Integrating Electrochemical CO2 Reduction on α-NiS with the Water or Organic Oxidations by Its Electro-Oxidized NiO(OH) Counterpart to an Artificial Photosynthetic Scheme
Source abstract
Abstract
Efficient hydrogen production, biomass up-conversion, and CO 2 -to-fuel generation are the key challenges of the present decade. Electrocatalysis in aqueous electrolytes by choosing suitable transition-metal-based electrode materials remains the green approach for the trio of sustainable developments. Given that, finding electrode materials with multifunctional capability would be beneficial. Herein, the nanocrystalline α-NiS, synthesized solvothermally, has been chosen as an electrode material. As the first step to construct an electrolyzer, α-NiS deposited on conducting nickel foam (NF) has been used as an anode, and under the anodic potential, the α-NiS particles have lost sulfides to the electrolyte and transform to amorphous electro-derived NiO(OH) (NiO(OH) ED ), confirmed by different spectroscopic and microscopic studies. In situ transformation of α-NiS to amorphous NiO(OH) ED results in an enhancement of the electrochemical surface area and not only becomes active toward oxygen evolution reaction (OER) at a moderate overpotential of 264 mV (at 20 mA cm –2 ) but also can convert a series of biomass-derived organic compounds, namely, 2-hydroxymethylfurfural (HMF), 2-furfural (FF), ethylene glycol (EG), and glycerol (Gly), to industrially relevant feedstocks with a high (∼96%) Faradaic efficiency. During these organic oxidations, NiO(OH) ED /NF participate in the multiple-electron oxidation process (up to 8e – ) including C–C bond cleavages of EG and Gly. During the cathodic performance of the α-NiS/NF, the structural integrity has been retained and the unaltered α-NiS/NF electrode remains more effective cathode for alkaline hydrogen evolution reaction (HER) and CO 2 reduction (CO 2 R) compared to its in situ-derived NiO(OH) ED /NF. α-NiS/NF can reduce the CO 2 predominantly to CO even at a higher potential like −0.8 V ( vs RHE). The fabricated cell with α-NiS and its electro-oxidized NiO(OH) ED counterpart, α-NiS/NF(−)/(+)NiO(OH) ED /NF, is able to show an artificial photosynthetic scheme in which the NiO(OH) ED /NF anode oxidizes water to O 2 and the α-NiS cathode reduces CO 2 majorly to CO in a moderate cell potential. In this study, α-NiS has been utilized as a single electrode material to perform multiple sustainable transformations.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Electrocatalysts for Energy Conversion · Advanced battery technologies research · Supercapacitor Materials and Fabrication
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Department of Chemistry, Indian Institute of Technology Delhi, Hauz Khas, 110016 New Delhi, India
Funding
Department of Science and Technology, Ministry of Science and Technology, India
References (70)
Show source-provided references
1. Darmawan A. · 2022 · 14910.1016/B978-0-323-85477-1.00006-3 ↗
2. 10.1021/cs400456310.1021/cs4004563 ↗
3. Gupta M. K. · 2017 · 17110.1016/B978-1-63067-050-4.00007-6 ↗
4. 10.1039/C9EE01673B10.1039/C9EE01673B ↗
5. 10.1038/ncomms1148110.1038/ncomms11481 ↗
6. 10.1038/s41467-021-24529-310.1038/s41467-021-24529-3 ↗
7. 10.1021/acs.chemmater.7b0266610.1021/acs.chemmater.7b02666 ↗
8. 10.1126/science.aaf505010.1126/science.aaf5050 ↗
9. 10.1021/ja407115p10.1021/ja407115p ↗
10. 10.1021/acsami.8b0081310.1021/acsami.8b00813 ↗
11. 10.1002/anie.20160889910.1002/anie.201608899 ↗
12. 10.1021/jacs.8b0222510.1021/jacs.8b02225 ↗
13. 10.1038/s41586-022-04595-310.1038/s41586-022-04595-3 ↗
14. 10.1039/D1GC00914A10.1039/D1GC00914A ↗
15. 10.1021/acsenergylett.6b0021410.1021/acsenergylett.6b00214 ↗
16. 10.1002/aenm.20200137710.1002/aenm.202001377 ↗
17. 10.1002/adma.20200409810.1002/adma.202004098 ↗
18. 10.1002/cssc.20170207510.1002/cssc.201702075 ↗
19. 10.1039/JR954000140610.1039/JR9540001406 ↗
20. 10.1021/acs.chemrev.0c0033510.1021/acs.chemrev.0c00335 ↗
21. 10.1021/acscatal.8b0101710.1021/acscatal.8b01017 ↗
22. 10.1039/D0TA08393C10.1039/D0TA08393C ↗
23. 10.1038/s41929-017-0009-x10.1038/s41929-017-0009-x ↗
24. 10.1038/s41598-020-59714-910.1038/s41598-020-59714-9 ↗
25. 10.1103/RevModPhys.40.75210.1103/RevModPhys.40.752 ↗
26. 10.1016/j.jallcom.2019.07.22210.1016/j.jallcom.2019.07.222 ↗
27. 10.1002/anie.20191283610.1002/anie.201912836 ↗
28. 10.1007/s10008-017-3600-910.1007/s10008-017-3600-9 ↗
29. 10.1021/acs.inorgchem.2c0116710.1021/acs.inorgchem.2c01167 ↗
30. 10.1021/acs.jpcc.2c0519610.1021/acs.jpcc.2c05196 ↗
31. 10.1039/C7TA06671F10.1039/C7TA06671F ↗
32. 10.1021/jacs.5b0818610.1021/jacs.5b08186 ↗
33. 10.1021/acsami.8b0936110.1021/acsami.8b09361 ↗
34. 10.1039/D0CS00962H10.1039/D0CS00962H ↗
35. 10.1021/acsenergylett.6b0008410.1021/acsenergylett.6b00084 ↗
36. 10.1002/adma.20150390610.1002/adma.201503906 ↗
37. 10.1002/adfm.20160056610.1002/adfm.201600566 ↗
38. 10.1039/D2TA02620A10.1039/D2TA02620A ↗
39. 10.1002/cphc.20190051110.1002/cphc.201900511 ↗
40. 10.1021/acsaem.8b0071010.1021/acsaem.8b00710 ↗
41. 10.1021/acsami.2c0130210.1021/acsami.2c01302 ↗
42. 10.1021/acsnano.8b0631210.1021/acsnano.8b06312 ↗
43. 10.1021/acsenergylett.7b0067910.1021/acsenergylett.7b00679 ↗
44. 10.1021/acsami.5b1009910.1021/acsami.5b10099 ↗
45. 10.1021/acscatal.8b0383510.1021/acscatal.8b03835 ↗
46. 10.1002/smsc.20210003010.1002/smsc.202100030 ↗
47. 10.1021/acsami.6b1398410.1021/acsami.6b13984 ↗
48. 10.1021/acsami.7b1643010.1021/acsami.7b16430 ↗
49. 10.1021/acs.jpcc.5b0010510.1021/acs.jpcc.5b00105 ↗
50. 10.1021/acs.jpcc.1c0617010.1021/acs.jpcc.1c06170 ↗
51. 10.1016/j.ijhydene.2022.07.18210.1016/j.ijhydene.2022.07.182 ↗
52. 10.1021/acs.nanolett.0c0084010.1021/acs.nanolett.0c00840 ↗
53. 10.1021/acscatal.8b0400310.1021/acscatal.8b04003 ↗
54. 10.1021/jacs.6b0712710.1021/jacs.6b07127 ↗
55. 10.1039/D2TA00863G10.1039/D2TA00863G ↗
56. 10.1021/acs.joc.1c0152010.1021/acs.joc.1c01520 ↗
57. 10.1021/acscatal.0c0149810.1021/acscatal.0c01498 ↗
58. 10.1002/anie.20200548910.1002/anie.202005489 ↗
59. 10.1002/cctc.20110002310.1002/cctc.201100023 ↗
60. 10.1021/acsenergylett.0c0138510.1021/acsenergylett.0c01385 ↗
61. 10.1039/C5CY01111F10.1039/C5CY01111F ↗
62. 10.1039/C8SC03555E10.1039/C8SC03555E ↗
63. 10.1021/acscatal.2c0262710.1021/acscatal.2c02627 ↗
64. 10.1039/D0TA11518E10.1039/D0TA11518E ↗
65. 10.1002/aenm.20220184310.1002/aenm.202201843 ↗
66. 10.1039/c3ee40534f10.1039/c3ee40534f ↗
67. 10.1021/acscatal.2c0175010.1021/acscatal.2c01750 ↗
68. 10.1021/jacs.7b0489210.1021/jacs.7b04892 ↗
69. 10.1002/adfm.20200944910.1002/adfm.202009449 ↗
70. 10.1039/C9FD00141G10.1039/C9FD00141G ↗