纳米棒
催化作用
甲烷氧化偶联
溴化物
化学
甲烷
高分辨率透射电子显微镜
肺表面活性物质
氧气
聚乙烯吡咯烷酮
热液循环
煅烧
无机化学
化学工程
核化学
材料科学
高分子化学
纳米技术
有机化学
透射电子显微镜
工程类
生物化学
作者
Junrong Yue,Qingyue Xiao,Dawei Zhao,Yu Guan,Jiao Liu,Guangwen Xu
出处
期刊:Energy & Fuels
[American Chemical Society]
日期:2023-09-28
卷期号:37 (20): 15986-15994
被引量:3
标识
DOI:10.1021/acs.energyfuels.3c02246
摘要
It is generally agreed upon that oxidative coupling of methane is structure-sensitive over the La2O3 catalysts and that morphology such as nanowire or nanorod exhibited the highest activity. Therefore, three crystalline La2O3 catalysts were synthesized by the hydrothermal method without (denoted as La-NS) or with polyvinylpyrrolidone (PVP) (denoted as La-PVP) or cetyltrimethylammonium bromide (denoted as La-CTAB) as the surfactant. The HRTEM results suggested (110) and (101) planes were both exposed in La-PVP, while only the (101) facet in La-NS and the (002) facet in La-CTAB were exposed. CO2-TPD characterization showed that La-PVP exhibited a larger capacity of CO2 adsorption and more amounts of moderate basic sites than La-NS and La-CTAB. Then, the formation of the chemisorbed oxygen species O2– was facilitated. In situ DRIFT spectra revealed that surface O2– species are the activated oxygen species which would convert methane to a methyl radical and then couple to C2+ hydrocarbons during the OCM reaction over the nanorod La2O3 catalysts. Therefore, the La-PVP catalyst outperformed its peers in both activity and selectivity.
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