Transient intermediate in the formation of an amorphous metal-organic framework

被引:2
|
作者
Sapnik, Adam F. [1 ]
Thorne, Michael F. [1 ]
Castillo-Blas, Celia [1 ]
Keenan, Luke [2 ]
Johnson, Timothy [3 ]
Bennett, Thomas D. [1 ]
机构
[1] Univ Cambridge, Dept Mat Sci & Met, Cambridge CB3 0FS, England
[2] Diamond Light Source Ltd, Diamond House,Harwell Campus, Didcot OX11 0DE, Oxon, England
[3] Johnson Matthey Technol Ctr, Sonning Common RG4 9NH, England
基金
英国工程与自然科学研究理事会;
关键词
MIL-100(FE); CRYSTALLIZATION; KINETICS; ACID; NMR;
D O I
10.1039/d3sm01658g
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
Amorphous metal-organic frameworks are rarely formed via direct synthesis. Our limited understanding of their atomic assembly in solution prevents full exploitation of their unique structural complexity. Here, we use in situ synchrotron X-ray absorption spectroscopy with sub-second time resolution to probe the formation of the amorphous Fe-BTC framework. Using a combination of spectral fingerprinting, linear combination analysis, and principal component analysis coupled with kinetic analyses, we reveal a multi-stage formation mechanism that, crucially, proceeds via the generation of a transient intermediate species. Amorphous metal-organic frameworks are rarely formed via direct synthesis. Here, in situ synchrotron X-ray absorption spectroscopy probes the formation of Fe-BTC, revealing a multi-stage mechanism that proceeds via a transient intermediate species.
引用
收藏
页码:2338 / 2347
页数:10
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