4.8 Article

Colloidal Synthesis and Charge-Carrier Dynamics of Cs2AgSb1-yBiyX6 (X: Br, Cl; 0 ≤y ≤1) Double Perovskite Nanocrystals

期刊

ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
卷 58, 期 8, 页码 2278-2283

出版社

WILEY-V C H VERLAG GMBH
DOI: 10.1002/anie.201811610

关键词

carrier-phonon coupling; perovskites; hot-carrier cooling; nanocrystals; trapped state

资金

  1. National Natural Science Foundation of China [21833009, 21533010, 21525315]
  2. National Key Research and Development Program of China [2017YFA0204800]
  3. DICP [DMTO201601, ZZBS201703]
  4. Science Challenging Program [JCKY2016212A501]

向作者/读者索取更多资源

A series of lead-free double perovskite nanocrystals (NCs) Cs2AgSb1-yBiyX6 (X: Br, Cl; 0 <= y <= 1) is synthesized. In particular, the Cs2AgSbBr6 NCs is a new double perovskite material that has not been reported for the bulk form. Mixed Ag-Sb/Bi NCs exhibit enhanced stability in colloidal solution compared to Ag-Bi or Ag-Sb NCs. Femtosecond transient absorption studies indicate the presence of two prominent fast trapping processes in the charge-carrier relaxation. The two fast trapping processes are dominated by intrinsic self-trapping (ca. 1-2 ps) arising from giant exciton-phonon coupling and surface-defect trapping (ca. 50-100 ps). Slow hot-carrier relaxation is observed at high pump fluence, and the possible mechanisms for the slow hot-carrier relaxation are also discussed.

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