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Effect of CeO2 support properties on structure of Pt-Cu nanoparticles synthesized by electron beam irradiation method for preferential CO oxidation

机译:CeO2负载性能对电子束辐照优先CO氧化合成Pt-Cu纳米粒子结构的影响

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摘要

The influence of surface properties of CeO2 support on the structure of Pt-Cu bimetallic system in an aqueous-phase synthesis process using electron beam irradiation and the resulting impact on PROX performance were investigated. The exposed hydroxyls on CeO2 surface with low hydrogen-bonding water led to cluster-like Pt-Cu phase with low crystallinity and high oxidation state. It was attributed to a strong interaction of CeO2 and Pt-Cu phase. In CO atmosphere, such oxidic or fine Pt-Cu phase was reduced to platinum and partially reduced CuO_x, and CeO2 was concomitantly reduced to retain carbonate species on its surface. This in turn affected catalytic performance, i.e., a significant increase in O2 conversion was observed in an oxygen-rich PROX condition compared to a stoichiometric condition while selectivity was retained in higher level than monometallic PL The higher oxidation state of Pt in the excess O2 was suggested to be responsible for the drastic change in activity. The surface chemical property of CeO2 was shown to affect PROX activity through the structure and oxidation state of Pt-Cu species which originates from metal-ceria interaction in the synthesis stage.
机译:研究了CeO2载体的表面性能对水相合成过程中使用电子束辐照的Pt-Cu双金属体系结构的影响及其对PROX性能的影响。低氢键水在CeO2表面暴露的羟基导致低结晶度和高氧化态的簇状Pt-Cu相。这归因于CeO2和Pt-Cu相之间的强相互作用。在CO气氛中,这种氧化的或细的Pt-Cu相被还原成铂并部分还原了CuO x,并且CeO 2被同时还原以在其表面上保留碳酸盐种类。这反过来影响了催化性能,即与化学计量条件相比,在富氧的PROX条件下观察到O2转化率显着提高,而选择性保持在比单金属PL更高的水平。过量O2中Pt的较高氧化态为建议对活动的急剧变化负责。结果表明,CeO2的表面化学性质会通过Pt-Cu物种的结构和氧化态影响其PROX活性,而Pt-Cu物种的合成态是由金属-二氧化铈相互作用引起的。

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