Ruthenium-Based High-Entropy Alloys Expediting Hydrogen Evolution through Catalytic Hydrolysis of Ammonia Borane
Source abstract
Abstract
Currently, ammonia borane (AB, NH 3 BH 3 ) hydrolysis is considered an available tactic for hydrogen evolution under ambient conditions, which includes many complex reaction steps, such as the activation and adsorption of AB and water molecules on the catalyst. Therefore, exploiting the high-performance catalysts with multiple active sites to match the multistep catalytic processes in AB hydrolysis is a critical and urgent task but a tough challenge. Herein, we propose a synthesis scheme for a high-entropy alloy (HEA) catalyst for hydrogen liberation from AB hydrolysis. The FeCoNiMnRu HEA with face-centered cubic (fcc) phase was synthesized by the polymer fiber nanoreactor method using low-cost transition metals of Co, Fe, Mn, and Ni as basic elements combined with the precious metal Ru, which facilitates the electron transfer and enhances the synergistic interaction between these elements, hence enhancing the catalytic activity toward AB hydrolysis to release hydrogen. For instance, the as-synthesized Fe 23 Co 27 Ni 27 Mn 12 Ru 11 HEA catalyst shows superior activity in catalyzing AB hydrolysis with an apparent activation energy ( E a ) of 42.3 kJ·mol –1 and a turnover frequency (TOF) of 55.3 mol H2 ·mol Ru –1 ·min –1 at 298 K. This work affords a facile approach for the synthesis of low-cost and high-efficiency catalysts for AB hydrolysis to produce hydrogen.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Hydrogen Storage and Materials · Advanced Chemical Physics Studies · Nuclear Materials and Properties
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Guangxi Key Laboratory of Information Materials, School of Materials Science and Engineering, Guilin University of Electronic Technology, Guilin 541004, China
Funding
Natural Science Foundation of Guangxi Zhuang Autonomous Region · National Natural Science Foundation of China · Science and Technology Major Program of Guangxi Province · Innovation Platform and Talent Program Project of Guilin · Guilin Lijiang Scholar Foundation
References (55)
Show source-provided references
1. 10.1016/j.ijhydene.2018.02.19010.1016/j.ijhydene.2018.02.190 ↗
2. 10.1016/j.ijhydene.2009.01.00210.1016/j.ijhydene.2009.01.002 ↗
3. 10.1016/j.ijhydene.2010.07.16410.1016/j.ijhydene.2010.07.164 ↗
4. 10.1016/j.jallcom.2022.16620710.1016/j.jallcom.2022.166207 ↗
5. 10.1016/j.jpowsour.2005.05.04310.1016/j.jpowsour.2005.05.043 ↗
6. 10.1021/acsaem.2c0363610.1021/acsaem.2c03636 ↗
7. 10.1039/D1SE00079A10.1039/D1SE00079A ↗
8. 10.1021/acsaem.9b0099710.1021/acsaem.9b00997 ↗
9. 10.1021/acsanm.0c0120810.1021/acsanm.0c01208 ↗
10. 10.1016/j.ijhydene.2017.12.07910.1016/j.ijhydene.2017.12.079 ↗
11. 10.1007/s12274-024-6750-y10.1007/s12274-024-6750-y ↗
12. 10.1016/j.ijhydene.2019.01.24810.1016/j.ijhydene.2019.01.248 ↗
13. 10.1039/D2SE01542K10.1039/D2SE01542K ↗
14. 10.1002/adsu.20220046410.1002/adsu.202200464 ↗
15. 10.1039/C9GC03986D10.1039/C9GC03986D ↗
16. 10.1016/j.ijhydene.2018.06.05810.1016/j.ijhydene.2018.06.058 ↗
17. 10.1016/j.jcis.2017.11.03710.1016/j.jcis.2017.11.037 ↗
18. 10.1039/D0SE00660B10.1039/D0SE00660B ↗
19. 10.1016/j.jpowsour.2014.01.12210.1016/j.jpowsour.2014.01.122 ↗
20. 10.1016/j.apcatb.2012.05.04810.1016/j.apcatb.2012.05.048 ↗
21. 10.1002/anie.20231655010.1002/anie.202316550 ↗
22. 10.1016/j.jallcom.2013.12.13410.1016/j.jallcom.2013.12.134 ↗
23. 10.1016/j.matchemphys.2024.12939810.1016/j.matchemphys.2024.129398 ↗
24. 10.1002/adsu.20210020910.1002/adsu.202100209 ↗
25. 10.1007/s12274-023-5667-110.1007/s12274-023-5667-1 ↗
26. 10.1002/adem.20030056710.1002/adem.200300567 ↗
27. 10.1038/s41467-019-10303-z10.1038/s41467-019-10303-z ↗
28. 10.1126/science.abn310310.1126/science.abn3103 ↗
29. 10.1016/j.esci.2024.10029510.1016/j.esci.2024.100295 ↗
30. 10.1002/adfm.20200961310.1002/adfm.202009613 ↗
31. 10.1021/jacs.2c0354410.1021/jacs.2c03544 ↗
32. 10.1021/jacs.1c0764310.1021/jacs.1c07643 ↗
33. 10.1039/D2RA01064J10.1039/D2RA01064J ↗
34. 10.1038/s41467-019-11848-910.1038/s41467-019-11848-9 ↗
35. 10.1126/science.aan541210.1126/science.aan5412 ↗
36. 10.1126/science.aaf840210.1126/science.aaf8402 ↗
37. 10.1002/smll.20190418010.1002/smll.201904180 ↗
38. 10.1002/adma.20200038510.1002/adma.202000385 ↗
39. 10.1016/j.matt.2020.07.02710.1016/j.matt.2020.07.027 ↗
40. 10.1038/s41467-024-50009-510.1038/s41467-024-50009-5 ↗
41. 10.3866/PKU.WHXB20230705710.3866/PKU.WHXB202307057 ↗
42. 10.1038/s41467-023-44261-410.1038/s41467-023-44261-4 ↗
43. 10.1002/adma.20230545310.1002/adma.202305453 ↗
44. 10.1021/jacs.1c1361610.1021/jacs.1c13616 ↗
45. 10.1126/sciadv.adl369310.1126/sciadv.adl3693 ↗
46. 10.1038/s41929-019-0376-610.1038/s41929-019-0376-6 ↗
47. 10.1051/epjap/202322033010.1051/epjap/2023220330 ↗
48. 10.1016/j.apcatb.2021.12009410.1016/j.apcatb.2021.120094 ↗
49. 10.1002/anie.20240819310.1002/anie.202408193 ↗
50. 10.1016/j.mtnano.2024.10048510.1016/j.mtnano.2024.100485 ↗
51. 10.1039/D2EE03185J10.1039/D2EE03185J ↗
52. 10.1038/s41467-022-30379-410.1038/s41467-022-30379-4 ↗
53. 10.1007/s40820-022-00986-310.1007/s40820-022-00986-3 ↗
54. 10.1016/j.cej.2021.13325110.1016/j.cej.2021.133251 ↗
55. 10.1016/j.jcis.2017.02.03010.1016/j.jcis.2017.02.030 ↗