3-Acetylpyridine (AcP), as an organic hydrogen carrier, and Pd nanoparticles, as a catalyst, were incorporated into MIL-101­(Cr) for chemical hydrogen storage. AcP was first grafted into MIL-101­(Cr), and then Pd (0.5–4.0 wt %) was encapsulated by a double-solvent adsorption process. Thermogravimetric analysis, inductively coupled plasma–optical emission spectrometry, X-ray photoelectron spectroscopy, transmission electron microscopy, in situ X-ray adsorption near-edge structure analysis, 1H nuclear magnetic resonance (NMR), and elemental analysis suggested the existence of AcP and Pd nanoparticles (NPs) inside the MIL-101­(Cr) cages. The chemical hydrogen storage of samples was evaluated by H2 temperature-programmed reaction. In situ Fourier transform infrared and 1H NMR techniques verified the hydrogenated and dehydrogenated forms of AcP upon hydrogen uptake. Reversible hydrogenation/dehydrogenation can be readily regulated by H2 partial pressure and temperature. The chemical hydrogen storage could be accomplished only when AcP and Pd NPs were adjacently present. The chemical hydrogen storage was enhanced with an increased Pd loading up to 0.33 mmol H2·g–1 per cycle. With the manipulation of hydrogenation and dehydrogenation temperatures at 150 °C, the chemical hydrogen storage can be maintained for up to 10 cycles. The material reported herein is one of the noncryogenic chemical hydrogen storages that can be operated at constant temperature and atmospheric pressure.

Highly stable Pd2+ species were anchored in ethylenediamine-grafted on MIL-101(Cr). The ethylenediamine (0.3-1.2 mmol/g) was first grafted onto MIL-101(Cr), then Pd2+ (0.03-0.2 mmol Pd/g) was incorporated by double-solvent adsorption. Fourier...