Dehydrogenation of Ammonia Borane Confined by Low-Density Porous Aromatic Framework
Source abstract
Abstract
Ammonia borane (AB) has been considered as an outstanding candidate material for on-board hydrogen storage due to its high stoichiometric hydrogen content (19.6 wt %) and moderate dehydrogenation temperature. However, slow dehydrogenation kinetics below 100 °C and release of volatile byproducts (ammonia, borazine, and diborane) limited its practical applications. In this work, low-density and highly porous aromatic framework (PAF-1; BET, 4657 cm 2 g –1; pore volume, 2.55 cm 3 g –1 ) was utilized as a template for the first time to nanoconfine AB molecules. The dehydrogenation behavior of the confined AB was studied by temperature-programmed desorption mass spectrometry (TPD-MS) and pressure–composition–temperature (PCT) analyses. It was found that the AB molecules can be fully confined within the nanopores when the weight ratio of AB/PAF-1 is around 1:1. More importantly, AB started to dehydrogenate at very low temperature (around 50 °C) with the peak of 77 °C in the absence of any volatile byproducts such as ammonia, borazine, or diborane. Furthermore, about 4 wt % of hydrogen was evolved in the first 25 min at 75 °C which is 27 times higher than the pristine AB, displaying higher kinetics at low temperatures. Compared with other porous supports such as MOFs, the PAF-1 has a very low framework density because it is built up only by light C and H elements. This could significantly improve the hydrogen systemic gravimetric capacity of the AB-confined system and thus increase feasibility in practical applications.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Hydrogen Storage and Materials · Metal-Organic Frameworks: Synthesis and Applications · Covalent Organic Framework Applications
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
State Key Laboratory of Inorganic Synthesis and Preparative Chemistry, Jilin University, 130012 Changchun, P. R. China
Queensland Micro- and Nanotechnology Centre, Griffith University, Nathan, Queensland 4111, Australia
ARC Centre of Excellence for Functional Nanomaterials, The University of Queensland, St. Lucia, Queensland 4072, Australia
Centre for Clean Energy and Environment, Griffith University, Gold Coast Campus, Queensland 4222, Australia
References (28)
Show source-provided references
1. Liu C. · Adv. Mater. · 2010 · 22 · E2810.1002/adma.200903328 ↗
2. Lim K. L. · Chem. Eng. Technol. · 2010 · 33 · 21310.1002/ceat.200900376 ↗
3. Yildirim T. · Phys. Rev. Lett. · 2005 · 94 · 17550110.1103/PhysRevLett.94.175501 ↗
4. Rowsell J. L. C. · Angew. Chem., Int. Ed. · 2005 · 44 · 467010.1002/anie.200462786 ↗
5. Assfour B. · Int. J. Hydrogen Energy · 2011 · 36 · 600510.1016/j.ijhydene.2011.02.044 ↗
6. Shao H. · Nanotechnology · 2011 · 22 · 23540110.1088/0957-4484/22/23/235401 ↗
7. Sakintunaa B. · Int. J. Hydrogen Energy · 2007 · 32 · 112110.1016/j.ijhydene.2006.11.022 ↗
8. Liu C. · Carbon · 2010 · 48 · 45210.1016/j.carbon.2009.09.060 ↗
9. Satyapal, S.; Read, C.; Ordaz, G.; Thomas, G.DOE Hydrogen Program Annual Merit Review Proceedings, 2006, http://www.hydrogen.energy.gov/annual_review06_plenary.html.
10. Yan Y. · J. Am. Chem. Soc. · 2010 · 132 · 409210.1021/ja1001407 ↗
11. Dinca M. · Angew. Chem., Int. Ed. · 2007 · 46 · 141910.1002/anie.200604362 ↗
12. Liu Y. · Langmuir · 2008 · 24 · 477210.1021/la703864a ↗
13. Bogdanovic B. · Int. J. Hydrogen Energy · 1993 · 18 · 57510.1016/0360-3199(93)90178-D ↗
14. Chen P. · Nature · 2002 · 420 · 30210.1038/nature01210 ↗
15. Graham T. W. · Angew. Chem., Int. Ed. · 2010 · 49 · 870810.1002/anie.201003074 ↗
16. Xiong Z. · Nat. Mater. · 2008 · 7 · 13810.1038/nmat2081 ↗
17. Gutowska A. · Angew. Chem., Int. Ed. · 2005 · 44 · 357810.1002/anie.200462602 ↗
18. Li Z. · J. Am. Chem. Soc. · 2010 · 132 · 149010.1021/ja9103217 ↗
19. Gadipelli S. · Chem.–Eur. J. · 2011 · 17 · 604310.1002/chem.201100090 ↗
20. Srinivas G. · Int. J. Hydrogen Energy · 2011 · 37 · 363310.1016/j.ijhydene.2011.04.008 ↗
21. Li L. · Adv. Funct. Mater. · 2009 · 19 · 26510.1002/adfm.200801111 ↗
22. Ren H. · Chem. Commun. · 2010 · 46 · 29110.1039/B914761F ↗
23. Ben T. · Angew. Chem., Int. Ed. · 2009 · 48 · 945710.1002/anie.200904637 ↗
24. Ben T. · Energy Environ. Sci. · 2011 · 4 · 399110.1039/c1ee01222c ↗
25. Ben T. · Energy Environ. Sci. · 2012 · 5 · 837010.1039/c2ee21935b ↗
26. GrantGlover T. · Chem. Eng. Sci. · 2011 · 66 · 16310.1016/j.ces.2010.10.002 ↗
27. Stowe A. C. · Phys. Chem. Chem. Phys. · 2007 · 9 · 183110.1039/b617781f ↗
28. Lee S. M. · Chem. Phys. Chem. · 2009 · 10 · 182510.1002/cphc.200900283 ↗