Self-organized Ruthenium-Barium Core-Shell Nanoparticles on a Mesoporous Calcium Amide Matrix for Efficient Low-Temperature Ammonia Synthesis

被引:165
|
作者
Kitano, Masaaki [1 ]
Inoue, Yasunori [2 ]
Sasase, Masato [1 ]
Kishida, Kazuhisa [1 ]
Kobayashi, Yasukazu [1 ]
Nishiyama, Kohei [1 ]
Tada, Tomofumi [1 ]
Kawamura, Shigeki [1 ]
Yokoyama, Toshiharu [1 ]
Hara, Michikazu [2 ,3 ]
Hosono, Hideo [1 ,2 ,3 ]
机构
[1] Tokyo Inst Technol, Mat Res Ctr Element Strategy, Midori Ku, 4259 Nagatsuta, Yokohama, Kanagawa 2268503, Japan
[2] Tokyo Inst Technol, Lab Mat & Struct, Midori Ku, 4259 Nagatsuta, Yokohama, Kanagawa 2268503, Japan
[3] Japan Sci & Technol Agcy, ACCEL, 4-1-8 Honcho, Kawaguchi, Saitama 3320012, Japan
基金
日本科学技术振兴机构;
关键词
alkaline-earth-metal amides; core-shell structures; low-temperatures; mesoporous; ruthenium; MEDIATED NITROGEN TRANSFER; PROMOTED TRANSITION-METAL; SYNTHESIS CATALYSTS; ALKALI-METAL; ACTIVATION; DINITROGEN; HYDROGEN; REDUCTION; ELECTRIDE; MECHANISM;
D O I
10.1002/anie.201712398
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
A low-temperature ammonia synthesis process is required for on-site synthesis. Barium-doped calcium amide (Ba-Ca(NH2)(2)) enhances the efficacy of ammonia synthesis mediated by Ru and Co by 2 orders of magnitude more than that of a conventional Ru catalyst at temperatures below 300 degrees C. Furthermore, the presented catalysts are superior to the wustite-based Fe catalyst, which is known as a highly active industrial catalyst at low temperatures and pressures. Nanosized Ru-Ba core-shell structures are self-organized on the Ba-Ca(NH2)(2) support during H-2 pretreatment, and the support material is simultaneously converted into a mesoporous structure with a high surface area (>100m(2)g(-1)). These self-organized nanostructures account for the high catalytic performance in low-temperature ammonia synthesis.
引用
收藏
页码:2648 / 2652
页数:5
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