1994
DOI: 10.1063/1.112530
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Self-holding photochromic polymer Mach–Zehnder optical switch

Abstract: Record-low propagation losses of 154dB/cm for substrate-type W1 photonic crystal waveguides by means of hole shape engineering Appl. Phys. Lett. 101, 131108 (2012) Electro-optic polymer/TiO2 multilayer slot waveguide modulators Appl. Phys. Lett. 101, 123509 (2012) Efficient broadband energy transfer via momentum matching at hybrid junctions of guided-waves Appl. Phys. Lett. 101, 123115 (2012) Silicon waveguides and devices for the mid-infrared Appl.

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Cited by 80 publications
(42 citation statements)
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“…The typical refractive index difference between the core and cladding for a single-mode waveguide is known to be about 0.3%. [13] Hence, the large photoinduced refractive index change (A 0.01) in the present results demonstrates that it is possible to make a thermostable optical waveguide device utilizing an alicyclic polyimide film containing phenylazide as a photoreactive electron-donor generator.…”
Section: Resultsmentioning
confidence: 84%
“…The typical refractive index difference between the core and cladding for a single-mode waveguide is known to be about 0.3%. [13] Hence, the large photoinduced refractive index change (A 0.01) in the present results demonstrates that it is possible to make a thermostable optical waveguide device utilizing an alicyclic polyimide film containing phenylazide as a photoreactive electron-donor generator.…”
Section: Resultsmentioning
confidence: 84%
“…a photocyclization and photocycloreversion reaction. Besides color, photochromic molecules or compounds can also change refractive index and redox potentials or other properties digitally between two states [126][127][128]. Furthermore, molecular crystals based on photochromic compounds can exhibit light-induced rapid and reversible macroscopic changes in shape and size.…”
Section: Photochromic Conjugatesmentioning
confidence: 99%
“…Relative coloring quantum yields for silsesquioxane film and polysiloxane solution samples, I 0 N U AeB , were calculated from the slopes, e A , C 0 /C B (v) (=100/Conv(C)) values as shown in Tab. 5. The values for the samples having methyl-substituted dithienylethene (PMC, MMC, SMC) were larger than those for the samples having methoxy-substituted dithienylethene (POC, MOC, SOC).…”
Section: Photoisomerizationmentioning
confidence: 94%
“…5. The activation energy values obtained from the slope were 0 -1 and 1 -3 kcal/ mol for coloring and bleaching processes, respectively.…”
Section: Photoisomerizationmentioning
confidence: 99%