journal article·2021-06

Stabilizing Black Phosphorus via Covalent Functionalization of Solvent Formamide

Zuoliang He, Rui Liu, Wanyu Shan, Huachao Zhao, Yujian Lai, Peng Li, Jingfu Liu

Advanced Materials Interfaces· Volume 8· Issue 11
Publisher page

Abstract

Abstract Black phosphorus (BP) has been attracting increasing scientific and technological interest for its excellent materials properties, but suffers from the intrinsic easy oxidization due to the high reactivity of lone‐pair electrons in each phosphorus atom. Herein, solvent formamide (FM) is proposed for the covalent modification of BP by a one‐step ultrasonication without any additive. FM is demonstrated to functionalize BP by the formation of single covalent bond PN, thus occupying the active lone‐pair electrons of P atoms and leading to the significant enhancement of the antioxidative capacity of BP. Density functional theory calculations also rationalize the formation of stable PN bond and its contribution to the high solvent‐exfoliated efficiency during the exfoliation of BP. The plausible reaction mechanism of FM with BP and the final 5‐membered ring structure of products are also proposed to explain the formation process of the stable PN bonds.
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Research context

OpenAlex topics: 2D Materials and Applications · MXene and MAX Phase Materials · Advanced Photocatalysis Techniques

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

Affiliations

State Key Laboratory of Environmental Chemistry and Ecotoxicology Research Center for Eco‐Environmental Sciences Chinese Academy of Sciences Beijing 100085 China

College of Resources and Environment University of Chinese Academy of Sciences Beijing 100049 China

School of Environment Hangzhou Institute of Advanced Study University of Chinese Academy of Sciences Hangzhou 310024 China

Funding

National Natural Science Foundation of China

References (35)

Show source-provided references
1. 10.1038/nnano.2014.8510.1038/nnano.2014.85 ↗
2. 10.1038/nnano.2014.3510.1038/nnano.2014.35 ↗
3. 10.1038/nnano.2015.7110.1038/nnano.2015.71 ↗
4. 10.1088/2053-1583/1/2/02500110.1088/2053-1583/1/2/025001 ↗
5. 10.1002/smll.20180170110.1002/smll.201801701 ↗
6. 10.1126/science.aaa648610.1126/science.aaa6486 ↗
7. 10.1021/nl500808510.1021/nl5008085 ↗
8. 10.1002/adma.20160577610.1002/adma.201605776 ↗
9. 10.1016/j.apcatb.2017.09.01010.1016/j.apcatb.2017.09.010 ↗
10. 10.1021/jacs.5b0602510.1021/jacs.5b06025 ↗
11. 10.1002/adma.20180364110.1002/adma.201803641 ↗
12. 10.1002/smll.20180456510.1002/smll.201804565 ↗
13. 10.1002/adma.20190235210.1002/adma.201902352 ↗
14. 10.1002/adma.20170694510.1002/adma.201706945 ↗
15. 10.1039/C9NR04348A10.1039/C9NR04348A ↗
16. 10.1002/anie.20160516810.1002/anie.201605168 ↗
17. 10.1021/jacs.8b0215610.1021/jacs.8b02156 ↗
18. 10.1002/anie.20170501210.1002/anie.201705012 ↗
19. 10.1021/acs.jpclett.5b0168610.1021/acs.jpclett.5b01686 ↗
20. 10.1002/adma.20170474910.1002/adma.201704749 ↗
21. 10.1002/adfm.20190341910.1002/adfm.201903419 ↗
22. 10.1002/anie.20160478410.1002/anie.201604784 ↗
23. 10.1002/anie.20170572210.1002/anie.201705722 ↗
24. 10.1002/anie.20151203810.1002/anie.201512038 ↗
25. 10.1002/anie.20181321810.1002/anie.201813218 ↗
26. 10.1002/aenm.20160045310.1002/aenm.201600453 ↗
27. 10.1007/s12274-014-0446-710.1007/s12274-014-0446-7 ↗
28. 10.1002/adfm.20150290210.1002/adfm.201502902 ↗
29. 10.1016/j.saa.2019.11789210.1016/j.saa.2019.117892 ↗
30. 10.1021/acs.langmuir.8b0419010.1021/acs.langmuir.8b04190 ↗
31. 10.1038/nmat429910.1038/nmat4299 ↗
32. 10.1021/ja963942610.1021/ja9639426 ↗
33. 10.1038/nchem.250510.1038/nchem.2505 ↗
34. 10.1002/adma.20170015210.1002/adma.201700152 ↗
35. 10.1021/jacs.7b0497110.1021/jacs.7b04971 ↗