Capping Black Phosphorene by h-BN Enhances Performances in Anodes for Li and Na Ion Batteries
Source abstract
Abstract
Black phosphorus (BP), despite possessing a favorable direct band gap, suffers from structural instability at ambient conditions that limits its utility for lithium ion batteries (LIB). In this Letter, we have proposed h-BN as an effective capping agent for black-phosphorene (Pn) for application as an anode material in both LIBs and sodium ion batteries (SIBs). The binding energy of Li/Na in the h-BN/black-Pn heterostructure is greatly enhanced (2.81 eV/2.55 eV) vis-a-vis pristine Pn (1.80 eV/1.59 eV) along with reduction in the barrier for movement of Li/Na within the layers. Significantly, lithiation/sodiation of these heterostructures does not alter the packing patterns due to insignificant volume changes (∼1.5–2.0%). The theoretical specific capacities for h-BN/black-Pn is 607 and 445 mA h g –1 for LIB and SIB, respectively, which are larger than those for existing commercial anode materials. Clearly, the high capacity, low open-circuit voltage, small volume change, and high mobility of Li/Na within the layers make h-BN-capped black-Pn an excellent anode material in LIBs/SIBs. The heterostructure exhibits an interesting semiconductor → metal electronic phase transition upon lithiation/sodiation.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: 2D Materials and Applications · MXene and MAX Phase Materials · Advancements in Battery Materials
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Department of Spectroscopy, Indian Association for the Cultivation of Science, Jadavpur 700032, West Bengal, India
Funding
Indian National Science Academy · Council of Scientific and Industrial Research · Science and Engineering Research Board · Board of Research in Nuclear Sciences
References (42)
Show source-provided references
1. 10.1016/j.jpowsour.2013.11.10310.1016/j.jpowsour.2013.11.103 ↗
2. 10.1126/science.110289610.1126/science.1102896 ↗
3. 10.1038/nmat184910.1038/nmat1849 ↗
4. 10.1126/science.270.5236.59010.1126/science.270.5236.590 ↗
5. 10.1002/anie.20100348510.1002/anie.201003485 ↗
6. 10.1021/jz400005k10.1021/jz400005k ↗
7. 10.1039/c2cp40727b10.1039/c2cp40727b ↗
8. 10.1021/nl200658a10.1021/nl200658a ↗
9. Chen H. J. · Int. J. Electrochem. Sci. · 2013 · 8 · 219610.1016/S1452-3981(23)14301-X ↗
10. 10.1021/ja308463r10.1021/ja308463r ↗
11. 10.1021/ja501520b10.1021/ja501520b ↗
12. 10.1021/nl400830u10.1021/nl400830u ↗
13. 10.1021/nl101223k10.1021/nl101223k ↗
14. 10.1021/am300096210.1021/am3000962 ↗
15. 10.1103/PhysRevB.32.253810.1103/PhysRevB.32.2538 ↗
16. 10.1016/j.electacta.2013.01.05710.1016/j.electacta.2013.01.057 ↗
17. 10.1038/nnano.2014.3510.1038/nnano.2014.35 ↗
18. 10.1021/nn501226z10.1021/nn501226z ↗
19. 10.1038/506019a10.1038/506019a ↗
20. 10.1039/C4TA04368E10.1039/C4TA04368E ↗
21. 10.1021/nl504336h10.1021/nl504336h ↗
22. 10.1039/C5CP01502B10.1039/C5CP01502B ↗
23. 10.1039/C5CP02419F10.1039/C5CP02419F ↗
24. 10.1088/2053-1583/2/1/01100210.1088/2053-1583/2/1/011002 ↗
25. 10.1038/ncomms831510.1038/ncomms8315 ↗
26. 10.1021/acs.nanolett.5b0064810.1021/acs.nanolett.5b00648 ↗
27. 10.1021/acsnano.5b0028910.1021/acsnano.5b00289 ↗
28. 10.1021/acs.jpcc.5b0263410.1021/acs.jpcc.5b02634 ↗
29. 10.1021/acs.jpclett.5b0251310.1021/acs.jpclett.5b02513 ↗
30. 10.1038/nnano.2015.19410.1038/nnano.2015.194 ↗
31. 10.1088/0953-8984/21/39/39550210.1088/0953-8984/21/39/395502 ↗
32. 10.1103/PhysRevLett.77.386510.1103/PhysRevLett.77.3865 ↗
33. 10.1103/PhysRevB.41.789210.1103/PhysRevB.41.7892 ↗
34. 10.1002/jcc.2049510.1002/jcc.20495 ↗
35. 10.1103/PhysRevB.47.55810.1103/PhysRevB.47.558 ↗
36. 10.1016/j.commatsci.2005.04.01010.1016/j.commatsci.2005.04.010 ↗
37. 10.1063/1.216119310.1063/1.2161193 ↗
38. 10.1039/C5CP07128C10.1039/C5CP07128C ↗
39. 10.1021/am501144q10.1021/am501144q ↗
40. 10.1021/jp410969u10.1021/jp410969u ↗
41. 10.1021/nl501617j10.1021/nl501617j ↗
42. 10.1039/c3ta10380c10.1039/c3ta10380c ↗