4.8 Article

Surface versus Bulk Currents and Ionic Space-Charge Effects in CsPbBr3 Single Crystals

Journal

JOURNAL OF PHYSICAL CHEMISTRY LETTERS
Volume 13, Issue 17, Pages 3824-3830

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acs.jpclett.2c00804

Keywords

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Funding

  1. Erlangen Graduate School in Advanced Optical Technologies (SAOT) by the Bavarian State Ministry for Science and Art
  2. Deutsche Forschungsgemeinschaft (DFG) [MA 6617/1-1]
  3. CRUE-Universitat Jaume I
  4. European Union's Horizon 2020 research and innovation program under the Photonics Public Private Partnership [871336]

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CsPbBr3 single crystals with optimal optoelectronic properties have potential applications in ionizing-radiation detection devices. However, their mixed ionic-electronic conductivity leads to instability and hysteresis, which hinders long-term operation. Electrical characterization of CsPbBr3 single crystals reveals voltage bias-dependent bulk mobilities and qualitative and quantitative transport differences between bulk and surface mobilities. The formation of space-charge-limited current (SCLC) associated with mechanisms similar to Poole-Frenkel ionized-trap-assisted transport is observed.
CsPbBr3 single crystals have potential for application in ionizing-radiation detection devices due to their optimal optoelectronic properties. Yet, their mixed ionic-electronic conductivity produces instability and hysteretic artifacts hindering the long-term device operation. Herein, we report an electrical characterization of CsPbBr3 single crystals operating up to the time scale of hours. Our fast time-of-flight measurements reveal bulk mobilities of 13-26 cm(2) V-1 s(-1) with a negative voltage bias dependency. By means of a guard ring (GR) configuration, we separate bulk and surface mobilities showing significant qualitative and quantitative transport differences. Our experiments of current transients and impedance spectroscopy indicate the formation of several regimes of space-charge-limited current (SCLC) associated with mechanisms similar to the Poole-Frenkel ionized-trap-assisted transport. We show that the ionic-SCLC seems to be an operational mode in this lead halide perovskite, despite the fact that experiments can be designed where the contribution of mobile ions to transport is negligible.

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