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空间受限催化增强高温二氧化碳电解

Spatially confined catalysis-enhanced high-temperature carbon dioxide electrolysis.

作者信息

Yang Liming, Xue Xingjian, Xie Kui

机构信息

School of Materials Science and Engineering, Hefei University of Technology, No. 193 Tunxi Road, Hefei, Anhui 230009, China.

出版信息

Phys Chem Chem Phys. 2015 May 7;17(17):11705-14. doi: 10.1039/c4cp06125j.

Abstract

In this study, a potential ilmenite cathode material Ni0.9TiO3 is designed for efficient CO2 electrolysis in an oxide-ion-conducting solid-oxide electrolyzer. Spatially confined catalysis has been successfully achieved to substantially improve cathode activity by in situ growth of catalytically active nickel nanoparticles on a ceramic skeleton. The combined analysis of XRD, SEM, EDS, XPS, TGA and Raman results together confirm that the growth of nickel catalyst is completely reversible in redox cycles. The n-type electrical properties of cathodes are systematically investigated and correlated to electrochemical performance. Efficient CO2 electrolysis with a Faraday efficiency above 90% has been demonstrated with Ni0.9TiO3 in contrast to 60% for a TiO2 cathode at 800 °C.

摘要

在本研究中,设计了一种潜在的钛铁矿阴极材料Ni0.9TiO3,用于在氧化物离子传导固体氧化物电解槽中进行高效二氧化碳电解。通过在陶瓷骨架上原位生长具有催化活性的镍纳米颗粒,成功实现了空间受限催化,从而大幅提高了阴极活性。XRD、SEM、EDS、XPS、TGA和拉曼结果的综合分析共同证实,镍催化剂的生长在氧化还原循环中是完全可逆的。系统研究了阴极的n型电学性质,并将其与电化学性能相关联。在800℃下,Ni0.9TiO3实现了法拉第效率高于90%的高效二氧化碳电解,相比之下,TiO2阴极的法拉第效率为60%。

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