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4 protocols using aniline

1

Polymer Characterization for Material Synthesis

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MC powder with a viscosity of 4,000 cP (in 2% solution) and HPMC powder with a viscosity of 4,260 cP (in 2% solution) were obtained from LOTTE Fine Chemical Co., Ltd (Incheon, Korea). CMC sodium salt with a viscosity of 50 to 200 cp (in 4% solution) was obtained from Sigma Chemical CO., (St. Louis, MO, USA). Yeast extract and peptone were purchased from BD Biosciences (San Jose, CA, USA). Glucose, hydrogen peroxide (34.5%), sodium hydroxide, ethyl alcohol (99.9%) and acetic acid were supplied by Duksan Pure Chemical Co., Ltd. (Seoul, Korea). Dodecylbenzene sulfonic acid (DBSA) and trifluoroacetic acid (TFA) were purchased from Sigma-Aldrich (St. Louis, MO, USA). Aniline and acetonitrile were purchased from Junsei Chemical Co., Ltd. (Tokyo, Japan). Ammonium peroxydisulfate (APS) was supplied by Kanto Chemical Co., Inc. (Tokyo, Japan). All chemical reagents were used as received.
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2

Enzymatic Laccase Catalysis for Oxidative Reactions

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Glucose (Duksan Pure Chemicals Co., Seoul, South Korea) was used as carbon source. A mixture of yeast extract (Becton, Dickinson and Company, Sparks, Unitesd States) and peptone (Becton, Dickinson, Sparks, United States) were used as nitrogen sources. The following chemicals were used without further purification: acetic acid (Duksan Pure Chemicals Co., Seoul, South Korea), sodium acetate (Sigma, Saint Louis, MO, United States), hydrogen peroxide (Duksan Pure Chemicals Co., South Korea), aniline (Junsei Chemical Co. Ltd., Tokyo, Japan), KHCF (Fisher Scientific, Loughborough, United Kingdom), AOT (Tokyo Chemical Industry Co., Tokyo, Japan). Laccase (EC 1.10.3.2.) from Myceliophthora thermophila was obtained from Novozymes (Bagsvaerd, Denmark). Citric acid monohydrate (Sigma, Saint Louis, MO, United States), sodium phosphate dibasic dehydrate (Riedel-de Haën, Seelze, Germany), and CMC (Sigma, Saint Louis, MO, United States).
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3

Synthesis of Metal-Doped Nitrogen-Enriched Carbon

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The metal (Fe, Co) phthalocyanine (~ 95%, Sigma-Aldrich, Korea) was dissolved in aniline (100 mL; > 99%, Junsei Chemical Co., Ltd., Japan) for 1 h upon magnetic stirring to achieve a concentration of 1 mM. Then, two high-purity graphite electrodes were discharged in this solution at a voltage of 1.2 kV, a frequency of 25 kHz, and a pulse width of 0.9 μs for 20 min (Pulse Modulator, MPP04-A4-200. Japan), with the assistance of an ultrasonic homogenizer (Korea Process Technology Co., Ltd., KSC-80, 25 kHz) [31 (link)]. The liquid phase was passed through a 55-mm-diameter polytetrafluoroethylene filter and evaporated at 80 °C for 10 h. The resulting product was heated at 550 °C for 2 h in N2 to enhance conductance and denoted as Fe-N4/NC and Co-N4/NC.
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4

Plasma Synthesis of Cobalt Nanoparticles

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Plasma synthesis was performed between a pair of high purity transition cobalt electrodes (99.999%, Nilaco Co., Ltd., Tokyo, Japan, diameter of 1 mm) inside an organic solution of aniline (A-Co), quinolone (Q-Co), and aniline-quinoline 1:1: mixed solution (Quinoline, aniline, >99%, Junsei Chemical Co., Ltd., Tokyo, Japan) using a bipolar pulse power supply (MPP-HV02, KURITA, Kyoto, Japan). The plasma was discharged at a voltage of ~4 kV, a frequency of 50 kHz, and a pulse width of 1.0 μs. Stable plasma was discharged for 30 min to obtain cobalt nanoparticles/N-doped carbon (Co-N/C). The solution was filtered using a ϕ 55 mm polytetrafluoroethylene filter, and the resulting filtered carbon powder samples were dried in an oven for 10 h at 80 °C, then heated at 700 °C for 1 h with 1.0 cc/min nitrogen atmosphere to improve their electrical conductivity. The schematic of the plasma synthesis is illustrated in Figure 1.
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