21:I[432972,["/_next/static/chunks/bb923814e1f4d2e9.js","/_next/static/chunks/dd3ee9f5b7716ca6.js","/_next/static/chunks/4204a0ae82542ca8.js","/_next/static/chunks/30036bedc5269936.js","/_next/static/chunks/6e1aa89a642f40be.js","/_next/static/chunks/cd5e572bc3e4eb92.js","/_next/static/chunks/8ffd0b71567920d8.js","/_next/static/chunks/959ed6555b8dc5ff.js","/_next/static/chunks/24eb4379f68013fd.js","/_next/static/chunks/b8cd775ffdf935bd.js","/_next/static/chunks/983103cd9eb7b428.js","/_next/static/chunks/d4ac9dcf27f6ff52.js","/_next/static/chunks/294b9525248c8e5f.js"],"default"] 22:T541,Direct ethanol fuel cells (DEFCs), which use ethanol as a fuel, have attracted considerable attention due to their relatively high energy density, the nontoxicity of ethanol, and the abundance of ethanol sources. However, since the crossover of ethanol as a fuel in DEFCs can deteriorate the cell performance due to the oxidation of ethanol (EtOH) at the cathode during oxygen reduction reaction (ORR), nonprecious metal (NPM) cathode catalysts for ORR have been studied using carbon-based nanostructures as promising alternatives to Pt-based catalysts. Herein, the doped carbon nanostructures (C/Fe-TMPP and C/Fe-Pc) as cathode catalysts were synthesized using a template method with iron(III) 5,10,15,20-(tetra-4-methoxyphenyl) porphyrin chloride (Fe-TMPP) and iron(II) phthalocyanine (Fe-Pc). In the half-cell test, C/Fe-TMPP exhibited an enhanced ORR activity in 0.5 M H2SO4 (i.e., high half-wave potential and specific current density) and maintained ORR performance in the presence of crossover ethanol, compared to a commercial Pt/C. Moreover, C/Fe-TMPP exhibited high performance in the DEFC supplied with high-concentrated EtOH as a fuel at the cathode. The excellent ORR activity of C/Fe-TMPP for the DEFC can be attributed to ethanol tolerance in the ORR and low ethanol adsorption energy of the active sites for the ORR of C/Fe-TMPP.23:T524,To develop doped carbon nanostructures as non-precious metal cathode catalysts, nanocomposites were synthesized by using SBA-15 and 5,10,15,20-tetrakis(4-methoxyphenyl)porphyrin-iron(III) chloride with different ratios of amorphous MoS₂ precursor. From various analyses, it was found that, during pyrolysis at 900 °C under an N₂ atmosphere, the amorphous MoS₂ precursor decomposed into Mo and S, facilitating the formation of graphene sheet-like carbon with MoC and doping of sulfur in the carbon. In the nanocomposite formed from 10 wt % MoS₂ precursor (denoted as Mo/S/PC-10), most of the MoS₂ was decomposed, thus forming S-doped carbon, which was grown on the MoC phase without crystalline MoS₂ . Furthermore, Mo/S/PC-10 exhibited better performance in the oxygen reduction reaction (specific activity of 1.23 mA cm^-2 at 0.9 V and half-wave potential of 0.864 V) than a commercial Pt catalyst, owing to a heteroatom-doped carbon nanostructure with a fairly high specific surface area. In the polarization curve of the unit-cell performance measured at 80 °C under ambient pressure, Mo/S/PC-10 as a cathode catalyst exhibited an optimal power density of 314 mW cm^-2 and a current density of 280 mA cm^-2 at 0.6 V.

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