歧化
催化作用
碳纤维
材料科学
双功能
化学工程
分解
甲烷
二氧化碳重整
合金
双金属片
纳米技术
化学
合成气
冶金
有机化学
复合材料
工程类
复合数
作者
Sun-Kyu Kim,Jochen Lauterbach,Erdem Sasmaz
出处
期刊:ACS Catalysis
[American Chemical Society]
日期:2021-06-21
卷期号:11 (13): 8247-8260
被引量:114
标识
DOI:10.1021/acscatal.1c01223
摘要
Herein, we report a highly carbon resistant nanotubular yolk–shell Pt-NiCe@SiO2 single-atom-alloy (SAA) catalyst for low-temperature dry reforming of methane (DRM). A synergetic combination of the confined yolk–shell morphology and Pt–Ni SAA structures prevents carbon formation and provides excellent catalyst stability. The confined morphology of the yolk–shell structures can impede carbon deposition due to the facile CO desorption from the surface. Carbon formation can be further minimized by 0.25 wt % Pt promotion, showing an excellent stability for 120 h during DRM at 500 °C. The enhanced stability of the Pt0.25-NiCe@SiO2 catalyst can be attributed to the atomically dispersed Pt on the yolks forming Pt–Ni SAA structures encapsulated by a nanotubular SiO2 shell. The Pt–Ni SAA facilitates Pt–Ni interactions and enhances the reducibility of the Ni species, which further suppresses carbon formation during DRM. The developed bifunctional catalyst exhibits excellent resistance to coking by decreasing the effect of both main carbon formation reactions: i.e., CO disproportionation and CH4 decomposition. When the Pt loading is increased above 0.25 wt %, Pt nanoparticles form, leading to oligomerization of C–H species. Our results show that advantageous effects of both confined morphology and Pt–Ni SAA structures can lower the operating temperature of DRM without showing any catalyst deactivation.
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