journal article·2018-02-21

CoHPi Nanoflakes for Enhanced Oxygen Evolution Reaction

Jingjing Wang, Hua Chun Zeng

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Abstract

Electrochemical splitting of water to produce hydrogen and oxygen is an important process for many energy storage and conversion devices. Developing efficient, robust, low-cost, and earth-abundant electrocatalysts for the oxygen evolution reaction (OER) is therefore of great importance. Herein, we report a novel method to prepare two-dimensional cobalt hydrogen phosphate (CoHPi) through chemical conversion of α-Co(OH) 2 precursor at room temperature. The CoHPi nanoflakes with the thickness of 3 nm contain HPO 4 2– anions, which have been demonstrated to serve as a proton acceptor in proton-coupled electron-transfer (PCET) process of OER. Due to their ultrathin structure and the PCET merit of anions, the CoHPi nanoflakes show enhanced OER activity as well as excellent stability in prolonged OER operation. Through further mechanism study, the observed performances can be ascribed to enriched active sites, surface superhydrophilicity, and rapid electron/proton and mass transfers.
Source: openalex_inverted_index · Quality: baseline

Research context

OpenAlex topics: Electrocatalysts for Energy Conversion · Advanced battery technologies research · Electrochemical Analysis and Applications

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

Affiliations

Department of Chemical and Biomolecular Engineering, Faculty of Engineering, National University of Singapore, 10 Kent Ridge Crescent, Singapore 119260, Singapore

Funding

Ministry of Education - Singapore · National Research Foundation Singapore · National University of Singapore

References (47)

Show source-provided references
1. 10.1039/c4cs00470a10.1039/c4cs00470a ↗
2. 10.1016/j.nanoen.2015.12.03210.1016/j.nanoen.2015.12.032 ↗
3. 10.1021/jacs.6b1225010.1021/jacs.6b12250 ↗
4. 10.1002/aenm.20140188010.1002/aenm.201401880 ↗
5. 10.1039/C5EE03453A10.1039/C5EE03453A ↗
6. 10.1038/nmat308710.1038/nmat3087 ↗
7. 10.1039/C6CC05699G10.1039/C6CC05699G ↗
8. 10.1021/jacs.5b0246510.1021/jacs.5b02465 ↗
9. 10.1039/C5CS00434A10.1039/C5CS00434A ↗
10. 10.1038/ncomms1232410.1038/ncomms12324 ↗
11. 10.1038/nmat331310.1038/nmat3313 ↗
12. 10.1021/ja407115p10.1021/ja407115p ↗
13. 10.1021/ja502128j10.1021/ja502128j ↗
14. 10.1021/acs.chemrev.6b0039810.1021/acs.chemrev.6b00398 ↗
15. 10.1021/ja412886e10.1021/ja412886e ↗
16. 10.1002/anie.20140933310.1002/anie.201409333 ↗
17. 10.1021/acs.chemmater.6b0152210.1021/acs.chemmater.6b01522 ↗
18. 10.1002/smll.20120320210.1002/smll.201203202 ↗
19. 10.1039/C6TA01929C10.1039/C6TA01929C ↗
20. 10.1039/B802885K10.1039/B802885K ↗
21. 10.1002/anie.20140684810.1002/anie.201406848 ↗
22. 10.1002/anie.20161041310.1002/anie.201610413 ↗
23. 10.1039/C4CS00160E10.1039/C4CS00160E ↗
24. 10.1021/ja052333810.1021/ja0523338 ↗
25. 10.1016/S0167-577X(98)00195-510.1016/S0167-577X(98)00195-5 ↗
26. 10.1016/j.jelechem.2014.03.01910.1016/j.jelechem.2014.03.019 ↗
27. 10.1039/C6CY01861K10.1039/C6CY01861K ↗
28. 10.4067/S0717-9707201500020000510.4067/S0717-97072015000200005 ↗
29. 10.1016/j.cej.2013.09.10310.1016/j.cej.2013.09.103 ↗
30. 10.1002/aenm.20160062110.1002/aenm.201600621 ↗
31. 10.1002/adma.20150269610.1002/adma.201502696 ↗
32. 10.1021/nn506983610.1021/nn5069836 ↗
33. 10.1002/aenm.20150166110.1002/aenm.201501661 ↗
34. 10.1002/adfm.20140011810.1002/adfm.201400118 ↗
35. 10.1039/c1ee02444b10.1039/c1ee02444b ↗
36. 10.1002/adfm.20160632510.1002/adfm.201606325 ↗
37. 10.1038/s41598-017-03526-x10.1038/s41598-017-03526-x ↗
38. 10.1002/anie.20150222610.1002/anie.201502226 ↗
39. 10.1039/C4RA13993C10.1039/C4RA13993C ↗
40. 10.1021/acscatal.6b0349710.1021/acscatal.6b03497 ↗
41. 10.1002/aenm.20150024510.1002/aenm.201500245 ↗
42. 10.1021/nl504872s10.1021/nl504872s ↗
43. 10.1002/aenm.20160155510.1002/aenm.201601555 ↗
44. 10.1002/adfm.20120092010.1002/adfm.201200920 ↗
45. 10.1002/anie.20160437210.1002/anie.201604372 ↗
46. 10.1021/jacs.6b0539810.1021/jacs.6b05398 ↗
47. 10.1021/jacs.6b0076210.1021/jacs.6b00762 ↗