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University of Cambridge

Charge and Thermoelectric Transport in Metal Halide Perovskite Semiconductors

Abstract

dc:description.abstract

Metal halide perovskites exhibit optoelectronic properties that hold significant potential for applications in photovoltaics, light-emitting diodes, photodetectors, X-ray detectors, and field-effect transistors (FETs). Rapid and substantial enhancements in the performance of perovskite-based optoelectronic devices have been achieved, that recent records indicate power conversion efficiency (PCE) of single-junction solar cells exceeding 26%, and FET mobility surpassing 50 cm<sup>2</sup>V<sup>-1</sup>s<sup>-1</sup>. These advancements in metal halide perovskites have been paralleled by efforts to understand the material's fundamental chemistry and physical properties from a bottom-up perspective, providing extensive theoretical optimization guidance. In this thesis, efforts to improve device performance have been paralleled by a focus to understand the underlying charge transport physics in these lead-based and tin-based perovskite systems. In Chapter 3, we identified a strong causal relationship between metal contact reaction and non-ideal FET characteristics in CsFAMAPbI<sub>3</sub> perovskite FETs. Prolonged channel bias leads to enhanced n-type doping at the contact interface, resulting in increased device conductivity. This research also extended to investigating electroactive A-site molecules on charge transport in alkyl-diammonium 2D/3D perovskite FETs (Chapter 4.1), and pure *n*=1 2D perovskite diodes (Chapter 4.2). Carbazole alkylammonium molecules were found to accept transferred holes and increase electron-hole pair separation, consequently enhancing charge carrier mobility in the out-of-plane direction. Tin-based perovskites have gained significant attention since 2022, as they are found to be less susceptible to ion migration and exhibit *p*-type FET mobility exceeding 10 cm<sup>2</sup>V<sup>-1</sup>s<sup>-1</sup>. Here, we optimized tin perovskite compositions with mixed A-site cations and de-doping additives, achieving *p*-type FET mobility above 2 cm<sup>2</sup>V<sup>-1</sup>s<sup>-1</sup> at room temperature. However, the reported high FET mobility exceeding 10 cm<sup>2</sup>V<sup>-1</sup>s<sup>-1</sup> in these tin-based perovskites is sometimes controversial. In Chapter 4.3, we conducted a comprehensive analysis of the impact of device geometry on mobility extraction and demonstrated more reliable mobility results using gated four-point probe measurements on tin perovskite FETs. In Chapter 5, we conducted a comprehensive analysis of charge transport characterization in tin-based perovskite systems. We precisely measured the hole concentration and mobility of CsSnI<sub>3</sub> films across varying grain sizes and Pb-substitution ratios. A transition in charge transport mechanisms was observed, shifting from predominantly band-like in larger grains to being dominated by grain boundary effects in smaller grains and films alloyed with Pb. Films with the largest grains exhibited a Hall effect mobility of 60 cm<sup>2</sup>V<sup>-1</sup>s<sup>-1</sup> at room temperature and between 100-160 cm<sup>-2</sup>V<sup>-1</sup>s<sup>-1</sup> at low temperatures, while maintaining a constant hole density of 1.6x10<sup>-19</sup> cm<sup>-3</sup>. This transition is thoroughly explained using a mixed transport model that integrates band-like, grain boundary thermal activation, and grain boundary site semi-metallic or impurity scattering mechanisms. To assess their thermoelectric performance and probe their electronic structure, we measured the temperature-dependent Seebeck coefficient. From a Seebeck coefficient of 85 μV K<sup>-1</sup> in CsSnI<sub>3</sub> we derived a DOS effective mass of 0.25 to 0.3*m*<sub>e</sub>, which remains consistent regardless of temperature and grain size and is slightly higher in samples with Pb-substitution. Finally, with thermal conductivity measurements, our best CsSnI<sub>3</sub> film exhibited a high thermoelectric power factor of 118 μW m<sup>-1</sup>K<sup>-2</sup> and a thermoelectric figure-of-merit of 0.11 at room temperature. We demonstrate that enhancing sample grain size and crystallinity is a viable strategy for optimizing the thermoelectric performance of tin perovskites.

Degree

thesis:*
Name dc:type.qualificationname
Doctor of Philosophy (PhD)
Level dc:type.qualificationlevel
Doctoral
Grantor dc:publisher.institution
University of Cambridge
Year dc:date.issued
2024

Author and committee

dc:creator, dc:contributor.*
Author dc:creator
  • Zhang, Youcheng
Advisor dc:contributor.advisor
  • Sirringhaus, Henning

Subjects

dc:subject × 7

Rights

dc:rights
Language dc:language
eng

Identifiers

dc:identifier.*
Author Identifier
0000-0003-4233-9769
OAI identifier oai:identifier
oai:www.repository.cam.ac.uk:1810/375249

Chain of custody

source
Harvested from
Cambridge University
Base URL
api.repository.cam.ac.uk/server/oai/request
Last updated
2026-07-22
Source record
OAI-PMH GetRecord
citation

Zhang, Youcheng. Charge and Thermoelectric Transport in Metal Halide Perovskite Semiconductors. Doctoral thesis, University of Cambridge, 2024. https://doi.org/10.17863/CAM.112999