Embedded MoN@C nanocomposites as an advanced catalyst for ammonia decomposition to COx-free hydrogen

被引:26
作者
Li, Lei [1 ]
Chu, Wei [2 ,3 ]
Ding, Cheng [2 ]
Xi, Xinguo [1 ]
Jiang, Ruiyu [1 ]
Yan, Jinlong [2 ]
机构
[1] Yancheng Inst Technol, Sch Chem & Chem Engn, Yancheng 224051, Peoples R China
[2] Yancheng Inst Technol, Sch Environm Sci & Engn, Yancheng 224051, Peoples R China
[3] Sichuan Univ, Dept Chem Engn, Chengdu 610065, Sichuan, Peoples R China
基金
中国国家自然科学基金;
关键词
Embedded structure; MoN nanoparticles; Porous carbon; Ammonia decomposition; Hydrogen production; BIMETALLIC CATALYSTS; CARBON NANOFIBERS; NH3; DECOMPOSITION; NI NANOPARTICLES; GENERATION; NITRIDE; PERFORMANCE; MORPHOLOGY; MO2N;
D O I
10.1016/j.ijhydene.2017.10.174
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Mo-based nanoparticles (MoO2 and Mo2C) embedded in porous carbon matrix have been synthesized by a successive hydrothermal and thermal treatment strategy. The synthesized materials were tested for COx-free H-2 production via ammonia decomposition. Various characterizations, including N-2-sorption, TGA, FTIR, TEM, XRD, EDX and XPS, were employed to investigate the morphology, component and structure of fresh and used catalysts. In terms of fresh Mo@C sample, tiny Mo-based nanoparticles (3-6 nm) are homogeneously dispersed in porous carbon matrixes, which were rapidly nitridized to MoN phases during reaction process. Most of MoN species were still embedded in carbon matrixes after 25 h stability test. For comparison, MoN@C sample was achieved via temperature-programmed ammonolysis of Mo@C sample, demonstrating the formation of MoN species and enhanced activities. The ammonia decomposition activity (similar to 90% conversion) is obtained over MoN@C catalyst at 600 degrees C and 15,000 h(-1), which is higher than that of non-pretreated Mo@C catalyst. This embedded structure also endows them with a relatively stable performance even at high temperature. (C) 2017 Hydrogen Energy Publications LLC. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:30630 / 30638
页数:9
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