4.6 Article

In Situ Fabrication of Ultrasmall Ni Nanoparticles from Ni(OH)2 Precursors for Efficient CO2 Reforming of Methane

期刊

INDUSTRIAL & ENGINEERING CHEMISTRY RESEARCH
卷 61, 期 1, 页码 198-206

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acs.iecr.1c03590

关键词

-

资金

  1. National Natural Science Foundation of China [21776007, 21811530293]
  2. National Key Research and Development Project [2018YFE0107400]
  3. Fundamental Research Funds for the Central Universities [XK1802-1]

向作者/读者索取更多资源

In this study, ultrasmall Ni nanoparticles were successfully fabricated via a simple solution method and H-2 reduction, showing competitive reforming performance in CO2 reforming of methane. The bifunctional reaction mechanism on the Ni/Al2O3 catalyst was identified, facilitating the activation of reactant molecules near metal-support interfaces. This work provides new insights into the structure-activity relationships in methane reforming.
Metal size is a critical structural parameter for Ni-based catalysts in CO2 reforming of methane. Herein, ultrasmall Ni nanoparticles (3.7 nm) were fabricated from Ni(OH)(2) precursors on gamma-Al2O3 nanoplates via a simple solution method followed by H-2 reduction. The resultant Ni/Al2O3-IS catalyst showed competitive reforming performance. The turnover frequency reached 15.3 s at 700 degrees C under atmospheric pressure. Methane (CH4) conversion declined marginally from 79.8 to 70.2% after 20 h of reaction. Characterization results reveal that high activity and good stability were endowed by the ultrasmall Ni size and superior coke resistance, respectively. A bifunctional reaction mechanism was identified on the Ni/Al2O3-IS catalyst, wherein the activation of the reactant molecules was facilitated near metal-support interfaces. This work offers a novel strategy to fabricate ultrasmall Ni particles and provides new insights into structure-activity relationships in CO2 reforming of methane.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.6
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据