This thesis deals with exciton relaxation processes in thin polycrystalline films and matrix-isolated molecules of the perylene derivatives PTCDA (3,4,9,10-perylenetetracarboxylic dianhydride) and MePTCDI (N,N'-dimethylperylene-3,4,9,10-dicarboximide). Using femtosecond pump-probe spectroscopy, transient absorption spectra, excitonic relaxation in the lowest excited state subsequent to excitation, and exciton-exciton interaction and annihilation at high excitation densities have been addressed. Transient absorption spectroscopy in the range 1.2eV-2.6eV has been applied to thin polycrystalline films of PTCDA and MePTCDI and to solid solutions of PTCDA and MePTCDI molecules (monomers) in a SiO2 matrix. We are able to ascribe the respective signal contributions to ground state bleaching, stimulated emission, and excited state absorption. Both systems exhibit broad excited-state absorption features below 2.0eV, with dominant peaks between 1.8eV and 2.0eV. The monomer spectra can be consistently explained by the results of quantum-chemical calculations on single molecules, and the respective experimental polarization anisotropies for the two major transitions agree with the calculated polarizations. Dimer calculations allow to qualitatively understand the trends visible in the experimental results from monomers to thin films. The broad excited state absorption band between 1.8eV and 2.0eV allows to probe the population dynamics in the first excited state of thin films. We show that excitons created at the Gamma point relax towards the border of the Brillouin zone on a 100fs time scale in both systems. Excitonic relaxation is accelerated by increase of temperature and/or excitation density, which is attributed to stimulated phonon emission during relaxation in k-space. Lower and upper limits of the intraband relaxation time constants are 25fs (resolution limit) and 250fs (100fs) for PTCDA (MePTCDI). These values agree with the upper limit for the intraband relaxation time of 10ps, evaluated from time-resolved luminescence measurements. While the luminescence anisotropy is in full accordance with the predictions made by a luminescence anisotropy model being consistent with the exciton model of Davydov-split states, the pump-probe anisotropy calls for an explanation beyond the models presently available. At excitation densities 10^(19)cm^(-3), the major de-excitation mechanism for the relaxed excitons is exciton-exciton annihilation, resulting in a strongly reduced exciton life time. Three different models for the microscopic behavior have been tested: a diffusion-limited annihilation model in both three and one dimensions (with diffusion constant D as fit parameter) as well as a long-range single-step Förster-type annihilation model (with Förster radius RF as fit parameter). For PTCDA, the latter two, being structurally equivalent, allow to fit a set of multiexponential decay curves for multiple initial exciton densities with high precision. In contrast, the three-dimensional diffusion-limited model is clearly inferior. For all three models, we extract annihilation rates, diffusion constants and diffusion lengths (or Förster radii), for both room and liquid helium temperature. Temperature dependence and orders of magnitude of the obtained parameters D or RF correspond to the expectations. For MePTCDI, the 1D and the Förster model are in good agreement for a smaller interval of excitation densities. For a initial exciton densities higher than 5 x 10^(19)cm^(-3), the 3D model performs significantly better than the other two.

The effects of surface plasmon for InGaN/GaN multi-quantum wells and ZnO nanoparticles optical linear and nonlinear emission efficiency had been experimentally studied. Due to the critical design for InGaN MQWs with inverted hexagonal pits based on GaN, both contribution of surface plasmon effect and image charge effect at resonant and off resonant frequencies were experimentally and theoretically investigated. With off- resonant condition, the InGaN MQWs emission significantly enhanced by metal nanoparticles. This enhancement was caused by the image charge effect, due to the accumulation of carriers to NPs region. When InGaN emission resonated with metal particles SP modes, surface Plasmon effect dominated the emission process. We also studied the surface plasmon effect for ZnO nanoparticles nonlinear optical processes, SHG and TPE. Defect level emission had more contribution at high incident intensity. Emissions are different for pumping deep into the bulk and near surface. A new assumption to increase the TPE efficiency was studied. We thought by using Au nanorods localized surface plasmon mode to couple the ZnO virtual state, the virtual state’s life time would be longer and experimentally lead the emission enhancement. We studied the TPE phenomena at high and near band gap energy. Both emission intensity and decay time results support our assumption. Theoretically, the carriers dynamic mechanism need further studies.

The aim of the current work was to investigate the photo-induced charge transport at low temperatures, allowing more sensitive, detailed measurements of the first steps in the build-up of space charge fields, which modify the refractive index, leading to modern applications like volume holographic storage. We investigated the light-induced properties of SBN:Ce, KTO and KTN materials like origin of trapping centers which are involved in the charge transport process, characterization of trapping centers, like temperature dependence, illumination intensity dependence, evolution with time, spectral response, activation energies, the basic properties of the electronic excitations and photo-carriers localization based on results of absorption, light-induced absorption, photoluminescence, and photocurrent. The main contributions of this dissertation are summarized as follows: The experimental intensity dependence, temperature dependence, and decay process of the light-induced polaron (NIR) and VIS center absorption can be fitted with the help of a simplified charge transfer model (for SBN). The decay observed of the NIR polaron and the VIS centers is present due to the Fourier spectrometer light. The dissociation of the VIS centers into NIR centers under red light was observed. The model proposed for the VIS-centers in SBN is a triad structure related to the simultaneous bonding of two hole polarons and one electronic polaron.In KTN the emergence of the UV-light induced wide absorption bands in the NIR region with maxima at 0.69 0.8 eV at low temperatures is treated as a manifestation of the localization of photo-induced electrons and the formation of small electron polarons in close-neighbor Nb-Nb pair centers. Also, these properties in KTN can be fitted with the help of the simplified charge transfer model.

Accurate energetic modeling of large molecular systems is always desired by chemists. For example, ligand-protein binding simulations and enzymatic catalysis studies all involve with a small energy difference. The energetic accuracy depends largely on a proper handling of electronic correlations. Molecular mechanics (MM) methods deliver a parameterized Newtonian treatment to these problems. They show great capability in handling large calculations but give only qualitatively good results. Quantum mechanics (QM) methods solve Schrödinger equations and exhibit much better energy accuracy, though the computational cost can be prohibitive if directly applied to very large systems. Fragment-based methods have been developed to decompose large QM calculations into fragment calculations. However, most current schemes use a self- consistent field (SCF) method on fragments, in which no electronic correlation is accounted for. The super-system energy is computed as a sum of fragment energies plus two-body corrections and, possibly, three-body corrections (a "body" is a fragment). Higher order corrections can be added. Nevertheless, many problems require the treatment of high order electronic correlations. The coupled-cluster (CC) theory is the state-of-the-art QM method for handling electronic correlations. The CC wavefunction contains correlated excitations up to a given truncated level and coincidental excitations for all possible electronic excitations. It is a brilliant way of including more electronic correlations while maintaining a low-order scaling. In the proposed excitonic coupled-cluster (X-CC) theory, substantial modifications have been made to allow CC algorithms to act on the collective coordinates of fragment fluctuations to obtain super-system energy. The X-CC theory is designed to achieve accurate energetic modeling results for large chemical systems with much improved affordability and systematic improvability. The test system used in this work is a chain of beryllium atoms. A 30-fragment X-CCSD(2) calculation delivered matching accuracy with traditional CCSD method. An X-CCSD(2) calculation on a chain of 100 bonded fragments finished in 7 hours on a single 2.2 GHz CPU core. The X-CC scheme also demonstrates the ability in handling charge transfer problems. Due to the use of fluctuation basis in the test cases, the excitonic algorithms can be easily generalized to inhomogeneous systems. This will be investigated in future work.

京都大学 / 0048 / 新制・課程博士 / 博士(工学) / 甲第18593号 / 工博第3954号 / 新制||工||1608(附属図書館) / 31493 / 京都大学大学院工学研究科高分子化学専攻 / (主査)教授 伊藤 紳三郎, 教授 木村 俊作, 教授 辻井 敬亘 / 学位規則第4条第1項該当 / Doctor of Philosophy (Engineering) / Kyoto University / DFAM

No description available.

Semilocal density functionals up to the generalized gradient approximation (GGA) level cannot accurately describe band gaps of bulk solids. Meta-GGA density functionals with a dependence on the kinetic energy density ingredient (τ) can potentially give wider band gaps compared with GGAs. The recently developed TASK meta-GGA functional yields excellent band gaps of bulk solids. The accuracy of the TASK functional for band gaps of bulk solids cannot be straightforwardly transferred to low-dimensional materials due to reduced screening in low-dimensional materials. We have developed mTASK from TASK by changing (a) the tight upper-bound for one or two-electron systems (h0X) from 1.174 to 1.29 and (b) the limit of the interpolation function fX(α → ∞) of the TASK functional that interpolates the exchange enhancement factor FX(s,α) from α = 0 to 1, so that mTASK has the screening appropriate for low-dimensional materials. These two conditions guarantee the increased nonlocality within the generalized Kohn-Sham scheme in the mTASK functional and yield a better description of band gaps of low-dimensional materials. We computed the band gaps of bulk solids from mTASK having a wide range of gaps such as Ge, CdO, ZnS, MgO, NiF, Ar. The improvement in the band gaps from mTASK is more consistent than TASK for the large-gaps crystals. We have studied the band structures in two forms of transition metal dichalcogenide (TMD) monolayers, i.e., monolayer hexagonal (1H) and monolayer trigonal (1T) and their nanoribbons. The mTASK functional systematically improves the band gaps and is in close agreement with the experiments or the hybrid level HSE06 density functional for 2D single-layer and nanoribbon systems. In the second part of this assessment, we explore the large tunability of band gaps and optical absorption of phosphorene nanoribbons under mechanical bending from first-principles. Bending can induce an unoccupied edge state in armchair phosphorene nanoribbons. The electronic and optical properties of nanoribbons drastically change because of this edge state. GW-Bethe–Salpeter equation calculations for armchair phosphorene nanoribbons at different bending curvatures show that the absorption peaks generally shift toward the high energy direction with increasing curvature. Our study suggests that bright excitons can also be formed from the transition from the valence bands to the edge state when the edge state completely separates out from the continuum conduction bands. We systematically study the role of the edge state to form bound excitons at large curvatures. Our analysis suggests that the optical absorption peaks of zigzag phosphorene nanoribbons shift toward the low-energy region, and the height of the absorption peaks increases while increasingthe bending curvature. In the third part of this assessment, we extend our study of phosphorene nanoribbons to MoS2 nanoribbons under bending from GW and Bethe-Salpeter equation approaches. We find three critical bending curvatures for armchair MoS2 nanoribbons, and the edge and non-edge band gaps show a non-monotonic trend with bending. The edge band gap shows an oscillating feature with ribbon width n, with a period of ∆n=3. The binding energy and the lowest exciton energy decrease with the curvature. The large tunability of optical properties of bent MoS2 nanoribbon is applicable in tunable optoelectronic nanodevices. / Physics

No description available.

No description available.

<p> Excitons represent the electronic excited state of organic semiconductor and many low-dimensional inorganic semiconductors. In solar energy conversion systems, exciton transport affects how fast the charges reach the electrodes thus governs the performance of photovoltaic cells. In optoelectronic applications such as semiconductor lasers and light-emitting diodes, exciton radiative rate determines the efficiency of luminescence in competition to various nonradiative processes. Therefore, understanding how exciton migrates over space as well as its decay dynamics are vital for the design of highly efficient optoelectronic devices. To interrogate these photophysical processes requires experimental tools with simultaneous high temporal and spatial resolution. In this thesis, I introduce two transient imaging systems (photoluminescence imaging with 300 ps time resolution, and transient absorption microscopy with 200 fs time) that are innovative tools to directly probe excited state dynamics and transport in sub-μm domains. The techniques were applied to a type of promising semiconductor, perovskites, including surface-passivated hybrid perovskite and 2D layered perovskites to explore the fundamental mechanisms that affect exciton transport. The fundamental understanding of excitons shed light on the underlying physics such as exciton delocalization, exciton-exciton interaction, and how these properties affected by the static and dynamic disorders of the material. We further demonstrated a novel twisted superlattice using ultrathin perovskites that confines excitons due to increased density of state from the moiré flat bands. In addition, excitons can be accelerated by strongly interacts photons, forming polariton quasiparticles that possess small effective mass. This is demonstrated by coupling 2D layered perovskites to a plasmonic array. We further showcase the formation of bulk polaritons without an external optical cavity in a self-assembled organic aggregate. Experimental investigation into these intriguing phenomena provide an approach to study fundamental processes such as many-body interaction and quantum coherence. </p>