Scholarship & Research
Permanent URI for this communityhttps://scholarworks.montana.edu/handle/1/1
Browse
2 results
Search Results
Item Elucidating the impacts of structural heterogeneity on excited state dynamics in solution-processed materials(Montana State University - Bozeman, College of Letters & Science, 2024) Afrin, Sajia; Chairperson, Graduate Committee: Erik Grumstrup; This is a manuscript style paper that includes co-authored chapters.Solution-processed inorganic and organic semiconductors hold enormous promises due to their low manufacturing cost, scalability, and compatibility with flexible substrates. However, solution processing techniques do not require control over crystal growth, which can lead to structural defects within the crystal structure. The defects within solution-processed semiconductors can create significant challenges in optimizing device functionality; therefore, it is crucial to understand the impact of structural defects on photophysical properties. Traditional ensemble measurement techniques can conceal the effects of microscale structural defects on functional properties in the structure-averaged observation of solution-processed materials. The work presented in this dissertation employs time-resolved and spectrally resolved microscopy techniques to investigate the influence of structural heterogeneity on the photophysical properties of microscale solution-processed materials. Measurements collected across multiple discrete and highly crystalline domains of multiple classes of solution-processed materials have helped establish a relationship between the functionality and the local structure of these materials. Initially, the focus was on elucidating anisotropic carrier transport in lead halide perovskites by investigating lattice strain and energetic distribution in microcrystals. Later, the focus shifted towards characterizing and understanding the impact of structural defects on the excited state dynamics in another class of solution-processed material called metal-organic frameworks (MOFs). PCN-222 exhibited rapid exciton transport with time-averaged diffusion coefficients ranging from 0.27 to 1.0 cm2/s and subdiffusive behavior, showing transport slowing on the tens of ps time scale. Subdiffusivity indicated that excited states were rapidly transported through the porphyrin network of PCN-222 before being trapped. Moreover, the first transport measurements and transient absorption microscopic measurements in PCN-222 are reported here. Photoluminescence quenching and heterogeneous relaxation pathways were noted in regions with higher structural heterogeneity. Furthermore, the spectral evolution of porphyrinic PCN-222 MOF was investigated, which revealed excitation-dependent chromophore coupling in the MOF structure. Soret band excitation with enhanced coupling can create more mobile excited states, whereas Q band excitation with reduced coupling will generate fewer mobile excited states. Excitation-dependent chromophore coupling strongly dictates the transport and relaxation properties in MOF microstructures that also illustrate the impact of structural defects on the excited state transport and relaxation dynamics. A significant spectral shift has also been observed in microrods stemming from structural heterogeneity. These findings contribute to a deeper understanding of the impact of structural defects on the photophysical properties of solution-processed materials, facilitating the development of optimized semiconductor devices for various applications. The results reported in this dissertation will not only continue to aid in the characterization of MOFs but will also advance our understanding of excited state dynamics in a variety of solution-processed materials.Item Characterizing excited state dynamics and carrier transport in hybrid organic-inorganic lead halide perovskites via ultrafast microscopy(Montana State University - Bozeman, The Graduate School, 2018) Hill, Andrew Hinson; Chairperson, Graduate Committee: Erik Grumstrup; Kori E. Smyser, Casey L. Kennedy, Eric S. Massaro and Erik M. Grumstrup were co-authors of the article, 'Ultrafast microscopy of methylammonium lead iodide perovskite thin films: heterogeneity of excited state spatial and temporal evolution' which is contained within this thesis.; Kori E. Smyser, Casey L. Kennedy, Eric S. Massaro and Erik M. Grumstrup were co-authors of the article, 'Screened charge carrier transport in methylammonium lead iodide perovskite thin films' in the journal 'Journal of physical chemistry letters' which is contained within this thesis.; Casey L. Kennedy, Eric S. Massaro and Erik M. Grumstrup were co-authors of the article, 'Perovskite carrier transport: disentangling the impacts of effective mass and scattering time through microscopic optical detection' in the journal 'Journal of physical chemistry letters' which is contained within this thesis.; Casey L. Kennedy and Erik M. Grumstrup were co-authors of the article, 'Determining the effects of A-site cation substitution on the optical response and transport properties of lead tri-bromide perovskites' submitted to the journal 'Journal of physical chemistry letters' which is contained within this thesis.Lead tri-halide perovskites have recently emerged as cost-effective alternatives to silicon for use in photovoltaic devices. A large contributor to their reduced cost compared to silicon is the simple solution processed techniques employed in their fabrication. While these methods can produce effective photovoltaic devices, heterogeneity endemic to solution processing makes characterization of tri-halide perovskites a challenging task. Most spectroscopic techniques use large sample interrogation volumes which often results in the indiscriminate sampling of grain boundaries and other heterogeneities which impact the spectroscopic observable. To circumvent this issue, pump-probe microscopy is used to dramatically shrink the sample volume, reducing the contributions from chemical and morphological heterogeneities and providing a more accurate measure of the sample's inherent properties. This work begins with a study of the recombination and transport dynamics methylammonium lead tri-iodide (MAPbI 3) perovskite. After identifying the main recombination pathways and contributions to the transient signal, experimental focus is shifted to the transport properties of MAPbI 3. The key contributing factors to the high diffusivities reported in MAPbI 3 are found to be strong electron-phonon coupling and a high static dielectric constant which serves to screen carriers from interactions with charged defects and other carriers. Then the development a new all-optical method capable of uniquely determining the two fundamental parameters that govern carrier transport (the mean scattering time and optical mass of photogenerated carriers) is reported. This method was applied to a series of different perovskite materials including MAPbI 3, cesium lead bromide di-iodide (CsPbBrI 2), methylammonium lead tri-bromide (MAPbBr 3), formamidinium lead tri-bromide (FAPbBr 3), and cesium lead tri-bromide (CsPbBr 3). The results of these experiments have led to the characterization of the role each perovskite constituent (namely, the identity of the organic cation and the halide stoichiometry) plays in determining the transport properties of the resulting material. The work presented in this dissertation characterizes the transport properties of lead halide perovskites. Measurements collected across multiple discrete and highly crystalline domains of multiple perovskite species have helped establish a relationship between the functionality and the local structure of these materials. Additionally, the design and first application of a new methodology to disentangle the effects of mean scattering time and the photogenerated carrier mass on carrier transport is reported. This technique will not only continue to aid in the characterization of lead-halide perovskites but will likely also see use on a host of other material systems to advance understanding of carrier transport in a variety of materials.