One-Pot Synthesis of B/P-Codoped Co-Mo Dual-Nanowafer Electrocatalysts for Overall Water Splitting
Source abstract
Abstract
Exploring electrocatalysts with satisfactory activity and durability has remained a long-lasting target for electrolyzing water, which is particularly significant for sustainable hydrogen fuel production. Here, we report a quaternary B/P-codoped transition metal Co-Mo hybrid as an efficient alternative catalyst for overall water splitting. The Co-Mo-B-P/CF dual nanowafers were deposited on a copper foam by double-pulse electrodeposition, which is favorable for achieving a nanocrystalline structure. The Co-Mo-B-P/CF catalyst shows a high catalytic activity along with good long-term stability in 1.0 M KOH solutions for both the hydrogen and oxygen evolution reactions, requiring 48 and 275 mV to reach 10 mA cm–2, respectively. The synergetic effect between Co-Mo and doped B and P elements is mainly attributed to the excellent bifunctional catalysis performance, while the dual-nanowafer structure endows Co-Mo-B-P with numerous catalytical active sites enhancing the utilization efficiency of atoms. Moreover, the catalytic capability of Co-Mo-B-P/CF as a bifunctional electrocatalyst for the overall water splitting is proved, with the current density of 10 mA cm–2 accomplished at 1.59 V. After the stability test for overall water splitting at 1.59 V for 24 h, the activity almost remains unchanged. The features of excellent electrocatalytic activity, simple preparation, and inexpensive raw materials for Co-Mo-B-P/CF as a bifunctional catalyst hold great potentials for overall water splitting.
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
School of Physics and Electronic Engineering, Jiangsu Normal University, Xuzhou, Jiangsu 221116, China
Department of Physics and Astronomy, University of California, Irvine, California 92697, United States
School of Chemical Engineering & Technology, China University of Mining and Technology, Xuzhou, Jiangsu 221116, China
Funding
National Natural Science Foundation of China · H.L.X.?s startup funding
References (65)
Show source-provided references
1. 10.1039/D0NR00752H10.1039/D0NR00752H ↗
2. 10.1016/j.elecom.2017.12.00810.1016/j.elecom.2017.12.008 ↗
3. 10.1016/j.ijhydene.2016.12.13010.1016/j.ijhydene.2016.12.130 ↗
4. 10.1016/j.apsusc.2020.14605910.1016/j.apsusc.2020.146059 ↗
5. 10.1038/s41560-019-0326-110.1038/s41560-019-0326-1 ↗
6. 10.1038/s41929-019-0246-210.1038/s41929-019-0246-2 ↗
7. 10.1016/j.ijhydene.2016.11.13410.1016/j.ijhydene.2016.11.134 ↗
8. 10.1002/cctc.20160160710.1002/cctc.201601607 ↗
9. 10.1002/chem.20180209210.1002/chem.201802092 ↗
10. 10.1038/nchem.163410.1038/nchem.1634 ↗
11. 10.1039/C8TA02999G10.1039/C8TA02999G ↗
12. 10.1016/j.ijhydene.2017.08.14810.1016/j.ijhydene.2017.08.148 ↗
13. 10.1021/ja510442p10.1021/ja510442p ↗
14. 10.1002/adfm.20150366610.1002/adfm.201503666 ↗
15. 10.1016/j.cattod.2015.08.01410.1016/j.cattod.2015.08.014 ↗
16. 10.1039/C7TA02333B10.1039/C7TA02333B ↗
17. 10.1016/j.nanoen.2018.05.03310.1016/j.nanoen.2018.05.033 ↗
18. 10.1021/acscatal.8b0156710.1021/acscatal.8b01567 ↗
19. 10.1002/chem.20170356510.1002/chem.201703565 ↗
20. 10.1038/nchem.269510.1038/nchem.2695 ↗
21. 10.1038/s41560-019-0355-910.1038/s41560-019-0355-9 ↗
22. 10.1021/ja01097a05710.1021/ja01097a057 ↗
23. 10.1002/smll.20170080510.1002/smll.201700805 ↗
24. 10.1021/jacs.7b0633710.1021/jacs.7b06337 ↗
25. 10.1039/C8CC03902J10.1039/C8CC03902J ↗
26. 10.1021/acsami.7b0103710.1021/acsami.7b01037 ↗
27. 10.1016/j.chempr.2017.09.00310.1016/j.chempr.2017.09.003 ↗
28. 10.1021/ja408105610.1021/ja4081056 ↗
29. 10.1016/j.jcat.2018.03.00410.1016/j.jcat.2018.03.004 ↗
30. 10.1007/s11467-019-0950-z10.1007/s11467-019-0950-z ↗
31. 10.1021/jacs.9b0121410.1021/jacs.9b01214 ↗
32. 10.1016/j.jpowsour.2020.22785810.1016/j.jpowsour.2020.227858 ↗
33. 10.1039/C5GC02073E10.1039/C5GC02073E ↗
34. 10.1039/C4TA03962A10.1039/C4TA03962A ↗
35. 10.1039/C7TA11033B10.1039/C7TA11033B ↗
36. 10.1039/C3CS60468C10.1039/C3CS60468C ↗
37. 10.1002/chem.20200191710.1002/chem.202001917 ↗
38. 10.1002/aenm.20160206810.1002/aenm.201602068 ↗
39. 10.1021/acsami.9b0464810.1021/acsami.9b04648 ↗
40. 10.1039/C5EE01155H10.1039/C5EE01155H ↗
41. 10.1021/acs.nanolett.5b0344610.1021/acs.nanolett.5b03446 ↗
42. 10.1002/celc.20170111210.1002/celc.201701112 ↗
43. 10.1021/acsami.7b0615210.1021/acsami.7b06152 ↗
44. 10.1016/j.apcatb.2019.01.03410.1016/j.apcatb.2019.01.034 ↗
45. 10.1021/jacs.6b0849110.1021/jacs.6b08491 ↗
46. 10.1021/acscentsci.8b0073410.1021/acscentsci.8b00734 ↗
47. 10.1021/acsami.7b0615210.1021/acsami.7b06152 ↗
48. 10.1016/j.molcata.2007.05.02710.1016/j.molcata.2007.05.027 ↗
49. 10.1007/s11426-018-9397-510.1007/s11426-018-9397-5 ↗
50. 10.1016/j.apcatb.2016.03.03210.1016/j.apcatb.2016.03.032 ↗
51. 10.1002/adma.20170457410.1002/adma.201704574 ↗
52. 10.1039/C7TA02644G10.1039/C7TA02644G ↗
53. 10.1016/j.ijhydene.2019.01.03610.1016/j.ijhydene.2019.01.036 ↗
54. 10.1016/j.apsusc.2020.14649110.1016/j.apsusc.2020.146491 ↗
55. 10.1007/s11244-012-9889-910.1007/s11244-012-9889-9 ↗
56. 10.1016/j.elecom.2017.12.01110.1016/j.elecom.2017.12.011 ↗
57. 10.1039/C8NR02198H10.1039/C8NR02198H ↗
58. 10.1021/acsami.6b0581110.1021/acsami.6b05811 ↗
59. 10.1016/j.elecom.2017.04.01410.1016/j.elecom.2017.04.014 ↗
60. 10.1021/ja407115p10.1021/ja407115p ↗
61. 10.1021/acs.chemmater.6b0279610.1021/acs.chemmater.6b02796 ↗
62. 10.1002/cssc.20130101910.1002/cssc.201301019 ↗
63. 10.1007/s11244-012-9889-910.1007/s11244-012-9889-9 ↗
64. 10.1021/acsami.0c1744510.1021/acsami.0c17445 ↗
65. Gong Z. · J. Funct. Mater. · 2006 · 06 · 940