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通过脱合金法制备的用于低温CO氧化的SmO/CoO催化剂。

SmO/CoO catalysts prepared by dealloying for low-temperature CO oxidation.

作者信息

Duan Dong, Hao Chunxi, Shi Wenyu, Wang Haiyang, Sun Zhanbo

机构信息

School of Science, MOE Key Laboratory for Non-Equilibrium Synthesis and Modulation of Condensed Matter, Key Laboratory of Shaanxi for Advanced Functional Materials and Mesoscopic Physics, Xi'an Jiaotong University Xi'an 710049 PR China

出版信息

RSC Adv. 2018 Mar 21;8(21):11289-11295. doi: 10.1039/c8ra01219a.

Abstract

A series of CoO catalysts modified by Sm were prepared by a combined dealloying and calcination approach, and the catalytic activities were evaluated using CO catalytic oxidation. The SmO/CoO catalysts were composed of a large number of nanorods and nanosheets, and exhibited a three-dimensional supporting structure with pores. The experimental results revealed that the addition of a small amount of Sm into the precursor AlCo alloy led to a dealloyed sample with improved catalytic activity, and the dealloyed AlCoSm ribbons (0.5 SmO/CoO) calcined at 300 °C showed the highest activity for CO oxidation with complete CO conversion at 135 °C, moreover, CO conversion almost no attenuation, even after 70 hours of catalytic oxidation, which is superior to that of CoO. The enhanced catalytic activity of the SmO/CoO catalyst can be attributed to the large specific surface area, more reactive oxygen species and Co ion, as well as electronic interactions between Sm and Co.

摘要

通过脱合金和煅烧相结合的方法制备了一系列经Sm改性的CoO催化剂,并采用CO催化氧化对其催化活性进行了评价。SmO/CoO催化剂由大量纳米棒和纳米片组成,呈现出具有孔隙的三维支撑结构。实验结果表明,向前驱体AlCo合金中添加少量Sm可得到催化活性提高的脱合金样品,在300℃煅烧的脱合金AlCoSm带材(0.5 SmO/CoO)在135℃时对CO氧化表现出最高活性,CO完全转化,而且即使经过70小时的催化氧化,CO转化率几乎没有衰减,优于CoO。SmO/CoO催化剂催化活性增强可归因于大比表面积、更多的活性氧物种和Co离子,以及Sm和Co之间的电子相互作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0c80/9079130/8af1d988179e/c8ra01219a-f1.jpg

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