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Methanol oxidation on MoO_3 promoted Pt/C electrocatalyst

机译:MoO_3促进Pt / C电催化剂上的甲醇氧化

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摘要

MoO_3 is incorporated into Vulcan carbon XC-72R by solid—state reaction under intermittent microwave heating (IMH) method. The Pt nanoparticles are dispersed by microwave-assisted polyol process. The physicochemical characterization reveals that MoO_3 and Pt nanoparticles are evenly deposited on Vulcan carbon XC-72R. The non-conducting MoO_3 is electrochemically reduced to nonstoichiometric and electroconductive hydrogen molybdenum bronze (H_xMoO_3) in acidic solution. The peak current for methanol electrooxidation is about 128% higher on Pt-MoCVC electrode than Pt-Ru/C electrode. Also, there is a significant increase in the electrode response toward stability test which can be attributed to hydrogen molybdenum bronze phase and its direct role in the conversion of CO to CO_2. Intermittent microwave heating method is effective for incorporating oxide materials in Vulcan XC-72R in a short span of time which is evidenced by the formation of hydrogen molybdenum bronze phase during the CV measurements.
机译:MoO_3在间歇微波加热(IMH)方法下通过固相反应掺入Vulcan碳XC-72R中。通过微波辅助多元醇工艺分散Pt纳米颗粒。理化特性表明,MoO_3和Pt纳米颗粒均匀地沉积在Vulcan碳XC-72R上。非导电MoO_3在酸性溶液中被电化学还原为非化学计量和导电氢钼钼青铜(H_xMoO_3)。在Pt-MoCVC电极上,甲醇电氧化的峰值电流比Pt-Ru / C电极高约128%。同样,电极对稳定性测试的响应也显着增加,这归因于氢钼青铜相及其在CO转化为CO_2中的直接作用。间歇式微波加热方法可在短时间内有效地将氧化物材料掺入Vulcan XC-72R中,这可通过在CV测量过程中形成氢钼青铜相来证明。

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