<p>New acceptor moieties with extended conjugation have been developed  for further understanding of structure-property relationships in donor-acceptor type semiconducting polymers. These diketopyrrolopyrrole or isoindigo based conjugated polymers have been demonstrated as functional materials in organic field effect transistors, photoacoustic imaging and organic electrochemical transistors. With demonstrations of semiconducting molecular design, we hope to spark new research directions especially on deeper investigation of charge transport dependence on chemical structures, and new design strategies of acceptor moieties with extended conjugation could be applied for targeted applications.</p>

京都大学 / 新制・課程博士 / 博士(情報学) / 甲第24040号 / 情博第796号 / 新制||情||135(附属図書館) / 京都大学大学院情報学研究科システム科学専攻 / (主査)教授 加納 学, 教授 大塚 敏之, 教授 下平 英寿 / 学位規則第4条第1項該当 / Doctor of Informatics / Kyoto University / DGAM

In traditional electronics, inorganic materials such as silicon and germanium are used as semiconductors due to their outstanding semiconducting properties. Unfortunately, inorganic materials are rigid due to their high crystalline nature, and processing these materials is complex and expensive. Furthermore, traditional semiconducting materials do not have favorable mechanical properties in applications such as wearable devices and large-area applications with complicated shapes. Conjugated conducting polymers (CCPs) are being explored as alternative materials to conventional semiconductors due to their mechanical properties and high conductivity. CCPs offer properties such as solution and low-temperature processability, flexibility, thermal and optical properties that traditional semiconductors could not provide. These characteristics are essential in Organic Light-Emitting Diodes (OLEDs), Organic Field-Effect Transistors (OFETs), and Photovoltaic (PVs) devices. This dissertation focuses on synthesizing rhodamine- and diketopyrrolopyrrole- containing CCPs. Chapter I focuses on the synthesis, and characterization of polyrhodamine (PRho), a semiconducting conjugated polymer containing the rhodamine core in the polymer’s backbone. PRho was synthesized by the Buchwald-Hartwig polycondensation and characterized for its optical and electrochemical properties. We have discovered that the polymer is electrochemically reversible and stable up to 1000 cycles as recorded by cyclic voltammetry between -0.4 and 1.0 V vs. Ag/AgCl and stable to extreme acidic and basic conditions without noticeable degradation. Remarkably, the polymer has a conductivity in the semiconductor range of 8.38 x 10-2 S cm–1 when treated with 20% HCl. Chapter II focuses on the synthesis and characterization of four different alkenyl flanked diketopyrrolopyrrole (DPP) polymers ( PDPPVTV, PDPPVTT, PDPPV3T, and PDPPV4T) synthesized via Stille polycondensation. Different pi-conjugated segments (alkenyl/ PDPPVTV, thiophene/ PDPPVTT, thienothiophene/ PDPPV3T, and dithienothiophene/ PDPPV4T) were used to tune the optoelectrical properties of the polymers. The effect of the alkenyl groups and different pi-conjugated segments on the optoelectrical and charge mobility properties were determined by UV/visible spectroscopy, cyclic voltammetry, and FET characteristics. Three of the four polymers, except PPP4T, showed good solubility in chloroform. All the polymers showed high thermal stabilities in TGA and semi-crystalline nature in X-Ray diffraction patterns. PDPPVTV and PDPPVTT exhibited hole mobilities of 1.8 x 10-3 cm2 V-1 s-1 and 0.25 cm2 V-1 s-1, respectively. .

This dissertation focuses on the design, synthesis, and characterization of a variety of organic dyes, semiconducting materials, and surface redox-active modifiers of potential interest to organic-based emerging photovoltaics. A discussion of the materials’ optoelectronic properties, their ability to modify and promote electron transfer through an organic/transparent conducting-oxide interface, and finally their effect on the photovoltaic properties of devices utilizing them as light-harvesters is provided where relevant. The first two research chapters discuss mono-chromophoric asymmetric squaraine-based sensitizers and covalently linked, dual-chromophoric, porphyrin-squaraine sensitizers as light absorbers in dye-sensitized solar cells (DSSCs), in an attempt to address two problems often encountered with DSSCs utilizing this class of near infra-red sensitizers; The lack of panchromatic absorption and aggregation on the surface. Also, this dissertation discusses the design and synthesis of asymmetric perylene diimide phosphonic acid (PDI-PA) redox-active surface modifiers, and reports on the electron-transfer rates and efficiencies across the interface of an ITO electrode (widely used in organic-electronic devices) modified with these perylene diimides. Finally two series of hole-transport materials based on oligothiophenes and benzodithiophenes are reported: optoelectronic properties and preliminary performance of organic photovoltaic (OPV) devices fabricated with them is discussed.

This thesis presents a study of lasing properties and optical amplification in semiconducting conjugated polymers and dendrimers. Configured as surface-emitting distributed feedback lasers, the effect of incorporating wavelength-scale microstructure on the output of the devices is examined along with the ability to create such structures using simplified fabrication processes such as soft lithography. Conjugated materials have received a great deal of interest due to their broad spectral absorption, emission, ability to exhibit gain and ease of processing from solution. As a result, they show great potential for a variety of applications such as photovoltaics, displays, amplifiers and lasers. To date however, there has only been one demonstration of a polymer optical amplifier. A broadband, solution based polymer amplifier is presented where the gain overlaps with the transmission window of polymer optical fibres. The effect of transitions that reduce the availability of gain in conjugated polymers is also examined by studying saturation of absorption in thin films. Producing wavelength scale microstructure is traditionally a slow, expensive technique. Here, solvent assisted micromoulding is used to pattern polymer films in less than two minutes. The effect of the variations in the pattern transfer on the laser characteristics is examined. The micromoulding technique is then applied to fabricating novel device types such as circular gratings and flexible plastic lasers. Encapsulation of the micromoulded laser is then shown to improve the lifetime of the device by over three orders of magnitude. The degradation effects witnessed during this extended operation are characterised quantitatively, an area of study where little data exists in the literature. A novel class of branched dendrimer materials whose properties can be independently tuned due to their modular architecture are configured as blue-emitting distributed feedback lasers. The ability to tune the emission wavelength by varying the film thickness is demonstrated. By changing the chemical groups contained within the molecule, further tuning of the emission can be obtained along with the demonstration of a highly efficient blue-emitting dendrimer laser. Chemosensing using dendrimer lasers is presented by demonstrating the incredibly sensitive response of the laser device to trace vapours of nitro-benzene compounds. The future application of which could be highly beneficial in the detection of explosives.

Les polymères semi-conducteurs semicristallins sont utilisés au sein de diodes électroluminescentes, transistors ou dispositifs photovoltaïques organiques. Ces matériaux peuvent être traités à partir de solutions ou directement à partir de leur état solide et forment des agrégats moléculaires dont la morphologie dicte en grande partie leurs propriétés optoélectroniques. Le poly(3-hexylthiophène) est un des polymères semi-conducteurs les plus étudiés. Lorsque le poids moléculaire (Mw) des chaînes est inférieur à 50 kg/mol, la microstructure est polycristalline et composée de chaînes formant des empilements-π. Lorsque Mw>50 kg/mol, la morphologie est semicristalline et composée de domaines cristallins imbriquées dans une matrice de chaînes amorphes. À partir de techniques de spectroscopie en continu et ultrarapide et appuyé de modèles théoriques, nous démontrons que la cohérence spatiale des excitons dans ce matériau est légèrement anisotrope et dépend de Mw. Ceci nous permet d’approfondir la compréhension de la relation intime entre le couplage inter et intramoléculaire sur la forme spectrale en absorption et photoluminescence. De plus, nous démontrons que les excitations photogénérées directement aux interfaces entre les domaines cristallins et les régions amorphes génèrent des paires de polarons liés qui se recombinent par effet tunnel sur des échelles de temps supérieures à 10ns. Le taux de photoluminescence à long temps de vie provenant de ces paires de charges dépend aussi de Mw et varie entre ∼10% et ∼40% pour les faibles et hauts poids moléculaires respectivement. Nous fournissons un modèle permettant d’expliquer le processus de photogénération des paires de polarons et nous élucidons le rôle de la microstructure sur la dynamique de séparation et recombinaison de ces espèces. / Microstructure plays a crucial role in defining the optoelectrical properties of conjugated polymeric semiconductors which can be used in light harvesting and generating devices such as organic light emitting diodes, field effect transistors or photovoltaic devices. These polymers can be processed from solution or solidstate and form photophysical aggregates, consequently providing a complex network which controls the fate of any photogenerated species. poly(3-hexylthiopene) is one of the most studied polymeric semiconductor. In this material, the molecular weight (Mw) of the polymer governs the microstructure and highly impact the optical and electronic properties. Below Mw≈ 50 kg/mol, the polymer chains forms polycrystalline domains of π-stacked molecules while high Mw (>50 kg/mol) consists of a two-phase morphology of molecularly ordered crystallites that are embedded in amorphous regions. Such morphology provides a bidimensionnal network hosting both neutral excitations, known as Frenkel excitons, and polarons. By means of steady-state and ultrafast spectroscopy experiment and backed up theoretical modeling, we demonstrate that the spatial coherence of such excitations are anisotropic in the lattice and depends on the Mw of the polymer, providing a deep understanding of the interplay between interchain (excitonic) and intrachain coupling in polymer aggregates. Moreover, we show that direct excitation at the interface between molecularly ordered and amorphous regions generates tightlybound charge pairs which decay via quantum tunneling over >10 ns. The yield of delayed photoluminescence arising from the recombination of those charge pairs varies between ∼10% and ∼40% for low and high Mw films respectively. We provide a quantitative model that describes the photogeneration process of those geminate polaron pairs and determine the role of the microstructure in the charge separation and recombination processes.

La durabilité chimique des alliages métalliques résulte notamment de la nature des défauts ponctuels assurant le transport au travers du film d’oxydation formé en surface. L'élaboration de couches d'oxyde modèles par oxydation thermique en pression contrôlée et ALD (Atomic Layer Deposition) et l'étude de leurs propriétés semi conductrices (conditionnées par la nature des défauts ponctuels) devrait permettre une meilleure compréhension des mécanismes de formation de ces couches d'oxyde. / The chemical durability of the metal alloy results in particular from the nature of point defects providing transport through the oxidation film formed on the surface. Models oxide layers, grown by thermal oxidation and Alomic Layer Deposition, will be studied by photoelectrochemistry. This will provide us information about the semiconductive properties of the oxide, determined by the point defect in the oxide layer, and should allow us a better understanding of the formation mechanism of these oxide.

Cette thèse rapporte l’étude des propriétés de films transparents conducteurs obtenus à partir de dispersions de nanotubes de carbone. La formulation des dispersions représente une étape clé dans le but d’obtenir des films homogènes avec de bonnes propriétés électro-optiques. Plus particulièrement, la création d’interactions attractives en solution entre les nanotubes de carbone permet d’une part de modifier le comportement rhéologique des dispersions et d’améliorer leur dépôt en couche mince par enduction. D’autre part, les travaux présentent une étude concernant l’influence des interactions sur la structuration du réseau de nanotube de carbone qui constitue les films. Ces changements de structuration sont notamment mis en parallèle avec les propriétés électriques des films selon leur épaisseur. L’utilisation de polymères semi-conducteurs a aussi fait l’objet de travaux expérimentaux pour améliorer la formation et les propriétés des films transparents conducteurs. / This thesis reports the study of the properties of transparent conductive films obtained from carbon nanotube dispersions. The dispersion formulation is a key step in order to obtain uniform films with good opto-electrical properties. In particular, the formation of attractive interactions between dissolved carbon nanotubes allows the modification of the rheological behavior of the dispersions and the improvement of their deposition in thin layer by coating. Also, the influence of the interactions on the carbon nanotube network morphology is presented. The structural changes of the networks are then related to both electrical properties and thickness of the films. Finally, the use of semiconducting polymers was analyzed in order to improve the fabrication and the properties of transparent conductive films.

The rapid development in perovskite solar cells (PSC) has generated a tremendous interest in the photovoltaic community. The power conversion efficiency (PCE) of these devices has increased from 3.8% in 2009 to a recent certified efficiency of over 20% which is mainly the product of the remarkable properties of the perovskite absorber material. One of the most important advances occurred with the replacement of the liquid electrolyte with a solid state hole conductor which enhanced PCE values and improved the device stability. Spiro-OMeTAD (2,2',7,7'-tetrakis(N,N'-di-p-methoxyphenylamine)- 9,9'-spirobifluorene) is the most common hole transport material in perovskite solar cells. Nevertheless, the poor conductivity, low charge transport and expensive synthetic procedure and purification have limited its commercialisation. Triphenylamines (TPA) like Spiro-OMeTAD are commonly employed due to the easy oxidation of the nitrogen centre and good charge transport. Other triarylamines have similar properties to Spiro-OMeTAD but are easier to synthesise. The aim of this doctoral thesis is to investigate different types of hole transport materials in perovskite solar cells. Three different series of triphenylamine-based HTM were designed, synthesised, characterised and studied their function in perovskite solar cells. A series of five diacetylide-triphenylamine (DATPA) derivatives (Chapter 3) with different alkyl chain length in the para position was successfully synthesised through a five step synthesis procedure. A range of characterisation techniques was carried out on the molecules including; optical, electrochemical, thermal and computational methods. The results show that the new HTMs have desirable optical and electrochemical properties, with absorption in the UV, a reversible redox property and a suitable highest occupied molecular orbital (HOMO) energy level for hole transport. Perovskite solar cell device performances were studied and discussed in detail. This project studied the effect of varying the alkyl chain length on structurally similar triarylamine-based hole transport materials on their thermal, optical, electrochemical and charge transport properties as well as their molecular packing and solar cell parameters, thus providing insightful information on the design of hole transport materials in the future. The methoxy derivative showed the best semiconductive properties with the highest charge mobility, better interfacial charge transfer properties and highest PCE value (5.63%). The use of p-type semiconducting polymers are advantageous over small molecules because of their simple deposition, low cost and reproducibility. Styrenic triarylamines (Chapter 4) were prepared by the Hartwig-Buchwald coupling followed by their radical polymerization. All monomers and polymers were fully characterised through electrochemical, spectroscopic and computational techniques showing suitable HOMO energy levels and desirable optoelectrochemical properties. The properties and performance of these monomers and polymers as HTMs in perovskite solar cells were compared in terms of their structure. Despite the lower efficiencies, the polymers showed superior reproducibility on each of the device parameters in comparison with the monomers and spiro-OMeTAD. Finally, star-shaped structures combine the advantages of both small molecules, like well-defined structures and physical properties, and polymers such as good thermal stability. Two star-shaped triarylamine-based molecules (Chapter 5) were synthesised, fully characterised and their function as hole-transport materials in perovskite solar cells studied. These materials afford a PCE of 13.63% and high reproducibility and device stability. In total this work provided three series of triarylamine-based hole transport materials for perovskite solar cells application and enabled a comparison of the pros and cons of different design structures: small-molecule, polymeric and star-shaped.

ZnO window layers for CIGS solar cells are grown with a DC sputtering technique instead of a conventional RF sputtering technique. Transparent window layers and buffer layers are sputtered from the Zn target in the presence of Oxygen. The window layer is doped with Aluminum in order to achieve high electrical conductivity and thermal stability. The effect of different sputtering parameters on the electrical and optical properties of the films is elaborately studied. Sets of annealing experiments are also performed. Combinations of different deposition parameters are examined to design the optimum fabrication conditions. We are able to deposit 85% transparent, Al doped ZnO films having 002-axis orientation and 4e-4 ohm-cm resistivity, which is successfully, used on CIGS solar cells. Resistivity of undoped ZnO buffer layers is varied form 10-2 ohm-cm to unmeasurable by varying the sputtering parameters. The performance of a reactively sputtered window layer and a buffer layer have matched the performance of the RF sputtered ZnO on CIGS solar cells. There has been considerable effort to eliminate Chemical Bath Deposition of the CdS buffer layer from CIS solar cell fabrication. The performance of an undoped DC sputtered ZnO layer is examined on Cd free CIGS solar cells. The ZnO buffer layer is directly sputtered on an underlying CIGS material. The performance of Cd free solar cells is highly susceptible to the presence of Oxygen in the sputtering ambient of the buffer layer deposition [6]. As Oxygen is a growth component in reactive sputtering, the growth mechanisms of the DC-sputtered buffer layer are studied to improve the understanding. The performance of all reactively sputtered ZnO devices matched the values reported in the literature and the results for DC sputtered ZnO on Cd-free solar cells were encouraging.