Transparent-to-Dark Electrochromic Behavior in Naphthalene-Diimide-Based Mesoporous MOF-74 Analogs

被引:153
作者
AlKaabi, Khalid [1 ]
Wade, Casey R. [1 ]
Dinca, Mircea [1 ]
机构
[1] MIT, Dept Chem, 77 Massachusetts Ave, Cambridge, MA 02139 USA
关键词
METAL-ORGANIC FRAMEWORKS; CHARGE-TRANSFER; THIN-FILMS; CONDUCTIVITY; CHEMISTRY; MN;
D O I
10.1016/j.chempr.2016.06.013
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The deliberate insertion of redox-active naphthalene diimide ligands into the versatile family of metal-organic frameworks known as MOF-74 (CPO-27) gives rise to a mesoporous electrochromic MOF that can be switched from transparent to dark, a desirable feature in electrochromic devices such as smart windows. Specifically, we report two new materials that have the MOF-74 topology and display redox activity stemming from a naphthalene diimide salicylic acid (NDISA) ligand. We show that these materials can be deposited as thin films on fluorine-doped tin oxide glass. The surprisingly different morphologies of MOF films obtained from Mg2+ and Ni2+ ions is likely controlled by the nucleation kinetics of Mg-2(NDISA) and Ni-2(NDISA), respectively. Both materials exhibit well-behaved quasi-reversible redox events associated with the [NDI]/[NDI](center dot-) and [NDI](center dot-)/[NDI](2-) redox couples, which are also responsible for the electrochromic switching.
引用
收藏
页码:264 / 272
页数:10
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