Phosphorus (P) one of the essential elements to plants and animals, is a non-renewable resource and accuatlly high demanded in agriculture. The World\'s population growth and future estimatives on food demands raises the question about the sustainability of the current agriculture systems, speccially concerns about the low P use efficiency in agroecosystems. Brazilian agriculture requires high P inputs and many researches has been developed to increase the crops yield and, consequently, food production efficiency. However, this development was achieved at the high costs of mineral fertilisers (specially P) and long-term perspectives about the costs of the intensification in the tropical agriculture is accuattly in debate. In this conxtext, in the present thesis chapter two we evaluated the evolution of the Brazilian cropland basis and P demands, quantifying the Brazil P Legacy and, based on scenarios involving the cropland area and yield expansion, we estimated the future (up to 2050) Legacy P and P fertilisers demand. We also estimated the potential aleviation that could be achieved in the mineral fertilizers consumption by utilisation and improvements on manure P recycling. Alternatively, considering the systems intensification and its effects on P availability, we proposed alternative scenarios to promote the Legacy P utilisation in Brazil\'s improved agriculture systems to grant the agriculture expansion without huge increments on the national P fertilisers consumption. A worldwide recognized advance in Brazilian agriculture is the Cerrado, where large cropland areas accually are cultivated twice a year, improving the food and fiber production without any additional disturbance of natural ecossystems. In this context, no-tillage (NT) agriculture has been widely used and, as consequence, soil fertility has been improved, which could be also farorable to the P availability, when rotation with crop species with P mobilization mechanisms are introduced, such as cover crops utilisation. However, the effects of these improved rotated systems on P bioavailability in long-term in tropical soils remains uncert in the literature and was our objective in the chapter three, where is described a study envolving the evaluation of long-term changes on P fractions in tropical Oxisols, from two long-term field trials involving tillage systems (NT and conventional tillage, CT) and cover crops (millet, brachiaria, maize and control, fallow). The long-term cultivation generated large amounts of legacy P in the soil and with the brachiaria introduction as cover crop, more P was recycled in the topsoil and labile P and all the organic P fractions increased. Based on the cover crop effects, we proposed that the bioavailability of the legacy P could be represented by the P extracted by the labile fractions + moderately labile P fractions. In the chapter four, we used other techniques actually widely applied to P speciation, and we applied in tropical soils affected by the native Cerrado conversion into NT and CT agriculture. A multiple approach to identify and quantify the P forms in tropical soils were proposed by the utilisation of Hedley\'s fractionation togheter with P K-edge XANES for P-bindings into inorganic soil matrix and liquid 31P-NMR spectroscopy to complement the organic P species in tropical soils. / Fósforo (P), um dos elementos essenciais às plantas e animais, é um recurso não-renovável e altamente demandado na agricultura atualmente. O crescimento da população mundial e as estimativas futuras da demanda de alimentos aumentam os questionamentos sobre a sustentabilidade dos sistemas agrícolas atuais, especialmente no que se refere a baixa eficiência no uso do P na agricultura. A agricultura brasileira requer altas quantidades de P e muitas pesquisas tem sido desenvolvidas para aumentar a produtividades das culturas e, conseequentemente, a eficiencia da produção de alimentos. Entretanto, este desenvolvimento tem sido alcançado a altos custos com uso de fertilizantes minerais (sobretudo P) e as perspectivas de longo prazo sobre os custos da intensificação da agricultura tropical estão atualmente em debate. Nesse contexto, no capítulo dois da presente tese avaliamos a evolução da área cultivada no Brasil e das demandas de P, quantificando o legado do P no Brasil e, baseado em cenários envolvendo a expansão da área cultivada e da produtividade, estimamos o futuro (até 2050) legado de P e as demandas por fertilizantes fosfatados. Ainda estimamos a potencial redução no consumo de fertilizantes fosfatados que pode ser alcançada pela utilização e melhorias na reciclagem do P oriundo de dejetos. Alternativamente, considerando a intensificação dos sistemas e seus efeitos na disponibilidade de P, propusemos cenários alternativos visando a utilização do \"Legacy P\" em sistemas agrícolas melhorados para garantir a expansão agrícola sem drásticos incrementos no consumo nacional de fertilizantes fosfatados. Um avanço internacionalmente reconhecido na agricultura Brasileira é o Cerrado, onde extensas áreas agrícolas são cultivadas duas vezes ao ano, incrementando assim a produção de alimentos e fibras sem qualquer custo aos ecossistemas naturais. Nesse contexto, a agricultura sob plantio direto (PD) tem sido amplamente difundida e, como consequencia, a fertilidade dos solos tem-se elevado, o que pode também favorecer a disponibilidade de P, quando são introduzidas rotações com espécies de plantas que apresentam mecanismos de mobilização do P, como o uso de plantas de cobertura. Entretanto, os efeitos desses sistemas melhorados de rotação na biodisponibilidade de P em solos tropicais no longo prazo permanecem incertos na literatura e foram objeto de estudo no capítulo três, onde está descrito um estudo envolvendo a avaliação das mudanças de longo-prazo nas frações de P em Latossolos, oriundos de dois experimentos de campo de longa duração no Cerrado, envolvendo a avaliação de sistemas de preparo (PD e preparo convencional, PC) e plantas de cobertura (milheto, braquiária milho e um controle, apenas pousio). O cultivo por longo tempo resultou em grandes quantididades de \"Legacy P\" acumulado no solo e, com o uso de braquiária como cultura de cobertura, maior quantidade de P foi reciclado para as camadas superiores do solo e as frações de P lábil e todas as frações organicas aumentaram. Baseado nos efeitos das plantas de cobertura, sugerimos que a biodisponibilidade do \"Legacy P\" pode ser representada pelo P extraído nas frações lábeis + o P de frações moderadamente lábeis. No capítulo quatro, utilizamos outras técincas atualmente difundidas para a especiação de P, aplicando-as em solos tropicais influenciados pela conversão do Cerrado nativo em agricultura sob PD e PC. Uma abordagem múltipla para identificação e quantificação de formas de P em solos tropicais foi proposta através da utilização do fracionamento de P proposto por Hedley em conjunto com a especiação de P por XANES da borda K do P para identificação de ligação do P a matrix inorgânica do solo, e espectroscopia de ressonância magnética nuclear (NMR) para complementação da identificação de espécies orgânicas de P em solos tropicais.

Phosphorus (P) one of the essential elements to plants and animals, is a non-renewable resource and accuatlly high demanded in agriculture. The World\'s population growth and future estimatives on food demands raises the question about the sustainability of the current agriculture systems, speccially concerns about the low P use efficiency in agroecosystems. Brazilian agriculture requires high P inputs and many researches has been developed to increase the crops yield and, consequently, food production efficiency. However, this development was achieved at the high costs of mineral fertilisers (specially P) and long-term perspectives about the costs of the intensification in the tropical agriculture is accuattly in debate. In this conxtext, in the present thesis chapter two we evaluated the evolution of the Brazilian cropland basis and P demands, quantifying the Brazil P Legacy and, based on scenarios involving the cropland area and yield expansion, we estimated the future (up to 2050) Legacy P and P fertilisers demand. We also estimated the potential aleviation that could be achieved in the mineral fertilizers consumption by utilisation and improvements on manure P recycling. Alternatively, considering the systems intensification and its effects on P availability, we proposed alternative scenarios to promote the Legacy P utilisation in Brazil\'s improved agriculture systems to grant the agriculture expansion without huge increments on the national P fertilisers consumption. A worldwide recognized advance in Brazilian agriculture is the Cerrado, where large cropland areas accually are cultivated twice a year, improving the food and fiber production without any additional disturbance of natural ecossystems. In this context, no-tillage (NT) agriculture has been widely used and, as consequence, soil fertility has been improved, which could be also farorable to the P availability, when rotation with crop species with P mobilization mechanisms are introduced, such as cover crops utilisation. However, the effects of these improved rotated systems on P bioavailability in long-term in tropical soils remains uncert in the literature and was our objective in the chapter three, where is described a study envolving the evaluation of long-term changes on P fractions in tropical Oxisols, from two long-term field trials involving tillage systems (NT and conventional tillage, CT) and cover crops (millet, brachiaria, maize and control, fallow). The long-term cultivation generated large amounts of legacy P in the soil and with the brachiaria introduction as cover crop, more P was recycled in the topsoil and labile P and all the organic P fractions increased. Based on the cover crop effects, we proposed that the bioavailability of the legacy P could be represented by the P extracted by the labile fractions + moderately labile P fractions. In the chapter four, we used other techniques actually widely applied to P speciation, and we applied in tropical soils affected by the native Cerrado conversion into NT and CT agriculture. A multiple approach to identify and quantify the P forms in tropical soils were proposed by the utilisation of Hedley\'s fractionation togheter with P K-edge XANES for P-bindings into inorganic soil matrix and liquid 31P-NMR spectroscopy to complement the organic P species in tropical soils. / Fósforo (P), um dos elementos essenciais às plantas e animais, é um recurso não-renovável e altamente demandado na agricultura atualmente. O crescimento da população mundial e as estimativas futuras da demanda de alimentos aumentam os questionamentos sobre a sustentabilidade dos sistemas agrícolas atuais, especialmente no que se refere a baixa eficiência no uso do P na agricultura. A agricultura brasileira requer altas quantidades de P e muitas pesquisas tem sido desenvolvidas para aumentar a produtividades das culturas e, conseequentemente, a eficiencia da produção de alimentos. Entretanto, este desenvolvimento tem sido alcançado a altos custos com uso de fertilizantes minerais (sobretudo P) e as perspectivas de longo prazo sobre os custos da intensificação da agricultura tropical estão atualmente em debate. Nesse contexto, no capítulo dois da presente tese avaliamos a evolução da área cultivada no Brasil e das demandas de P, quantificando o legado do P no Brasil e, baseado em cenários envolvendo a expansão da área cultivada e da produtividade, estimamos o futuro (até 2050) legado de P e as demandas por fertilizantes fosfatados. Ainda estimamos a potencial redução no consumo de fertilizantes fosfatados que pode ser alcançada pela utilização e melhorias na reciclagem do P oriundo de dejetos. Alternativamente, considerando a intensificação dos sistemas e seus efeitos na disponibilidade de P, propusemos cenários alternativos visando a utilização do \"Legacy P\" em sistemas agrícolas melhorados para garantir a expansão agrícola sem drásticos incrementos no consumo nacional de fertilizantes fosfatados. Um avanço internacionalmente reconhecido na agricultura Brasileira é o Cerrado, onde extensas áreas agrícolas são cultivadas duas vezes ao ano, incrementando assim a produção de alimentos e fibras sem qualquer custo aos ecossistemas naturais. Nesse contexto, a agricultura sob plantio direto (PD) tem sido amplamente difundida e, como consequencia, a fertilidade dos solos tem-se elevado, o que pode também favorecer a disponibilidade de P, quando são introduzidas rotações com espécies de plantas que apresentam mecanismos de mobilização do P, como o uso de plantas de cobertura. Entretanto, os efeitos desses sistemas melhorados de rotação na biodisponibilidade de P em solos tropicais no longo prazo permanecem incertos na literatura e foram objeto de estudo no capítulo três, onde está descrito um estudo envolvendo a avaliação das mudanças de longo-prazo nas frações de P em Latossolos, oriundos de dois experimentos de campo de longa duração no Cerrado, envolvendo a avaliação de sistemas de preparo (PD e preparo convencional, PC) e plantas de cobertura (milheto, braquiária milho e um controle, apenas pousio). O cultivo por longo tempo resultou em grandes quantididades de \"Legacy P\" acumulado no solo e, com o uso de braquiária como cultura de cobertura, maior quantidade de P foi reciclado para as camadas superiores do solo e as frações de P lábil e todas as frações organicas aumentaram. Baseado nos efeitos das plantas de cobertura, sugerimos que a biodisponibilidade do \"Legacy P\" pode ser representada pelo P extraído nas frações lábeis + o P de frações moderadamente lábeis. No capítulo quatro, utilizamos outras técincas atualmente difundidas para a especiação de P, aplicando-as em solos tropicais influenciados pela conversão do Cerrado nativo em agricultura sob PD e PC. Uma abordagem múltipla para identificação e quantificação de formas de P em solos tropicais foi proposta através da utilização do fracionamento de P proposto por Hedley em conjunto com a especiação de P por XANES da borda K do P para identificação de ligação do P a matrix inorgânica do solo, e espectroscopia de ressonância magnética nuclear (NMR) para complementação da identificação de espécies orgânicas de P em solos tropicais.

In this work systematic studies of the organic semiconductor CuPc have been presented. In general the investigation can be devided in three parts. In the first one we have studied the electronic structure of clean CuPc thin film. The next two parts are devoted to organic-organic and metal–organic interface formation, where one of the interface components is CuPc thin film. The main results of this thesis are: - The electronic structure of the pristine organic semiconductor CuPc (valence band and empty states) has been obtained by a combination of conventional and resonant photoemission, near-edge X-ray absorption, as well as by theoretical ab initio quantum-chemical calculations. A qualitative assignment of different VB structures has been given, or in other words the contributions of different atomic species as well as sites of the CuPc molecule to the electronic DOS has been established. In particular, it was shown, that the HOMO is mainly comprised of the spectral weights from the orbitals of carbon pyrolle atoms. Additional contributions to the HOMO stems from the benzene atoms. A combined experimental and theoretical study of the unoccupied electronic density of states of CuPc was presented. Our study allows identifying the contributions from different parts of the molecule to the unoccupied DOS and the measured spectra, which lays grounds for future studies of the evolution of the CuPc electronic states upon e.g. functionalization or doping. Application of similar studies to other organic semiconductors will also provide significant insight into their unoccupied electronic states. - The electronic properties of the organic heterointerfaces between fullerite and pristine copper phthalocyanine were studied. Both interfaces, CuPc/C60 and C60/CuPc, were found to be non-reactive with pronounced shifts of the vacuum level pointing to the formation of an interfacial dipole mainly at the CuPc side of the heterojunctions. The dipole values are close to the difference of the work functions of the two materials. Important interface parameters and hole-injection barriers were obtained. The sequence of deposition does not influence the electronic properties of the interfaces. - CuPc doped with potassium was studied by means of photoemission and photoabsorption spectroscopy. A detailed analysis of the core-level PE spectra allows one to propose possible lattice sites, which harbor the potassium ions. Contrasting to a few results reported in the literature, the films prepared in this thesis showed no finite electronic density of states at the Fermi level. - Two stages of the In/CuPc interface formation have been distinguished. The low-coverage stage is characterized by a strong diffusion of the In atoms into the organic film. Metal ions occupy sites close to the pyrolle nitrogen and strongly interact with molecules transferring negative charge to CuPc. Indium diffusion into the organic films saturates at a stoichiometry of In2CuPc. Subsequently, in the second stage the formation of a metallic indium film occurs on the top of the In2CuPc film. - Upon deposition on CuPc film Sn and Ag atoms do not diffuse into the organic film forming metallic clusters and/or thin metallic overlayer. Sharp metal-organic film interface is formed, in contrast to indium and potassium deposition. Presented experimental results also give evidence for absence of noticeable chemical reaction of Sn and Ag with CuPc thin film. - The systematic investigation of interface formation between CuPc thin film and various metals gives us the possibility to summarize all results with demonstrating similarities and differences for all systems studied.

No description available.

In this work systematic studies of the organic semiconductor CuPc have been presented. In general the investigation can be devided in three parts. In the first one we have studied the electronic structure of clean CuPc thin film. The next two parts are devoted to organic-organic and metal–organic interface formation, where one of the interface components is CuPc thin film. The main results of this thesis are: - The electronic structure of the pristine organic semiconductor CuPc (valence band and empty states) has been obtained by a combination of conventional and resonant photoemission, near-edge X-ray absorption, as well as by theoretical ab initio quantum-chemical calculations. A qualitative assignment of different VB structures has been given, or in other words the contributions of different atomic species as well as sites of the CuPc molecule to the electronic DOS has been established. In particular, it was shown, that the HOMO is mainly comprised of the spectral weights from the orbitals of carbon pyrolle atoms. Additional contributions to the HOMO stems from the benzene atoms. A combined experimental and theoretical study of the unoccupied electronic density of states of CuPc was presented. Our study allows identifying the contributions from different parts of the molecule to the unoccupied DOS and the measured spectra, which lays grounds for future studies of the evolution of the CuPc electronic states upon e.g. functionalization or doping. Application of similar studies to other organic semiconductors will also provide significant insight into their unoccupied electronic states. - The electronic properties of the organic heterointerfaces between fullerite and pristine copper phthalocyanine were studied. Both interfaces, CuPc/C60 and C60/CuPc, were found to be non-reactive with pronounced shifts of the vacuum level pointing to the formation of an interfacial dipole mainly at the CuPc side of the heterojunctions. The dipole values are close to the difference of the work functions of the two materials. Important interface parameters and hole-injection barriers were obtained. The sequence of deposition does not influence the electronic properties of the interfaces. - CuPc doped with potassium was studied by means of photoemission and photoabsorption spectroscopy. A detailed analysis of the core-level PE spectra allows one to propose possible lattice sites, which harbor the potassium ions. Contrasting to a few results reported in the literature, the films prepared in this thesis showed no finite electronic density of states at the Fermi level. - Two stages of the In/CuPc interface formation have been distinguished. The low-coverage stage is characterized by a strong diffusion of the In atoms into the organic film. Metal ions occupy sites close to the pyrolle nitrogen and strongly interact with molecules transferring negative charge to CuPc. Indium diffusion into the organic films saturates at a stoichiometry of In2CuPc. Subsequently, in the second stage the formation of a metallic indium film occurs on the top of the In2CuPc film. - Upon deposition on CuPc film Sn and Ag atoms do not diffuse into the organic film forming metallic clusters and/or thin metallic overlayer. Sharp metal-organic film interface is formed, in contrast to indium and potassium deposition. Presented experimental results also give evidence for absence of noticeable chemical reaction of Sn and Ag with CuPc thin film. - The systematic investigation of interface formation between CuPc thin film and various metals gives us the possibility to summarize all results with demonstrating similarities and differences for all systems studied.

<p>Oligo(phenyleneethynylene) (OPE) molecules are a class of fully conjugated aromatic molecules, that attract attention for their application as “molecular wires” in molecular electronic devices. In this thesis work, self-assembled monolayers (SAMs) formed from a variety of OPE derivatives have been studied. The chemical properties, structure, and packing density of the SAMs have been characterized utilizing techniques such as high-resolution X-ray photoemission spectroscopy (HRXPS), near-edge X-ray absorption fine structure spectroscopy (NEXAFS), Infrared reflection absorption spectroscopy (IRRAS), contact angle measurements, and atomic force microscopy (AFM).</p><p>In a first study, three OPE-derivatives, with benzene, naphthalene and anthracene, respectively, inserted into the backbone, and an acetyl-protected thiophenol binding group were found to form SAMs on Au(111) substrates with lower molecular surface densities and larger molecular inclination as the lateral π-system increases.</p><p>In a second study, porphyrin was introduced as the end group to a wire-like molecule such as OPE. The purpose was to obtain well-organized and functionalized surfaces with optical and redox properties. Three porphyrin-functionalized OPEs had different binding groups, an acetyl-protected thiophenol, a benzylic thiol, and a trimethylsilylethynylene group, and were found to form SAMs on gold surfaces with difference in structure and degree of order. The molecules with the acetyl-protected thiophenol binding group were found to form a high quality SAM compared to the other two. This SAM exhibits a well-ordered and densely packed layer.</p><p>This study gives rise to a better understanding of SAM formation of OPE derivatives, and will form a base for further investigations of charge transport properties of these molecular films, which is of interest for applications in molecular electronic devices.</p>

Les spectroscopies de photoémission, d'absorption X –assistées par des calculs DFT d'états de coeur excités – et la microscopie tunnel, ont permis de déterminer avec précision les géométries d'adsorption, sur la surface Si(001)-2×1, de quatre molécules possédant un groupe cyano, monofonctionnelle - comme l'acétonitrile - ou polyfonctionnelles - comme le benzonitrile, l'acrylonitrile et le cyanure de vinyle. La chimie organique fournit le cadre général des réactions possibles à la surface. Ce sont des considérations d'ordre cinétique qui sélectionnent les modes d'adsorption des molécules organiques. Un réglage fin des conditions expérimentales permettrait donc d'obtenir les modes d'adsorption désirés en vue d'application dans le domaine de l'électronique moléculaire.

Oligo(phenyleneethynylene) (OPE) molecules are a class of fully conjugated aromatic molecules, that attract attention for their application as “molecular wires” in molecular electronic devices. In this thesis work, self-assembled monolayers (SAMs) formed from a variety of OPE derivatives have been studied. The chemical properties, structure, and packing density of the SAMs have been characterized utilizing techniques such as high-resolution X-ray photoemission spectroscopy (HRXPS), near-edge X-ray absorption fine structure spectroscopy (NEXAFS), Infrared reflection absorption spectroscopy (IRRAS), contact angle measurements, and atomic force microscopy (AFM). In a first study, three OPE-derivatives, with benzene, naphthalene and anthracene, respectively, inserted into the backbone, and an acetyl-protected thiophenol binding group were found to form SAMs on Au(111) substrates with lower molecular surface densities and larger molecular inclination as the lateral π-system increases. In a second study, porphyrin was introduced as the end group to a wire-like molecule such as OPE. The purpose was to obtain well-organized and functionalized surfaces with optical and redox properties. Three porphyrin-functionalized OPEs had different binding groups, an acetyl-protected thiophenol, a benzylic thiol, and a trimethylsilylethynylene group, and were found to form SAMs on gold surfaces with difference in structure and degree of order. The molecules with the acetyl-protected thiophenol binding group were found to form a high quality SAM compared to the other two. This SAM exhibits a well-ordered and densely packed layer. This study gives rise to a better understanding of SAM formation of OPE derivatives, and will form a base for further investigations of charge transport properties of these molecular films, which is of interest for applications in molecular electronic devices.

In the present work a Metal / organic / inorganic semiconductor hybrid heterostructure (Ag / DiMe−PTCDI / GaAs) was built under UHV conditions and characterised in situ. The aim was to investigate the influence of the organic layer in the surface properties of GaAs(100) and in the electrical response of organic−modified Ag / GaAs Schottky diodes. The device was tested by combining surface−sensitive techniques (Photoemission spectroscopy and NEXAFS) with electrical measurements (current−voltage, capacitance−voltage, impedance and charge transient spectroscopies). Core level examination by PES confirms removal of native oxide layers on sulphur passivated (S−GaAs) and hydrogen plasma treated GaAs(100) (H+GaAs) surfaces. Additional deposition of ultrathin layers of DiMe−PTCDI may lead to a reduction of the surface defects density and thereby to an improvement of the electronic properties of GaAs. The energy level alignment through the heterostructure was deduced by combining UPS and I−V measurements. This allows fitting of the I−V characteristics with electron as majority carriers injected over a barrier by thermionic emission as a primary event. For thin organic layers (below 8 nm thickness) several techniques (UPS, I−V, C−V, QTS and AFM) show non homogeneous layer growth, leading to formation of voids. The coverage of the H+GaAs substrate as a function of the nominal thickness of DiMe−PTCDI was assessed via C−V measurements assuming a voltage independent capacitance of the organic layer. The frequency response of the device was evaluated through C−V and impedance measurements in the range 1 kHz−1 MHz. The almost independent behaviour of the capacitance in the measured frequency range confirmed the assumption of a near geometrical capacitor, which was used for modelling the impedance with an equivalent circuit of seven components. From there it was found a predominance of the space charge region impedance, so that A.C. conduction can only takes place through the parallel conductance, with a significant contribution of the back contact. Additionally a non linear behaviour of the organic layer resistance probably due to the presence of traps was deduced. ( ) ω ' R QTS measurements performed on the heterostructure showed the presence of two relaxations induced by deposition of the organic layer. The first one is attributed to the presence of a deep trap probably located at the metal / organic interface, while the second one has very small activation energy ( ~ 20 meV) which are probably due to disorder at the organic film. Those processes with small activation energies proved to be determinant for fitting the I−V characteristics of DiMe−PTCDI organic modified diodes using the expressions of a trapped charge limited current regime TCLC. Such a model was the best analytical approach found for fitting the I−V response. Further improving probably will involve implementation of numerical calculations or additional considerations in the physics of the device.

Bibliografische Beschreibung, Referat und Schlagwörter M.S. Chem. Ing. Sung Gook Park Thema: Organic Modified GaAs Schottky Contacts Einreichungsdatum: 28. September 2001 Im Rahmen dieser Arbeit wurden organische Halbleitermaterialien verwendet, um damit die Transporteigenschaften von Metal/GaAs(100) Schottky-Kontakten zu kontrollieren. Ziel ist es, Strom-Spannungs- (J-V) und Kapazitäts-Spannungs-Kennenlien (C-V) zu verstehen. Zur chemischen und elektronischen Charakterisierung der GaAs(100)-Oberflächen, organische Molekül/GaAs(100)-Grenzflächen und der Metall/organische Molekül-Grenzflächen wurden die Photoelektronenspektroskopie (PES) und Nahkantenröntgenabsorptionsspektroskopie (NEXAFS) eingesetzt. Verschiedene GaAs(100)-Oberflächen, wie die reine GaAs(100)-c(4x4)-, die Wasserstoff-Plasma behandelte GaAs(100)- und die chalkogenpassivierte GaAs-Oberflächen, wurden als Substrate für die organische Molekularstrahldeposition (OMBD) verwendet. In der Arbeit wird der Einfluss der chemischen und elektronischen Eigenschaften dieser Substratoberflächen auf das Wachstum von organischen Molekülen auf deren Oberflächen untersucht. 3,4,9,10-Perylentetracarboxylic Dianhydrid (PTCDA) und Dimethyl-3,4,9,10-Perylentetracarboxyl Diimid wurden zur organischen Modifizierung von Metall/GaAs(100)-Schottky-Kontakten verwendet. Die organischen Moleküle werden anfänglich an Defekten der GaAs(100)-Oberflächen adsorbiert. Die Adsorption an Defekten führt zu einer Reduktion der inhomogenen Bandverbiegung der GaAs(100)-Oberfläche. Aus den PES-Spektren wurden Energiebanddiagramme für organische Schicht/GaAs(100)-Grenzflächen und Metall/organische Grenzflächen abgeleitet. Entsprechend der relativen energetischen Lagen des Leitungsbandminimums von GaAs(100)-Oberflächen und des niedrigsten unbesetzten Molekülorbitals der organischen Schichten werden Interfacedipole ausgebildet. Die Verwendung von anorganischen Substraten mit systematisch variierender Elektronenaffinität (EA) stellt eine neue Methode zur Bestimmung des Transportniveaus von Elektronen in der organischen Schicht dar. Bei Einfügung von dünnen PTCDA-Schichten zwischen Ag-Elektrode und GaAs(100)-Oberfläche, wurde beobachtet, dass die J-V-Kennlinien in Abhängigkeit von der Dicke der organischen Schicht und der Behandlung der GaAs-Oberflächen systematisch variierte. Dieses Verhalten kann unter Verwendung des Energieniveaudiagramms, das mittels PES bestimmt wurde, und durch eine Barrierenerniedrigung infolge von Bildkräften gut erklärt werden. Durch die Kombination von Oberflächenbehandlung und Einfügen einer dünnen definierten organischen Schicht kann die effektive Barrierenhöhe in einem breiten Bereich verändert, d. h. letztendlich definiert eingestellt und kontrolliert werden. Daraus ergibt sich die Möglichkeit, die Leistungsaufnahme von GaAs-Schottky-Kontakten zu reduzieren. <Schlagwörter> Organische Moleküle, Organische Molekularstrahldeposition (OMBD), GaAs(100), Metall/Hableiter- Schottky-Kontakt, Photoemissionspektroskopie (PES), Nahkantenröntgenabsorptionsspektroskopie (NEXAFS), Elektrische Messungen