The Package Matters
Tucking ammonia borane in mesoporous silica results in high-quality hydrogen at lower temperatures
Results: When it comes to squeezing hydrogen out of ammonia borane, the packaging matters, according to scientists from three national labs. Ammonia borane releases hydrogen with heating by a multi-step reaction, but the nominal heating required to release that hydrogen requires additional energy, decreasing the overall efficiency. The scientists found that less heat is needed to free the hydrogen when the ammonia borane is confined in a mesoporous form of silica.
In a recent study, they demonstrated the power of a relatively new method called "atomic pair distribution function" to study how mesoporous materials influence the molecules they confine. This new method provides far more insight into the nature of nanophase materials than conventional techniques.
This study was done by an interdisciplinary team from Los Alamos National Laboratory, Pacific Northwest National Laboratory, and Argonne National Laboratory.
Why it matters: Remote outposts, such as telecommunications towers, or emergency back-up power in isolated locations could benefit from reliable long lasting power supplies. While conventional methods are cumbersome or severely limited, hydrogen or other chemical bonds coupled with fuel cells could provide the needed energy. One of the stumbling blocks to making this happen is understanding and ultimately controlling the reactions that release and store the hydrogen.
Methods: The team began with synchrotron x-ray powder diffraction experiments on ammonia borane or NH3BH3 embedded in a form of mesoporous silica known as MCM-41. The silica contained pockets measuring between 2 and 50 nanometers across. The scientists obtained diffraction patterns for ammonia borane across a temperature range from 80K to 300K, which translates to about -315 to 80 degrees Fahrenheit.
The x-ray powder diffraction experiments were done at the XOR/BESSRC 11-ID-B beamline at the Advanced Photon Source at Argonne National Laboratory.
Next, the team used an analytical technique known as atomic pair distribution function or PDF to unravel the x-ray data. "This type of analysis tells you about the nanoscale ordering of the material," said Dr. Tom Autrey, a Pacific Northwest National Laboratory scientist on the team. "This analysis lets you look at atom pairs and understand group interactions."
The researchers found that ammonia borane changed from a well-ordered molecular crystal to a disordered solid at temperatures around 270K (26.33°F). Further, the ammonia borane skipped a structural change that the unconfined molecules experience at 225K (54°F).
The results of the atomic pair distribution analysis, combined with their earlier studies, suggested that a mesoporous silica packaging could play a key role in allowing hydrogen-rich molecules to release hydrogen at lower temperatures, costing less energy to get the reaction going, and providing hydrogen with fewer impurities.
What's next: At Pacific Northwest National Laboratory, Dr. Tom Autrey and his colleagues are looking at using mesoporous silica and similar materials to develop new approaches for the activation of molecular hydrogen. The activated hydrogen could be used to produce higher quality biofuels or be used to convert carbon dioxide to renewable fuels without the use of expensive metal catalysis.
"Catalysis is critical to a whole range of different energy applications, but catalytic activation of hydrogen without metals, well, that can be a game changer," said Autrey.
The Advanced Photon Source at Argonne National Laboratory was used in this research.
The work was done by Hyunjeong Kim and Thomas Proffen of Los Alamos National Laboratory; Abhi Karkamkar and Tom Autrey of Pacific Northwest National Laboratory; and Peter Chupas of Argonne National Laboratory.
Reference: Kim H, A Karkamkar, T Autrey, P Chupas, and T Proffen. 2009. "Determination of Structure and Phase Transition of Light Element Nanocomposites in Mesoporous Silica: Case Study of NH3BH3 in MCM-41," Journal of the American Chemical Society 131(38):13749-13755. DOI: 1021/ja904901d