journal article·2022-02-08

Synergistic Effect of Nickel Oxyhydroxide and Tungsten Carbide in Electrocatalytic Alcohol Oxidation

Mengrui Zhang, Jianping Zhu, Rong Wan, Bin Liu, Dongdi Zhang, Chao Zhang, Jingping Wang, Jingyang Niu

Chemistry of Materials· Volume 34· Issue 3
Publisher page

Abstract

Design and synthesis of efficient small organic molecule-based electrooxidation catalysts in replacing conventional oxygen evolution reaction (OER) catalysts has been considered as an alternative path to enable large-scale renewable energy storage. In contrast to OER, alcohol oxidation reactions can be implemented at lower applied potentials along with generating higher value-added byproducts than oxygen. Here, the ultrafine Ni/WC hybrid nanoparticles (NPs) were successfully synthesized via an in situ trapping and space-confinement pyrolysis strategy. The as-synthesized Ni/WC hybrid NPs exhibit high electrooxidation performances in oxidizing methanol, ethanol, iso-propanol, ethylene glycol, and propylene glycol in alkaline solution. Particularly, for the methanol oxidation reaction, Ni/WC NPs demonstrate high reaction activity (specific activity: 325 mA cm–2 at 0.6 V vs Ag/AgCl/3.5 M KCl; mass activity: 1363 mA mg–1) and excellent stability (catalytic current drops ∼6.8% after 4 h). In the first 6 h of the electrolysis process, methanol was effectively converted into formate with ca. 93.8% Faraday efficiency. Based on in situ IR spectra and control catalyst experiments, tungsten carbide (WC) and nickel oxyhydroxide (NiOOH, derived from Ni) species are capable of activating different functional groups of methanol. More interestingly, their hybrid structure (Ni/WC) demonstrates improved catalytic performance in converting methanol into a formate product for the synergistic effect.
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

Henan Key Laboratory of Polyoxometalate Chemistry, Institute of Molecular and Crystal Engineering, College of Chemistry and Chemical Engineering, Henan University, Kaifeng, Henan 475004, P. R. China

Funding

National Natural Science Foundation of China · Henan University · Program for Science and Technology Innovation Talents in the Universities of Henan Province

References (54)

Show source-provided references
1. 10.1021/acscatal.7b0155110.1021/acscatal.7b01551 ↗
2. 10.1002/adfm.20200693910.1002/adfm.202006939 ↗
3. 10.1021/jacs.5b0818610.1021/jacs.5b08186 ↗
4. 10.1038/s41467-018-03429-z10.1038/s41467-018-03429-z ↗
5. 10.1021/jacs.6b0519010.1021/jacs.6b05190 ↗
6. 10.1002/celc.20140226210.1002/celc.201402262 ↗
7. 10.1039/C6CS00328A10.1039/C6CS00328A ↗
8. 10.1039/C5EE02463C10.1039/C5EE02463C ↗
9. 10.1002/anie.20170243010.1002/anie.201702430 ↗
10. 10.1021/ja405351s10.1021/ja405351s ↗
11. 10.1002/anie.20140394610.1002/anie.201403946 ↗
12. 10.1021/cs300309810.1021/cs3003098 ↗
13. 10.1021/acsenergylett.6b0057410.1021/acsenergylett.6b00574 ↗
14. 10.1039/c2ee21928j10.1039/c2ee21928j ↗
15. 10.1016/j.jpowsour.2008.03.07510.1016/j.jpowsour.2008.03.075 ↗
16. 10.1038/s41467-020-18461-110.1038/s41467-020-18461-1 ↗
17. 10.1039/C2EE02552C10.1039/C2EE02552C ↗
18. 10.1126/sciadv.170058010.1126/sciadv.1700580 ↗
19. 10.1002/anie.20170114910.1002/anie.201701149 ↗
20. 10.1021/cr400389f10.1021/cr400389f ↗
21. 10.1016/j.apcatb.2018.12.01710.1016/j.apcatb.2018.12.017 ↗
22. 10.1021/acscatal.8b0036610.1021/acscatal.8b00366 ↗
23. 10.1002/adma.20170565310.1002/adma.201705653 ↗
24. 10.1021/acscatal.0c0149810.1021/acscatal.0c01498 ↗
25. 10.1016/S0022-0728(99)00235-110.1016/S0022-0728(99)00235-1 ↗
26. 10.1007/s10800-008-9636-x10.1007/s10800-008-9636-x ↗
27. 10.1021/acscatal.0c0375610.1021/acscatal.0c03756 ↗
28. 10.1007/s12274-020-2649-410.1007/s12274-020-2649-4 ↗
29. 10.1021/am506554b10.1021/am506554b ↗
30. 10.1016/j.apcatb.2014.02.01910.1016/j.apcatb.2014.02.019 ↗
31. 10.1039/c7ta01982c10.1039/c7ta01982c ↗
32. 10.1016/j.ijhydene.2018.04.16510.1016/j.ijhydene.2018.04.165 ↗
33. 10.1021/acsami.5b1250910.1021/acsami.5b12509 ↗
34. 10.1002/cctc.20150064610.1002/cctc.201500646 ↗
35. 10.1021/acsaem.9b0133210.1021/acsaem.9b01332 ↗
36. 10.1021/ic50174a06010.1021/ic50174a060 ↗
37. 10.1039/DT992000190110.1039/DT9920001901 ↗
38. 10.1021/acsami.6b1441210.1021/acsami.6b14412 ↗
39. 10.1021/acscatal.9b0122610.1021/acscatal.9b01226 ↗
40. 10.1039/D1CC03446D10.1039/D1CC03446D ↗
41. 10.1016/j.ijhydene.2011.05.02810.1016/j.ijhydene.2011.05.028 ↗
42. 10.1039/C8EE01129J10.1039/C8EE01129J ↗
43. 10.1016/j.jelechem.2015.03.02410.1016/j.jelechem.2015.03.024 ↗
44. 10.1149/2.078403jes10.1149/2.078403jes ↗
45. 10.1002/smll.20120083910.1002/smll.201200839 ↗
46. 10.1002/anie.20190713610.1002/anie.201907136 ↗
47. 10.1016/j.apcatb.2018.12.01310.1016/j.apcatb.2018.12.013 ↗
48. 10.1016/j.apcatb.2018.10.04710.1016/j.apcatb.2018.10.047 ↗
49. 10.1021/acsami.8b1625610.1021/acsami.8b16256 ↗
50. 10.1002/anie.20190713610.1002/anie.201907136 ↗
51. 10.1038/s41563-021-01006-210.1038/s41563-021-01006-2 ↗
52. 10.1007/s10973-005-0466-010.1007/s10973-005-0466-0 ↗
53. 10.3847/1538-4357/ab3c4f10.3847/1538-4357/ab3c4f ↗
54. 10.1016/j.bbabio.2008.04.02510.1016/j.bbabio.2008.04.025 ↗