焦炭
二氧化碳重整
甲烷
催化作用
合成气
材料科学
镍
原材料
化学工程
分解
纳米技术
碳纤维
化学
冶金
有机化学
复合材料
工程类
复合数
作者
Mohcin Akri,Shu Zhao,Xiao‐Yu Li,Ketao Zang,Adam F. Lee,Mark A. Isaacs,Wei Xi,Yuvaraj Gangarajula,Jun Luo,Yujing Ren,Yi‐Tao Cui,Lei Li,Yang Su,Xiaoli Pan,Wu Wen,Yang Pan,Karen Wilson,Lin Li,Botao Qiao,Hirofumi Ishii
标识
DOI:10.1038/s41467-019-12843-w
摘要
Abstract Dry reforming of methane (DRM) is an attractive route to utilize CO 2 as a chemical feedstock with which to convert CH 4 into valuable syngas and simultaneously mitigate both greenhouse gases. Ni-based DRM catalysts are promising due to their high activity and low cost, but suffer from poor stability due to coke formation which has hindered their commercialization. Herein, we report that atomically dispersed Ni single atoms, stabilized by interaction with Ce-doped hydroxyapatite, are highly active and coke-resistant catalytic sites for DRM. Experimental and computational studies reveal that isolated Ni atoms are intrinsically coke-resistant due to their unique ability to only activate the first C-H bond in CH 4 , thus avoiding methane deep decomposition into carbon. This discovery offers new opportunities to develop large-scale DRM processes using earth abundant catalysts.
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