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2 protocols using ircl3 3h2o

1

Preparation of PtIr/C Electrocatalyst on Carbon Cloth

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Plain carbon fibre cloth (0.35 mm thickness, E-TEK) was used as the substrate for the catalysts. The carbon cloth electrode (1 × 1 cm2) was sonicated in diluted hydrochloric acid, deionized water, and isopropanol for 1 min respectively. PtIr/C catalysts (20 wt% of metals loading) were prepared by the borohydride reduction process88 (link) using K2PtCl6 (Pt 39.6%, Thermo Scientific™), IrCl3 ∙ 3H2O (53–56% Ir, Thermo Scientific™) and Vulcan XC72 carbon black (Cabot) as precursors. The atomic ratio of Pt:Ir is 50:50. The catalyst ink was made up of 80 mg PtIr/C powder, 500 μL isopropanol and 145 μL 5 wt% Nafion solution (Sigma Aldrich). The ink slurry was ultrasonicated for 1 h and then brushed onto the pre-treated carbon cloth. The electrode was dried in an oven at 80 °C. The loading of PtIr was about 1.2 mg cm-2. The Pt/C electrode (20 wt% Pt on carbon black, Alfa Aesar) was prepared in the same way and the loading of Pt was about 1.3 mg cm-2.
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2

Synthesis of Metal Oxide Nanoparticles

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Precursor salts of Ni(NO3)2•6H2O (99%), Mg(NO3)2•6H2O (99 + %), Al(NO3)3•9H2O (99 + %), ZrO(NO3)2•H2O (99.5%), Co(NO3)2•6H2O (99 + %), Ga(NO3)3•H2O (99.99%), Ce(NO3)3•6H2O (99.5%), and Cr(NO3)3•9H2O (99%) were purchased from Acros Organics; In(NO3)3•H2O (99.99%), Nd(NO3)3•6H2O (99.9%), Er(NO3)3•5H2O (99.9%), and Pt(NO3)4 solution (Pt 15 w/w) were purchased from Alfa Asear; Fe(NO3)3•9H2O was purchased from Fisher Chemical; Zn(NO3)2•6H2O (98%) was purchased from Sigma Aldrich; Pd(NO3)2•H2O (99.8%, Pd 39% min) and IrCl3•3H2O (Ir 53–56%) were purchased from Thermo Scientific. NaOH pellets were purchased from Sigma Aldrich. Hexadecyltrimethylammonium bromide (CTAB, 99 + %) and HCl (37%) were purchased from Acros Organics. Ethanol (200 proof) was obtained from Decon Labs, Inc.
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