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3 protocols using pmma a4

1

PMMA Thin Film Deposition on Silicon

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The substrate used was a standard 4-inch (100) silicon wafer coated with a 0.5 μm thermally grown silicon dioxide layer. First, the wafer was cleaved into 1 cm × 1 cm pieces, then cleaned by sequential sonication baths in acetone and 2-propanol (both purchased from Sigma-Aldrich, St. Louis, MO, USA). The samples were rinsed under deionized water flow and dried out under nitrogen gas flow. A thin layer of PMMA A4 (950 kDa, in solvent anisole, MicroChem, Berlin, Germany) was spun for 30 s at 4000 rpm using a semiautomatic spinner DELTA 80T (SUSS MicroTec Corp, Garching, Germany); finally, the samples were baked on a hotplate for 90 s at 180 °C to remove anisole solvent. The thickness of the PMMA layer was measured with an Alpha-Step P6 profilometer (KLA-Tencor Corporation, Milpitas, CA, USA).
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2

Fabrication of Ti/Au Thin Film Patterns on Si and Optical Fiber Substrates

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For the Si substrate sample, a 1 μm of SiO2 film was grown on a Si substrate through thermal oxidation. The SiO2/Si substrate was spin-coated with poly(methyl methacrylate) (PMMA A4, MicroChem) and was patterned using e-beam lithography (e-line, Raith). Then, a 3 nm/60 nm of Ti/Au film was deposited on the substrate using e-beam evaporation (Denton Vacuum Explorer 14, Denton Vacuum). Here, the Ti was used to enhance the adhesion between the Au and SiO2 films. Lastly, the Ti/Au film on the poly(methyl methacrylate) was lifted-off in a solvent stripper (Remover PG, MicroChem). The thickness of the Ti/Au film was measured to be approximately 68 nm using a profilometer (Alpha step 200, Tencor). For the optical fiber sample, a single-mode optical fiber (SMF-28, Corning) was cleaved, so that the fiber end-face was perpendicular to the waveguide direction. The fiber end-face was cleaned by acetone, isopropyl alcohol, and deionized water followed by nitrogen blow. A 3 nm/60 nm of Ti/Au film was deposited on the fiber end-face using e-beam evaporation. The Ti/Au film on the fiber end-face was patterned to the square and rectangular nanopatch array using FIB lithography (GAIA3, Tescan). Note that the Ti/Au films for both optical fiber sample and Si substrate sample were deposited in the same chamber at the same time.
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3

Fabrication of Glucose Sensing Hydrogels

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The following chemicals
were supplied by Sigma-Aldrich (now MERCK): phosphate buffered saline
(PBS), N,N′-diisopropylcarbodiimide
(DIC), 1-hydroxybenzotriazole (HOBt), Anthraquinone-2-carboxylic acid
(AQCA), d-glucose (GLU), PEG-diacrylate Mn575 (PEGDA), pentaerythritol
tetraacrylate, diphenyl(2,4,6-trimethylbenzoyl)phosphine oxide (DTPO),
agar (A1296 powder), tetrakis(dimethylamido) hafnium(IV), glucose
oxidase (GOX; G2133), N,N-diethylhydroxylamine
(DEHA), sodium l-lactate (LAC), and tetramethylammonium hydroxide
(TMAH). Dimethyl sulfoxide (DMSO), hydrogen peroxide (H2O2), and sulfuric acid were supplied by Biolab. N-Methyl-2-pyrrolidone (NMP), acetone, and 2-isopropanol
(IPA) were supplied by J.T Baker. LOR5A, SF15, PMMA A4, and MMA el6
were supplied by Microchem (now Kayaku Advanced Materials). Lactate
oxidase was from A.G Scientific. Hexamethyldisilazane (HMDS), AZ1505,
and AZ4562 were supplied by Microchemicals. (3-Aminopropyl)-dimethyl-ethoxysilane
was supplied by Gelest. SOI and Si wafers were supplied by SOITEC
and University Wafers (device layer 50 nm 10 Ω per cm, BOX 150
nm, handle 725 μm, 10 Ω per cm, both handle and device
layers were ⟨0-0-1⟩).
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