共 44 条
Sustaining metal-organic frameworks for water-gas shift catalysis by non-thermal plasma
被引:161
作者:
Xu, Shaojun
[1
]
Chansai, Sarayute
[1
]
Stere, Cristina
[1
]
Inceesungvorn, Burapat
[2
]
Goguet, Alexandre
[3
]
Wangkawong, Kanlayawat
[1
,2
]
Taylor, S. F. Rebecca
[1
]
Al-Janabi, Nadeen
[1
]
Hardacre, Christopher
[1
]
Martin, Philip A.
[1
]
Fan, Xiaolei
[1
]
机构:
[1] Univ Manchester, Sch Chem Engn & Analyt Sci, Manchester, Lancs, England
[2] Chiang Mai Univ, Dept Chem, Fac Sci, Chiang Mai, Thailand
[3] Queens Univ Belfast, Sch Chem & Chem Engn, Belfast, Antrim, North Ireland
基金:
英国工程与自然科学研究理事会;
关键词:
HETEROGENEOUS CATALYSIS;
HYDROGEN-PRODUCTION;
ACTIVE-SITES;
IN-SITU;
ADSORPTION;
MECHANISM;
BTC;
STABILITY;
OXIDATION;
VAPOR;
D O I:
10.1038/s41929-018-0206-2
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:
The limited thermal and water stability of metal-organic frameworks (MOFs) often restricts their applications in conventional catalysis that involve thermal treatment and/or use of water. Non-thermal plasma (NTP) is a promising technique that can overcome barriers in conventional catalysis. Here we report an example of an NTP-activated water-gas shift reaction (WGSR) over a MOF (HKUST-1). Significantly, the exceptional stability of HKUST-1 was sustained under NTP activation and in the presence of water, which led to a high specific rate of 8.8 h(-1). We found that NTP-induced water dissociation has a twofold promotion effect in WGSR, as it facilitates WGSR by supplying OH and sustains the stability and hence activity of HKUST-1. In situ characterization of HKUST-1 revealed the critical role of open Cu sites in the binding of substrate molecules. This study paves the way to utilize MOFs for a wider range of catalysis.
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页码:142 / 148
页数:7
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