Academic literature on the topic '(Photo)stability'
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Journal articles on the topic "(Photo)stability":
Schallreuter, Karin U., Jeremy Moore, and John M. Wood. "On Photo-Stability of Oxybenzone." Journal of Investigative Dermatology 110, no. 1 (January 1998): 96–97. http://dx.doi.org/10.1038/sj.jid.5602936.
Santoro, Ettore. "On Photo-Stability of Oxybenzone." Journal of Investigative Dermatology 110, no. 1 (January 1998): 95–96. http://dx.doi.org/10.1046/j.1523-1747.1998.00082.x.
Abid, Abdul Rahman, Bronisław Marciniak, Tomasz Pędziński, and Muhammad Shahid. "Photo-stability and photo-sensitizing characterization of selected sunscreens’ ingredients." Journal of Photochemistry and Photobiology A: Chemistry 332 (January 2017): 241–50. http://dx.doi.org/10.1016/j.jphotochem.2016.08.036.
Wang, Jian‐Hua, Shao‐Peng Wang, Pavel N. Melentiev, Bin Kang, Jing‐Juan Xu, and Hong‐Yuan Chen. "Photo‐stability and Photo‐damage of SPASER Nanoparticles under Nanosecond Pulsed‐laser." Chinese Journal of Chemistry 40, no. 4 (December 24, 2021): 507–14. http://dx.doi.org/10.1002/cjoc.202100629.
LIU, Minghua. "Surfactant Enhancing Photo-Stability of Folic Acid." Acta Physico-Chimica Sinica 35, no. 7 (2019): 663–64. http://dx.doi.org/10.3866/pku.whxb201811042.
Bulloch, R. H., and J. R. Reynolds. "Photostability in dioxyheterocycle electrochromic polymers." Journal of Materials Chemistry C 4, no. 3 (2016): 603–10. http://dx.doi.org/10.1039/c5tc03536h.
Pandey, Krishna K., Jayashree, and H. C. Nagaveni. "Study of dimensional stability, decay resistance, and light stability of phenylisothiocyanate modified rubberwood." BioResources 4, no. 1 (January 11, 2009): 257–67. http://dx.doi.org/10.15376/biores.4.1.257-267.
Ruqaya Raad and Mustafa Abdallh. "Surface modification to enhance photo-stability of polymers." GSC Advanced Research and Reviews 11, no. 2 (May 30, 2022): 080–88. http://dx.doi.org/10.30574/gscarr.2022.11.2.0130.
Fahmy, Hassnaa M., Nabel A. Negm, Ahmed H. M. Elwahy, and Maram T. H. Abou Kana. "Laser induced fluorescence, photo-physical parameters and photo-stability of new fluorescein derivatives." Journal of Molecular Liquids 229 (March 2017): 31–44. http://dx.doi.org/10.1016/j.molliq.2016.12.047.
Chen, Shaoyu, Chaoxia Wang, Yunjie Yin, and Kunlin Chen. "Synthesis of photo-responsive azobenzene molecules with different hydrophobic chain length for controlling foam stability." RSC Advances 6, no. 65 (2016): 60138–44. http://dx.doi.org/10.1039/c6ra06459k.
Dissertations / Theses on the topic "(Photo)stability":
Razzell, Hollis Joseph. "Understanding morphology and photo-stability of organic solar cells via advanced structural probes." Thesis, Imperial College London, 2016. http://hdl.handle.net/10044/1/32271.
Mouri, Shinichiro. "Dynamical properties of photo-induced spin conversion in the spin crossover complex with multi-stability." 京都大学 (Kyoto University), 2009. http://hdl.handle.net/2433/124406.
Zhang, Chaohong [Verfasser], and Christoph [Gutachter] Brabec. "Influence of Microstructure on Thermo- and Photo-stability in Organic Bulk-heterojunction Solar Cell / Chaohong Zhang ; Gutachter: Christoph Brabec." Erlangen : Friedrich-Alexander-Universität Erlangen-Nürnberg (FAU), 2018. http://d-nb.info/1150967692/34.
Mabrouk, Salima. "Synthèse par voie colloïdale et étude des propriétés optiques et structurales de nanocristaux ternaires ZnSeS dopés." Electronic Thesis or Diss., Université de Lorraine, 2022. http://www.theses.fr/2022LORR0169.
In recent years, ternary QDs have experienced an exponential development thanks to their properties, especially their photoluminescence, which can be controlled not only by their size but also by their composition. As part of this thesis, we developed a new "green" synthesis in aqueous media of ZnSeS-doped ternary QDs and we studied the effect of the variation of the dopant (Mn2+, Cu2+, or Cu2+/Al3+) as well as its localization (in the core or in the shell) on their optical and structural properties. The first part of this work describes the synthesis of ZnSeS:Mn ternary QDs and ZnSeS:Mn/ZnS core/shell using 2-MPA as a ligand. The results obtained show that these nanocrystals can be prepared with quantum yields of 22% and 41%, respectively. These QDs have shown excellent photostability under UV irradiation and can easily be transferred to the organic phase using the hydrophobic octanethiol ligand without altering their optical properties. Subsequently, core/shell ZnSeS/ZnS:Cu/ZnS QDs for which the Cu dopant is introduced into the first shell were prepared using 3-MPA as a ligand. Excellent (photo)stability in the presence of air and oxygen was observed. ZnSeS/ZnS:Cu/ZnS core/shell QDs have a 20% photoluminescence quantum yield and have been used as photoluminescent probes for the detection of Pb2+ ions in aqueous media. A selective extinction of the photoluminescence emission in the presence of Pb2+ ions was observed. Finally, Cu and Al co-doped QDs, ZnSeS/ZnS:Cu/ZnS:Al/ZnS (first shell doped with Cu2+ and second shell doped with Al3+) were prepared. Co-doping allows the improvement of the optical properties, including quantum efficiency (up to 32%) as well as the photoluminescence lifetime of Cu-doped QDs
Hansson, Rickard. "Morphology and material stability in polymer solar cells." Licentiate thesis, Karlstads universitet, Institutionen för ingenjörsvetenskap och fysik, 2015. http://urn.kb.se/resolve?urn=urn:nbn:se:kau:diva-37843.
The performance of polymer solar cells depends strongly on the distribution of electron donor and acceptor material in the active layer. Understanding the connection between morphology and performance as well as how to control the morphology, is therefore of great importance. Furthermore, improving the lifetime has become at least as important as improving the efficiency for polymer solar cells to become a viable technology. In this work, the relation between morphology and solar cell performance is studied as well as the material stability for polymer:fullerene blend films. A combination of microscopic and spectroscopic methods is used to investigate the lateral and vertical morphology as well as the surface composition. Lateral phase-separated domains are observed whose size is correlated to the solar cell performance, while the observed surface enrichment of polymer does not affect the performance. Changes to the unoccupied molecular states as a result of illumination in ambient air are observed for the fullerene, but not for the polymer, and fullerenes in a blend change more than pristine fullerenes. Solar cells in which the active layer has been illuminated exhibit greatly reduced electrical performance, mainly attributed to fullerene degradation at the active layer surface.
Paper 2 ingick som manuskript i avhandlingen. Nu publicerad.
Shehayeb, Sanaa. "Récepteur solaire photo-thermique obtenu par électrophorèse de nanoparticules à propriété optique sélective." Thesis, Montpellier, 2017. http://www.theses.fr/2017MONTT195/document.
The production of hot water by using efficient photothermal solar collectors is growing in importance to limit the use of fossil fuels. Black copper (CuO) has proved to be one of the viable solar-selective coatings owing to its nearly intrinsic properties. The formation of a tandem absorber based on CuO thin film deposited onto a highly IR reflecting metallic substrate is processed by electrophoretic deposition (EPD).In this way, the stabilization of a CuO colloidal suspension is studied previously by adding Mg(NO3)2 in isopropanol (IPA) or polyethylenimine (PEI) in water suspension. Both acts as positively charging agents and allow the realisation of a cathodic EPD. The colloidal stability as a function of the stabilizing agent content is studied prior to EPD, by dynamic light scattering (DLS) coupled with laser doppler velocimetry.CuO tandem absorbers are obtained by varying different EPD parameters to control the final thickness and also the morphology. Consequently, the optical selectivity of the tandem material is tuned and optimized. The deposition yield is compared relative to the different applied voltage range, deposition time and nanoparticle concentrations. Homogeneous deposits are obtained for [CuO]=5x10-4 g/cm3 from both suspensions. The optimum applied voltage is found to be 50 V.cm-1 for IPA suspension and 2 V.cm-1 for H2O suspension, for deposition times of 30 mins and 120 mins, respectively. The composition and the thickness of the coatings are analysed by Grazing Incidence X-ray diffraction (GIXRD), scanning electron microscopy (SEM) and the density is obtained from energy-dispersive X-ray spectroscopy (EDX). For the previously mentioned optimized conditions, CuO tandem absorbers derived from IPA suspension possess a density of 1.69 g/cm3 with high surface roughness. In contrast, homogeneous and regular surfaces is obtained from water suspensions having a higher density of 5.7 g/cm3.Moreover, absorptance (α) and emittance (ԑ) are calculated from the reflectance spectra of the UV-Vis-NIR and the Fourier transform InfraRed (FTIR) spectroscopy, respectively. α and ԑ were combined to determine the efficiency (ƞ) of the tandem material. Tandems obtained from water suspension has ƞ=0.8 -0.87 while from IPA ƞ=0.7. Besides, the applicability of this EPD is checked by performing other deposit of CuO on metallic substrates of different types.CuO tandems obtained from water suspensions are clearly more prominent to be used as solar selective tandem absorbers due to the high calculated ƞ value reported. The efficiency of such selective tandem absorbers was further enhanced by carbonization (pyrolysis under inert atmosphere) of the polymer (PEI) embedded in the coating. Otherwise, a thin film of SiO2 nanoparticles was deposited at the surface of the selective tandem absorbers to protect them. Both routes were successfully processed and proved to raise ƞ to 0.9
Peng, Yong. "Hybrid Lead Perovskites as Photocatalysts and Materials for Photo- and Electrocatalytic N2 Reduction." Doctoral thesis, Universitat Politècnica de València, 2021. http://hdl.handle.net/10251/171731.
[ES] La conversión de energía solar a productos químicos se considera una de las estrategias más viables para abordar los problemas derivados del uso masivo de combustibles fósiles y la excesiva emisión antropogénica de CO2. En catálisis asistida con luz, incluida la fotocatálisis y la catálisis fototérmica, el punto clave es el desarrollo de fotocatalizadores eficientes y robustos que puedan utilizar al máximo la energía solar y que sean lo suficientemente estables como para su comercialización. Los materiales basados en perovskitas híbridas orgánicas-inorgánicas han revolucionado el campo de la fotovoltaica en la última década, alcanzando una eficiencia de conversión de luz solar del 23%. Dado que los campos de la fotocatálisis y la fotovoltaica comparten procesos comunes, se abre la posibilidad de aplicación de estos materiales en fotocatálisis. Con el objetivo de confirmar esta posible aplicación de las perovskitas híbridas en fotocatálisis, en esta Tesis Doctoral, se han sintetizado nuevos materiales híbridos de perovskita con el objetivo de mejorar su estabilidad frente a la humedad aprovechando la gran variedad de ligandos orgánicos disponibles, que además pueden ser usados para promover modificaciones superficiales capaces de ajustar las propiedades hidrofílicas / hidrofóbicas. La actividad fotocatalítica de estos nuevos materiales de perovskita se ha estudiado en reacciones modelo para confirmar su estabilidad en las condiciones de reacción. Por otro lado, la reacción de fijación de nitrógeno fotoasistida también ha sido estudiada en detalle en esta Tesis Doctoral. Por un lado, se han sintetizado, caracterizado y testado nuevos complejos organometálicos como foto- y electrocatalizadores homogéneos para esta reacción. Estos han demostrado ser capaces de activar la molécula de dinitrógeno bajo un potencial electroquímico de reducción para formar amoníaco. Por otro lado, se han preparado nanopartículas de rutenio depositadas sobre un material de perovskita a base de titanato como fotocatalizador heterogéneo para la producción de amoniaco en flujo continuo. Además, se ha demostrado que la incorporación de metales alcalinos a este fotocatalizador puede potenciar su actividad fotocatalítica en esta reacción. Así, este material compuesto ha demostrado estar entre los fotocatalizadores más eficientes del estado del arte en la actualidad para esta reacción demostrando además una su elevada estabilidad en las condiciones de reacción.
[CA] La conversió d'energia solar en productes químics es considera una de les estratègies més viables per abordar els problemes derivats de l'ús massiu de combustibles fòssils i l'excessiva emissió antropogènica de CO2. En catàlisi assistida amb llum, inclosa la fotocatàlisi i la catàlisi fototèrmica, el punt clau és el desenvolupament de fotocatalitzadors eficients i robustos que puguen utilitzar al màxim l'energia solar i que siguen prou estables com per a la seva comercialització. Els materials basats en perovskites híbrides orgàniques-inorgàniques han revolucionat el camp de la fotovoltaica en l'última dècada, aconseguint una eficiència de conversió de llum solar del 23%. Atès que els camps de la fotocatàlisi i la fotovoltaica comparteixen processos comuns, s'obre la possibilitat d'aplicació d'aquests materials en fotocatàlisi. Amb l'objectiu de confirmar aquesta possible aplicació de les perovskites híbrides en fotocatàlisi, en aquesta tesi doctoral, s'han sintetitzat nous materials híbrids de perovskita amb l'objectiu de millorar la seva estabilitat enfront de la humitat aprofitant la gran varietat de lligands orgànics disponibles, que amés poden ser usats per a promoure modificacions superficials capaços d'ajustar les propietats hidrofíliques / hidrofòbiques. L'activitat fotocatalítica d'aquests nous materials de perovskita s'ha estudiat en reaccions model per confirmar la seva estabilitat en les condicions de reacció. D'altra banda, la reacció de fixació de nitrogen fotoassistida també ha sigut estudiada en detall en aquesta tesi doctoral. D'una banda, s'han sintetitzat, caracteritzat i testat nous complexos organometàl·lics com foto- i electrocatalitzadors homogenis per a aquesta reacció. Aquests han demostrat ser capaços d'activar la molècula de dinitrogen sota un potencial electroquímic de reducció per formar amoníac. D'altra banda, s'han preparat nanopartícules de ruteni depositades sobre un material de perovskita a força de titanat com fotocatalitzador heterogeni per a la producció d'amoníac en flux continu. A més, s'ha demostrat que la incorporació de metalls alcalins a aquest fotocatalitzador pot potenciar la seva activitat fotocatalítica en aquesta reacció. Així, aquest material compost ha demostrat estar entre els fotocatalitzadors més eficients de l'estat de l'art actualment per a aquesta reacció seva demostrant amés una elevada estabilitat en les condicions de reacció.
[EN] Solar energy to chemicals conversion is regarded to be one of the most plausible strategies addressing the issues of fossil fuel crisis and excessive anthropogenic CO2 emission. For photo-assisted catalysis, including photocatalysis and photothermal catalysis, the key point is the development of efficient and robust photocatalysts that can efficiently utilize the solar energy as well as they are stable enough that meets the requirements for commercialization. Hybrid organic-inorganic perovskites have revolutionized the photovoltaic field in the last decade, reaching a certified sunlight conversion efficiency of 20 %. Since photocatalysis and photovoltaics share common processes, the application of these materials in photocatalysis would be possible. In this Doctoral Thesis, novel hybrid perovskite materials have been synthesized with the aim to improve their stability against moisture by taking advantage large variety of the available organic ligand, which can promote surface modifications capable to adjust the hydrophilic/hydrophobic properties. Additionally, the photocatalytic activity of these novel perovskite materials has been studied in model reactions in order to confirm their stability under reaction conditions. On the other hand, the photo-assisted nitrogen fixation reaction has been also studied in detail in this Doctoral Thesis. on one hand, new organometallic complexes have been synthetized, characterized and tested as homogeneous photo and electrocatalysts for this reaction. They have been demonstrated to be able to activate dinitrogen molecule under electrochemical cathodic potentials to form ammonia. On the other hand, ruthenium nanoparticles deposited on a titanate-based perovskite material have been prepared and tested as heterogeneous photocatalyst for ammonia production in continuous flow. Moreover, it has been demonstrated that the addition of alkali metals to this photocatalyst can boost the photocatalytic activity of this reaction. Thus, this composite material has demonstrated to be among the most efficient photocatalysts in the current state-of-the art for this reaction, as well as very stable under reaction conditions. Considering the large industrial importance of N2 fixation and the mild conditions of pressure and temperature used in the present study, the results of the photo-assisted N2 hydrogenation to ammonia can have a large impact in the area.
Peng, Y. (2021). Hybrid Lead Perovskites as Photocatalysts and Materials for Photo- and Electrocatalytic N2 Reduction [Tesis doctoral]. Universitat Politècnica de València. https://doi.org/10.4995/Thesis/10251/171731
TESIS
Compendio
Huang, Shang-Chieh, and 黃尚頡. "Investigation of photo-stability and photo-oxidation mechanism for colloidal quantum dots." Thesis, 2018. http://ndltd.ncl.edu.tw/handle/jyx729.
Yu, Weilai. "Stability of Photo-Electrochemical Interface for Solar Fuels." Thesis, 2021. https://thesis.library.caltech.edu/14107/1/202104_Weilai_Thesis_Final.pdf.
Photoelectrochemical (PEC) water splitting is a promising approach to convert renewable solar energy to clean hydrogen (H2) fuels in one simple step. Although Ⅲ-Ⅴ semiconductors are attractive candidates as light-absorbers in tandem solar-fuel devices, their long-term stability for the hydrogen-evolution reaction (HER) in either acidic or alkaline aqueous electrolytes needs to be established. Chapter 2-5 of this thesis first aims at revealing the underlying corrosion chemistry for a variety of Ⅲ-Ⅴ semiconductors specifically under the HER conditions, offering a rational understanding towards the stability of semiconductor photoelectrode.
In Chapter 2, we start from p-InP and reveal its susceptibility to cathodic photocorrosion forming metallic In0, which however can be completely mitigated by the presence of Pt catalyst due to kinetic stabilization. We also show that the resulting PEC performance of p-InP/Pt electrodes is sensitive to the changes in surface stoichiometry, whereas an InOx-rich surface developed in KOH caused a substantial degradation in the current density-potential (J-E) behavior. In Chapter 3, we discovered that a non-stoichiometric and As0-rich surface of p-GaAs, resulting from a galvanic corrosion by Pt, led to mid-gap surface states as well as a complete loss in photoactivity. In Chapter 4-5, we demonstrate similar kinetic stabilization applied to both p-InGaP2/Pt and pn+-InGaP2/Pt photocathodes for the HER at both pH 0 and pH 14. Additionally, we found that the corrosion of underlying GaAs substrates for the pn+-InGaP2/Pt photocathodes at positive potentials caused damage of structural integrity as well as instability in electrode performance. Altogether these works underscore the mutual dependence of the physical and electrochemical stability of semiconductor photoelectrodes during the HER, which also need to be considered separately. Moreover, both catalytic kinetics and surface stoichiometry are crucial factors for defining long-term corrosion chemistry for semiconductor photoelectrode.
In Chapter 6-7, we further explore solar fuels beyond H2, namely electrochemical N2-to-NH3 conversion. We first establish a new analytical method to isotopically quantify the concentrations of 15NH3 in aqueous solutions with a high sensitivity and a low limit-of-detection of <1 μM. Further we applied this advanced method to rigorously verify the electrocatalytic activity of a CoMo electrode for reducing N2(g) to NH3. We show that the additional ammonia detected in electrolyte was instead attributed to the corrosion of N impurities present in the CoMo electrode under cathodic bias, thus giving false positive results. These works emphasize the importance of both rigorous product analysis and experiment design in further catalyst development.
Kuo, Yang-Kuao, and 郭養國. "The Stability Control of Semiconductor Photo Lithography in Nano Size." Thesis, 2004. http://ndltd.ncl.edu.tw/handle/24083135967809487005.
國立交通大學
材料科學與工程系所
93
A new reticle is designed that takes advantage of the high value of thermal conductivity of diamond to add a layer of diamond film to the bottom of traditional pellicle-reticle; that is, the new reticle replaces the pellicle with a diamond material. This method may help maintain the future manufacturing process of photo-lithography below 35 nm and can improve the problem of slightly out of shape reticle caused by the long-term effects of light and thermal energy. Exposure dose is one of the most important factors that affects CD (Critical Dimension) bar since it can change the dimension of line-width and white wall. In this work, both line-width and white wall present a linear relationship ( >0.85) with respect to the exposure dose. However, too high or too low of exposure dose would impose the instability of line-width. The reason for exposure dose to affect CD bar is that when absorbing high energy the photo-resist (PR) can produce more severely neutralized reaction as it in contact with developer. Therefore, the higher the exposure dose the smaller is the line-width. Also, CD bar would reveal inhomogeneous phenomenon caused by absorbing high energy via the edge of PR. Due to this reason, increasing the exposure dose intentionally is not an appropriate method to obtain a smaller CD bar. When it comes to using exposure energy to obtain the desirable CD, PR capable of being exposed with higher energy should be considered. If it becomes necessary to obtain much smaller line width, then it is necessary to use PR of better resolution in conjunction with a light source containing a much lower wavelength. But, higher exposure dose would cause the bottom of PR to absorb more reflective energy and make white wall become smaller. On the contrary, if exposure dose becomes too low, PR would not form a pattern due to the fact that the absorption of exposure energy by PR is not strong enough to produce a neutralized reaction when in contact with TMAH (Tetramethylammonium Hydroxide).
Books on the topic "(Photo)stability":
Schuett-Hames, Joanne. Germany Creek photo points and channel stability evaluation, 1990-2000. Olympia, Wash: Washington State Dept. of Ecology, Southwest Regional Office, Water Quality Program, 2000.
Pozhidaeva, Nina. Reversible photo-control of peptide helix content: Adjusting thermal stability of the cis state. 2004.
ALBINI, A., and E. FASINI. DRUGS:PHOTOCHEMISTRY AND PHOTO (Special Publications). Royal Society of Chemistry, 1998.
Book chapters on the topic "(Photo)stability":
YAN, HOH-JIEAR, and ELI M. PEARCE. "Thermal and Photo Stability of Polyarylates." In ACS Symposium Series, 209–23. Washington, D.C.: American Chemical Society, 1985. http://dx.doi.org/10.1021/bk-1985-0282.ch018.
Im, Seongil, Youn-Gyoung Chang, and Jae Kim. "Device Stability and Photo-Excited Charge-Collection Spectroscopy." In SpringerBriefs in Physics, 1–16. Dordrecht: Springer Netherlands, 2013. http://dx.doi.org/10.1007/978-94-007-6392-0_1.
Sandford, Scott A., Partha P. Bera, Timothy J. Lee, Christopher K. Materese, and Michel Nuevo. "Photosynthesis and Photo-Stability of Nucleic Acids in Prebiotic Extraterrestrial Environments." In Photoinduced Phenomena in Nucleic Acids II, 123–64. Cham: Springer International Publishing, 2014. http://dx.doi.org/10.1007/128_2013_499.
Aht-Ong, Duangdao, Chiravoot Pechyen, and Duangduen Atong. "Evaluation of the Influence of Additives on the Mechanical Properties and Photo-Stability of Glass Fiber Reinforced Epoxy Pipes Using Central Composite Design." In Advanced Materials Research, 349–52. Stafa: Trans Tech Publications Ltd., 2007. http://dx.doi.org/10.4028/0-87849-463-4.349.
Sumino, Ken-ichi, Kazuo Asuka, Boping Liu, Masayuki Yamaguchi, Minoru Terano, Takanobu Kawamura, and Koh-hei Nitta. "Influence of polymer morphology on photo-stability of polypropylene/SiO2 nanocomposites." In Studies in Surface Science and Catalysis, 229–32. Elsevier, 2006. http://dx.doi.org/10.1016/s0167-2991(06)80463-5.
Chandran, Senthilkumar, and Srinivasan Manikam. "Optical Properties of Single Crystals." In Optoelectronics. IntechOpen, 2021. http://dx.doi.org/10.5772/intechopen.95607.
Ielo, I., A. M. Cancelliere, A. Arrigo, and G. La Ganga. "Metal-based chromophores for photochemical water oxidation." In Photochemistry, 384–409. Royal Society of Chemistry, 2023. http://dx.doi.org/10.1039/bk9781837672301-00384.
Juvekar, Vinayak, and Hwan Myung Kim. "Two-photon Fluorescent Probes." In Fluorescent Chemosensors, 106–23. The Royal Society of Chemistry, 2023. http://dx.doi.org/10.1039/9781839167324-00106.
Natesan, Subramanian, Nidhi Singh, Victor Hmingthansanga, Pallab Datta, Sai Hanuman Sagar Boddu, and V. Ravichandiran. "Nanoemulsions for the Delivery of Anti-Hypertensive Drugs." In Handbook of Research on Nanoemulsion Applications in Agriculture, Food, Health, and Biomedical Sciences, 378–400. IGI Global, 2022. http://dx.doi.org/10.4018/978-1-7998-8378-4.ch017.
Cetindere, Seda. "BODIPY Dyes in Solar Energy." In Eco-Friendly and Agile Energy Strategies and Policy Development, 119–42. IGI Global, 2022. http://dx.doi.org/10.4018/978-1-7998-9502-2.ch006.
Conference papers on the topic "(Photo)stability":
Bar-Yam, Y., J. D. Joannopoulos, and D. Adler. "Photo-induced degradation and stability in semiconductor devices." In AIP Conference Proceedings Volume 157. AIP, 1987. http://dx.doi.org/10.1063/1.36487.
Sinha, Abhishek Kumar, and Amita Amita. "Transient Stability Improvement of Grid Using Photo-Voltaic Solar Farm." In 2018 International Conference on Intelligent Circuits and Systems (ICICS). IEEE, 2018. http://dx.doi.org/10.1109/icics.2018.00081.
Shi, Yongqiang, David J. Olson, James H. Bechtel, Srinath Kalluri, William H. Steier, Wenshen Wang, Datong Chen, and Harold R. Fetterman. "Photo excitation stability and bias voltage stability of electro-optic polymer modulators for broadband analog transmission systems." In Organic Thin Films for Photonic Applications. Washington, D.C.: Optica Publishing Group, 1995. http://dx.doi.org/10.1364/otfa.1995.wb.8.
Abbas, Sikandar, and Linda Peteanu. "Effects of plasmonic substrates on the photo-stability of organic polymer." In SPIE Nanoscience + Engineering, edited by Artem A. Bakulin, Robert Lovrincic, and Natalie Banerji. SPIE, 2016. http://dx.doi.org/10.1117/12.2238261.
Kusevic, Maja, Arto Maaninen, Jussi Hiltunen, Marianne Hiltunen, Jarkko Tuominen, and Pentti Karioja. "Photo-crosslinkable hybrid material with improved aging stability for integrated optics." In Photonics Europe, edited by Giancarlo C. Righini and Seppo Honkanen. SPIE, 2004. http://dx.doi.org/10.1117/12.545488.
de Andrés, Alicia, Carlos Redondo-Obispo, Esteban Climent-Pascual, Javier Bartolomé-Vilchez, Carlos Zaldo, and Carmen Coya. "Light Induced Ion Migration in Bi-Doped MAPbI3 for Enhanced Photo-Stability." In 2nd nanoGe International Conference on Perovskite Thin Film Photovoltaics and Perovskite Photonics and Optoelectronics. València: Fundació Scito, 2019. http://dx.doi.org/10.29363/nanoge.nipho.2020.051.
Ravichandran, Sharon, S. G. Bharathi Dasan, and R. P. Kumudini Devi. "Small signal stability analysis of grid connected Photo Voltaic distributed generator system." In 2011 International Conference on Power and Energy Systems (ICPS). IEEE, 2011. http://dx.doi.org/10.1109/icpes.2011.6156620.
Sarkas, H. W., S. R. Flom, F. J. Bartoli, and Z. H. Kafafi. "Enhanced Photo-oxidative Stability and Nonlinear Optical Response of a Dialkoxy-Substituted Poly-Phenylenevinylene through C60 Addition." In Organic Thin Films for Photonic Applications. Washington, D.C.: Optica Publishing Group, 1995. http://dx.doi.org/10.1364/otfa.1995.md.34.
Hossain, Istiaque, Liang Zhang, Ranjith Kottokkaran, Mohamed El-Henawey, Pranav Joshi, Max Noack, and Vikram Dalal. "Influence of Grain Size and Interfaces on Photo-Stability of Perovskite Solar Cells." In 2017 IEEE 44th Photovoltaic Specialists Conference (PVSC). IEEE, 2017. http://dx.doi.org/10.1109/pvsc.2017.8366303.
Kaneki, Takayuki, Yu Shoji, Chika Hibino, and Hitoshi Araki. "Negative-Tone Photo-Definable Polyimide with High Thermal Stability and Thick Film Processability." In 2023 24th European Microelectronics and Packaging Conference & Exhibition (EMPC). IEEE, 2023. http://dx.doi.org/10.23919/empc55870.2023.10418340.
Reports on the topic "(Photo)stability":
Christopher, David A., and Avihai Danon. Plant Adaptation to Light Stress: Genetic Regulatory Mechanisms. United States Department of Agriculture, May 2004. http://dx.doi.org/10.32747/2004.7586534.bard.