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4 protocols using gold etchant

1

Plasmonic DNA Sensor Fabrication

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All solutions were prepared with deionized, ultrafiltered water (Fisher Scientific). The following reagents were used as received: 4-(2-hydroxyethyl)-1-piperazineethanesulfonic acid (HEPES) and sodium perchlorate from Alfa Aesar; tris(2-carboxyethyl) phosphine hydrochloride (TCEP), mercaptohexanol, gold etchant, and chromium etchant from Sigma-Aldrich. Methylene blue (MB)-conjugated DNA was purchased from Biosearch Technologies (Novato, CA), purified by RP-HPLC. All other DNA sequences (listed in Table S-1) were obtained from Integrated DNA Technologies (IDT; Coralville, Iowa), with purity confirmed by mass spectrometry. Gold-sputtered glass slides (100 nm Au with 5 nm Cr adhesion layer) were purchased from Deposition Research Lab (St. Charles, MO), with dimensions of 1.0 in. × 3.0 in. × 0.44 in. (width, length, thickness). AZ 40XT (positive photoresist) and AZ 300 MIF developer was obtained from MicroChemicals GmbH. Polydimethylsiloxane (PDMS) was purchased from Dow Corning, and dimethyl sulfoxide (DMSO) was purchased from VWR/Anachemia.
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2

Transfer and Isolation of Graphene Nanoribbons

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The procedure to transfer the films, we employed a technique which we have reported previously17 (link): After the CVD growth of the GNRs, a thin layer of poly(methyl methacrylate) (PMMA) was spun onto the GNR/gold/mica stack which provided additional mechanical stability and facilitated the transfer of intact films over a large area. Carefully, the resulting stack was floated on concentrated HF for several hours to delaminate the PMMA/GNR/gold film from the mica slab. After the delamination was complete, the gold was etched away in a gold etchant (Sigma-Aldrich). We then transferred the PMMA/GNR film to the target substrate with Au electrodes. To dissolve the PMMA, the PMMA/GNR/substrate stack was immersed in an acetone bath. Finally, we rinsed the chip with isopropanol and dry blow the GNR film.
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3

Fabrication of Plasmonic Au Nanodisk Array

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A sapphire wafer (University wafer) was spin-coated with poly(methyl methacrylate) resist (MicroChem, 950 PMMA C4) at 3000 r.p.m. for 60 s, followed by thermal curing on a hot plate at 180 °C for 15 min. After a 20-nm-thick Au layer was sputtered on the electron-beam resist to prevent electrons from piling up, a nanohole array (250 nm diameter and 500 nm period) was patterned via electron-beam lithography (VISTEC, EBPG5000+) at 100 KeV beam energy and 1000 μC/cm2 exposure dose. After removal of Au in gold etchant (Sigma-Aldrich) and developing with a solution of MIBK:IPA (1:3) for 90 s, 3-nm Ti and 200-nm Au film were then directionally deposited on the patterned substrate using electron-beam evaporator (CHA, SEC 600). After a lift-off process in acetone and an oxygen plasma cleaning (STS, 320PC) at 100 W for 30 s to remove resist residue, the resultant Au nanodisk array was coated with an Al2O3 film using ALD (Cambridge Nano Tech Inc., Savannah) at a typical deposition rate of 1 Å per cycle at 250 °C, followed by conformal deposition of a 400 nm Au film using an electron-beam evaporator (CHA, SEC 600) with a planetary fixture. Finally, the structures were planarized via ion milling (Intlvac, Nanoquest) with an Ar beam of 130 mA and 36 V incident at 10º from the horizontal plane.
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4

Fabrication of Optical Fiber-Based Sensors

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All materials used in this study were purchased as follows without any purification. Optical fibre with square-shaped silica core (FP150QMT, Thorlabs), gold (Au, 99.99%, TAEWON SCIENTIFIC), chromium (Cr, CR-090010, 99.9%, Nilaco), nickel (Ni, NI-311165, 99.9%, Nilaco), IGZO sputtering target (In2O3: Ga2O3: ZnO = 1: 1: 1 in atom%, 99.99%, Advanced Engineering Materials), Au etchant (Gold Etchant, Sigma Aldrich), Cr etchant (CR-7, KMG Electronic Chemicals), Ni etchant (Nickel Etchants, TRANSENE), Al2O3 etchant (Aluminium Etch ANPE 80/5/5/10 Microchem), IGZO etchant (HCl, 35%, Wako), Positive photoresist (AZ GXR 601, AZ Electronic Materials), Developer (AZ 300 MIF Developer, Merck).
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