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7 protocols using agnws

1

Synthesis of Graphene on Ag Nanowires

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First, a 0.5 wt.% solution of commercially available Ag NWs (Sigma Aldrich, diameter: 60 nm and length: 10 μm) in isopropyl alcohol was spin-coated onto a hydrophilic-treated SiO2 (300 nm)/Si(001) substrate at a rotational speed of 3000 rpm for 30 s, and then immediately heated to 150 °C for 5 min to remove the solvent. Next, graphene was synthesized using a conventional thermal chemical vapor deposition (TCVD) system. A 25 μm-thick Cu foil (Alfa Aesar, 99.8% purity) was utilized as a catalytic substrate for the synthesis of graphene. The Cu foil was loaded into the TCVD chamber and pre-annealed at 1050 °C with introducing H2 (200 sccm) under a pressure of ~3.6 Torr for 2 h in order to reduction and surface flattening of the Cu catalytic substrate. After the pre-annealing process, the graphene was immediately synthesized through the introduction of CH4 (2 sccm) and H2 (200 sccm) for 80 min. Following the growth of the graphene, the TCVD reactor was cooled down to room temperature with H2.
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2

Flexible Transparent Conductive Composite Fabrication

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Poly(3,4-ethylenedioxythiophene):poly(styrenesulfonate)
(PEDOT:PSS) (PH 1000) was purchased from Ossila, and poly(ethylene
oxide) (PEO) (Mn: 100 kDa) was purchased from Alfa Aesar. Dimethylformamide
(DMF), Triton X-100, AgNWs (0.5% isopropyl alcohol suspension in IPA)
with aspect ratios of 120 (diameter × length, 50 nm × 6
μm) and 330 (diameter × length, 120–150 nm ×
20 μm), the CuNWs (5 mg/mL in IPA, diameter × length, 100
nm × 25 μm, aspect ratio: 250), and poly(caprolactone)
(PCL) (Mn: 45 kDa) were purchased from Sigma-Aldrich. Kapton substrates
were purchased from DuPont, and cotton fabric was procured from a
local seller. All chemical reagents were used as received without
further purification.
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3

Electrochemical Acetylcholinesterase Biosensor

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AChE (from electric eel), ATCl, AgNWs and DDVP were from Sigma-Aldrich. CS (viscosity > 400 mPa s) and Gra (stripped by 1-methyl-2-pyrrolidinone (NMP)) were from Aladdin Bio-Chem Technology (Shanghai, China). Glucose was from Sangon Biotech (Shanghai, China), ethanol absolute, glacial acetic acid, tetra-n-butyl titanate, hydrochloric acid, N,N-dimethylformamide (DMF), isopropanol, potassium ferricyanide, potassium ferrocyanide trihydrate, potassium chloride, sodium chloride, sodium dihydrogen phosphate, disodium hydrogen phosphate were from Sinopharm Chemical Reagent Co., Ltd (Shanghai, China). All chemical reagents used are of analytical grade. Nitrogen with a purity of 99.9% comes from Air Liquide (China) Holding Co., Ltd. The deionized water (DI water) used in the whole experiment was obtained by ion exchange method. Vegetable juice is a supernatant obtained by washing, grinding, filtering, and centrifuging fresh lettuce purchased from a nearby vegetable market (ESI).
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4

Synthesis and Characterization of Silver Nanowire Networks

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The investigated NWN were synthesized starting from Ag NWs (Sigma-Aldrich, prod. no. 739448) of length 20μm to 50μm , diameter 115±(15)nm , coated with 1–2 nm of PVP24 (link) and concentration 0.5 wt.% in isopropyl alcohol (IPA). By the dilution of the original suspension by additional IPA we obtained NWN of AMD in the range between 70mgm-2 and 120mgm-2 (calculated). NWs were dispersed on a square quartz substrate of size 1×1cm2 . A detailed structural and chemical characterisation of these nanostructures is reported in our previous work23 (link).
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5

Graphene Oxide and Silver Nanowire Coatings

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GO solution was purchased from Graphenea Inc., San Sebastián, Spain. The GO was dispersed in deionized (DI) water with a 4-mg/mL concentration. The GO was diluted using isopropanol (IPA) and then coated on an optical grade PET substrate (Nan Ya Plastics, BH215, New Taipei City, Taiwan) via spin-coating with 1000-rpm spin speed for 30 s to form GO sheets. Hereafter, these prepared samples are labeled “GO/PET.” Subsequently, the GO/PET was baked to remove the solvent thoroughly using a hot plate at 60 °C for 10 min. The thickness of as-prepared GO film was about 30 nm measured by atomic force microscope. The details were described in Supplementary Materials Figure S1. In addition, AgNWs were purchased from Sigma-Aldrich, Saint Louis, MO, USA (average diameter: 35 μm; length: 115 μm). The AgNWs were dispersed in IPA with a 0.5 wt % concentration. Before being coated onto PET substrate via drop casting, which was followed by drying at 60 °C for 30 min, the AgNWs were also diluted in IPA at various concentrations. This AgNW/IPA solution was then coated on the PET followed by the GO coating under the same conditions as those used for the GO/PET samples. The prepared samples, hereafter, are referred to as GO/AgNWs/PETs.
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6

Deposition of Silver Nanowires on Patterned Membranes

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The patterned membranes were exposed to O2-plasma (100 W, 4 min) and soaked in DI water containing detergent (Triton X100, Sigma Aldrich). AgNWs (60 nm diameter, 10 μ m long, Sigma Aldrich) were dispersed in ethanol, vortexed and briefly ultrasonicated. Immediately prior to filtration, the AgNWs were diluted in 15 ml DI water and vortexed. The dispersion was filtered through the membrane and the membrane with the deposited AgNWs was dried on a hotplate (50 °C, 10 min). The surface coverage of AgNWs on the patterned membrane area was approximately 0.17 mg/cm2.
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7

Conductive PEDOT:PSS and Silver Nanowire Solutions

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PH1000 (Clevios), which is a mixture of PEDOT:PSS (1:2.5 by weight) in aqueous solution, was used as the conducting solution for the anode. PH1000 had a solid content of 1.0–1.3%, a viscosity of 15–50 mPa·s, and a conductivity of ~850 S/cm. To increase the conductivity, PH1000 and 5 wt% DMSO (99.9% ACS reagent, Sigma-Aldrich) were mixed and stirred for 24 h. The conducting solution for the cathode consisted of 0.5 wt% Ag NWs (Sigma-Aldrich) in IPA. The average diameter and length of the Ag NWs were ~60 nm and ~10 μm, respectively.
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