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.
引用
收藏
页码:142 / 148
页数:7
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