Dissertations / Theses on the topic 'Photoluminescence'
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Chiu, Sheng-Kuei. "Photoluminescent Silicon Nanoparticles: Fluorescent Cellular Imaging Applications and Photoluminescence (PL) Behavior Study." PDXScholar, 2015. http://pdxscholar.library.pdx.edu/open_access_etds/2455.
Full textVijh, Uma Parvathy. "Photoluminescence by Interstellar Dust." See Full Text at OhioLINK ETD Center (Requires Adobe Acrobat Reader for viewing), 2005. http://www.ohiolink.edu/etd/view.cgi?toledo1122478565.
Full textTypescript. "A dissertation [submitted] as partial fulfillment of the requirements of the Doctor of Philosophy degree in Physics." Bibliography; leaves 209-225.
Al-Ajili, Adwan Nayef Hameed. "Photoluminescence of nanostructured silicon." Thesis, Loughborough University, 1996. https://dspace.lboro.ac.uk/2134/26999.
Full textXiao, Bin, and 肖斌. "Photoluminescence study of ZnO materials." Thesis, The University of Hong Kong (Pokfulam, Hong Kong), 2011. http://hub.hku.hk/bib/B47153593.
Full textpublished_or_final_version
Physics
Master
Master of Philosophy
Alrrshedan, Marrwa. "Photoluminescence from Bulk GaN Substrates." VCU Scholars Compass, 2012. http://scholarscompass.vcu.edu/etd/2802.
Full textZheng, Wan Hua. "Photoluminescence study of porous silicon." HKBU Institutional Repository, 1998. http://repository.hkbu.edu.hk/etd_ra/138.
Full textNgan, Mei Lun. "Photoluminescence excitation of porous silicon." HKBU Institutional Repository, 1998. http://repository.hkbu.edu.hk/etd_ra/139.
Full textFaklaris, Orestis. "Photoluminescent diamond nanoparticles as labels in cells : study of their optical properties and investigation of their cellular uptake mechanism." Cachan, Ecole normale supérieure, 2009. http://tel.archives-ouvertes.fr/tel-00439561/fr/.
Full textThis thesis work studies the use of Photoluminescent NanoDiamonds (PNDs) for bio-imaging applications. Nanodiamonds are photoluminescent thanks to embedded nitrogen-vacancy (NV) color centers. The thesis is divided in two parts. The first part concerns the study of the optical properties of NV color centers in nanodiamonds. After optimization of the NV center concentration, we compared the photoluminescence of PNDs to commercial Quantum Dots (QDs) and conclude that it can be similar or even higher in the case of PNDs. To enhance the imaging contrast of internalized by cells PNDs, we studied the 2-photon excitation properties of NV centers. While implementing a pulsed excitation laser, we discovered that simultaneous one- and two-photon excitation (IR+VIS pulses) quenches the photoluminescence signal of PNDs. We examined how this effect can serve for super-resolution imaging of NV color centers in nanodiamonds. The second part of the work is devoted to the applications of PNDs as bio-imaging probes. In the prospect of applications of PNDs as drug delivery vehicles, we studied the uptake mechanisms of PNDs and elucidated their intracellular localization by blocking different entry mechanisms and by immunofluorescence experiments. Moreover, we ensured that PNDs are not toxic for cells in culture. As a first try of vectorization we covered PNDs with plasmid DNA and examined the transfection efficiency
Wilde, Fabian. "Unidirectional photoluminescence emission of pierced microdisks /." München : Dr. Hut Verlag, 2009. http://bvbr.bib-bvb.de:8991/F?func=service&doc_library=BVB01&doc_number=017120456&line_number=0001&func_code=DB_RECORDS&service_type=MEDIA.
Full textSeyhan, Ayse. "Photoluminescence Specroscopy Of Cds And Gase." Master's thesis, METU, 2003. http://etd.lib.metu.edu.tr/upload/1258383/index.pdf.
Full textRatmann, Cristiane Wienke Raubach. "Metal sulfides: photoluminescence and photocatalytic properties." Universidade Federal de São Carlos, 2013. https://repositorio.ufscar.br/handle/ufscar/6279.
Full textUniversidade Federal de Minas Gerais
In this work we report an experimental and theoretical study of photoluminescence (PL) and photocatalytic activity of pure metal sulfides and systems furnished prepared by microwave assisted solvothermal (MAS) method. The theoretical model of the decorated system was created in order to analyze the electronic transition, especially in their interfaces. The results show that the system interface decorated (core-shell) produces an electron charge transfer of holes from cadmium sulfide (CdS) to zinc sulfide (ZnS), which helps increase the PL and photocatalytic activity of the system. For the pure systems, was observed the efficacy of the method synthesis employed verified that the process for obtaining the ZnS and calcium sulfide (CaS) was extremely important. Through the theoretical models was possible to evaluate the influence caused by the solvothermal influence caused by the MAS method. The variation in the synthesis parameters shows a direct influence on the PL properties of sulfides obtained which can be attributed to structural organization. The theoretical results how this order and disorder of the system can affect these properties of the obtained materials.
Neste trabalho relata-se um estudo teórico e experimental da atividade fotoluminescente (FL) e fotocatalítica de sulfetos metálicos puros e em sistemas decorados preparados por intermédio do método solvotérmico assistido por micro-ondas. O modelo teórico do sistema decorado foi criado de forma a analisar a transição eletrônica, principalmente nas suas interfaces. Os resultados mostram que a interface do sistema decorado (core-shell) produz uma transferência de carga do elétron do sulfeto de cádmio (CdS) para os buracos do sulfeto de zinco (ZnS), o que ajuda a aumentar a atividade fotoluminescente e fotocatalítica do sistema. Para os sistemas puros, observou-se a eficácia do método de síntese empregado, sendo verificado que o processo de obtenção do ZnS e sulfeto de cálcio (CaS) foi de extrema importância. Por intermédio dos modelos teóricos foi possível avaliar a influência causada pelo método. A variação nos parâmetros de síntese mostra uma influência direta nas propriedades FL dos sulfetos obtidos que pode ser atribuída a organização estrutural. O modelo teórico mostra como essa ordem e desordem do sistema podem afetar essas propriedades dos materiais obtidos.
Mosor, Sorin. "Photoluminescence of Quantum Confined Semiconductor Structures." Diss., Tucson, Arizona : University of Arizona, 2005. http://etd.library.arizona.edu/etd/GetFileServlet?file=file:///data1/pdf/etd/azu%5Fetd%5F1309%5F1%5Fm.pdf&type=application/pdf.
Full textMakuc, Boris. "Photoluminescence of ZnSe grown by MOVPE." Thesis, McGill University, 1988. http://digitool.Library.McGill.CA:80/R/?func=dbin-jump-full&object_id=61819.
Full textGower, Joanne Elizabeth. "Photoluminescence of point defects in silicon." Thesis, King's College London (University of London), 1998. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.300758.
Full textSun, Ye. "Synthesis and photoluminescence of ZnO nanostructures." Thesis, University of Bristol, 2007. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.440141.
Full textHouse, Jody L. (Jody Lee) 1970. "Optical characterization of ZnSe by photoluminescence." Thesis, Massachusetts Institute of Technology, 1994. http://hdl.handle.net/1721.1/36430.
Full textWilkinson, Victoria Ailsa. "High pressure photoluminescence of semiconductor structures." Thesis, University of Surrey, 1990. http://epubs.surrey.ac.uk/844514/.
Full textLefez, Benoît. "Caractérisation d'oxydes de cuivre par photoluminescence." Rouen, 1991. http://www.theses.fr/1991ROUES047.
Full textIslangulov, Radiy Rashitovich. "Low Power Photoluminescence and Photochemical Upconversion." Bowling Green State University / OhioLINK, 2006. http://rave.ohiolink.edu/etdc/view?acc_num=bgsu1162244082.
Full textOlsen, Anita. "Thermal Quenching of Photoluminescence from GaN." VCU Scholars Compass, 2012. http://scholarscompass.vcu.edu/etd/2796.
Full textJain, Swati. "Photoluminescence study of cadmium zinc telluride." Morgantown, W. Va. : [West Virginia University Libraries], 2001. http://etd.wvu.edu/templates/showETD.cfm?recnum=1876.
Full textTitle from document title page. Document formatted into pages; contains x, 84 p. : ill. (some col.). Includes abstract. Includes bibliographical references (p. 79-83).
Patel, Bhavnesh. "Photoluminescence and kinetics of zinc oxide doped with rare earths." Ohio : Ohio University, 1998. http://www.ohiolink.edu/etd/view.cgi?ohiou1176402695.
Full textPemasiri, Karunananda. "Investigation of zincblende, wurtzite, and mixed phase InP nanowires by photocurrent, photoluminescence and time-resolved photoluminescence spectroscopies." University of Cincinnati / OhioLINK, 2013. http://rave.ohiolink.edu/etdc/view?acc_num=ucin1377873494.
Full textZhao, Shen. "Propriétés optiques de nanorubans et boites quantiques de graphène." Thesis, Université Paris-Saclay (ComUE), 2018. http://www.theses.fr/2018SACLN032/document.
Full textThis manuscript presents an experimental study on the optical properties of graphene nanoribbons (GNRs) and graphene quantum dots (GQDs) synthesized by bottom-up chemistry.For the part on GNRs, the optical absorption and photoluminescence spectra as well as the life-time measurements on the dispersion of solution-mediated synthesized GNRs implies the formation of excimer states as a result of aggregation of GNRs. By means of confocal fluorescence microscopy and atomic force microscopy, we observe the emission of small GNR aggregates confirming the ability of GNRs to emit light in the solid state. On the other hand, the optical characterizations of on-surface synthesized GNRs shows remarkable Raman features, implying the distinct vibrational properties of GNRs compared to graphene and carbon nanotubes. The observed PL is spectrally broad with higher energy instead of a bright bandgap emission, which might be related to the defects created during the sample preparation.For the part on GQDs, the optical spectroscopy results indicate that GQDs are individualized in dispersions rather than in the form of aggregates. Then by means of microphotoluminescence, we directly address the intrinsic properties of single GQDs. Second-order photon correlation measurements reveal that GQDs exhibit single-photon emission with a high purity. Notably, the emission of GQDs has good photo-stability with high brightness. As a first example of the optical tunability of GQDs through the control of their structure, we observe that the emission of single edge-chlorinated GQDs is redshifted by almost 100 nm while maintaining the single-photon emission
Feng, Lin. "Photoluminescence studies of single zinc oxide nanostructures /." View abstract or full-text, 2010. http://library.ust.hk/cgi/db/thesis.pl?PHYS%202010%20FENG.
Full textMbulanga, Crispin Munyelele. "Defect-related photoluminescence of zinc oxide nanorods." Thesis, Nelson Mandela Metropolitan University, 2015. http://hdl.handle.net/10948/10318.
Full textDegliame, Gary. "Thermométrie par photoluminescence, application en micro/nanothermique." Thesis, Reims, 2017. http://www.theses.fr/2017REIMS021/document.
Full textThis PhD work focuses on the study of microcrystals photoluminescence in order to design a hybrid probe allowing micro/nano-scales measurements of a sample’s temperature and the thermal conductivity. Thus, a Wollaston thermoresistive probe used in thermal microscopy (SThM), was coupled to an Erbium doped microcrystal of Cd0.7Sr0.3F2 (4% Er3+), whose emission spectrum is sensitive to the temperature.At first, for its applications in thermometry, the optical properties of the bulk crystal have been studied. We worked on the interpretation of its luminescence spectrum obtained by up-conversion using a laser diode centered at 655 nm and 4mW. Then, we proposed three methods to determine the fluorescence intensities to access this temperature via the RIF (Fluorescence Intensity Ratio) technique. We have shown that it is possible to determine its temperature using the Stark sub-levels of the thermalized levels emissions intensities.Furthermore, we studied the temperature behavior of the microcrystals individually fixed at the end of thermoresistive probes. The experimental results made it possible to deduce the optimal size of the microcrystal and the most adapted intensity determination method for nano/microthermometry.After validating our microcrystal temperature approach, we focused on the principle of temperature imaging from photoluminescence spectra. We present an application on a microsystem composed of wires with a diameter of 350nm covered by a SiO2 thin film
Harrison, Dale A. "Photoluminescence spectroscopy of D§- states in GaAs." Thesis, National Library of Canada = Bibliothèque nationale du Canada, 1998. http://www.collectionscanada.ca/obj/s4/f2/dsk2/tape15/PQDD_0006/NQ37711.pdf.
Full textDybiec, Maciej. "Spatially resolved photoluminescence spectroscopy of quantum dots." [Tampa, Fla] : University of South Florida, 2006. http://purl.fcla.edu/usf/dc/et/SFE0001767.
Full textMcGhee, Ewan James. "The photoluminescence spectroscopy of single quantum dots." Thesis, Heriot-Watt University, 2004. http://hdl.handle.net/10399/1116.
Full textWinser, Andrew James. "Photoluminescence studies of arsenic-doped gallium nitride." Thesis, University of Nottingham, 2004. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.405387.
Full textToft, Ian. "Fibre optic micro-photoluminescence of quantum nanostructures." Thesis, University of Cambridge, 2006. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.614103.
Full textStarck, Christophe. "Caractérisation de doubles hétérostructures laser par photoluminescence." Toulouse, INSA, 1990. http://www.theses.fr/1990ISAT0008.
Full textShevchenko, D., V. V. Kononets, D. Dobrovolskas, S. Neicheva, N. G. Starzhinskiy, O. Ts Sidletskiy, K. Lebbou, and G. Tamulaitis. "Photoluminescence Inhomogeneity of LGSO : Ce Scintillator Crystal." Thesis, Sumy State University, 2013. http://essuir.sumdu.edu.ua/handle/123456789/35261.
Full textTsagli, Kelvin Xorla. "Temperature Dependence of Photoluminescence Spectra in Polystyrene." University of Akron / OhioLINK, 2021. http://rave.ohiolink.edu/etdc/view?acc_num=akron1625744248503334.
Full textJohnson, Matthew Bruce McGill T. C. McGill T. C. "Ultrafast time-resolved photoluminescence studies of GaAs /." Diss., Pasadena, Calif. : California Institute of Technology, 1989. http://resolver.caltech.edu/CaltechETD:etd-02062007-105824.
Full textSun, Yuxuan. "Setup for Micro Photo- and Electro-Luminescence of Optoelectronic Device Structures." Thesis, KTH, Skolan för informations- och kommunikationsteknik (ICT), 2015. http://urn.kb.se/resolve?urn=urn:nbn:se:kth:diva-175708.
Full textVautravers, Nicolas R. "Polyhedral oligomeric silsesquioxanes in catalysis and photoluminescence applications." Thesis, St Andrews, 2009. http://hdl.handle.net/10023/729.
Full textSkarpeteig, Jon. "Cryogenic micro-photoluminescence of silicon solar cell materials." Thesis, Norges teknisk-naturvitenskapelige universitet, Institutt for elektronikk og telekommunikasjon, 2010. http://urn.kb.se/resolve?urn=urn:nbn:no:ntnu:diva-11106.
Full textCrandles, David A. "Photoconductivity and photoluminescence in ZnIn(2)S(4)." Thesis, University of Ottawa (Canada), 1985. http://hdl.handle.net/10393/4565.
Full textSong, Young Wook. "Photoluminescence of InN with Mg and Zn Dopants." Thesis, University of Canterbury. Physics and Astronomy, 2008. http://hdl.handle.net/10092/1638.
Full textThảo. "Photoluminescence spectroscopy on erbium-doped and porous silicon." Amsterdam : Amsterdam : [s.n.] ; Universiteit van Amsterdam [Host], 2000. http://dare.uva.nl/document/83659.
Full textSong, Young-Wook. "Photoluminescence of High Quality Epitaxial p-type InN." Thesis, University of Canterbury. Physics and Astronomy, 2013. http://hdl.handle.net/10092/8101.
Full textRichter, Robert [Verfasser]. "Photoluminescence of Diamondoids: Experiment and Theory / Robert Richter." Berlin : epubli GmbH, 2015. http://d-nb.info/1078816085/34.
Full textEdiger, Matthias. "Photoluminescence from charged excitons in single quantum dots." Thesis, Heriot-Watt University, 2006. http://hdl.handle.net/10399/196.
Full textCheng, Yu-li, and 鄭育俐. "Photoluminescence, Photoluminescence Excitation and Absorption of m-GaN." Thesis, 2007. http://ndltd.ncl.edu.tw/handle/bj6tyu.
Full text國立中山大學
物理學系研究所
95
Group III nitrides have recently attracted great interest and are intensively studied for that cover continuously from the ultraviolet to nearinfrared region by proper alloying.Therefore, group III nitrides have wide applications inoptoelectronic devices, such as light-emitting diodes,ultraviolet or blue lasers, and full color displays. Unintentionally doped m-GaN thin films have been epitaxially grown on LAO by PAMBE. The optical characteristics were investigated with photoluminescence (PL), photoluminescence excitation (PLE), and absorption spectrum.
Wang, Wen-Han, and 王文瀚. "Photoluminescence of CulnS2." Thesis, 1997. http://ndltd.ncl.edu.tw/handle/59588748655310179611.
Full textLai, Jui-Feng, and 賴瑞豐. "Photoluminescence from nc-SiOx:H." Thesis, 2005. http://ndltd.ncl.edu.tw/handle/51235886546820410587.
Full text國立中興大學
精密工程研究所
93
Abstract In this thesis, the amorphous silicon oxide (SiOx) films with various O/Si ratios were deposited by plasma-enhanced chemical vapor deposition with the pulse-modulated RF power. The influence of the pulse-on time (ton) on the O/Si ratio of the SiOx films was elucidated. These amorphous SiOx films were then annealed in N2 atmosphere at 1100℃ for 30 min to be converted into nc-SiOx films. The intensities and the peak positions of the photoluminescence (PL) of these nc-SiOx films were measured to explore how the O/Si ratio of the as-deposited amorphous SiOx films affects the PL signals of the obtained nc-SiOx films after annealing. The chamber pressure, SiH4/N2O/H2, the plasma power, the pulse-off time (toff), and the substrate temperature were fixed at 0.3 torr, 4/12/80 sccm, 30 W, 50 ms, and 70 ℃, respectively. The ton was varied from 2, 5, 12, 25, 50, 100, 150, 200, 325, 450, 800, 1200 ms, to continuous wave (cw). The thickness of all SiOx thin films was fixed at 310 nm, and the Si-O bonding modes of the SiOx films were measured by Fourier transform infrared spectrometer (FTIR). Energy dispersive spectrometer (EDS), Raman scattering spectrometer, x-ray diffraction (XRD), and high resolution transmission electron microscope (HRTEM) were used to measure and analyze the O/Si ratio and the crystalline structures and sizes of the nc-SiOx films. EDS results show that, the O/Si ratio of the SiOx films can be controlled between 0.1 and 0.57 for ton changed from 5 to 800 ms in the condition of N2O/SiH4 = 3. FTIR measurements display that there are three peaks of 850 cm-1 (Si-O bending mode), 1060 cm-1 (Si-O-Si stretching mode), and 2240 cm-1 (H-Si-O stretching mode) in each samples. For the ton = 200 ms sample, which the O/Si ratio is 0.57, the intensities of the 850 cm-1 and 2240 cm-1 peaks are in between those of the other samples, and the intensity of the 1060 cm-1 peak is close to the maximum value of all samples. The background fluorescence intensities of the Raman scattering of the nc-SiOx films obtained after annealing is lager than those of as-deposited amorphous SiOx films about 1 to 2 orders. Especially, the ton = 200 ms sample has the maximum value about 92 times. The results indicate that the increasing of the background fluorescence of Raman scattering is due to light scattering from the nanocrystalline silicon (nc-Si) existed in the nc-SiOx films. XRD results present that there are four distinct crystalline signals at , , , and in the ton = 200 ms sample. The peak positions of the PL signals of all nc-SiOx films are located at about 800 nm. The PL intensity of the nc-SiOx film is increased as the O/Si ratio increases from 0.1 to 0.57. The ton = 200 ms sample exhibiting maximum O/Si ratio (0.57) has the strongest PL intensity. Notely, the small variation of peak positions of all samples implies that there is little change in the size of nc-Si in all samples. The variation of PL intensity is mainly influenced by the fraction of nc-Si in nc-SiOx films. The HRTEM data of ton = 200 ms sample shows that the size of the nc-Si is about 3 nm. The fraction of nc-Si in nc-SiOx film is about 33 %, which is estimated from the area ratio of the nc-Si in nc-SiOx film. The O/Si ratio of the SiOx thin films can be effectively controlled by modulating ton of the pulse-modulated RF power. The PL intensity of the nc-SiOx thin films increases as the O/Si ratio increases from 0.1 to 0.57. The PL intensity of the nc-SiOx films is mainly affected by the fraction of nc-Si in nc-SiOx films.
Li, Chung-li, and 李中立. "Photoluminescence of Stereoregular Polymers." Thesis, 2012. http://ndltd.ncl.edu.tw/handle/01855021877245218250.
Full text國立中山大學
材料與光電科學學系研究所
100
A series of stereoregular polymers including atactic, syndiotactic and isotactic poly 4(N, N-diphenyl)styrene (PNNDPS) and poly 4(N, N-ethylphenyl)styrene (PNNEPS) were synthesized to exam the tacticity effect on the photoluminescence (PL) behavior. Also, different degrees of the regularity as well as the chemical modification of the fluorophor were explored in the stereoregular polymers. Because of the increase of the steric hindrance among the bulky triphenylamine pendants in the polymer chains, a red shift of the PL emission with an accompanying increase in the emissive intensity was found in contrast to the weakened emission of triphenylamine monomers. In solution state, the PL spectra of these stereoregular polymers reveal multiple PL emissive bands including monomeric and aggregation emissions as evidenced by the time-resolved lifetime measurement. Because of the huge triphenylamine pendants, the triphenylamine pendants attached on the iPNNDPS17 (mmmmmm~50%) might encounter higher steric hindrance than that in the sPNNDPS23 (rrrrrr~59%) due to the stereoregularity evidenced by simulation. Accordingly, the iPNNDPS17 (mmmmmm~50%) exhibits more emissive intensity than the sPNNDPS23 (rrrrrr~59%) due to the effective blockage of the intramolecular rotation of the phenyl blade i.e., the restriction of intramolecular rotation (RIR). Accordingly, the RIR-active PNNDPS is highly sensitive to the temperature variations. The chemical modification of the fluorophor was carried out to examine the effect of the chemical structure. By comparison, the sPNNDPS2 (rrrrrr~70%) with high regularity exhibits much higher emissive intensity than the sPNNDPS23 (rrrrrr~59%) with low regularity due to the less solubility. However, more intense PL emission can be found in the sPNNEPS17 than aPNNEPS8 due to the ethyl substitution of the fluorophor. In aggregation solution, with the increase of the poor water contents, the PL emission decreases significantly in the sPNNDPS23 (rrrrrr~59%) and sPNNDPS2 (rrrrrr~70%) due to the formation of H-aggregate in which extra energetic loss is conducted. By contrast, the PL spectra display that the emissive intensity decreases first as fw=0.1~0.5 and then intensifies later as fw=0.6~0.9. This might be resulted from the competition between the π-π interaction and RIR effect. Interestingly, the PL emissive intensity drops down significantly in the sPNNEPS, whereas the PL emissive intensity is almost unchanged in the aPNNEPS8 with the increase of the poor water contents. We suggest that because the aPNNEPS8 might contain both syndiotactic and isotactic configurations, the isotactic configurations having the ethyl group pointing out of the plane may prevent the formation of the π-stacking between the fluorophors. The PL behavior in thin film is also explored for these stereoregular polymers. After slow cooling from melt, the crystalline sPNNDPS2 (rrrrrr~70%) thin film exhibits very strong emission in comparison with the thin film after quenching from melt, indicating the crystallization-induced emission enhancement. Although the iPNNDPS17 (mmmmmm~50%) is noncrystallizable as evidenced by differential scanning calorimetry (DSC) and polarized light microscope (PLM), the PL emissive intensity of the iPNNDPS17 (mmmmmm~50%) thin film is significantly stronger after slow cooling from melt than that after quenching from melt. We suggest that this might be attributed to the free volume effect varied with the thermal history associated with the steric hindrance. Notably, this enhanced PL emission in the iPNNDPS17 (mmmmmm~50%) thin film is extremely larger than that in the sPNNDPS23 (rrrrrr~59%) and aPNNDPS8, indicating the stereoregularity effect associated with the RIR effect. By contrast, this free volume effect is not significant in the PNNEPS thin film due to the flexible ethyl substitutions. As a result, the stereoregular polymers with different tacticities and regularities indeed exhibit distinct PL behavior in solution and thin film.
Yang, Tun-Chun, and 楊敦鈞. "Studies of Surface V-Defect on AlGaN Films by Micro-Photoluminescence and Photoluminescence Excitation." Thesis, 2003. http://ndltd.ncl.edu.tw/handle/97941997470701756550.
Full text國立交通大學
電子物理系
91
We have studied optical properties of AlGaN films grown by metal organic chemical vapor phase epitaxy under various ammonia flow rate. From micro-photoluminescence (Micro-PL) spectra, there is an extra peak in the V-defect, which is 0.1 eV lower than the near band edge emission. The origin of this extra peak is the defect band induced by V-defect. In order to determine the characteristics of Inbe, and IV, the excitation power dependent measurements were carried out indicating that they are not from donor-acceptor pair (DAP) transitions. Furthermore, the temperature dependence of Micro-PL was studied and the S-shape behavior was observed in the spectrum as due to the spatial fluctuation, for instance, Ga vacancy formed localized states. For Al0.9Ga0.91N, the activation energy of 27.8 meV and the exciton localization energy of 6.1 meV film for Inbe were obtained from the Arrhenius plot. However, for IV, the activation energy increases to 65.1 meV and the localization energy increases to 7.6 meV. By using the photoluminescence excitation (PLE) technique, we found that the V-defect created new energy levels that are responsible for the new IV emissions. We suggested that the broad band from the V-defect is probably related to acceptor-like level due to Ga vacancy.