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Topochemical conversion of a dense metal-organic framework from a crystalline insulator to an amorphous semiconductor.


ABSTRACT: The topochemical conversion of a dense, insulating metal-organic framework (MOF) into a semiconducting amorphous MOF is described. Treatment of single crystals of copper(i) chloride trithiocyanurate, CuICl(ttcH3) (ttcH3 = trithiocyanuric acid), 1, in aqueous ammonia solution yields monoliths of amorphous CuI1.8(ttc)0.6(ttcH3)0.4, 3. The treatment changes the transparent orange crystals of 1 into shiny black monoliths of 3 with retention of morphology, and moreover increases the electrical conductivity from insulating to semiconducting (conductivity of 3 ranges from 4.2 × 10-11 S cm-1 at 20 °C to 7.6 × 10-9 S cm-1 at 140 °C; activation energy = 0.59 eV; optical band gap = 0.6 eV). The structure and properties of the amorphous conductor are fully characterized by AC impedance spectroscopy, X-ray photoelectron spectroscopy, X-ray pair distribution function analysis, infrared spectroscopy, diffuse reflectance spectroscopy, electron spin resonance spectroscopy, elemental analysis, thermogravimetric analysis, and theoretical calculations.

SUBMITTER: Tominaka S 

PROVIDER: S-EPMC5811114 | biostudies-literature | 2015 Feb

REPOSITORIES: biostudies-literature

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Topochemical conversion of a dense metal-organic framework from a crystalline insulator to an amorphous semiconductor.

Tominaka S S   Hamoudi H H   Suga T T   Bennett T D TD   Cairns A B AB   Cheetham A K AK  

Chemical science 20141201 2


The topochemical conversion of a dense, insulating metal-organic framework (MOF) into a semiconducting amorphous MOF is described. Treatment of single crystals of copper(i) chloride trithiocyanurate, Cu<sup>I</sup>Cl(ttcH<sub>3</sub>) (ttcH<sub>3</sub> = trithiocyanuric acid), <b>1</b>, in aqueous ammonia solution yields monoliths of amorphous Cu<sup>I</sup><sub>1.8</sub>(ttc)<sub>0.6</sub>(ttcH<sub>3</sub>)<sub>0.4</sub>, <b>3</b>. The treatment changes the transparent orange crystals of <b>1</  ...[more]

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