銅銦鎵硒薄膜太陽能電池因為其高效率及相對低廉的成本，商業應用已經開始陸續出現。我們自主研發的集成式銅銦鎵硒薄膜電池生產系統可以全程製作襯底大小為10cm x 10cm 的電池及剃型組件。本研究工作主要分為兩個方向:第一個方向是研究及測試生長高效率太陽能電池及組件的具體條件。通過儀器改進及電池每層鍍膜的條件優化，能夠重複的生長高效率電池及組件; 第二個方向是通過減少銅銦鎵硒吸光習的厚度從而達到降低電池生產成本的目的。 / 銅銦鎵硒採用三步共蒸法製備吸收層。第一步先蒸發銦、鎵、硒三種元素形成n型硒化銦(鎵)薄膜;第二步蒸發銅、硒形成銦鎵硒半導體薄膜; 第三步蒸發一層額外的型硒化銦(鎵)薄膜保證整體電池是p型半導體。三步期間的襯底溫度經過小心調試，以使得合適的鎵梯度能夠在吸收層裹形成。通過每一層的條件優化我們能夠生長出高光電轉換效率的太陽能電池(17%)及組件(12%)。 / 太陽能電池的變溫測試及弱光測試對瞭解其應用潛能存在非常重要的作用。通過多組對比實驗發現銅銦鎵硒電池的溫度係數可以通過增加鎵在吸收層的組分而得到改善。同時，電池的弱光表現可以通過減少銅的量得到很大的提高。STM 的研究發現弱光表現得到改善是因為吸收層顆粒介面電阻的增加而導致的。 / 減少吸收層的厚度有利於進一步減少太陽能電池的材料成本。當電池的吸收層厚度小於一微米時，開路電壓跟短路電流都明顯有所減少，從而導致太陽能電池效率降低。更薄電池效率的提高可以從兩個方面來實現:氧化鋅表面的陷光結構及更加合適的鎵含量的使用。通過這兩艇改進方法，電池效率被提高到14%以上，使得超薄電池有更好的應用前景。 / Cu(In,Ga)Se₂ (CIGS)-based thin film solar cell has been commercialized recently due to its high energy conversion efficiency. We have designed an integrated satellite deposition system for producing CIGS solar cell with substrate size of 10cm x 10cm. This work mainly contains two parts with first part focusing on growing and characterizing high quality baseline solar cells and solar modules and second part concentrating on further reducing the material costs by growing thinner absorber layer with high efficiency. / The most difficult part in growing high quality CIGS solar cells originate from the absorber layers which contain p-type chalcopyrite structures with four different elements: Cu, In, Ga and Se. The widely used three-stage process is employed to co-evaporate In, Ga and Se first, then Cu and Se are evaporated to form the chalcopyrite CIGS structure and additional In, Ga and Se are deposited in the end to ensure an overall Cu deficiency, which is important for getting p-type semiconductors. The substrate temperatures during these three stages are carefully adjusted to introduce proper gallium gradients which is important for collecting electrons efficiently. Together with optimizing other layers we are able to get cell efficiency (area around 0.5 cm²) over 17%. To produce CIGS mini-modules, laser scribing as well as mechanical scribing are employed for series interconnection of individual cells using monolithic integration. The power and speed of laser together with the condition of mechanical scriber are carefully adjusted to ensure a minimum dead area in the module. Module (area around 80 cm²) with efficiency over 12% is produced. / Solar cells were fabricated and tested under varied temperature and weak light conditions. Temperature coefficient is compared between CIGS solar cells and other types of solar cells. Temperature coefficient is improved a lot with higher gallium content in the absorber layer. Weak light performance is shown to be increased a lot when copper percentage is lowered down. In order to examine the origin of beneficial effects from Cu-poor absorber, solar cells are grown with comparable grain sizes using our technique and I-V performances are examined under STM in grain/atomic scale. Leakage current is found to be mainly originates from boundary area. CIGS solar cells with Cu-poor absorber benefit from the reduced leakage from boundary area. / CIGS solar cells with thinner absorber thickness are studied and compared with conventional CIGS solar cells. We have found that high conversion efficiency solar cells can be grown for absorber thickness as thin as 1.5μm. Further reduction in absorber thickness deteriorates solar cell performances in both V∝ and Jsc resulting in conversion efficiency as low as 11%. / Two major approaches are performed to improve solar cell performances. Light trapping by etching AZO top contact for creating pyramid-structures to enhance light scattering. Efficiency is increased by more than 1.5% for solar cells with etched AZO surfaces. Solar cells with efficiency larger than 13% can be grown by using AZO etching. Another approach is by using suitable Ga content in absorber layer. Solar cells with efficiency as high as 14.17% are grown which makes thinner CIGS solar cells very competitive. / Detailed summary in vernacular field only. / Detailed summary in vernacular field only. / Detailed summary in vernacular field only. / Detailed summary in vernacular field only. / Yang, Shihang = 高效率、低成本銅銦鎵硒薄膜太陽能電池的製造 / 楊世航. / Thesis (Ph.D.)--Chinese University of Hong Kong, 2012. / Includes bibliographical references (leaves 101-109). / Abstract also in Chinese. / Yang, Shihang = Gao xiao lu, di cheng ben tong yin jia xi bo mo tai yang neng dian chi de zhi zao / Yang Shihang. / Chapter 1 --- Introduction to Photovoltaics --- p.1 / Chapter 1.1 --- Energy crisis --- p.1 / Chapter 1.2 --- Physics of solar cells --- p.4 / Chapter 1.2.1 --- Light Absorption --- p.4 / Chapter 1.2.2 --- Charge Carrier Separation --- p.8 / Chapter 1.2.3 --- Solar Cell I-V Characteristics --- p.9 / Chapter 1.3 --- Classifications of Solar Cells --- p.11 / Chapter 1.3.1 --- Crystalline silicon solar cell --- p.11 / Chapter 1.3.2 --- Thin film solar cells --- p.12 / Chapter 1.3.3 --- Organic and polymer solar cells --- p.13 / Chapter 1.4 --- Cu(In,Ga)Se₂ (CIGS) based Solar Cells --- p.13 / Chapter 1.4.1 --- State of the art --- p.13 / Chapter 1.4.2 --- Material properties and structures --- p.14 / Chapter 1.4.3 --- CIGS advantages --- p.17 / Chapter 2 --- Integrated CIGS deposition system and fabrication process optimization --- p.21 / Chapter 2.1 --- Introduction to vacuum deposition system --- p.21 / Chapter 2.1.1 --- Integrated CIGS solar cell deposition system --- p.21 / Chapter 2.1.2 --- Ni-Al top grid evaporation system --- p.23 / Chapter 2.2 --- Fabrication processes --- p.23 / Chapter 2.2.1 --- Substrate treatment --- p.23 / Chapter 2.2.2 --- Molybdenum back contact deposition --- p.24 / Chapter 2.2.3 --- CIGS absorber layer formation --- p.26 / Chapter 2.2.4 --- Hetero-junction formation --- p.31 / Chapter 2.2.5 --- Window layer optimization --- p.32 / Chapter 2.2.6 --- Laser and mechanical scribing for mini-modules fabrication --- p.37 / Chapter 2.3 --- Equipment improvements --- p.42 / Chapter 2.3.1 --- Heating uniformity of substrate --- p.42 / Chapter 2.3.2 --- Use of pyrometer for improved control of absorber thickness/composition --- p.43 / Chapter 2.3.3 --- Se cracking unit --- p.45 / Chapter 2.4 --- Characterization of CIGS solar cells --- p.47 / Chapter 2.4.1 --- Morphology, composition and crystallinity --- p.47 / Chapter 2.4.2 --- Depth profile of CIGS --- p.49 / Chapter 2.4.3 --- Electrical property measurements --- p.51 / Chapter 2.5 --- Conclusion --- p.54 / Chapter 3 --- Performance of CIGS solar cells under non-standard test conditions --- p.56 / Chapter 3.1 --- Temperature coefficient measurement of CIGS --- p.57 / Chapter 3.1.1 --- Equipment set-up --- p.57 / Chapter 3.1.2 --- Temperature coefficients for different types of solar cells . --- p.60 / Chapter 3.1.3 --- CIGS solar cells with varied Ga/III composition --- p.65 / Chapter 3.2 --- Weak Light Performance of CIGS --- p.69 / Chapter 3.2.1 --- Introduction --- p.69 / Chapter 3.2.2 --- Experiment --- p.72 / Chapter 3.2.3 --- Results and discussion --- p.73 / Chapter 3.3 --- Conclusion --- p.81 / Chapter 4 --- CIGS solar cells with lower fabrication cost --- p.83 / Chapter 4.1 --- Fabrication cost analysis for commercial CIGS solar cells --- p.83 / Chapter 4.2 --- Thinner CIGS absorber layer --- p.84 / Chapter 4.2.1 --- Solar cell performances with different absorber thicknesses --- p.84 / Chapter 4.2.2 --- Performance improvement for thinner solar cell --- p.87 / Chapter 4.3 --- Conclusion --- p.96 / Chapter 5 --- Conclusion --- p.98 / Chapter 5.1 --- Summary of previous researches --- p.98 / Chapter 5.2 --- Future work --- p.99 / Bibliography --- p.101

在本篇論文中，我們成功地在透明導電襯底上製備了一系列準一維納米材料陣列。我們首先製備了氧化鋅納米線陣列，然後把它們用作氧化鋅/硒化鎘核殼納米線纜陣列中的核以及合成硒化鎘和碲化鎘納米管陣列所需的犧牲模板。最後，金納米管陣列則是利用之前製備的硒化鎘納米管陣列為模板合成的。氧化鋅納米線陣列是通過高溫的熱蒸法和低溫的水熱法製備的。水熱法製備的氧化鋅納米線陣列的電導高於熱蒸法製備的氧化鋅納米線陣列，這使得水熱法製備的氧化鋅納米線更適合採用與電相關的後續處理方法。當氧化鋅納米線陣列被用作犧牲模板來製備納米管時，水熱法製備的氧化鋅納米線能被輕易地完全去除。基於這些認識，我們主要採用電化學沉積法在水熱法製備的氧化鋅納米線陣列表面沉積硒化鎘，得到了氧化鋅/硒化鎘核殼納米線纜陣列。接下來，我們將納米線纜陣列光電極和沉積了鉑催化劑的對電極組裝成三文治結構的太陽能電池。研究發現，採用多硫電解液的電池性能比碘基電解液的電池好，其中成分為1摩爾每升硫化鈉，1摩爾每升硫和1摩爾每升氫氧化鈉的多硫電解液的電池效率最高。當去除電化學沉積法生長的氧化鋅/硒化鎘和氧化鋅/碲化鎘核殼納米線纜陣列中的氧化鋅核以後，便在導電襯底上得到了硒化鎘和碲化鎘的納米管陣列。儘管兩種納米管陣列都對可見光有很強的吸收，但是，硒化鎘納米管陣列相比碲化鎘納米管陣列，表現出較高的光響應和較好的光催化降解亞甲基藍的活性。這是因為該樣品中的光生載流子能有效分離，同時能參與化學反應的表面積也較大。最後，我們選用硒化鎘納米管陣列作為模板，利用化學方法製備了金納米管陣列。金納米管的尺寸可以通過控制硒化鎘納米管模板來加以調節。當我們將具有拉曼活性的4-巰基苯甲酸分子吸附到金納米管的表面時，其拉曼散射相比未吸附時，顯著地增強了約四個數量級，如此大的提高來源於金納米管表面附近的局域電場增強效應。 / In this thesis, we demonstrated the synthesis of a series of pseudo-one-dimensional nanostructure arrays on transparent conducting substrates. We started with ZnO nanowire arrays, which were then served as the core for the ZnO/CdSe core/shell nanocable arrays formation. Further taking the ZnO as sacrificial templates led to the formation of CdSe (and CdTe) nanotube arrays. Finally, Au nanotube arrays were fabricated using the CdSe nanotube arrays as the template. ZnO nanowire arrays were synthesized via high-temperature thermal evaporation method (TE) and low temperature hydrothermal method (HT). The electrical conductivity of HT samples on the substrates was higher than that of the TE counterparts, making it attractive for further electrical-based processing. When serving as the sacrificial templates for nanotube fabrication, HT nanowires can be completely removed with ease. Based on these understanding, ZnO/CdSe core/shell nanocable arrays were obtained mainly via electrochemical deposition of CdSe on HT ZnO nanowire arrays. Nanocable-array-photoelectrode was assembled with a Pt-coated counter electrode into a sandwiched solar cell. Polysulfide electrolytes with various compositions were found to work better than iodine-based ones for such cells, and the cell with the polysulfide electrolyte containing 1 M Na₂S, 1 M S and 1 M NaOH showed highest efficiency. Removal of the ZnO cores in the electrodeposited ZnO/CdSe and ZnO/CdTe nanocable arrays left CdSe and CdTe nanotube arrays on the conducting substrate. Although strong visible-light absorption was observed from both two nanotube arrays, higher photocurrent and better photocatalytic degradation activity of methlyene blue were recorded from CdSe-nanotube-array samples (as compared to the CdTe ones), owing to effective charge separation and large surface area for chemical reactions. Lastly, Au nanotube arrays were synthesized via chemical method using CdSe nanotube arrays as the template. The dimensions of the Au nanotubes, as replicated from CdSe nanotubes, were tunable. When absorbed on the Au nanotube arrays surface, the Raman scattering of 4-mercaptobenzoic acid (a Raman-active molecule) was greatly enhanced for~4 orders of magnitude compared to the signals from the dry powder of the same molecule. Such large increase was due to the strong local electrical field enhancement near the Au nanotubes surface. / Detailed summary in vernacular field only. / Zhu, Haojun = 準一維納米結構在光伏、光催化及等離子體激元方面的應用 / 朱浩君. / Thesis (Ph.D.)--Chinese University of Hong Kong, 2012. / Includes bibliographical references (leaves 141-168). / Electronic reproduction. Hong Kong : Chinese University of Hong Kong, [2012] System requirements: Adobe Acrobat Reader. Available via World Wide Web. / Abstract also in Chinese. / Abstracts in English and Chinese. / Zhu, Haojun = Zhun yi wei na mi jie gou zai guang fu, guang cui hua ji deng li zi ti ji yuan fang mian de ying yong / Zhu Haojun. / Abstract --- p.i / 摘要 --- p.iii / Acknowledgements --- p.iv / Contents --- p.v / List of Figures --- p.viii / List of Tables --- p.xviii / Chapter Chapter 1 --- Introductions --- p.1 / Chapter Chapter 2 --- Background --- p.4 / Chapter 2.1. --- Nanostructured Photovoltaic (PV) Solar Cells --- p.4 / Chapter 2.1.1. --- Fundamental physics of nanostructures for solar cell applications --- p.5 / Chapter 2.1.2. --- Inorganic nano-architectures for PV cells --- p.9 / Chapter 2.2. --- Nanostructures for Photocatalytic Degradation of Organic Pollutants --- p.18 / Chapter 2.2.1 --- Overview of photocatalytic degradation of organic pollutants --- p.19 / Chapter 2.2.2 --- Photocatalysis under visible light illumination --- p.24 / Chapter 2.3. --- Plamonic Noble Metal Nanostructures --- p.29 / Chapter 2.3.1 --- Surface plasmons of noble metal nanostructures --- p.29 / Chapter 2.3.2 --- Applications of plasmonic noble metal nanostructures in solar energy conversion and sensing --- p.35 / Chapter Chapter 3 --- Methodologies and Instrumentations --- p.45 / Chapter 3.1. --- Materials Growth Methodologies --- p.45 / Chapter 3.1.1. --- Thermal evaporation (TE) methods --- p.45 / Chapter 3.1.2. --- Hydrothermal (HT) methods --- p.47 / Chapter 3.1.3. --- Electrodeposition (ED) methods --- p.49 / Chapter 3.1.4. --- Prototype solar cells assemble --- p.52 / Chapter 3.2. --- Characterization Techniques --- p.53 / Chapter 3.2.1. --- Morphological, structural, and compositional analysis using electron microscopy based techniques --- p.53 / Chapter 3.2.2. --- Photoelectrochemical (PEC) performance test --- p.63 / Chapter 3.2.3. --- Photocatalytic degradation of organic pollutants --- p.65 / Chapter 3.2.4. --- Single-particle scattering imaging and spectroscopy --- p.67 / Chapter Chapter 4 --- ZnO Nanowire Arrays on Conducting Substrates -- A Comparison on the Growth Methodology --- p.71 / Chapter 4.1. --- Introduction --- p.71 / Chapter 4.2. --- Experimental --- p.72 / Chapter 4.3. --- Results and Discussions --- p.75 / Chapter 4.3.1 --- Morphologies, crystal structures and chemical compositions --- p.75 / Chapter 4.3.2 --- ZnO nanowire arrays used as electrodes --- p.80 / Chapter 4.3.3 --- ZnO nanowire arrays used as sacrificial templates in electroplating . --- p.85 / Chapter 4.4. --- Conclusions --- p.88 / Chapter Chapter 5 --- ZnO-core/CdSe-shell Nanocable Arrays for Photovoltaic Solar Cells --- p.89 / Chapter 5.1. --- Introduction --- p.89 / Chapter 5.2. --- Experimental --- p.90 / Chapter 5.3. --- Results and Discussions --- p.93 / Chapter 5.3.1 --- Synthesis of the ZnO-core/CdSe-shell nanocable arrays on ITO/glass --- p.93 / Chapter 5.3.2 --- The photovoltaic (PV) performance --- p.100 / Chapter 5.4. --- Conclusions --- p.107 / Chapter Chapter 6 --- CdSe and CdTe Nanotube Arrays as Visible-light-driven Photocatalyst for Organic Pollutant Degradation --- p.108 / Chapter 6.1. --- Introduction --- p.108 / Chapter 6.2. --- Experimental --- p.109 / Chapter 6.3. --- Results and Discussions --- p.112 / Chapter 6.3.1. --- Morphology, crystal structure, and chemical composition of the nanotube arrays --- p.112 / Chapter 6.3.2. --- Optical properties --- p.116 / Chapter 6.3.3. --- Photoelectrochemical (PEC) performance --- p.117 / Chapter 6.3.4. --- Photocatalytic activities --- p.120 / Chapter 6.4. --- Conclusions --- p.123 / Chapter Chapter 7 --- Fabrication of Au Nanotube Arrays and Their Plasmonic Properties --- p.124 / Chapter 7.1. --- Introduction --- p.124 / Chapter 7.2. --- Experimental --- p.125 / Chapter 7.3. --- Results and Discussions --- p.127 / Chapter 7.3.1. --- Morphology, crystalline structure, and chemical composition of Au nanotube arrays --- p.127 / Chapter 7.3.2. --- Au nanotube formation mechanism --- p.129 / Chapter 7.3.3. --- Plasmonic properties of Au nanotube arrays on ITO/glass substrates --- p.131 / Chapter 7.3.4. --- Plasmonic properties of single Au nanotubes --- p.133 / Chapter 7.3.5. --- Au nanotube arrays on ITO/glass as SERS substrates --- p.134 / Chapter 7.4. --- Conclusions --- p.138 / Chapter Chapter 8 --- Conclusions --- p.139 / Bibliography --- p.141

Wong, Man Keung. / "November 2010." / Thesis (M.Phil.)--Chinese University of Hong Kong, 2011. / Includes bibliographical references. / Abstracts in English and Chinese. / Abstract --- p.i / Table of contents --- p.iii / List of Figures --- p.vi / List of Tables --- p.ix / Chapter Chapter 1 --- Introduction --- p.1 / Chapter 1.1 --- Background --- p.1 / Chapter 1.2 --- History of organic photovoltaic cells --- p.2 / Chapter 1.2.1 --- Single layer organic photovoltaic cells --- p.2 / Chapter 1.2.2 --- Bilayer organic photovoltaic cells --- p.3 / Chapter 1.2.3 --- Bulk Heterojunction organic photovoltaic cells --- p.6 / Chapter 1.3 --- Device physics of organic photovoltaic cells --- p.9 / Chapter 1.4 --- Device fabrication and characterization --- p.12 / Chapter 1.5 --- Thesis outline --- p.14 / Chapter Chapter 2 --- Instrumentation --- p.18 / Chapter 2.1 --- Keithley 236 source measure unit --- p.18 / Chapter 2.2 --- CHI 660C electrochemical instrument --- p.18 / Chapter 2.3 --- Tensor Alpha Step 500 Profilometer --- p.19 / Chapter 2.4 --- Fourier Transform Infrared (FTIR) spectroscopy --- p.20 / Chapter 2.5 --- Thermogravimetric Analysis --- p.22 / Chapter 2.6 --- X-ray Diffraction --- p.23 / Chapter 2.7 --- Scanning electron microscopy --- p.24 / Chapter 2.8 --- Atomic force microscopy --- p.26 / Chapter Chapter 3 --- Surface functionalization of Carbon Nanotube --- p.28 / Chapter 3.1 --- Introduction --- p.28 / Chapter 3.2 --- Oxidative treatment --- p.28 / Chapter 3.2.1 --- Experimental procedures --- p.28 / Chapter 3.2.2 --- Characterization --- p.29 / Chapter 3.3 --- Hydrothermal treatment --- p.35 / Chapter 3.3.1 --- Experimental procedures --- p.35 / Chapter 3.3.1.1 --- Synthesis of MWCNTols --- p.35 / Chapter 3.3.1.2 --- Synthesis of MWCNT-PEDOT --- p.36 / Chapter 3.3.2 --- Characterization --- p.37 / Chapter 3.4 --- Summary --- p.42 / Chapter Chapter 4 --- P3HT/f-CNT/PCBM Composites for Organic Photovoltaic Cells --- p.45 / Chapter 4.1 --- Introduction --- p.45 / Chapter 4.2 --- Fabrication procedures --- p.48 / Chapter 4.3 --- IV characteristics of organic photovoltaic cells --- p.51 / Chapter Chapter 5 --- Vertically aligned poly(3-hexylthiophene) nanobrushes of high aspect ratio for photoelectrochemical solar cells --- p.60 / Chapter 5.1 --- Introduction --- p.60 / Chapter 5.2 --- Sample preparation --- p.63 / Chapter 5.3 --- IV characteristics of P3HT nanobrushes --- p.65 / Chapter 5.4 --- AFM and XRD analysis --- p.66 / Chapter 5.5 --- Summary --- p.71 / Chapter Chapter 6 --- Conclusions --- p.74 / Chapter 6.1 --- Conclusions --- p.74

Photovoltaic (PV) devices based on PbS quantum dot (QD) solids demonstrate high photon-to-electron conversion yields. However, record power conversion efficiencies remain limited mainly due to bulk and interfacial defects in the light absorbing material (QD solids). Interfacial defects can be formed when a semiconductor, such as QD solid, is contacted by another material and may predetermine the semiconductor/metal or semiconductor/metal-oxide junction properties. The objective of the work described in this dissertation was set to explore whether electrochemical contacting using liquid electrolytes can provide sufficient means of contacting the QD solids to investigate their PV performance without introducing the unwanted interfacial defects. I have initially focused on optimizing processing conditions for efficient QD solids deposition and studied their photovoltaic properties in a standardized solid-state, depleted heterojunction solar cell configuration. Further, a liquid contacting method was developed to study the relationship between photovoltages of QD solids and the energetics (e.g. reduction potentials) of the liquid contacting media. This electrochemical contacting of PbS QD solids was achieved by using anhydrous liquid electrolytes containing fast, non-coordinating, outer-sphere redox couples. Depending on the energetics of a redox couple, both rectifying and non-rectifying (Ohmic) PbS QD solid/electrolyte junctions were successfully formed with both p- and n-type QD solids. Furthermore, application of the liquid solution contacting method in studies of the PbS QD solids has unprecedentedly demonstrated that an ideal behavior of the photovoltage changes with respect to the changes in the energetics of the contacting media can be achieved. This fact supports the initially proposed hypothesis that such liquid contacting method will not introduce surface defects to the studied QD materials, allowing for their intrinsic properties to be better understood. The applicability of this method to both p- and n- type QD solids was demonstrated. Finally, a better understanding of the relationships between the surface and ligand chemistries of both p- and n-type QD solids and their photovoltaic properties was possible via applications of such method in conjunction with XPS and UPS studies.

Thesis (M.S.)--University of Missouri--Rolla, 2007. / Vita. The entire thesis text is included in file. Title from title screen of thesis/dissertation PDF file (viewed April 17, 2007) Includes bibliographical references (p. 88-91).

A pulse-laser based time-resolved photocurrent (TRPC) and photoluminescence (TRPL) system with a programmable Boxcar integrator/averager system incorporated was implemented to investigate the optical properties and charge carrier dynamics in a GaInP/GaAs single-junction photovoltaic device for the purposes of understanding fundamental optoelectronic processes in the solar cell. The implementation of whole system was realized by integrating the instrument of a Boxcar averager system with a pulse laser source + spectroscopic facilities. The delay time control and data acquisition were organized by the software code. The effects of the hardware configurations and the software parameters on the performance of the system were particularly addressed for the optimization of measurement conditions and precisions. Two main functions of TRPC and TRPL with a wide time range were demonstrated for the system. The system was employed to measure temperature- and bias voltages-dependent TRPC and TRPL spectra of a GaInP/GaAs single-junction photovoltaic device. The spectral data show a lot of information about the transient dynamic behaviors of photogenerated charge carriers in the device, including both the rise and decay processes. Interestingly, the measured time-resolved photocurrent curves are characterized by a fast rising edge followed by a relatively slow decay process as the temperature increases. Relevant theoretical calculations and analysis to the experimental curves were also carried out to understand diffusion and transport processes of charge carriers inside the device. The results show that the variation in temperature and reverse biases results in the structural change in the space charge region of the P-N junction and therefore affects the rise and decay time constants of the time-resolved photocurrent. The TRPL spectral data give information of mid-way radiative recombination of charge carriers in the device. / published_or_final_version / Physics / Master / Master of Philosophy

Ο σκοπός της διπλωματικής αυτής εργασίας είναι η βελτιστοποίηση της απόδοσης των επιταξιακών ηλιακών κυττάρων τύπου n+ p p+, ως προς τον πάχος της p περιοχής. Αναπτύχθηκε ένα 3D μοντέλο αυτού του τύπου πολυκρυσταλλικού πυριτίου και έγινε ανάλυση των φωτοβολταϊκών παραμέτρων αυτού. Για να έχουμε διαφορετικού μεγέθους κρυσταλλικών κόκκων κύτταρα χρησιμοποιήθηκαν πλακέτες από την βάση, την μέση και την κορυφή της κρυσταλλικής κολώνας βελτιωμένης ποιότητας μεταλλουργικού πυριτίου (UMG) πάνω στις οποίες έχει αναπτυχθεί λεπτό ή παχύ επιταξιακό στρώμα. / Thiw essay is about the optimization of the performance of the n+pp+ type epitaxial solar cells. The parameter that was optimized, is the thikness of the p area.

Ongoing efforts to improve the efficiency of organic photovoltaic cells emphasize the significance of the architecture of molecular assemblies in thin films, at nanometer and micron length scales, to enhance both exciton diffusion and charge transport, in donor and acceptor layers. Controlled growth of molecules via self-assembly techniques presents new opportunities to develop nano-structured organic thin films for electronic devices. This thesis is focused on controlling the orientation of phthalocyanine molecular assemblies in thin films in order to demonstrate the impact of microscopic control of molecular order on electrical properties and organic solar cell device performance.The studies performed here provide insights into the self-assembling behavior, film morphology, nanoscale electrical conductivity, and photovoltaic properties of a disk-shaped peripherally substituted phthalocyanine (Pc) molecule possessing amide functional groups in the side chains. Amide functionality was integrated in the side chains of this phthalocyanine molecule with the purpose of increasing the intra-columnar interaction through formation of a hydrogen bonding network between molecules, and to guide columnar orientation in a preferred direction via specific surface-molecule interactions. It is realized that molecule-substrate interactions must dominate over molecule-molecule interactions to achieve control over the deposition of molecules in a preferred direction for organic solar cell applications. Microscopic imaging and spectroscopic studies confirm the formation of flat-lying, well ordered, layered phthalocyanine films as anticipated.The remarkable electrical conductivity of the flat-lying phthalocyanine molecules, as studied by Conducting tip Atomic Force Microscopy (C-AFM) provide the impetus for the formation of organic solar cells based on layers of these hydrogen bonding phthalocyanine molecules. The photocurrent from devices that are made with the ordered Pc molecules and disordered Pc molecules as the primary photoactive donor layer, and vacuum deposited C60 as the acceptor material, were evaluated. The results presented here demonstrate the feasibility of increasing the photogenerated current by controlling the molecular organization in the photo active layer.

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