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.

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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.

The effect of cooling down to 150 K on the structures of