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The correlation of maximum hydrogen uptake with surface area and micropore volume was investigated.
Although some MOFs exhibit remarkable hydrogen storage capacity with maximum hydrogen uptake up to 11 wt%, which exceeds the 2010 DOE hydrogen storage target of 6.0 wt%, and the required low adsorption temperature impedes onboard storage applications.
The maximum hydrogen uptake capacity (0.36 wt.%) showed the material with the Pd nanoparticle diameter of 11 nm, and the hydrogen storage capacity was enhanced by the factor of two in respect to the pristine HCS.
Development of high-capacity hydrogen-storage systems utilizing physisorption at high pressure and low temperature is hindered by poor understanding of the pore size/shape requirements for achieving the maximum hydrogen uptake.
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The maximum hydrogen uptakes were measured to be 3.2 wt% at −196 °C and 0.28 wt% at 35 °C.
The electrode system has made feasible simultaneous measurements of the hydrogen uptake in PdHx films where the maximum composition reached was PdH0.81.
The behavior of all the components of the EEC undergoes a clear transition when the hydrogenation degree of the electrode is approximated to its maximum value (H to Y ratio 2.7) and electrochemical process changes from hydrogen uptake to hydrogen evolution.
The (3,3) K-decorated BNNT with maximum coverage of two fifth is found to adsorb at most 36 H2 with Eb of 0.41 eV/H2, corresponding to a hydrogen uptake of 8.5 % by weight.
Maximum hydrogen production is desired in optimization.
The Ir– and Rh SiO2 nano-hollows exhibited excess hydrogen uptake.
The hydrogen uptake mechanism of the modified CNTs was discussed.
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