4 in 1: multifunctional europium-organic frameworks with luminescence sensing properties, white light emission, proton conductivity and reverse acetylene-carbon dioxide adsorption selectivity.

Lanthanide metal-organic frameworks (Ln-MOFs) combine the lanthanide luminescence characteristics and the advantages of porous materials, which can be used in various research fields by exploring their multifunctional properties. A three-dimensional water-stable and high-temperature resistant Eu-MOF [Eu(H2O)(HL)]·0.5MeCN·0.25H2O (H4L = 4-(3,5-dicarboxyphenoxy)isophthalic acid), demonstrating a high photoluminescence quantum yield, was synthesized and structurally characterized. In terms of luminescence, the Eu-MOF exhibits excellent selectivity and quenching sensing for Fe3+ (LOD = 4.32 µM) and ofloxacin, as well as color modulation with Tb3+ and La3+ to develop white LED components with high illumination efficiency (color rendering index, CRI = 90). On the other hand, narrow one-dimensional channels of the Eu-MOF decorated with COOH groups enable a rare reverse adsorption selectivity in a CO2/C2H2 gas mixture. In addition, the protonated carboxyl groups in the Eu-MOF provide an efficient conducting platform for proton transfer with a conductivity value of 8 × 10-4 S cm-1 at 50 °C and RH 100%.

High proton conductivity and spectroscopic investigations of metal-organic framework materials impregnated by strong acids.

Strong toluenesulfonic and triflic acids were incorporated into a MIL-101 chromium(III) terephthalate coordination framework, producing hybrid proton-conducting solid electrolytes. These acid@MIL hybrid materials possess stable crystalline structures that do not deteriorate during multiple measurements or prolonged heating. Particularly, the triflic-containing compound demonstrates the highest 0.08 S cm(-1) proton conductivity at 15% relative humidity and a temperature of 60 °C, exceeding any of today's commercial materials for proton-exchange membranes. The structure of the proton-conducting media, as well as the long-range proton-transfer mechanics, was unveiled, in a certain respect, by Fourier transform infrared and (1)H NMR spectroscopy investigations. The acidic media presumably constitutes large separated droplets, coexisting in the MIL nanocages. One component of proton transfer appears to be related to the facile relay (Grotthuss) mechanism through extensive hydrogen-bonding interactions within such droplets. The second component occurs during continuous reorganization of the droplets, thus ensuring long-range proton transfer along the porous structure of the material.

Imparting high proton conductivity to a metal-organic framework material by controlled acid impregnation.

The extensive implementation of hydrogen-powered technology today is limited by a number of fundamental problems related to materials research. Fuel-cell hydrogen conversion technology requires proton-conducting materials with high conductivity at intermediate temperatures up to 120 °C. The development of such materials remains challenging because the proton transport of many promising candidates is based on extended microstructures of water molecules, which deteriorate at temperatures above the boiling point. Here we show the impregnation of the mesoporous metal-organic framework (MOF) MIL-101 by nonvolatile acids H(2)SO(4) and H(3)PO(4). Such a simple approach affords solid materials with potent proton-conducting properties at moderate temperatures, which is critically important for the proper function of on-board automobile fuel cells. The proton conductivities of the H(2)SO(4)@MIL-101 and H(3)PO(4)@MIL-101 at T = 150 °C and low humidity outperform those of any other MOF-based materials and could be compared with the best proton conductors, such as Nafion.