Oxygen Evolution Reaction Electrocatalytic Improvement in POM@ZIF Nanocomposites: A Bidirectional Synergistic Effect
Source abstract
Abstract
A bidirectional synergy involving Co-based polyoxometalates (POMs) incorporated in the Co-containing zeolitic imidazolate framework, ZIF-67, that promoted a notable improvement in the oxygen evolution reaction (OER) performance was unveiled for the first time. Two POM@ZIF nanocomposite materials—SiW9Co3@ZIF-8 and SiW9Co3@ZIF-67—were successfully prepared via a room temperature “in situ” approach, by the immobilization of POM anions [SiW9Co3(H2O)3O37]10– (SiW9Co3) in the cages of two isostructural ZIFs: ZIF-8 and ZIF-67, formed with Zn2+ and Co2+, respectively. Despite both SiW9Co3@ZIF-8 and SiW9Co3@ZIF-67 revealing similar and low occupancy degrees (ca. 6 POM units per 100 ZIF-cages), an intense synergy has been detected in the ZIF-67 based nanocomposite, while no synergistic interaction was found for POMs and ZIF-8. Due to this synergistic effect, the OER activity of SiW9Co3@ZIF-67 is significantly enhanced in comparison with that of ZIF-67: ∼110 mV decreased overpotential and double current density. Additionally, this nanocomposite exhibits excellent stability in the alkaline electrolyte. Insights into the nature and magnitude of the SiW9Co3–ZIF-67 synergy have shown up its interesting ZIF ↔ POM bidirectional nature that involves activation of the Co-based active sites in POM clusters as a consequence of a ZIF-67 → SiW9Co3 electron transfer, along with POM-induced generation of more active unsaturated Co-nodes in the ZIF-67 frameworks. These findings represent a promising “proof of concept” for the development of more efficient POM@MOF-based electrocatalysts in the future.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Electrocatalysts for Energy Conversion · Polyoxometalates: Synthesis and Applications · Advanced Nanomaterials in Catalysis
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
REQUIMTE/LAQV and Department of Chemistry and Biochemistry, Faculty of Sciences, University of Porto, 4169-007 Porto, Portugal
Funding
European Regional Development Fund · Funda??o para a Ci?ncia e a Tecnologia
References (52)
Show source-provided references
1. 10.1002/adma.20180152610.1002/adma.201801526 ↗
2. 10.1002/cssc.20180206910.1002/cssc.201802069 ↗
3. 10.1002/cctc.20170192610.1002/cctc.201701926 ↗
4. 10.1021/acscatal.8b0171510.1021/acscatal.8b01715 ↗
5. 10.1002/aenm.20170277410.1002/aenm.201702774 ↗
6. 10.1002/aenm.20170051810.1002/aenm.201700518 ↗
7. 10.1002/smll.20180357610.1002/smll.201803576 ↗
8. 10.1016/j.nanoen.2019.10393510.1016/j.nanoen.2019.103935 ↗
9. 10.1021/acscatal.6b0247910.1021/acscatal.6b02479 ↗
10. 10.1039/C9CC02845E10.1039/C9CC02845E ↗
11. 10.1021/acssuschemeng.9b0131510.1021/acssuschemeng.9b01315 ↗
12. 10.1021/acssuschemeng.8b0574410.1021/acssuschemeng.8b05744 ↗
13. 10.1002/celc.20170121010.1002/celc.201701210 ↗
14. 10.1016/j.jcat.2018.09.01110.1016/j.jcat.2018.09.011 ↗
15. 10.1039/C7CC09223G10.1039/C7CC09223G ↗
16. 10.1002/9781119242659.ch510.1002/9781119242659.ch5 ↗
17. 10.1016/j.ijhydene.2017.01.20710.1016/j.ijhydene.2017.01.207 ↗
18. 10.1021/acsami.7b0963410.1021/acsami.7b09634 ↗
19. 10.1016/j.apcatb.2016.12.01610.1016/j.apcatb.2016.12.016 ↗
20. 10.1021/acsami.7b1013810.1021/acsami.7b10138 ↗
21. 10.1039/C6TA09193H10.1039/C6TA09193H ↗
22. 10.1016/j.carbon.2015.12.04510.1016/j.carbon.2015.12.045 ↗
23. 10.1002/adma.20150504510.1002/adma.201505045 ↗
24. 10.1021/acsami.6b0697910.1021/acsami.6b06979 ↗
25. 10.1039/C9TA03833G10.1039/C9TA03833G ↗
26. 10.1021/cr960403a10.1021/cr960403a ↗
27. 10.1039/C7TA08268A10.1039/C7TA08268A ↗
28. 10.1002/anie.20090248310.1002/anie.200902483 ↗
29. 10.1039/c3nj00243h10.1039/c3nj00243h ↗
30. 10.1002/anie.20171192010.1002/anie.201711920 ↗
31. 10.1039/C7TA08683K10.1039/C7TA08683K ↗
32. 10.1016/j.electacta.2012.09.09910.1016/j.electacta.2012.09.099 ↗
33. 10.1021/am404256410.1021/am4042564 ↗
34. 10.1002/celc.20140209410.1002/celc.201402094 ↗
35. 10.1021/acsaem.8b0201010.1021/acsaem.8b02010 ↗
36. 10.1021/acs.inorgchem.7b0033310.1021/acs.inorgchem.7b00333 ↗
37. 10.1039/C5RA17427A10.1039/C5RA17427A ↗
38. 10.1016/j.nanoen.2016.08.04010.1016/j.nanoen.2016.08.040 ↗
39. 10.1002/admi.20160063210.1002/admi.201600632 ↗
40. 10.1021/ic50174a06010.1021/ic50174a060 ↗
41. 10.1039/DT992000190110.1039/DT9920001901 ↗
42. 10.1021/ic00144a00610.1021/ic00144a006 ↗
43. 10.1021/acsami.5b0394810.1021/acsami.5b03948 ↗
44. 10.1002/chem.20150449710.1002/chem.201504497 ↗
45. 10.1039/C7TA04662F10.1039/C7TA04662F ↗
46. 10.1039/C6RA25810G10.1039/C6RA25810G ↗
47. 10.1002/adma.20170087410.1002/adma.201700874 ↗
48. 10.1021/jp504105310.1021/jp5041053 ↗
49. 10.1039/C7TC03150E10.1039/C7TC03150E ↗
50. 10.1021/acsami.6b0798610.1021/acsami.6b07986 ↗
51. 10.1039/C6CS00328A10.1039/C6CS00328A ↗
52. 10.1039/C8MH01397G10.1039/C8MH01397G ↗