Transition metal inclusion in RhoZMOF materials

被引:4
作者
Calleja, Guillermo [1 ]
Martos, Carmen [1 ]
Orcajo, Gisela [1 ]
Botas, Juan A. [1 ]
Villajos, Jose A. [1 ]
机构
[1] Univ Rey Juan Carlos, Dept Chem & Energy Technol, ESCET, Madrid 28933, Spain
来源
CRYSTENGCOMM | 2015年 / 17卷 / 02期
关键词
ORGANIC FRAMEWORKS ZMOFS; ZEOLITIC IMIDAZOLATE FRAMEWORKS; CARBON-DIOXIDE; ION-EXCHANGE; ADSORPTION; CATALYSTS; HYDROGEN; BINDING; STORAGE; ENERGY;
D O I
10.1039/c4ce01401d
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Porous RhoZMOF is a negatively charged zeolite-like MOF material susceptible to post-synthesis modification by an ion-exchange process replacing as-synthesized organic cations with transition metals. This material exhibiting open transition metal sites is a very attractive candidate for industrial applications related to clean energy technologies, like electrochemistry and gas storage. In the present work, partial or total Co2+, Ni2+ and Cu2+ inclusions have been successfully carried out in the RhoZMOF structure by ion-exchange treatment. Particularly, complete exchange of HDMA(+) with Co2+ could be reached at room temperature after 12 h of contact time. For Cu2+ exchange, a rapid transformation of the RhoZMOF structure into a new Cu-rich, crystalline and practically non-porous phase was observed at room temperature; its appearance can be avoided and the desired structure can be preserved when ion-exchange treatment is carried out at -20 degrees C for 6 h, reaching a partial ion-exchange degree of 30%. Moreover, for Ni2+ ion-exchange treatment at 25 and 0 degrees C, a covering of an amorphous Ni-rich organometallic phase over the crystals was detected by SEM analysis; its appearance can be prevented by reducing the amount of HDMA(+) in the media by developing the ion-exchange process in two steps: exchanging HDMA(+) with Na+ and Na+ with Ni2+. The results provide a post-synthesis modification route for obtaining porous MOF materials containing open transition metal sites accessible for redox catalysis and selective gas adsorption.
引用
收藏
页码:338 / 343
页数:6
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