Improving Electrocatalytic Activity of MoO3 for the Oxygen Evolution Reaction by Incorporation of Li Ions
Source abstract
Abstract
Several polymorphs of MoO 3 with different crystal and electronic structures provide many opportunities to find suitable electrocatalysts for water splitting hydrogen generation. So far, promising electrocatalytic activity for hydrogen evolution reaction (HER) has been found for α-MoO 3 (orthorhombic), while the polymorph has shown a poor oxygen evolution reaction (OER) activity. In this work, it is found that the intrinsic OER activity of α-MoO 3 is remarkably improved by incorporating guest ions of lithium-ion (Li + ). α-MoO 3 nanoparticles were deposited on a carbon fiber paper (α-MoO 3 /CFP) by chemical vapor transport and a subsequent lithiation process was applied to prepare lithiated α-MoO 3 /CFP (Li-α-MoO 3 /CFP), showing the robust η 10 of 458 mV. The improved OER activity in the lithiated electrode is attributed to the incorporation of Li + into the MoO 3, which increases the electron carrier density and the corresponding electrical conductivity, thereby improving the interfacial charge transfer kinetics as well as activating a large number of ECSA.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Electrocatalysts for Energy Conversion · Advanced battery technologies research · Fuel Cells and Related Materials
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Department of Mechanical Engineering, Massachusetts Institute of Technology, Cambridge, Massachusetts 02139, Unites States of America
School of Advanced Materials and Chemical Engineering, Daegu Catholic University, Gyeongsan 38430, Gyeongbuk Republic of Korea
Department of Energy Science, Sungkyunkwan University, Suwon 16419, Republic of Korea
Department of Physics, Pusan National University, Pusan 46241, Republic of Korea
Funding
National Research Foundation of Korea
References (41)
Show source-provided references
1. 10.1021/cr100246c10.1021/cr100246c ↗
2. 10.1073/pnas.071068310410.1073/pnas.0710683104 ↗
3. 10.1021/jacs.8b0454610.1021/jacs.8b04546 ↗
4. 10.1039/C9EE01202H10.1039/C9EE01202H ↗
5. 10.1021/ja407115p10.1021/ja407115p ↗
6. 10.1021/ja510442p10.1021/ja510442p ↗
7. 10.1126/science.121285810.1126/science.1212858 ↗
8. 10.1039/C4EE03869J10.1039/C4EE03869J ↗
9. 10.1007/s12598-020-01384-710.1007/s12598-020-01384-7 ↗
10. 10.1002/celc.20190014310.1002/celc.201900143 ↗
11. 10.3390/catal1011130110.3390/catal10111301 ↗
12. 10.1039/C4CS00350K10.1039/C4CS00350K ↗
13. 10.1021/acs.cgd.8b0089410.1021/acs.cgd.8b00894 ↗
14. 10.3390/molecules2501001810.3390/molecules25010018 ↗
15. 10.1002/adma.20170161910.1002/adma.201701619 ↗
16. 10.1002/aenm.20160052810.1002/aenm.201600528 ↗
17. 10.1016/j.elecom.2009.07.00510.1016/j.elecom.2009.07.005 ↗
18. 10.1021/nl202047610.1021/nl2020476 ↗
19. 10.1002/smll.20170044110.1002/smll.201700441 ↗
20. 10.1039/D0TA12152E10.1039/D0TA12152E ↗
21. 10.1016/j.jallcom.2019.15334610.1016/j.jallcom.2019.153346 ↗
22. 10.1016/j.matchemphys.2020.12357010.1016/j.matchemphys.2020.123570 ↗
23. 10.1021/acssuschemeng.7b0426610.1021/acssuschemeng.7b04266 ↗
24. 10.1002/adma.20070088310.1002/adma.200700883 ↗
25. 10.1073/pnas.131679211010.1073/pnas.1316792110 ↗
26. 10.1007/s12678-019-00561-210.1007/s12678-019-00561-2 ↗
27. 10.1039/b107046k10.1039/b107046k ↗
28. 10.1016/j.solmat.2016.02.01010.1016/j.solmat.2016.02.010 ↗
29. 10.1039/C5NR08118A10.1039/C5NR08118A ↗
30. 10.1039/D1TA10492F10.1039/D1TA10492F ↗
31. Beamson G. · 1992
32. 10.1021/acs.jpcc.5b0260910.1021/acs.jpcc.5b02609 ↗
33. 10.1021/jp503065x10.1021/jp503065x ↗
34. 10.1002/adma.20120334610.1002/adma.201203346 ↗
35. 10.1021/jp106837g10.1021/jp106837g ↗
36. 10.1002/adfm.20200417210.1002/adfm.202004172 ↗
37. 10.1039/C7QI00780A10.1039/C7QI00780A ↗
38. 10.1039/C6CS00328A10.1039/C6CS00328A ↗
39. Krasil’shchikov A. I. · Zh. Fiz. Khim. · 1963 · 37 · 531
40. 10.1149/2.015303jes10.1149/2.015303jes ↗
41. 10.1021/cm102703s10.1021/cm102703s ↗