiba 277-8581, Japan.
  • Katayama T; Institute for Solid State Physics, University of Tokyo, Kashiwa, Chiba 277-8581, Japan.
  • Togashi T; Institute for Solid State Physics, University of Tokyo, Kashiwa, Chiba 277-8581, Japan.
  • Owada S; JASRI, Kouto, Sayo-cho, Hyogo 679-5198, Japan.
  • Yabashi M; RIKEN SPring-8 Center, Kouto Sayo-cho, Hyogo 679-5148, Japan.
  • Halisdemir U; JASRI, Kouto, Sayo-cho, Hyogo 679-5198, Japan.
  • Koster G; RIKEN SPring-8 Center, Kouto Sayo-cho, Hyogo 679-5148, Japan.
  • Yokoyama T; JASRI, Kouto, Sayo-cho, Hyogo 679-5198, Japan.
  • Weckhuysen BM; RIKEN SPring-8 Center, Kouto Sayo-cho, Hyogo 679-5148, Japan.
  • de Groot FMF; RIKEN SPring-8 Center, Kouto Sayo-cho, Hyogo 679-5148, Japan.
J Phys Chem C Nanomater Interfaces ; 125(13): 7329-7336, 2021 Apr 08.
Article in En | MEDLINE | ID: mdl-33859771
ABSTRACT
Copper tungstate (CuWO4) is an important semiconductor with a sophisticated and debatable electronic structure that has a direct impact on its chemistry. Using the PAL-XFEL source, we study the electronic dynamics of photoexcited CuWO4. The Cu L3 X-ray absorption spectrum shifts to lower energy upon photoexcitation, which implies that the photoexcitation process from the oxygen valence band to the tungsten conduction band effectively increases the charge density on the Cu atoms. The decay time of this spectral change is 400 fs indicating that the increased charge density exists only for a very short time and relaxes electronically. The initial increased charge density gives rise to a structural change on a time scale longer than 200 ps.

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: J Phys Chem C Nanomater Interfaces Year: 2021 Document type: Article Affiliation country: Netherlands

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: J Phys Chem C Nanomater Interfaces Year: 2021 Document type: Article Affiliation country: Netherlands