Solid-state dye-sensitized solar cells (ssDSSCs) and recently developed perovskite solar cells (PSCs) have attracted a great attention in the scientific field of photovoltaics due to their low cost, absence of solvent, simple fabrication and promising power conversion efficiency (PCE). In these types of solar cell, the dye molecule or the perovskite can harvest the light on the basis of electron excitation. Afterwards, the electron and hole are collected at the charge transport materials. Photoelectrochemical polymerization (PEP) is employed in this thesis to synthesize conducting polymer hole transport materials (HTMs) for ssDSSCs. We have for the first time developed aqueous PEP in comparison with the conventional organic PEP with acetonitrile as solvent. This water-based PEP could potentially provide a low-cost, environmental-friendly method for efficient deposition of polymer HTM for ssDSSCs. In addition, new and simple precursors have been tested with PEP method. The effects of dye molecules on the PEP were also systematically studied, and we found that (a) the bulky structure of dye is of key importance for blocking the interfacial charge recombination; and (b) the matching of the energy levels between the dye and the precursor plays a key role in determining the kinetics of the PEP process. In PSCs, the HTM layer is crucial for efficient charge collection and its long term stability. We have studied different series of new molecular HTMs in order to understand fundamentally the influence of alkyl chains, molecular energy levels, and molecular geometry of the HTM on the photovoltaic performance. We have identified several important factors of the HTMs for efficient PSCs, including high uniformity of the HTM capping layer, perovskite-HTM energy level matching, good HTM solubility, and high conductivity. These factors affect interfacial hole injection, hole transport, and charge recombination in PSCs. By systematical optimization, a promising PCE of 19.8% has been achieved by employing a new HTM H11. We believe that this work could provide important guidance for the future development of new and efficient HTMs for PSCs.

Metal and metal oxides are widely used in industry, and to optimize their performance their surfaces are commonly functionalized by the formation of thin films. Self-assembled monolayers (SAMs) are deposited on metals or metal oxides either from solution or by gas deposition. Thiols with polar terminal groups are utilized for creating the responsive surfaces which can interact electrostatically with other adsorbates. Surface charge effects wetting and adhesion, and many other surface properties. Polar terminal groups in thiols could be used to modify these factors. Mixed SAMs can provide more flexible surfaces, and could change the resulting surface properties under the influence of factors such as pH, temperature, and photo-illumination. Therefore, in order to control these phenomena by mixed polar-terminated thiols, it is necessary to understand the composition and conformation of the mixed SAMs and their response to these factors. In this work, mixtures of thiols with carboxylic and amino terminal groups were studied. Carboxylic and amino terminal groups of thiol interact with each other via hydrogen bonding in solution and form a complex. Complexes adsorb to the surface in non-conventional orientations. Unmixed SAMs from each type, either carboxylic terminated thiols or amino terminated thiols are in standing up orientation while SAMs from complexes are in an axially in-plane orientation. Selenol is an alternative to replace thiols for particular applications such as contact with biological matter which has a better compatibility with selenol than sulfur. However, the    Se-C bond is weaker than the S-C bond which limits the application of selenol. Understanding the selenol adsorption mechanism on gold surfaces could shed some light on Se-C cleavage and so is investigated in this work. Se-C cleavage happens in the low coverage areas on the step since atoms at steps have lower coordination making them more reactive than atoms on the terraces.  Another area where the self-assembly of molecules is of importance is for dye sensitized solar cells, which are based on the adsorption of the dye onto metal oxides surfaces such as TiO2.The interface between the SAM of dye and the substrate is an important factor to consider when designing dyes and surfaces in dye sensitized solar cells (DSSCs). The quality of the self-assembled monolayers of the dye on the TiO2 surface has a critical influence on the efficiency of the DSSCs.  Creation of just a monolayer of dye on the surface could lead to an efficient current of photo-excited electrons to the TiO2 and degeneration of the dye by redox. This work, T-PAC dye showed island growth with some ad-layer that is not in contact with the surface, whereas the MP13 dye adsorption is laminar growth.  Cuprite (Cu2O) is the initial and most common corrosion product for copper under atmospheric conditions. Copper could be a good replacement for noble metal as catalysts for methanol dehydrogenation. Knowledge about the structure of Cu2O(100) and Cu2O(111) surfaces could be used to obtain a deeper understanding of methanol dehydrogenation mechanisms with respect to adsorption sites on the surfaces. In this work, a detailed study was done of Cu2O(100) surface which revealed the possible surface structures as the result of different preparation conditions. Studies of the structure of Cu2O(100) and Cu2O(111) surfaces show that Cu2O(100) has a comparatively stable surface and reduces surface reactivity. As a consequence, dehydrogenation of methanol is more efficient on the Cu2O(111) surface. The hydrogen produced from methanol dehydrogenation is stored in oxygen adatom sites on both surfaces. / <p>QC 20161107</p>

Kesterite Cu2ZnSnS4 (CZTS) is interesting as a sustainable photovoltaic technology due to its earth-abundant elements and suitable semiconducting properties. To date, a record efficiency of 12.6% has been achieved but further improvements are required to reach high efficiency for industrial implementation. Among the limiting issues is the understanding of the annealing process, which is crucial in promoting high material quality. In particular, the knowledge of the effects of segregated secondary compounds on solar cell performance is lacking. In contrast to formation of ZnS particles throughout CZTS film, it is notable that SnS forms and usually segregates on the CZTS top and rear surfaces. The influence of SnS on CZTS solar cells was studied by electron beam induced current measurements. It is found that SnS presence on the CZTS surfacecan introduce “dead area”, whereas it seems beneficial for solar cell current when accumulates on the CZTS rear. For SnS passivation and from investigation of the passivation effect from an Al2O3 thin layer at the CZTS rear, improvement in overall device performance could not be demonstrated, due to either poor CZTS bulk or non-optimal device structure. The limitation in CZTS bulk quality was shown from a thickness study where carrier collection saturated already about 700-1000 nm CZTS thickness. Formation of SnS alongside CZTS implies the anneal is limited by a deficient sulfur partial pressure (PS2). By looking into Sn-S phase transformations in SnS2 films after annealing, we find that PS2 drops rapidly over the annealing time, which could be well-correlated to a series of changes in CZTS material quality including secondary phase formations and defect modifications. It is shown that annealing CZTS under sufficiently high PS2 is critical for CZTS solar cells with high open circuit voltage (upto 783mV was reached), possibly due to the defect modification. Besides SnS, it is observed that NaxS compounds are also readily formed on CZTS surfaces, due to Na diffusion from the glass substrate during annealing. NaxS negatively affects the formation of the CdS/CZTS interface during chemical bath deposition. It can be removed by an oxidation process or wet chemical etching.

The cost of the present generation of inorganic silicon solar cells is very high and further breakthroughs in cost and efficiency using traditional materials are becoming less and less likely after over 50 years of development. Next generation organic solar cells offer a solution to the limitations of silicon through the vision of low-cost, liquid-based, large area fabrication technology based on polymer and nanomaterials at room temperature. However, most polymers used in solar cells are dissolved in organic solvents such as xylene, toluene, chloroform, and chlorobenzene. Such solvents are harmful to people and environments, leading to higher costs due to complicated waste disposal processing. This is in conflict with the low cost, green, and renewable energy for which we are aiming. To realize a green organic solar cell, a novel solar cell has been created using an environmentally friendly water-soluble thiophene polymer [(Sodium poly[2-(3-thienyl)-ethoxy-4-butylsulfonate])] (PTEBS) and nanocrystalline TiO2. This novel system has shown great potential in photovoltaics the work has garnered the attention of the international community.In our innovative solar cells, the water-soluble polythiophene (PTEBS) is used as electron donor. Nanoparticle TiO2 acts as electron acceptor. PTEBS/TiO2 solar cells with various structures including bilayer heterojunctions, bulk heterojunctions and a hybrid of bilayer and bulk heterojunctions have been developed and explored. These results are comparable to the best polymer/metal-oxide solar cells reported by other groups using organic solvents.In summary, this is the first time that green solar cells have been fabricated from environmentally friendly water-soluble polymers. By using water as the solvent and utilizing liquid-based processing, the cost of the energy generated by this type of solar cell will be further lowered. In addition, the flexible polymer offers the ease of fabrication and integration into different devices.

This doctoral thesis deals with analysis of existing area defect detection methods in solar cells and with concept of its innovation and of the development of faster detection method. Results of measurement is analyzing in practical and theoretical part. The most important is LBIC (Light Beam Induced Current) method innovated of different wavelength light source usage and Electroluminescence method. On the bases of this knowledge is created Fast LBIC method and then is created catalog of defects in monocrystalline silicon solar cells.

Organic solar cells are one of the most promising candidates for future solar power generation. They are thin and lightweight with several additional advantages such as scalability, environmental sustainability and low cost for processing and installation. However, the low charge carrier mobility of the absorbing material for organic solar cells requires thin absorber layers, limiting photon harvesting and the overall power conversion efficiency. Several attempts, e.g., periodically patterned structures and scattering layers have been tried to enhance the absorption of thin-film solar cells as light trapping elements. However, much effort is required to introduce light trapping structures to conventional rigid metal oxide electrodes and glass substrate. For instance, almost 13 hours are required to fabricate micro structures of 1 m2 area on glass, in contrast, 1 minute on PET using a same laser set-up and an additional scattering layers are demanded for providing light trapping effects to solar cells. In the last years, flexibility is emerging as the one of the major advantages of organic solar cells. To realize flexibility of solar cells, the classically used glass substrates and ITO electrodes are too brittle. Therefore, polymer materials are promising candidates to replace them as flexible electrodes and substrates. In this thesis, the highly transparent conducting polymer, PEDOT:PSS and PET equipped with an AlOx encapsulation layer are used as electrode and substrate, respectively. Besides the flexibility, additional light trapping elements, e.g. scattering particles, nano- and microstructures can be easily applied to the polymer materials since they have the potential for easier shaping and processing. In this study, we apply different light trapping and in-coupling approaches to organic solar cells. First, PET substrates are structured with a direct laser interference patterning system, which is a powerful and scalable one-step technique for patterning polymers. Almost 80 % of the light is diffracted by these patterned PET substrates and thereby the light path in the absorption layer is increased. Optical display films, commercially developed to be used as back light units of liquid crystal displays are also examined as light trapping substrates and exhibit similar enhancement as patterned PET. Moreover, since PEDOT:PSS is prepared by a solution-based process, TiO2 nanoparticles are added as light scattering elements to the PEDOT:PSS electrodes. Consequently, those electrodes provide a dual function as electrical contact and light trapping element. Finally, 2- or 3-dimensional nanostructures are printed by a nano-imprinting technique onto the surface of PEDOT:PSS with PDMS stamps. By controlling the temperature and the time of PEDOT:PSS during an annealing step, nanostructures are transferred from PDMS masks to PEDOT:PSS. To evaluate the effects of light trapping for all above mentioned approaches, flexible organic solar cells are produced by vacuum evaporation using blends of DCV5T-Me and C60 as absorber layer. The substrates are optically characterized using UV-vis spectrometer and goniometer measurements. The topography of the samples is measured by atomic force microscopy, scanning microscopy and optical microscopy. Bending tests with various radii are performed to test the flexibility of the substrates. In summary, light trapping effects are successfully implemented in the electrodes and substrates for OPVs, giving efficiency improvements of up to 16 %. The light trapping mechanisms in our approaches are extensively discussed in this thesis. / Organische Photovoltaik ist einer der vielversprechendsten Kandidaten für die zukünftige Solarstromgewinnung auf flexiblen Substraten. Um diese Flexibilität zu ermöglichen, sind herkömliche Glassubstrate mit ITO-Elektroden zu spröde. Ein vielversprechender Kandidat, um sowohl flexible Elektroden als auch flexible Substrate herzustellen, sind Polymere, da diese sehr biegsam und leicht zu verarbeiten sind. Deshalb wird in dieser Arbeit das hoch transparente, leitfähige Polymer PEDOT:PSS als Elektrode und PET (mit einer AlOx Verkapselungsschicht) als Substrat untersucht. Aufgrund der guten Prozessierbarkeit der Polymere konnten wir zusätzlich zu den eigentlichen Funktionen des Substrates und der Elektrode noch den Mechanismus des Lichteinfangs hinzufügen. Zusätzlich zu ihrer Flexibilität haben organische Solarzellen noch weitere Vorteile: sie sind dünn, leicht, skalierbar und verursachen vergleichsweise geringe Kosten für Herstellung und Installation. Ein Nachteil organischer Solarzellen ist die vergleichsweise geringe Ladungsträgerbeweglichkeit der Absorbermaterialien, welche oft die Schichtdicke der Absorbermaterialien begrenzt. Dies hat weniger absorbierte Photonen, weniger Stromdichte und somit einen geringeren Wirkungsgrad zur Folge. In den letzten Jahren wurden periodisch strukturierte Substrate und streuende Schichten als Lichteinfangelemente eingesetzt, um den Wirkungsgrad organischer Solarzellen mit dünnen Absorberschichten zu erhöhen. Gestaltungsregeln für solche Lichteinfangelemente sind noch weitestgehend unbekannt. Im Rahmen dieser Arbeit strukturieren wir PET Substrate mit einem direkten Laserinterferenzsystem, welches ein leistungsfähiges, skalierbares Einschrittverfahren zur Polymerstrukturierung ist. Da PEDOT:PSS aus der Lösung prozessiert wird, können wir weiterhin Nanopartikel hinzufügen, die der Elektrode zusätzlich noch lichtstreuende Eigenschaften geben. Außerdem können 2- bzw. 3-dimensionale Nanostrukturen leicht mithilfe einer Stempeltechnik eingeprägt werden. Um die Effekte des Lichteinfangs, welcher durch die oben genannten Methoden erzeugt wird, zu untersuchen, werden flexible organische Solarzellen mittels Vakuumverdampfung prozessiert. DCV5T-Me und C60 bilden dabei die photoaktive Schicht. Somit werden die Licht fangenden Eigenschaften dieser flexiblen Solarzellen ausgenutzt und ausführlich in der Arbeit diskutiert.

Doctor of Philosophy / Department of Chemistry / Stefan H. Bossmann / Porin A from Mycobacterial smegmatis (MspA) is an octameric trans-membrane channel protein and is one of the most stable porins known to date. MspA has been successfully isolated and purified to obtain liquid extracts and crystals using a modified extraction procedure. A full analytical assessment has been carried out to authenticate its’ structure, including gel electrophoresis, spectroscopy (fluorescence, UV, FTIR, NMR), HPLC, Bradford protein assay, dynamic light scattering and X-ray crystallography. Nanoscopic vesicle formation of MspA molecules in aqueous media has been thoughroughly investigated. Temperature dependent dynamic light scattering experiments reveal that size of such vesicles is dependent on temperature but is independent of ionic strength of the medium. Zeta potential measurements reveal a steady build up of positive charge on the vesicle surface with increasing temperature. For the first time, wild type (WT) MspA has been utilized as a channel forming agent. This phenomenon has future potential in DNA sequencing and the development of antimycobacterial drugs. Channel activity of WT MspA and mutant A96C MspA has been investigated and has shown to form stable channels across DPhPC lipid bilayers. Blocking of the channel current via external molecules (i.e. channel blocking) is an extremely important process, which helps to evaluate the biosensor ability of the pore. In this regard, two Ruthenium based compounds, Ru(QP-C2)38+ (i.e. RuC2) and Ru(bpy)32+have been successfully employed as channel blocking agents. Both compounds show evidence for channel blocking of WT MspA. However, these results are not reproducible. Three dimensional aggregation behavior of RuC2-MspA vesicles have been thoughroughly investigated. It is evident that addition of RuC2 significantly increases vesicle size and polydispersity of MspA aggregates in solution. The results provide explanations onto the lack of channel blocking ability of MspA by RuC2. Development of a ‘greener’ dye sensitized solar cell with the use of MspA as an electron carrier is investigated for the first time. A series of Ru(II)-phenanthroline-based dyes have been synthesized as non-toxic dyes in this regard. Chemical binding between the dyes and MspA has been achieved successfully. Two types of solar cell prototypes, i.e. TiO2-based (Grätzel type) and FTO-based have been developed and tested. Significant current generation and conversion efficiencies have been achieved for both cell types. This marks the first development of a protein-based photovoltaic device, which has the potential to be developed as a new class of “hybrid soft solar cells”.

Doctor of Philosophy / Department of Chemistry / Jun Li / Solar energy as a sustainable resource is a promising alternative to fossil fuels to solve the tremendous global energy crisis. Development of three generation of solar cells has promoted the best sunlight to electricity conversion efficiency above 40%. However, the most efficient solar cells rely on expensive nonsustainable raw materials in device fabrication. There is a trend to develop cost-effective biophotovoltaics that combines natural photosynthetic systems into artificial energy conversion devices such as dye sensitized solar cells (DSSCs). In this research, a model system employs natural extract light-harvesting complex II (LHCII) as a light-absorbing sensitizer to interface with semiconductive TiO₂ and plasmonic nanoparticles in DSSCs. The goal of this research is to understand the fundamental photon capture, energy transfer and charge separation processes of photosynthetic pigment-protein complexes along with improving biophotovoltaic performance based on this model system through tailoring engineering of TiO₂ nanostructures, attaching of the complexes, and incorporating plasmonic enhancement. The first study reports a novel approach to linking the spectroscopic properties of nanostructured LHCII with the photovoltaic performance of LHCII-sensitized solar cells (LSSCs). The aggregation allowed reorganization between individual trimers which dramatically increased the photocurrent, correlating well with the formation of charge-transfer (CT) states observed by absorption and fluorescence spectroscopy. The assembled solar cells demonstrated remarkable stability in both aqueous buffer and acetonitrile electrolytes over 30 days after LHCII being electrostatically immobilized on amine-functionalized TiO₂ surface. The motivation of the second study is to get insights into the plasmonic effects on the nature of energy/charge transfer processes at the interface of photosynthetic protein complexes and artificial photovoltaic materials. Three types of core-shell (metal@TiO₂) plasmonic nanoparticles (PNPs) were conjugated with LHCII trimers to form hybrid systems and incorporated into a DSSC platform built on a unique open three-dimensional (3D) photoanode consisting of TiO₂ nanotrees. Enhanced photon harvesting capability, more efficient energy transfer and charge separation at the LHCII/TiO₂ interface were confirmed in the LHCII-PNP hybrids, as revealed by spectroscopic and photovoltaic measurements, demonstrating that interfacing photosynthesis systems with specific artificial materials is a promising approach for high-performance biosolar cells. Furthermore, the final study reveals the mechanism of hot electron injection by employing a mesoporous core-shell (Au@TiO₂) network as a bridge material on a micro-gap electrode to conduct electricity under illumination and comparing the photoconductance to the photovolatic properties of the same material as photoanodes in DSSCs. Based on the correlation of the enhancements in photoconductance and photovoltaics, the contribution of hot electrons was deconvoluted from the plasmonic near-field effects.

In this thesis, the process of fabricating PEDOT:PSS/c-Si hybrid solar cells has been investigated with the goal of performing a proof of concept as well as to determine the influence on solar cell performance of some processing parameters. Properties of PEDOT:PSS film formation and metal contact formation were investigated as a first step. Additionally, the surface passivation properties of PEDOT:PSS on n-Si have been studied and carrier lifetimes of 300 <img src="http://www.diva-portal.org/cgi-bin/mimetex.cgi?%5Cmu" />s were measured by quasi steady-state photoconductance and photoluminescence carrier lifetime imaging of silicon substrates that had PEDOT:PSS spin-coated onto both sides. Finally, working PEDOT:PSS/c-Si hybrid solar cells of both the FrontPEDOT and BackPEDOT concepts were successfully fabricated and their current-voltage characteristics were measured. The champion device showed a JSC of 23.0 mA/cm2, a VOC of 520 mV and a FF of 59% as measured directly after fabrication. Repeating the measurements the following day showed a strong degradation of the cells, particularly of the JSC. It can be concluded from this work that fully working PEDOT:PSS/c-Si hybrid solarcells of both the FrontPEDOT and BackPEDOT types can be fabricated through a simple and low-cost production route. The quality of the metal contacts is of very high importance for the function of the cells. The cells are heavily degraded within less than 24 hours when stored in atmoshperic conditions, but some of the function can be regained by annealing and edge isolation. Achieving better wetting on Si substrates after certain cleaning procedures is an important point for further study. PEDOT:PSS has been seen to have some excellent passivation properties on c-Si, although these results show a strong dependency on the specific type of PEDOT:PSS. / I denna uppsats har tillverkningen av PEDOT:PSS/c-Si hybridsolceller undersökts med målet att tillverka en fungerande solcell samt att bestämma påverkan på cellens prestanda av vissa processparametrar. Polymerfilmbildning och metallkontaktbildning undersöktes som ett första steg. Dessutom studerades polymerfilmens förmåga att passivera n-Si ytor, och livstider hos laddningsbärare på ca 300<img src="http://www.diva-portal.org/cgi-bin/mimetex.cgi?%5Cmu" />s mättes genom QSSPC och PL-I på kiselsubstrat med polymerfilmer på båda sidor. Slutligen tillverkades fungerande polymer/kisel hybridsolceller av både FrontPEDOT och BackPEDOT typ och de elektriska egenskaperna bestämdes. Den bästa cellen hade JSC=23.0 mA/cm2, VOC=520 mV och FF=59%, uppmätt direkt efter tillverkningen. Upprepning av mätningarna följande dag visade en stark degradering av cellerna, i synnerhet av kortslutningsströmmen. Man kan dra slutsatsen från detta arbete att fullt fungerande polymer/kisel hybridsolceller av både FrontPEDOT och BackPEDOT typ kan tillverkas genom en enkel och kostnadseffektiv produktionsväg. Kvaliteten på metallkontakterna är av mycket stor betydelse för cellernas funktion. Cellerna försämras kraftigt inom mindre än 24 timmar vid förvaring i atmosfäriska förhållanden, men en del av funktionen kan återfås genom upphettning och kantisolering. Att uppnå bättre vätning på kiselsubstrat efter vissa rengöringsmetoder är en viktig punkt för vidare studier. Polymerfilmer av PEDOT:PSS har visat sig ha utmärkta passiveringsegenskaper på kiselytor, även om dessa resultat visar ett starkt beroende på den specifika typen av PEDOT:PSS.

L'objectif d'amélioration des performances de cellules solaires sur des substrats de silicium cristallin de plus en plus en minces (< 200 µm) est indispensable à la réduction des coûts du module et donc à l'essor du photovoltaïque à l'échelle mondiale. Cette thèse se propose de répondre à la problématique d'amincissement des plaquettes sur substrats monocristallins (Cz) de type p de grande surface (239 cm2 - 180 µm) par le développement d'une structure en face arrière capable de générer un rendement de conversion élevé tout en limitant le degré de complexité du procédé de fabrication de la cellule. La solution explorée est celle des cellules à face arrière passivée et contacts localisés et les schémas de passivation étudiés s'appuient sur l'utilisation d'empilements diélectriques à base d'oxydes de silicium (SiO2) et d'aluminium (Al2O3) couplés au nitrure de silicium (SiNx). Ces travaux ont pour objectif d'optimiser les propriétés de passivation des couches diélectriques tout autant que les briques technologiques nécessaires à leur intégration dans la structure de cellule finale (conditionnement de surface, ablation laser sélective, métallisation par sérigraphie). Le procédé de fabrication résultant a permis d'obtenir des cellules avec un rendement de conversion de 19.1% pour l'empilement SiO2/SiNx. Il est cependant démontré que les limitations des performances de cette structure peuvent être partiellement compensées en introduisant une couche d'alumine, permettant d'atteindre un rendement remarquable de 19.5% (+0.4% par rapport à une structure standard). / Improving the solar cell efficiency on thin wafers (< 200 µm) has become a must in the industry in order to reduce the module cost and enhance the photovoltaics field growth worldwide. This work addresses the issues regarding the thickness reduction of large monocrystalline p-type wafers (239 cm2 - 180 µm) by developing a back side architecture capable of increasing the efficiency while limiting the cell fabrication level of complexity. Thus back passivated and local contacts, also known as PERC-type, solar cells are investigated. Those include passivation schemes relying on the use of dielectric stacks based on silicon oxide (SiO2), aluminum oxide (Al2O3) both coupled with silicon nitride layers (SiNx). This PhD study attempts to carry out an optimization of the passivation properties as well as of the technological steps required for a proper integration in the final cell structure (surface preparation, selective laser ablation, screen-printing metallization). The resulting optimized process led to the fabrication of solar cells displaying an 19.1% conversion efficiency by using SiO2/SiNx layers. Nevertheless it was shown evidence that the limited electrical performances can be overcome by introducing an Al2O3 layer, eventually reaching a remarkable 19.5% efficiency. This represents an absolute gain efficiency of +0.4% compared to the standard full-area Al-BSF solar cell architecture.