钙钛矿(结构)
分解
解吸
X射线光电子能谱
材料科学
相对湿度
催化作用
拉曼光谱
化学分解
化学工程
无机化学
化学
物理化学
结晶学
工程类
吸附
有机化学
物理
光学
热力学
作者
Shuyan Gong,Zheng Xie,Weiman Li,Xiaofeng Wu,Ning Han,Yunfa Chen
标识
DOI:10.1016/j.apcatb.2018.09.041
摘要
Nowadays, it is still challenging to prepare highly active O3 decomposition catalyst, especially with high water resistance used in harsh environments such as high relative humidity (RH). Herein, perovskite LaFeO3 based catalysts are synthesized by a facile sol-gel method, which show far higher O3 decomposition activity of 70–80% than the commonly used Fe2O3 counterpart of 0% at RH 90% and room temperature. Furthermore, 5% mol Ni is effectively doped into LaFeO3 substituting part of Fe as verified by X-ray diffraction and X-ray photoelectron spectroscopy, which enhances the RH resistance with a stable >90% conversion efficiency on 1000 ppm O3 at RH 90% and room temperature in a test period of 4.0 h. The temperature programmed desorption results show that the H2O desorption temperature decreases from 180 to 480 °C of Fe2O3 to <100 °C for LaFeO3 and LaFe0.95Ni0.05O3, which contributes to the easy desorption of H2O and thus high RH resistance of these perovskite materials. Importantly, the in-situ Raman spectra show deformation of Fe2O3 in O3 decomposition reaction at high RH, leading to accumulation of intermediate O22− and thus depression of catalytic activity. However, the perovskite materials show neither deformation nor O22− accumulation, corresponding well with the high activity at high RH. All these results show the potential of these highly active and RH resistive perovskite catalysts for decomposition of ozone under harsh environments.
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