Transition metal inclusion in RhoZMOF materials

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 a...

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Veröffentlicht in:CrystEngComm 2015-01, Vol.17 (2), p.338-343
Hauptverfasser: Calleja, Guillermo, Martos, Carmen, Orcajo, Gisela, Botas, Juan A., Villajos, José A.
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Sprache:eng
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Zusammenfassung: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 Co 2+ , Ni 2+ and Cu 2+ inclusions have been successfully carried out in the RhoZMOF structure by ion-exchange treatment. Particularly, complete exchange of HDMA + with Co 2+ could be reached at room temperature after 12 h of contact time. For Cu 2+ 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 °C for 6 h, reaching a partial ion-exchange degree of 30%. Moreover, for Ni 2+ ion-exchange treatment at 25 and 0 °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 Ni 2+ . 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.
ISSN:1466-8033
1466-8033
DOI:10.1039/C4CE01401D