In this thesis, we have developed a reproducible, safe, and scalable sequential thermal vapour deposition (STVD) method for the growth of quality 3D halide perovskite (HaP) thin films. High-quality methylammonium lead tri-bromide (MAPbBr3), methylammonium lead tri-iodide (MAPbI3), and methylammonium lead bromide-iodide (MAPb(I1-xBrx)3) thin films have been optimised using the STVD technique. The structural, optical, morphological, and electrical properties were tuned by varying the thicknesses of the organic (MAI, MABr) and inorganic (PbI2, PbBr2) precursor thin films and post-annealing times of the HaP. X-ray diffractograms confirmed the cubic MAPbBr3 structure with the Pm¯3 m space group, tetragonal MAPbI3 crystal structure with I4/mcm space group, and the tetragonal MAPbI3 structure being transformed to cubic MAPbBr3 system as MAPb(I1-xBrx)3 (x=0.89-0.95) forms. UV-Vis spectra revealed broad absorption bands with a redshift in absorption onset from 540 to 550 nm for MAPbBr3 and 750 to 780 nm for MAPbI3 as the thickness of respective organic precursors increased from 300 to 500 nm. The bandgap of MAPb(I1-xBrx)3 decreased from 2.21 to 2.14 eV as the thicknesses of MABr precursors increased from 300 to 500 nm. The crystallisation of the HaP started within the chamber, and prolonged post-annealing times exceeding 10 min caused the transformation of MAPbI3 to PbI2. Scanning Electron Micrographs show pin-hole-free and densely packed grains with an average size that increases as thicknesses increase. The charge carrier mobility increases while trap density decreases as the thickness of organic precursors increased. Besides, the thesis investigated the growth and stability of thin MAPbBr3 films at metal/MAPbBr3 interfaces. We studied the structure, morphology, and stability of the optimised MAPbBr3 perovskite on aluminium (Al), tin (Sn), silver (Ag), gold-zinc (Au-Zn) and gold (Au) electrodes, immediately and 60 days later. FE-SEM images show an average grain size that increased linearly with the work function from 294 nm for Al to 850 nm for Au. The MAPbBr3 grains remain glued to Sn, Ag, Au-Zn but delaminate quickly on Al. X-ray analysis of MAPbBr3 reveals variable crystallographic texturing for various metals and loss in intensity of prominent peaks at different rates over time. We found that the best thicknesses of 100 nm PbI2 and 500 nm MAI, and 100 nm PbBr2 and 500 nm MABr are needed for the preparation of quality MAPbI3 and MAPbBr3 thin films for solar cells, respectively. Quality thin MAPb(I0.11Br0.89)3 film is formed by inter-diffusion and halide exchange processes when optimised MAPbBr3 is grown on optimised MAPbI3 as a bottom layer. Al speeds up the degradation of MAPbBr3 at Al/MAPbBr3 while MAPbBr3 is relatively stable at Au-Zn/MAPbBr3 interfaces. / Thesis (PhD (Physics))--University of Pretoria, 2020. / University of Pretoria, the National Research Foundation/The World Academy of Sciences (NRF-TWAS), and NRF grant no N0115/115463 of the SARChI / Physics / PhD (Physics) / Restricted

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Les perovskites organiques-inorganiques en halogénures de plomb sont des matériaux très prometteurs pour la prochaine génération de cellules solaires avec des avantages intrinsèques tels que leur faible coût de fabrication (grande disponibilité des matériaux de base et leur mise en œuvre à basse température) et leur bon rendement de conversion photovoltaïque. Cependant, les cellules solaires pérovskites sont encore instables et montrent des effets d'hystérésis courant-tension délétères. Dans cette thèse, des résultats de l’analyse physique de couches minces de pérovskite à base de CH3NH3PbI3-xClx et de cellules solaires ont été présentés. Les caractéristiques de transport électrique et les processus de vieillissement ont été étudiés avec différentes approches.Dans une première étape, la synthèse du matériau pérovskite a été optimisée en contrôlant les conditions de dépôt des films en une seule étape telles que la vitesse de rotation (6000 rpm) de la tournette et la température de recuit des films (80 °C). Dans un second temps, des cellules solaires perovskites à base de CH3NH3PbI3-xClx ont été fabriquées en utilisant la structure planaire inversée et caractérisées optiquement et électriquement.Grace à l’utilisation de la spectroscopie optique à décharge luminescente (GDOES), un déplacement des ions halogénures a été observé expérimentalement et de façon directe sous l’application d’une tension électrique. Une longueur de diffusion ionique de 140 nm et un rapport de 65% d'ions mobiles ont été déduits. Il est montré que l'hystérésis courant-tension dans l'obscurité est fortement affectée par la migration des ions halogénures provoquant un écrantage substantiel du champ électrique appliqué. Nous avons donc trouvé sous obscurité un décalage de la tension à courant nul jusque 0,25 V et un courant de fuite jusque 0,1 mA / cm2 en fonction des conditions de mesure. Grâce aux courbes courant-tension en fonction de la température, nous avons déterminé la température de transition de la conductivité ions/électrons à 260K et analysé les résultats expérimentaux en utilisant l'équation de Nernst- Einstein donnant une énergie d'activation de 0.253 eV pour les ions mobiles.Enfin, le processus de vieillissement de la cellule solaire a été étudié avec des mesures optiques et électriques. Nous avons déduit que le processus de vieillissement apparaît d'abord à la surface des cristaux de pérovskite ainsi qu’aux joints de grains. Les mesures GDOES nous indiquent que les caractéristiques électriques des cellules pérovskites sont perdues par une corrosion progressive de l'électrode supérieure en argent causée par la diffusion des ions iodures. / Organic-inorganic lead halide perovskites are very promising materials for the next generation of solar cells with intrinsic advantages such as a low-cost material due to the availability of source materials and low-temperature solution processing as well as a high power conversion efficiency of the sunlight. However, perovskite solar cells are still unstable and show deleterious current-voltage hysteresis effects. Inthis thesis, analyses of CH3NH3PbI3-xClx based perovskite thin films and solar cells are presented. The electrical transport characteristics and the ageing processes are investigated using different approaches.The synthesis of the halide perovskite materials is optimized in a first step by controlling the deposition conditions such as annealing temperature (80°C) and spinning rate (6000 rpm) in the one step-spin-casted process. CH3NH3PbI3-xClx based perovskite solar cells are then fabricated in the inverted planar structure and characterized optically and electrically in a second step.Direct experimental evidence of the motion of the halide ions under an applied voltage has been observed using glow discharge optical emission spectroscopy (GDOES). Ionic diffusion length of 140 nm and ratio of mobile iodide ions of 65 % have been deduced. It is shown that the current-voltage hysteresis in the dark is strongly affected by the halide migration which causes a substantial screening of the applied electric field. Thus we have found a shift of voltage at zero current (< 0.25 V) and a leakage current (< 0.1 mA/cm2) in the dark versus measurement condition. Through the current-voltage curves as a function of temperature we have identified the freezing temperature of the mobile iodides at 260K. Using the Nernst-Einstein equation we have deduced a value of 0.253 eV for the activation energy of the mobile ions.Finally, the ageing process of the solar cell has been investigated with optical and electrical measurements. We deduced that the ageing process appear at first at the perovskite grain surface and boundaries. The electrical characteristics are degraded through a deterioration of the silver top-electrode due to the diffusion of iodides toward the silver as shown by GDOES analysis.

京都大学 / 0048 / 新制・課程博士 / 博士(エネルギー科学) / 甲第21884号 / エネ博第385号 / 新制||エネ||75(附属図書館) / 京都大学大学院エネルギー科学研究科エネルギー基礎科学専攻 / (主査)教授 佐川 尚, 教授 萩原 理加, 教授 野平 俊之 / 学位規則第4条第1項該当 / Doctor of Energy Science / Kyoto University / DGAM

京都大学 / 0048 / 新制・課程博士 / 博士(工学) / 甲第21786号 / 工博第4603号 / 新制||工||1717(附属図書館) / 京都大学大学院工学研究科物質エネルギー化学専攻 / (主査)教授 村田 靖次郎, 教授 辻 康之, 教授 小澤 文幸 / 学位規則第4条第1項該当 / Doctor of Philosophy (Engineering) / Kyoto University / DGAM

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Since their discovery, fullerenes and metallofullerenes have been investigated regarding their structures, synthesis, isolations, and applications. The highly symmetric structures of fullerenes and metallofullerenes lead to extraordinary physical properties, such as electron transfers, and attract major attention from the science community. It has been well established that the stabilities of fullerenes and metallofullerenes can be estimated by recognizing structural patterns. Recently, we developed a generalized spiral program and additional codes and believe they are useful for fullerene/metallofullerene researchers. The higher fullerenes, those with more than 90 carbon atoms, also follow certain structural patterns. In our studies, we have shown that the higher fullerenes with tubular structures are stable in thermodynamics and can survive the aminopropanol reaction, but other spherical fullerenes cannot. For the past three decades, great efforts have been devoted to applying fullerenes and metallofullerenes as electronic materials. In our studies, we find the ground state electron transfer properties endow metallofullerenes as an ideal material for perovskite solar cells to enhance the stabilities. It has been shown in our investigations that common metallofullerenes, such as Sc3N@C80, are capable to be as the electron transfer layers in perovskite solar cells, and the test demonstrates that our novel perovskite solar cells may achieve high stability and high efficiency. The electron transfer abilities of metallofullerenes are studied with the M2@C79N since electron densities located in between the two metal atoms convert between a single electron bond and a double electron bond. The huge spherical electron delocalized structures of fullerenes and metallofullerenes lead to strong interactions with other delocalized systems, such as graphene. Previous studies have shown that graphene has a unique ability in molecular adsorptions. However, the graphene surface is not always flat and the rippled areas have effects on the packing styles. Therefore, we examined the behavior of fullerenes on the rippled graphene surface and then compared with another flat molecule, PTCDA. The results show that the effect of rippled areas varies due to molecular structures. This study gives instructions for electronic device manufacturing using graphene and fullerenes. In our studies, polarizability is a key factor of fullerenes and metallofullerenes. It has been shown that the chromatographic retention behavior has a strong relationship with the average polarizability of a molecule. Based on the experimental data, we built a model for the prediction of chromatographic retention times using computational polarizabilities. After that, we validated the model by two series of chromatographic data. The characterization of carbon-based materials has been long investigated. In the last chapter, we introduce a dynamic nuclear polarization-based method to characterize the structures of chars and studied the adsorption of oxygen on the activated radical sites. Overall, the dissertation reports my Ph. D. studies in the areas including theoretical studies of fullerene geometries, chromatographic models, applications and also experimental studies of the applications of fullerenes/metallofullerenes and characterization. / Doctor of Philosophy / Fullerenes and metallofullerenes are important materials for engineering and science. In general, a fullerene cage contains only carbon atoms and has a closed spherical structure. Theoretically, for a given number of carbon atoms, there are thousands of different ways to assemble a fullerene structure, just like assembling Lego. However, just a limited number of fullerene molecules have been discovered. In the past four decades, several theories have been proposed to explain the fact. For example, an isolated pentagon rule shows that the fullerene structures should not have any conjugated pentagons, which will decrease the stabilities of fullerene molecules. In this dissertation, I would like to show our results, which demonstrate fullerenes that can be synthesized follow certain patterns. We apply experimental and theoretical methods to discover the patterns and explain the reason. The application of fullerenes/metallofullerenes is another hot topic. We consider the structures of fullerenes endow them extraordinary abilities of electron transfers. Therefore, we use metallofullerenes as electron transfer material in a solar cell, and we have a good solar cell with high efficiency. We also inspect the interactions between fullerenes and rippled graphene surface. The results are also extended to understand the chromatographic behavior of fullerenes. By considering the physical properties of fullerenes, we build up simple models to simulate the chromatographic retention behaviors of fullerene inside the chromatographic column. The characterization of carbon-based material is a big challenge and in this dissertation, we demonstrate our contributions of a novel method for characterization, which can detect activated carbons.

Perovskite solar cells (PSCs) have emerged as a promising renewable energy technology in recent years. However, their path towards industrial production and commercialization presents challenges that demand innovative solutions. This doctoral thesis is dedicated to addressing two pivotal issues in the development of PSCs: (1) the development of a fabrication method compatible with traditional semiconductor industry processes and (2) the exploration of approaches to improve device performance and stabilityThe present thesis separates these two issues into three parts. First, the fabrication method of MA-free perovskites via vacuum vapor deposition process is proposed. CsBr is added to FAPbI3giving FAxCs1-xPbI3-xBrx. to maintain the stable black perovskite phase. Furthermore, the effect of the thermal annealing process on perovskite films with different stoichiometric ratios was explored. It was found that thermal annealing enhances the crystallinity of both FAI-poor and stoichiometric films. For FAI-poor perovskite films, an increase in absorption as well as reduction in defect concentrations was achieved through annealing process. However, the opposite effect was observed for FAI-rich films. By optimizing the fabrication processes, a solar cell device with an efficiency of 16.6% was acquired. However, these vapor-deposited devices still exhibit lower performances compared to those prepared using solution processes, indicating the need for further improvements in perovskite layer composition and interfacial properties to enhance their efficiency. The second part of this dissertation demonstrates the concept of phase heterojunction (PHJ) solar cells by combining two polymorphs of the same material from the evaporation process (γ-CsPbI3) and solution process (β-CsPbI3). It was discovered that the photovoltaic parameters of these PHJ devices significantly surpass those of either single-phase device, resulting in a maximum power conversion efficiency of 20.1%. The enhancement comes from the following three factors: efficient passivation of the β-CsPbI3 by the larger bandgap γ-CsPbI3, an increase in the built-in potential of the PHJ devices enabled by the energetic alignment between the two phases, and enhanced absorption of light resulting from narrower band-gap β-CsPbI3 in the PHJ structure. The approach demonstrated here offers new possibilities for developing photovoltaic devices based on polymorphic materials. In the final part, a 1D-3D dimensional junction formed spontaneously by a two-step process is presented. It was found that the morphology, energy alignment, and defects of the buried interface were improved by creating 1D perovskites. In addition, strip-shaped PbI2 domains and voids are eliminated which ultimately enhances photovoltaic performance and stability. These improvements can be attributed to the passivation effect of the 1D perovskite and better energetic alignment. Furthermore, this dimensional junction strategy also shows potential for use in large-area devices.

<p dir="ltr">This research presents a comprehensive study of a 3D Perovskite Solar Cell model using Finite Element Analysis (FEA) and Machine Learning (ML). The research aims (i) to understand how material properties impact solar cell’s performance by applying basic semiconductor physics principles (ii) to investigate how interfacial delamination affects the performance of Perovskite solar cells (iii) to determine the optimum thickness of different layers of the solar cell (iv) to determine the fatigue life cycle of Perovskite layer.</p>

This thesis consists of three main studies: magnetic field effects in thermally activated delayed fluorescent (TADF) organic light emitting diodes (OLEDs), magnetic field effects in bipolar and unipolar polythiophene (P3HT) devices and a study of hybrid organic/inorganic perovskite devices. Spin-dependent transport and recombination processes of spin-pair species have been detected by magnetic field effect (MFE) technique in carbon-based semi- conductor devices. Magneto-electroluminescence (MEL) and magneto-conductivity have been measured as a function of the applied magnetic field, B, in light emitting diodes. TADF materials have been used instead of simple fluorescent materials in OLEDs. We have observed very large magnetic response with TADF materials. The second study is magnetic field effects of regio-regular P3HT based OLED devices. P3HT is a well known semiconducting polymer, and its electrical properties such as magneto-conductance can be affected by an applied magnetic field. P3HT was chosen because it exhibits a sign change in magnetoresistance (MR) as the bias is increased. Unipolar and bipolar devices have been fabricated with different electrode materials to understand which model can be best to explain organic magnetoresistance effect, possibly depending on the operating regime of the device. Transport and luminescence spectroscopies were studied to isolate the different mechanisms and identify their fingerprints. The third study is on hybrid organic-inorganic perovskite devices. With the potential of achieving very high efficiencies and the very low production costs, perovskite solar cells have become commercially attractive. Scanning electron microscopy (SEM) images and absorption spectrum of the films were compared in single-step solution, two-step solution and solution-assisted vapor deposition techniques. Grain size, morphology and thickness parameters of perovskite films were studied within these techniques. Perovskite solar cells were fabricated and their efficiencies were measured.