journal article·2021-02

B, N Co‐doped Nanocarbon Derived In Situ from Nanoboron Carbide as Electrocatalyst for Oxygen Reduction Reaction

Shuyu Zhou, Jianbing Zang, Wei Li, Pengfei Tian, Hongwei Gao, Shiwei Song, Xueqing Tian, Yanhui Wang

ChemNanoMat· Volume 7· Issue 2
Publisher page

Abstract

Abstract Heteroatom‐doped metal free carbon materials, especially boron and nitrogen co‐doped carbons have been widely researched as promising oxygen reduction electrocatalysts because of their low cost, high activity and environmental friendliness. However, B, N‐doped carbon electrocatalysts are usually prepared at high temperature and accompanied by the formation of B−N bonds resulting in the inactivation of the active sites. This paper proposed a strategy for synthesizing B and N co‐doped carbons for oxygen reduction reaction in‐situ derived from nano‐boron carbide by one‐step heat treatment at low temperature. This strategy can produce B‐ and N‐doped active sites while avoiding formation of B−N bonds, allowing electrocatalysts to exhibit excellent catalytic activities (Eonset=0.93 V, E1/2=0.79 V) and better stability (current density remained 93.3% after 12,000 s) comparable to commercial Pt/C (20 wt%). New ideas were provided by this work to massively produce the B and N co‐doped carbon electrocatalysts candidates for ORR.
Source: crossref · Quality: baseline

Research context

OpenAlex topics: Electrocatalysts for Energy Conversion · Fuel Cells and Related Materials · Advancements in Battery Materials

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

Affiliations

Institution State Key Laboratory of Metastable Materials Science and Technology College of Materials Science and Engineering Yanshan University Qinhuangdao 066004 P. R. China

References (52)

Show source-provided references
1. 10.1021/acscatal.5b0052410.1021/acscatal.5b00524 ↗
2. 10.1002/cssc.20190303510.1002/cssc.201903035 ↗
3. 10.1038/s41524-019-0210-310.1038/s41524-019-0210-3 ↗
4. 10.1016/j.ijhydene.2018.04.11810.1016/j.ijhydene.2018.04.118 ↗
5. 10.1016/j.jcis.2019.08.06410.1016/j.jcis.2019.08.064 ↗
6. 10.1016/j.jcis.2020.02.08910.1016/j.jcis.2020.02.089 ↗
7. 10.1016/j.apsusc.2020.14795010.1016/j.apsusc.2020.147950 ↗
8. 10.1002/smll.20177018710.1002/smll.201770187 ↗
9. Shao Y. · Chem. · 2019 · 12 · 2133
10. 10.1002/cctc.20190158410.1002/cctc.201901584 ↗
11. 10.1039/C8TA06743K10.1039/C8TA06743K ↗
12. 10.1016/j.eurpolymj.2018.01.00810.1016/j.eurpolymj.2018.01.008 ↗
13. Feng L. · Sci. Total Environ. · 2020 · 698 · 1
14. 10.1002/cplu.20190008310.1002/cplu.201900083 ↗
15. 10.1016/j.nanoen.2019.03.08410.1016/j.nanoen.2019.03.084 ↗
16. 10.1039/C8TA07994C10.1039/C8TA07994C ↗
17. 10.1016/j.electacta.2018.02.01710.1016/j.electacta.2018.02.017 ↗
18. 10.1016/j.nanoen.2017.11.00410.1016/j.nanoen.2017.11.004 ↗
19. 10.1002/chem.20170451510.1002/chem.201704515 ↗
20. 10.1002/anie.20110128710.1002/anie.201101287 ↗
21. 10.1002/ange.20110128710.1002/ange.201101287 ↗
22. 10.1016/j.electacta.2014.08.00110.1016/j.electacta.2014.08.001 ↗
23. 10.1039/C5CC01963J10.1039/C5CC01963J ↗
24. 10.1039/C7CS00690J10.1039/C7CS00690J ↗
25. 10.1021/acsami.7b1865110.1021/acsami.7b18651 ↗
26. 10.1002/cssc.20180296010.1002/cssc.201802960 ↗
27. Zhang M. · ACS Sustainable Chem. Eng. · 2019 · 7
28. Wang W. · Int. J. Hydrogen Energy. · 2019 · 44
29. Sun T. · Adv. Sci. · 2018 · 5 · 1
30. 10.1021/acsnano.6b0131810.1021/acsnano.6b01318 ↗
31. 10.1021/ja310566z10.1021/ja310566z ↗
32. 10.1002/anie.20110925710.1002/anie.201109257 ↗
33. 10.1016/j.electacta.2016.10.20110.1016/j.electacta.2016.10.201 ↗
34. 10.1039/C5CP04211A10.1039/C5CP04211A ↗
35. Vineesh T. V. · Adv. Energy Mater. · 2015 · 5
36. 10.1039/C9CC03413G10.1039/C9CC03413G ↗
37. Zhou Y. · Chem. Front. · 2018 · 5 · 2985
38. 10.1016/j.carbon.2016.04.01810.1016/j.carbon.2016.04.018 ↗
39. 10.1002/aenm.20190094510.1002/aenm.201900945 ↗
40. 10.1021/jp404409410.1021/jp4044094 ↗
41. 10.1016/j.jcis.2018.03.02210.1016/j.jcis.2018.03.022 ↗
42. 10.1016/j.carbon.2019.01.03910.1016/j.carbon.2019.01.039 ↗
43. 10.1021/acsanm.8b0143010.1021/acsanm.8b01430 ↗
44. 10.1021/acs.chemmater.8b0402710.1021/acs.chemmater.8b04027 ↗
45. 10.1002/anie.20120954810.1002/anie.201209548 ↗
46. 10.1039/C3EE42799D10.1039/C3EE42799D ↗
47. 10.1002/adma.20160039810.1002/adma.201600398 ↗
48. 10.1039/C6TA07214C10.1039/C6TA07214C ↗
49. 10.1039/C4RA10162F10.1039/C4RA10162F ↗
50. 10.1016/j.carbon.2019.01.10610.1016/j.carbon.2019.01.106 ↗
51. 10.1021/acssuschemeng.9b0142610.1021/acssuschemeng.9b01426 ↗
52. 10.1039/D0TA05908K10.1039/D0TA05908K ↗