Metal-free, polyether-mediated H-2-release from ammonia borane: roles of hydrogen bonding interactions in promoting dehydrogenation

Abstract

Polyetheral additives were found to be efficient promoters to enhance the rate of H-2-release from ammonia borane (AB) at various temperatures. In particular, tetraethylene glycol dimethyl ether (T4EGDE, 29 wt% relative to AB + T4EGDE) exhibited significantly improved activities for AB dehydrogenation, with the material-based hydrogen storage capacity of 10.3 wt% at 125 degrees C within 40 min. In situ FT-IR spectroscopy indicated the formation of B-(cyclodiborazanyl) amino-borohydride (BCDB), borazine, and mu-aminodiborane as gaseous byproducts. In addition, B-11 nuclear magnetic resonance (NMR) spectroscopy further revealed that diammoniate of diborane (DADB) was initially formed to give polyaminoborane as liquid and/or solid spent-fuel, consistent with previous reports. Density Functional Theory (DFT) calculations suggested that hydrogen bonding interactions between AB and a polyetheral promoter initially played an important role in increasing the reactivity of B-H bonds of AB by transferring electron density from oxygen atoms of the promoter into B-H bonds of AB. These partially activated, hydridic B-H bonds were proposed to help promote the formation of diammoniate of diborane (DADB), which is considered as a reactive intermediate, eventually enhancing the rate of H-2-release from AB. In addition, our in situ solid state B-11 magic angle spinning (MAS) NMR measurements further confirmed that the rate of DADB formation from AB with a small quantity of T4EGDE was found to be much faster than that of pristine AB even at 50 degrees C. This metal-free method for H-2-release from AB with an added, small quantity of polyethers would be helpful to develop feasible hydrogen storage systems for long-term fuel cell applications.