journal article·2021-06-28

ZnCl2 as a “Nitrogen Bank” to Inhibit Nitrogen Loss during the Thermal Conversion of Nitrogen-Containing Carbon Precursors to Nitrogen-Doped Carbon

Yuke Su, Suqin Liu, Guanying Ye, Weiwei Zhu, Kuangmin Zhao, Rongjiao Huang, Zhen He

ACS Applied Energy Materials· Volume 4· Issue 6
Publisher page

Abstract

A universal synthesis strategy for inhibiting the nitrogen loss during the thermal conversion of N-containing carbon precursors to nitrogen-doped carbon is developed. ZnCl2, as a sacrificial additive in the pyrolysis, acts like a “nitrogen bank” (“N-bank”) to accommodate the N-containing intermediates from the decomposed precursors and redopes the nitrogen back into the final carbon materials. The nitrogen-doped carbon synthesized by this N-bank synthesis strategy has a significantly elevated nitrogen content and shows an excellent catalytic performance toward the oxygen reduction reaction (E1/2 = 0.89 VRHE).
Source: openalex_inverted_index · Quality: baseline

Research context

OpenAlex topics: Ammonia Synthesis and Nitrogen Reduction · Nanomaterials for catalytic reactions · Catalytic Processes in Materials Science

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

Affiliations

College of Chemistry and Chemical Engineering, Central South University, Changsha, Hunan 410083, People’s Republic of China

Hunan Provincial Key Laboratory of Chemical Power Sources, Central South University, Changsha, Hunan 410083, People’s Republic of China

Funding

National Natural Science Foundation of China · Hunan Province

References (28)

Show source-provided references
1. 10.1002/adma.20180429710.1002/adma.201804297 ↗
2. 10.1002/anie.20201279810.1002/anie.202012798 ↗
3. 10.1002/adma.20150321110.1002/adma.201503211 ↗
4. 10.1039/C8SC01801D10.1039/C8SC01801D ↗
5. 10.1002/adfm.20200109710.1002/adfm.202001097 ↗
6. 10.1021/jacs.9b0935210.1021/jacs.9b09352 ↗
7. 10.1039/C9EE00162J10.1039/C9EE00162J ↗
8. 10.1039/C9TA04954A10.1039/C9TA04954A ↗
9. 10.1021/acsenergylett.9b0174010.1021/acsenergylett.9b01740 ↗
10. 10.1002/adfm.20170535610.1002/adfm.201705356 ↗
11. 10.1007/s10973-007-8615-510.1007/s10973-007-8615-5 ↗
12. 10.1007/s11243-009-9257-110.1007/s11243-009-9257-1 ↗
13. 10.1016/0040-6031(85)85006-110.1016/0040-6031(85)85006-1 ↗
14. 10.1016/S0010-8545(00)80404-X10.1016/S0010-8545(00)80404-X ↗
15. 10.1021/acssuschemeng.8b0410510.1021/acssuschemeng.8b04105 ↗
16. 10.1016/j.nanoen.2018.08.00310.1016/j.nanoen.2018.08.003 ↗
17. 10.1021/acsnano.7b0380710.1021/acsnano.7b03807 ↗
18. 10.1021/acssuschemeng.0c0728510.1021/acssuschemeng.0c07285 ↗
19. 10.1002/smll.20170416910.1002/smll.201704169 ↗
20. 10.1016/j.nanoen.2019.05.06610.1016/j.nanoen.2019.05.066 ↗
21. 10.1016/j.nanoen.2019.01.05710.1016/j.nanoen.2019.01.057 ↗
22. 10.1002/cssc.20180296010.1002/cssc.201802960 ↗
23. 10.1039/D0GC00168F10.1039/D0GC00168F ↗
24. 10.1021/acs.langmuir.0c0167010.1021/acs.langmuir.0c01670 ↗
25. 10.1016/j.jssc.2014.06.00510.1016/j.jssc.2014.06.005 ↗
26. 10.1016/j.chempr.2019.07.02010.1016/j.chempr.2019.07.020 ↗
27. 10.1039/C7TA06916B10.1039/C7TA06916B ↗
28. 10.1002/cssc.20190277610.1002/cssc.201902776 ↗