The highly unfavorable thermodynamics of direct aluminum hydrogenation can be overcome by stabilizing alane within a nanoporous bipyridine-functionalized covalent triazine framework (AlH₃ @CTF-bipyridine). This material and the counterpart AlH₃ @CTF-biphenyl rapidly desorb H₂ between 95 and 154 °C, with desorption complete at 250 °C. Sieverts measurements, ²⁷ Al MAS NMR and ²⁷ Al{¹ H} REDOR experiments, and computational spectroscopy reveal that AlH₃ @CTF-bipyridine dehydrogenation is reversible at 60 °C under 700 bar hydrogen, >10 times lower pressure than that required to hydrogenate bulk aluminum. DFT calculations and EPR measurements support an unconventional mechanism whereby strong AlH₃ binding to bipyridine results in single-electron transfer to form AlH₂ (AlH₃ )_n clusters. The resulting size-dependent charge redistribution alters the dehydrogenation/rehydrogenation thermochemistry, suggesting a novel strategy to enable reversibility in high-capacity metal hydrides.

Abstract: The highly unfavorable thermodynamics of direct aluminum hydrogenation can be overcome by stabilizing alane within a nanoporous bipyridine‐functionalized covalent triazine framework (AlH3@CTF‐bipyridine). This material and the counterpart AlH3@CTF‐biphenyl rapidly desorb H2 between 95 and 154 °C, with desorption complete at 250 °C. Sieverts measurements, 27Al MAS NMR and 27Al{1H} REDOR experiments, and computational spectroscopy reveal that AlH3@CTF‐bipyridine dehydrogenation is reversible at 60 °C under 700 bar hydrogen, >10 times lower pressure than that required to hydrogenate bulk aluminum. DFT calculations and EPR measurements support an unconventional mechanism whereby strong AlH3 binding to bipyridine results in single‐electron transfer to form AlH2(AlH3)n clusters. The resulting size‐dependent charge redistribution alters the dehydrogenation/rehydrogenation thermochemistry, suggesting a novel strategy to enable reversibility in high‐capacity metal hydrides.