Efficient Co-Nanocrystal-Based Catalyst for Hydrogen Generation from Borohydride
Source abstract
Abstract
Sodium borohydride (NaBH 4 ) has been proposed as a potential hydrogen storage material for fuel cells, and the development of highly active and robust catalysts for hydrolyzing NaBH 4 is the key for the practical usage of NaBH 4 for fuel cells. Herein we report Co-nanocrystal assembled hollow nanoparticles (Co-HNP) as an active and robust catalyst for the hydrolysis of NaBH 4 . A hydrogen generation rate of 10.8 L·min –1 ·g –1 at 25 °C was achieved by using the Co-HNP catalyst with a low activation energy of 23.7 kJ·mol –1, which is among the best performance of reported noble and non-noble catalysts for hydrolyzing NaBH 4 . Co-HNP also showed good stability in the long term cycling tests. The mechanism of the catalytic hydrolysis of NaBH 4 on Co-HNP was studied by using 1 H and 11 B solid-state NMR, which provided unambiguous experimental evidence of the Co–H formation. The systematically designed NMR experiments unveiled the key role of Co-HNP in the activation of borohydride and the subsequent transfer of H – to water for generating H 2 gas and helped to distinguish various hypotheses proposed for catalytic H 2 generation reactions. The porous hollow nanostructure of the Co-HNP catalyst provides large surface area and facilitates mass transfer. The facile preparation and outstanding performance of Co-HNP enables it as a very competitive catalyst for hydrogen production.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Hydrogen Storage and Materials · Hybrid Renewable Energy Systems · Superconductivity in MgB2 and Alloys
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
CAS Key Laboratory of Soft Matter Chemistry, iChEM (Collaborative Innovation Center of Chemistry for Energy Materials), Department of Chemistry, University of Science and Technology of China, Hefei, Anhui 230026, People’s Republic of China
Department of Chemistry and Biochemistry, Florida State University, Tallahassee, Florida 32306, United States
Funding
American Chemical Society Petroleum Research Fund · National Natural Science Foundation of China · Natural Science Foundation of Anhui Province
References (27)
Show source-provided references
1. 10.1038/3510463410.1038/35104634 ↗
2. 10.1039/C4EE03690E10.1039/C4EE03690E ↗
3. 10.1016/j.ijhydene.2009.01.00210.1016/j.ijhydene.2009.01.002 ↗
4. 10.1039/b900595a10.1039/b900595a ↗
5. 10.1021/acscatal.6b0071510.1021/acscatal.6b00715 ↗
6. 10.1002/cssc.20150022810.1002/cssc.201500228 ↗
7. 10.1016/j.ijhydene.2016.04.05810.1016/j.ijhydene.2016.04.058 ↗
8. 10.1039/C5CY01756D10.1039/C5CY01756D ↗
9. 10.1016/j.jpowsour.2015.03.01310.1016/j.jpowsour.2015.03.013 ↗
10. 10.1016/j.ijhydene.2015.11.07610.1016/j.ijhydene.2015.11.076 ↗
11. 10.1016/j.jpowsour.2008.11.12110.1016/j.jpowsour.2008.11.121 ↗
12. 10.1016/j.ijhydene.2009.02.00710.1016/j.ijhydene.2009.02.007 ↗
13. 10.1016/j.cattod.2010.09.00710.1016/j.cattod.2010.09.007 ↗
14. 10.1016/j.nanoen.2016.03.01710.1016/j.nanoen.2016.03.017 ↗
15. 10.1016/j.jallcom.2005.08.01910.1016/j.jallcom.2005.08.019 ↗
16. 10.1016/j.ijhydene.2012.06.11710.1016/j.ijhydene.2012.06.117 ↗
17. 10.1016/j.ijhydene.2008.09.05510.1016/j.ijhydene.2008.09.055 ↗
18. 10.1016/j.ijhydene.2008.12.09710.1016/j.ijhydene.2008.12.097 ↗
19. 10.1002/anie.20160136710.1002/anie.201601367 ↗
20. 10.1021/jp063362n10.1021/jp063362n ↗
21. 10.1002/cctc.20110010110.1002/cctc.201100101 ↗
22. 10.1016/j.jpowsour.2007.12.00610.1016/j.jpowsour.2007.12.006 ↗
23. 10.1021/jp805115m10.1021/jp805115m ↗
24. 10.1016/j.ijhydene.2014.07.09310.1016/j.ijhydene.2014.07.093 ↗
25. 10.1016/j.ijhydene.2011.04.22310.1016/j.ijhydene.2011.04.223 ↗
26. 10.1016/S0010-8545(02)00118-210.1016/S0010-8545(02)00118-2 ↗
27. 10.1021/acs.chemrev.6b0009110.1021/acs.chemrev.6b00091 ↗