Gallium Oxide Nanofibers for Hydrogen Evolution and Oxygen Reduction
Source abstract
Abstract
An effective, cost-efficient catalyst material that can replace platinum as electrode material in fuel cell has become the focus point of non-fossil fuel based alternate energy systems. Transition/post-transition metal oxide based catalyst development is now the thrust area in the above-mentioned context for efficient energy conversions, especially oxygen reduction reaction (ORR), oxygen evolution reaction (OER), and hydrogen evolution reaction (HER). Here, for the first time, application of electrospun β-gallium oxide (β-Ga2O3) nanofibers, a post-transition metal oxide, as an efficient bifunctional catalyst material is reported. These nanofibers are highly porous (specific surface area ∼100–300 m2/g) and exhibit a mesoporous architecture (pore size ∼1.5–2 nm) which facilitates better ion transport through the spongy morphology of individual nanofiber. The fabricated β-Ga2O3 nanofibers performed at par with the Pt/C catalyst, like for ORR the onset potential was 0.84 V (vs RHE) and for HER, although the onset potential was −0.34 V (vs RHE), the current density was visibly better than the latter catalyst. This catalyst also performed much better in methanol tolerance test and was near similar in current retention for 6 h, as measured in chronoamperometry. This performance was solely attributed to the large surface area and unique morphology presented by the material, via a rather simple fabrication technique, without addition of any dopant material.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Ga2O3 and related materials · ZnO doping and properties · Advanced Photocatalysis Techniques
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Department of Mechanical and Industrial Engineering, University of Illinois at Chicago, Chicago, Illinois 60607-7022, United States
Funding
Science and Engineering Research Board · Ministry of Human Resource Development · Indian Institute of Technology Mandi
References (61)
Show source-provided references
1. 10.1002/advs.20170051510.1002/advs.201700515 ↗
2. 10.1039/C5TA02974K10.1039/C5TA02974K ↗
3. 10.1007/s12274-014-0591-z10.1007/s12274-014-0591-z ↗
4. 10.1039/C3CS60468C10.1039/C3CS60468C ↗
5. 10.1126/science.110319710.1126/science.1103197 ↗
6. 10.1039/c0ee00558d10.1039/c0ee00558d ↗
7. 10.1016/B978-0-08-043877-1.50012-710.1016/B978-0-08-043877-1.50012-7 ↗
8. 10.1021/acsnano.5b0712610.1021/acsnano.5b07126 ↗
9. 10.1021/jacs.5b1198610.1021/jacs.5b11986 ↗
10. 10.1002/smll.20170114310.1002/smll.201701143 ↗
11. 10.1126/science.114048410.1126/science.1140484 ↗
12. 10.1039/C7NH00066A10.1039/C7NH00066A ↗
13. 10.1021/acs.jpcc.5b0387010.1021/acs.jpcc.5b03870 ↗
14. 10.1039/C4RA09341K10.1039/C4RA09341K ↗
15. 10.1007/s10562-012-0826-010.1007/s10562-012-0826-0 ↗
16. 10.1021/acs.jpcc.6b0031310.1021/acs.jpcc.6b00313 ↗
17. 10.1002/anie.20160156810.1002/anie.201601568 ↗
18. 10.1038/srep2339810.1038/srep23398 ↗
19. 10.1021/jacs.7b0658710.1021/jacs.7b06587 ↗
20. 10.1002/smll.20150292410.1002/smll.201502924 ↗
21. 10.1002/smll.20160005110.1002/smll.201600051 ↗
22. 10.1021/jp908322h10.1021/jp908322h ↗
23. 10.1016/j.electacta.2012.04.02810.1016/j.electacta.2012.04.028 ↗
24. 10.1149/06917.1237ecst10.1149/06917.1237ecst ↗
25. 10.1021/cs400944p10.1021/cs400944p ↗
26. 10.1039/C5CP01542A10.1039/C5CP01542A ↗
27. 10.1016/j.nanoen.2014.09.00910.1016/j.nanoen.2014.09.009 ↗
28. 10.1016/j.mtphys.2017.10.00210.1016/j.mtphys.2017.10.002 ↗
29. 10.1016/j.jcat.2005.03.00110.1016/j.jcat.2005.03.001 ↗
30. Ralph T. R. · Platinum Met. Rev. · 2002 · 46 · 11710.1595/003214002X463117135 ↗
31. 10.1016/j.electacta.2015.12.19310.1016/j.electacta.2015.12.193 ↗
32. 10.1155/2017/878601310.1155/2017/8786013 ↗
33. 10.1021/la034061x10.1021/la034061x ↗
34. 10.1295/polymj.29.55710.1295/polymj.29.557 ↗
35. 10.1016/S0167-577X(02)00713-910.1016/S0167-577X(02)00713-9 ↗
36. 10.1016/j.progpolymsci.2011.07.00110.1016/j.progpolymsci.2011.07.001 ↗
37. 10.1007/s10973-005-0909-x10.1007/s10973-005-0909-x ↗
38. 10.1002/chem.20120335910.1002/chem.201203359 ↗
39. 10.1016/S0022-3697(98)00047-X10.1016/S0022-3697(98)00047-X ↗
40. 10.1016/j.jiec.2013.12.08010.1016/j.jiec.2013.12.080 ↗
41. 10.1021/la047718310.1021/la0477183 ↗
42. 10.1063/1.485841910.1063/1.4858419 ↗
43. 10.1039/C7CE00553A10.1039/C7CE00553A ↗
44. 10.1002/pssa.20067530110.1002/pssa.200675301 ↗
45. 10.1002/app.2549810.1002/app.25498 ↗
46. 10.1016/S0032-3861(02)00136-210.1016/S0032-3861(02)00136-2 ↗
47. 10.1039/C7TA00828G10.1039/C7TA00828G ↗
48. 10.1021/cs500820610.1021/cs5008206 ↗
49. 10.1021/ja407552k10.1021/ja407552k ↗
50. 10.1149/1.277969210.1149/1.2779692 ↗
51. 10.1002/ange.20140384210.1002/ange.201403842 ↗
52. 10.1021/jacs.5b0268810.1021/jacs.5b02688 ↗
53. Sarno M. · Chem. Eng. Trans. · 2015 · 43 · 943
54. 10.1021/acsami.6b0874010.1021/acsami.6b08740 ↗
55. 10.1021/acsami.6b0126610.1021/acsami.6b01266 ↗
56. 10.1039/C8SC01710G10.1039/C8SC01710G ↗
57. 10.1039/C6CC04141H10.1039/C6CC04141H ↗
58. 10.1002/adma.20160166310.1002/adma.201601663 ↗
59. 10.1038/ncomms569510.1038/ncomms5695 ↗
60. 10.1039/C6TA05411K10.1039/C6TA05411K ↗
61. 10.1002/ange.20110017010.1002/ange.201100170 ↗