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      Unveiling hole trapping and surface dynamics of NiO nanoparticles†

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          Abstract

          Mesoporous NiO is used as p-type material in photoelectrochemical energy conversion devices. The presence of two kinds of hole traps can affect device performance. Here, after band-gap excitation, the relaxation of the hole into two different traps was observed and characterized.

          Abstract

          The research effort in mesoporous p-type semiconductors is increasing due to their potential application in photoelectrochemical energy conversion devices. In this paper an electron–hole pair is created by band-gap excitation of NiO nanoparticles and the dynamics of the electron and the hole is followed until their recombination. By spectroscopic characterization it was found that surface Ni 3+ states work as traps for both electrons and holes. The trapped electron was assigned to a Ni 2+ state and the trapped hole to a “Ni 4+” state positioned close to the valence band edge. The recombination kinetics of these traps was studied and related with the concept of hole relaxation suggested before. The time scale of the hole relaxation was found to be in the order of tens of ns. Finally the spectroscopic evidence of this relaxation is presented in a sensitized film.

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          Author and article information

          Journal
          Chem Sci
          Chem Sci
          Chemical Science
          Royal Society of Chemistry
          2041-6520
          2041-6539
          25 October 2017
          7 January 2018
          : 9
          : 1
          : 223-230
          Affiliations
          [a ] Department of Chemistry – Ångström Laboratory , Uppsala University , Box 523 , 751 20 Uppsala , Sweden . Email: leif.hammarstrom@ 123456kemi.uu.se ; Fax: +46 18 471 6844 ; Tel: +46 18 471 3648
          Author notes

          ‡These authors contributed equally to this work.

          Author information
          http://orcid.org/0000-0003-0510-5541
          http://orcid.org/0000-0002-9933-9084
          Article
          c7sc03442c
          10.1039/c7sc03442c
          5869301
          29629091
          3e0d8d95-b770-459a-94e0-f5e298a8bf8b
          This journal is © The Royal Society of Chemistry 2018

          This article is freely available. This article is licensed under a Creative Commons Attribution 3.0 Unported Licence (CC BY 3.0)

          History
          : 7 August 2017
          : 25 October 2017
          Categories
          Chemistry

          Notes

          †Electronic supplementary information (ESI) available. See DOI: 10.1039/c7sc03442c


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