During the last years, the phenomenon of ultra-fast fashion, specifically the retailer SHEIN, has grown massively and became popular among young female consumers. SHEIN is also known for their polluting productions, bad working conditions, violating (social) sustainable laws and stealing designs from other designers. Still, this does not seem to impact the consumers' attraction towards clothes from SHEIN. The purpose of this research is to investigate the appeal of SHEIN for young female consumers. This research employs qualitative research methods to examine the empirical material in relation to three prominent theories: Hawkin Stern's "impulse buying theory", John Schouten and James McAlexander's "consumption subculture theory", and Russel Belk's "extended self theory". The empirical material for this research was obtained through 10 semi-structured interviews. Given the limited existing research on the phenomenon of ultra-fast fashion, an exploratory research design was chosen to investigate this topic. The empirical findings of this research can be divided into three different themes: The contradicting appreciation, The irrelevance of socioeconomic status and The SHEIN consumption subculture. The central theme lies in SHEIN’s big collection and the respondents’ appreciation for it. Another theme shows that there is not a clear pattern found between the socioeconomic status of the respondents and their SHEIN consumption. Lastly, around the consumption of SHEIN clothes, a consumption subculture is formed. This research is believed to contribute to the under researched area of ultra-fast fashion, as well as further develop and question the selective theories.

This thesis consists of three main objectives: fundamental and literature review of EV batteries, experimental development, and validation of two liquid cooling battery modules, thermal modeling and comparison of the inter-cell cooling battery module. / The traditional vehicles with internal combustion engine have resulted in severe environmental pollution, which motivates the development of electric vehicles and hybrid electric vehicles. Due to a low energy density and long refueling time of the battery pack, it is still hard for electric vehicles and hybrid electric vehicles to be widely accepted by the consumers. As the batteries with a better ultra-fast charging capability are massively produced, the range anxiety issue is somewhat alleviated. During a charging with large current magnitude, the battery generally has a great amount of heat generation and evident temperature rise. Therefore, a thermal management system is necessary to effectively dissipate the battery loss and minimize the degradation mechanisms caused by extreme temperature. The motivation of this thesis is to study the discipline of the battery thermal management system as an application for electric vehicles. The design methodologies are presented in both experiment test and numerical simulation. For the comparative study between active liquid cooling methods for a lithium-ion battery module using experimental techniques, two battery modules with three Kokam Nickel Manganese Cobalt battery cells connected in parallel are developed. One has liquid coolant flowing along the edge of the model, and another with liquid coolant flowing between the cells. Several characterization tests, including thermal resistance tests, fast charging tests up to 5C, and drive cycle tests are designed and performed on the battery module. The inter-cell cooling module has a lower peak temperature rise and faster thermal response compared to the edge cooling module, i.e., 4.1⁰C peak temperature rise under 5C charging for inter-cell cooling method and 14.2⁰C for edge cooling method. The thermal models built in ANSYS represent the numerical simulation of the inter-cell cooling module as a comparison with the experiment. A cell loss model is developed to calculate the battery heat generation rate under ultra-fast charging tests and a road trip test, which are further adopted as the inputs to the thermal models. The simulation of the 5C ultra-fast charging test gives the peak temperature rise just 0.47⁰C lower than the experimental measurement, it indicates that the FEA thermal models can provide an accurate temperature prediction of the battery module. / Thesis / Master of Applied Science (MASc) / With a demanding market of electric vehicles, battery technologies have grown rapidly in recent years. Among all the battery research topics, the development of ultra-fast charging, that can fully charge the battery pack within 15 minutes, is the most promising direction to address the range anxiety and improve the social acceptance of electric vehicles. Nevertheless, the application of ultra-fast charging has many challenges. In particular, an efficient thermal management system is significant to guarantee the safety and prolong the service life of the battery pack. This thesis contributes to study the fundamentals of the battery field, and design liquid cooling systems to observe the thermal behavior of a battery prototype module under fast charging and general use. FEA thermal modeling of the battery module is developed to provide a guide for further test validation.

To our knowledge this is the first comprehensive study of laser-induced effects generated at intermediate distances using self-channeled femtosecond laser pulses. Studies performed were made both experimentally and theoretically with the use of novel modeling techniques. Peak laser pulse powers above 3 GW allow beam propagation without divergence for up to several kilometers. In this regime, experiments were performed at 30 meters from the laser system in a custom propagation and target range, utilizing the Laser Plasma Laboratory's Terawatt laser system. Experiments included investigations of laser ablation; electromagnetic pulsed (EMP) radiation generation over the 1-18 GHz region; shockwave formation in air and solid media; optical coupling of channeled pulses into transparent media; and, conservation of energy in these interactions. The use of bursts of femtosecond pulses was found to increase the ablation rate significantly over single-pulse ablation in both air and vacuum. EMP generation from near-field focused and distance-propagated pulses was investigated. Field strengths upwards of 400 V/m/[Lambda] for vacuum focusing and 25 V/m/[Lambda] for self-channeled pulses were observed. The total field strengths over 1-18 GHz measured at distance surpassed 12 kV/m. Shockwaves generated in transparent media at 30 meters were observed as a function of time. It was found that the interaction conditions control the formation and propagation of the shock fronts into the medium. Due to the processes involved in self-channeling, significant fractions of the laser pulse were coupled into the target materials, resulting in internal optical and exit-surface damage. Basic estimations on the conservation of energy in the interaction are presented. The results of the experiments are supported by hydrodynamic plasma physics code and acoustic modeling.

From space exploration and advanced aircraft to next generation weapons, achieving hypersonic speed is becoming increasingly important across a range of research domains. The immense challenge associated with this goal involves the development of suitable materials and systems for the different components of a hypersonic vehicle, each of which must have the inherent capability to resist extreme temperatures, high thermal shock due to high heat flux, and high oxidation and ablation. First, the ultra-high temperature ceramic (UHTC) zirconium diboride or ZrB2 was sintered by ultra-fast high temperature sintering (UHS). The UHS process was optimized and the sintering parameters for ZrB2 and other UHTCs were studied. ZrB2 is an ultra-high temperature ceramic (UHTC) with a very high melting point; thus, its densification is difficult, energy intensive, and time-consuming. Commercial ZrB2 powders were rapidly densified via UHS to >90% relative density within 60 second in vacuum without pressure. The effect of sintering time on densification and final grain size were studied. An innovative process for manufacturing bulk UHTC materials was studied and is detailed herein. Second, the work function (W_f) of electron emitting materials was reduced to improved performance. A reduction of W_f in multicomponent hexaborides was achieved by doping with highly electropositive Ba, which enhances electron emission. Single-phase bulk multicomponent polycrystalline hexaborides of La0.5Ba0.5B6, Ce0.5Ba0.5B6, and BaB6 powders were first synthesized and then densified by UHS sintering. W_f measurements were obtained by Kelvin probe force microscopy. Ba-substitution was found to lower W_f (~25%) in synthesized multicomponent hexaborides. The specific techniques required to engineer the W_f of these materials are also provided herein. Finally, combining low W_f materials with UHTCs was explored for thin film systems for the exterior surface of hypersonic vehicles. The thin films of CeB6, a low W_f material, was deposited on sintered ZrB2 by RF-sputtering and single crystalline SrTiO3 (STO) substrates. Epitaxial thin films of SrHfO3 (SHO) were also deposited on (100), (110) and (111) STO substrates at 600°C. X-ray diffraction (XRD) results confirmed the formation of epitaxial layer, and reciprocal space mapping (RSM) was used to characterize film's mosaicity / texture on different substrates. XRD and RSM data demonstrated that the most favorable film growth direction was (110). As detailed herein, an inexpensive thin film production process, RF-sputtering, was exploited to manufacture various epitaxial and non-epitaxial layers of low W_f materials on UHTC and single-crystal substrates for hypersonic vehicles. To summarize, a range of bulk UHTCs and low W_f materials were prepared by UHS, and various thin films of low W_f material were produced on UHTC. Thereafter, the properties of synthesized materials were studied to develop new material systems for hypersonic applications. The findings from this research shed light on the development of suitable materials for implementation of electron transpiration cooling for hypersonic vehicle development. / Doctor of Philosophy / Rapid sintering of ultra-high temperature ceramics (UHTCs) and synthesis of low work-function electron emitting materials have been performed by ultra-fast high temperature sintering technique (UHS). Sintering of UHTCs is a difficult process, due to their high melting temperature, presence of covalent bond, and slower diffusion coefficient. A long sintering duration is used to achieve a high relative density along with adding sintering aid, using fine powder (produced by milling), and utilizing pressure (such as field assisted sintering and hot-pressing technology) during sintering. Synthesis and densification of multicomponent hexaboride is difficult, involves multi-steps and complicated processes. These long and complicated processes not only prolong development of new materials but also cause chemical wastes. To overcome all the aforementioned processing issues, an advanced processing technique, UHS, is used and densified pure and commercially available UHTCs to >90% within 60 second without applying sintering aid, powder milling, and pressure. The outcome of this research demonstrates the potential for a simple, cost-effective, fast, and adjustable processes, UHS, to develop a wide range of bulk UHTCs and other technical ceramics, and it gives new insight into the mechanisms of rapid sintering of UHTCs by rapid heating. The first detailed studies (experimental report) on rapid sintering of ZrB2 (and other UHTCs) by UHS technique and a through characterizations of the UHS sintered sample were performed to understand rapid sintering mechanism and how the processing effects the microstructure and properties of UHS ZrB2. The rapid microstructural evolution during the UHS sintering is investigated at 10, 30, and 60 second sintering interval. The UHS technique enables a heating rate of 103 - 104 °C/min and reaches a sintering temperature of 2600 °C in 30 seconds. Microstructural analysis was conducted on polished sample surfaces by using ImageJ software (National Institutes of Health, version 1.53e), measuring the grain size perpendicular to two diagonals of each grain. A comparison of grain size from sample center and periphery showed a homogeneous microstructure after sintering. Furthermore, the rapid sintering did not change/effect crystallinity, boron to metal stoichiometry, and grain boundary elemental composition as observed by XRD and EDS analysis. Additional characterization of the UHS sintered ZrB2 shows a hardness and elastic modulus of 30 GPa and 412 GPa respectively by nanoindentation method. Finally, the oxidation test at 1100 °C in isothermal condition showed a weight gain of 1.4% in air. The low work-function (W_f) materials are famous for electron emitting applications like electron guns for scanning electron microscopy. DFT simulation predicts the W_f of the widely used electron emitters (such as LaB6 and CeB6) can be reduced by changing their compositions, which increase electron generation efficiency of those materials. Previously, those materials were synthesized by long processes that involved multiple processing steps, which required expensive starting materials and yielded chemical wastes. The advantages of rapid sintering technique, UHS, had been exploited to synthesize low work function electron emitting materials. Single-phase bulk polycrystalline hexaborides were produced by using electrically powered UHS technique using a vacuum atmosphere. A reaction synthesis route: B4C reduction technique was first used to form pure phase hexaboride. Then, the synthesized compositions were densified to ~90% theoretical density in 180 seconds by UHS densification. After UHS sintering, XRD analysis confirmed the presence of a phase pure cubic BaB6, La0.5Ba0.5B6, and Ce0.5Ba0.5B6. Additional analyses were conducted to determine an optimum reaction temperature 1500 and 2100 °C for the formation BaB6 and multi-component hexaborides. Microstructural analyses were conducted to observe both reaction-synthesized and densified products. EDS compositional analysis and elemental mapping revealed a stoichiometric reaction product with homogeneous metal cation and boron distributions. The W_f of BaB6, La0.5Ba0.5B6, and Ce0.5Ba0.5B6 was determined to be 1.95 ± 0.1, 2.05 ± 0.1 and 2.0 ± 0.1 eV, respectively. The addition of BaB6 in La0.5Ba0.5B6, and Ce0.5Ba0.5B6 resulted in a 25% decrease in W_f for LaB6 from 2.7 ± 0.1 to 2.00 ± 0.1 eV and a 23% decrease in W_f for CeB6 from 2.68 ± 0.08 to 2.05 ± 0.1 eV. Ba substitution is shown to be a general method for lowering W_f in a variety of multicomponent hexaborides. Finally, the polycrystalline thin films of CeB6, a low W_f material, was deposited on sintered ZrB2 by RF-sputtering technique. Additionally, epitaxial thin films of SrHfO3 (SHO) were also deposited on (100), (110) and (111) STO single crystalline substrates. Both types of thin films were deposited at 600 °C temperature and at a vacuum pressure of 10-3 Torr. After deposition of the SHO films, X-ray diffraction (XRD) was conducted to confirm the formation of epitaxial layer, and reciprocal space mapping (RSM) was used to characterize film's mosaicity / texture on different substrates. XRD and RSM data demonstrated that the most favorable film growth direction was (110). The XRD of the CeB6 film showed highly crystalline film was formed. For both the films, a detailed microstructural analysis was performed by scanning electron microscopy and film smoothness was characterized by atomic force microscopy method. As detailed herein, an inexpensive thin film production process, RF-sputtering, was exploited to manufacture various epitaxial and non-epitaxial layers of low W_f materials on UHTC and single-crystal substrates for hypersonic vehicles applications.

Ultra-fast charging of electric vehicles will soon be available to charge the batteries in less than 15 minutes to 80% state of charge. However, very few studies of batteries under these conditions exist. To design a battery pack with ultra-fast charging in mind, more information about batteries is needed, both electrically and thermally. In this thesis, the performance of three specific commercial lithium-ion batteries during ultra-fast charging is investigated and their thermal behaviour is simulated for use in the battery pack design process. The cells are charged at 1C to 6C current rates, or as high as 10C, and the surface temperature of each cell is measured. The loss calculated from the charging tests are used in a thermal analysis of the three batteries using finite element analysis. The batteries are modeled in a simple cooling apparatus to determine their thermal management requirements in a pack, i.e., how effectively must the heat be removed from the cells to obtain a specific temperature in a pack. Test results show that ultra-fast charging is possible with very little loss; but, it is dependent on the battery. The analysis illustrates important trade-offs between the battery type, charge rate, and the thermal management system. This thesis presents a holistic view to the study of the batteries for eventual use in the design of a battery pack. The thermal performance of the batteries is equally important as their electrical (charge) performance. It also attempts to justify the observed behaviour of the batteries by their underlying chemical behaviour. The work here can be used as a jumping-off point for further work on the ultra-fast charging of batteries or the design of a battery pack. / Thesis / Master of Applied Science (MASc) / Ultra-fast charging of electric vehicles, i.e., fully charging the vehicle in less than 15 minutes, will soon be more available. However, literature on the ultra-fast charging of the batteries used in these vehicles is limited. It is not widely known whether the batteries can effectively achieve ultra-fast charging or how the batteries behave under these conditions. Charging batteries this fast means that the battery cells will heat up. The temperature of the cell greatly impacts its longevity and safety. The thesis attempts to address these questions by studying three commercial lithium-ion batteries, selected for specific characteristics, that show potential for ultra-fast charging. The batteries are charged at different rates to ultra-fast charging levels and the charge performance at each rate is determined. The temperature of the batteries is simulated with different cooling systems to determine how effectively must heat be removed from the batteries to maintain the cells at a specific temperature.

A técnica de eco de fótons com luz temporalmente incoerente (EFLI) foi utilizada neste trabalho para a medida do tempo de relaxação transversal T2 do Iodeto de 3-3´-Dietiloxadicarbonocianina (DODCI) como função da temperatura. Nestes experimentos foi utilizado um laser de corante de banda larga, bombeado pelo 2&#176 harmônico de um laser de Nd+3 : YAG Q-switched. Este laser operou com os corantes Kiton Red 620 e rodamina 640, cujos máximos do espectro de emissão estão respectivamente em 598 e 610 nm. O tempo de relaxação T2, que é proporcional ao inverso da largura de linha homogênea, segue uma dependência funcional com a temperatura do tipo T-1,9. Encontramos o valor de T2 entre 0 e 30fs para &#955 = 598nm e entre 30 e 590fs para &#955 = 610nm, no intervalo de temperatura entre 300 e 60k. Os perfis das medidas de EFLI podem ser descritos por um modelo baseado num sistema quântico de dois níveis / The photon echo with incoherent light technique (EFLI) has been used in this work for the measurement of the transverse relaxation time T2 in 3-3´-Dietiloxadicarboncyanine Iodide (DODCI) as a function of the temperature. A broad-band dye laser, pumped by the second harmonic of a Q-switched Nd+3 : YAG laser, was used in this experiment. The laser used Kiton Red 620 and rodamine 640 dyes, whose maxima output power are respectively around 598 and 610nm. The relaxation time T2 , which is inversely proportional to the homogeneous linewidth, depends on the temperature according to a T-1,9 Law. We found the value of T2 ranging from 0 to 30fs at 598nm and from 30 to 590fs at 610nm in the temperature range between 300 and 60K. The EFLI profiles can be described by means of a two-level quantum system model

"There is plenty of room at the bottom." This bold and prophetic statement from Nobel laureate Richard Feynman back in 1950s at Cal Tech launched the Nano Age and predicted, quite accurately, the explosion in nanoscience and nanotechnology. Now this is a fast developing area in both science and technology. Many think this would bring the greatest technological revolution in the history of mankind. To understand electronic and optical properties of nanostructures, the following problems have been studied. In particular, intensity of mid-infrared light transmitted through a metallic diffraction grating has been theoretically studied. It has been shown that for s-polarized light the enhancement of the transmitted light is much stronger than for p-polarized light. By tuning the parameters of the diffraction grating enhancement can be increased by a few orders of magnitude. The spatial distribution of the transmitted light is highly nonuniform with very sharp peaks, which have the spatial widths about 10 nm. Furthermore, under the ultra fast response in nanostructures, the following two related goals have been proved: (a) the two-photon coherent control allows one to dynamically control electron emission from randomly rough surfaces, which is localized within a few nanometers. (b) the photoelectron emission from metal nanostructures in the strong-field (quasistationary) regime allows coherent control with extremely high contrast, suitable for nanoelectronics applications. To investigate the electron transport properties of two dimensional carbon called graphene, a localization of an electron in a graphene quantum dot with a sharp boundary has been considered. It has been found that if the parameters of the confinement potential satisfy a special condition then the electron can be strongly localized in such quantum dot. Also the energy spectra of an electron in a graphene quantum ring has been analyzed. Furthermore, it has been shown that in a double dot system some energy states becomes strongly localized with an infinite trapping time. Such states are achieved only at one value of the inter-dot separation. Also a periodic array of quantum dots in graphene have been considered. In this case the states with infinitely large trapping time are realized at all values of inter-dot separation smaller than some critical value.

A técnica de eco de fótons com luz temporalmente incoerente (EFLI) foi utilizada neste trabalho para a medida do tempo de relaxação transversal T2 do Iodeto de 3-3´-Dietiloxadicarbonocianina (DODCI) como função da temperatura. Nestes experimentos foi utilizado um laser de corante de banda larga, bombeado pelo 2&#176 harmônico de um laser de Nd+3 : YAG Q-switched. Este laser operou com os corantes Kiton Red 620 e rodamina 640, cujos máximos do espectro de emissão estão respectivamente em 598 e 610 nm. O tempo de relaxação T2, que é proporcional ao inverso da largura de linha homogênea, segue uma dependência funcional com a temperatura do tipo T-1,9. Encontramos o valor de T2 entre 0 e 30fs para &#955 = 598nm e entre 30 e 590fs para &#955 = 610nm, no intervalo de temperatura entre 300 e 60k. Os perfis das medidas de EFLI podem ser descritos por um modelo baseado num sistema quântico de dois níveis / The photon echo with incoherent light technique (EFLI) has been used in this work for the measurement of the transverse relaxation time T2 in 3-3´-Dietiloxadicarboncyanine Iodide (DODCI) as a function of the temperature. A broad-band dye laser, pumped by the second harmonic of a Q-switched Nd+3 : YAG laser, was used in this experiment. The laser used Kiton Red 620 and rodamine 640 dyes, whose maxima output power are respectively around 598 and 610nm. The relaxation time T2 , which is inversely proportional to the homogeneous linewidth, depends on the temperature according to a T-1,9 Law. We found the value of T2 ranging from 0 to 30fs at 598nm and from 30 to 590fs at 610nm in the temperature range between 300 and 60K. The EFLI profiles can be described by means of a two-level quantum system model

Nous avons appliqué notre interface QM/MM pour modéliser les propriétés photophysiques et photochimiques du chromophore rétinal dans plusieurs environnements.Nous avons commencé par montrer que la méthylation du squelette carbonné du rétinal, qui transforme une photochimie lente en un processus ultra-rapide, comme dans une protéine, dans une solution de méthanol, modifie l’interaction entre les états excités du rétinal, et favorise la formation d’une espèce transitoire réactive. Nous avons ensuite étudié l’effet direct de l’environnement dans le cas de mimiques de la rhodopsine, où des mutations ponctuelles de quelques acides aminés donnent des systèmes qui absorbent sur toute la gamme du visible. En combinaison avec la spectroscopie pompe-sonde ultra-rapide, notre méthode a montré que le potentiel électrostatique autour du rétinal peut affecter la forme des surfaces d’énergies potentielles excitées, et peut moduler le temps de vie de l’état excité ainsi que le lieu de photo-isomérisation. Ensuite, nous avons montré que l’état de protonation standard des acides aminés proches du rétinal dans la bacteriorhodopsine mènent à une surestimation de l’énergie d’absorption,alors que la protonation du résidu Asp212 donne des résultats plus précis ; nous souhaitons maintenant valider ce modèle par le calcule des propriétés de fluorescence et de temps de vie de l’état excité. Enfin, nous avons modélisé la photophysique de la base de Schiff non-protonée d’un pigment UV, où une photochimie originale, et non encore documentée, a lieu, impliquant notamment un état doublement excité. Ces études ont montré la robustesse de notre potentiel QM/MM pour modéliser une large gamme d’environnements. / We have used our QM/MM interface to model the photochemical and photophysical properties of the retinal chromophore in several environments.First, we proved that methylation of the retinal backbone, which converts a slow photochemistry to an ultra-fast protein-like behaviour in methanol solution, modifies the interplay between the retinal excited states, favouring the formation of a photo-active transient intermediate. Then, we have studied the direct effect of the environment in the case of rhodopsin mimics, where point mutations of a few amino-acids lead to systems that can absorb in the wide visible range. Combined with ultra-fast pump-probe spectroscopy, our method has shown that the electrostatic potential around the retinal can affect the shape of the excited potential energy surface, and is able to tune the excited state lifetime as well as the location of the photoisomerization. Next, we showed that the currently accepted protonation state of amino-acids in the vicinity of the retinal in bacteriorhodopsin leads to a strongly blue shifted absorption, while the protonation of Asp212 leads to accurate results; we now aim toward a validation of this protonation by computation of fluorescence and excited state lifetime. Finally, we have modeled the photophysics of the unprotonated Schiff base in a UV-pigment, where an original an previously unreported photochemistry takes place, especially with the direct involvement of a doubly excited state. These studies have shown the reliability of our QM/MM potential for modeling a wide range of different environments.

Nous nous intéressons au développement ainsi qu’à la modélisation théorique de techniques de spectroscopie optique de champ lointain capables de coupler résolutions spatiale et temporelle grâce à l’utilisation de faisceaux d'excitation mis en forme spatialement. Nous établissons, théoriquement et expérimentalement, que dans une expérience de mélange de quatre ondes réalisée avec des faisceaux de Laguerre-Gauss, la charge totale du moment orbital est conservée. Nous montrons comment cette propriété peut être mise à profit pour travailler en géométrie colinéaire dans le but d’améliorer la résolution spatiale des expériences. Dans une deuxième partie, nous présentons une technique de spectroscopie « pompe-sonde » résolue spatialement que nous avons conçue et développée : l’imagerie temporelle est obtenue via la détection interférométrique des variations d’indice d’un matériau vues par une sonde étendue et consécutives à l’excitation par une impulsion pompe focalisée à la limite de diffraction. Nos modélisations démontre d’un tel montage associé à l’emploi d’une impulsion pompe modulée spatialement doit permettre, grâce au battement entre les fréquences spatiales des inhomogénéités de l’échantillon et de la modulation spatiale de l’excitation, de dépasser la limite de Rayleigh. / This work focuses on developing and modelling far-field spectroscopic methods that couple spatial and time resolutions by using beam-shaping. In a first part, we demonstrate, theoretically and experimentally, that generating a signal in a four-wave mixing experiment performed with Laguerre-Gauss beams, implies the conservation of the total charge of the orbital momentum. We show that this specificity can be used to perform experiments with collinear beams in order to improve spatial resolution. In a second part, we present a time- and spatially-resolved pump-probe technique of our own design: time-resolved imaging is obtained by the interferometric detection of variations in the refraction index of a material, undergone by a wide probe and induced by a diffraction-limited pump-pulse. Improving such an experiment set-up with a spatially-modulated pump-pulse should enable, thanks to the beating between spatial frequencies of sample inhomogeneities and the excitation spatial-modulation, to increase spatial resolution go the Rayleigh criterion.