journal article·2015-03-24

Chemically Reduced Organic Small-Molecule-Based Lithium Battery with Improved Efficiency

Manik E. Bhosale, Kothandam Krishnamoorthy

Chemistry of Materials· Volume 27· Issue 6
Publisher page

Abstract

Organic lithium batteries are attractive because of the possibility of fabricating lightweight and flexible devices. However, the organic lithium batteries have a few drawbacks. The specific capacity is usually lower than the theoretical capacity, which further decreases upon cycling. Often, the specific capacity is very low compared to theoretical capacity while discharging the battery at moderate and high C rates. To circumvent this issue, we chemically reduced carboxylic acid functionality substituted perylene diimide (benzoic-PDI) with hydrazine. Indeed, we found that the rate of redox reaction as well as the conductivity of the benzoic-PDI increased upon chemical reduction. The battery comprising reduced benzoic-PDI exhibits 100% Coulombic efficiency and specific capacity while discharging at 20 C . The battery also exhibits very high specific energy (213 Wh/kg) and specific power (8548 W/kg). The control experiments confirm our hypothesis of using chemical reduction to improve the performance of organic lithium battery.
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Research context

OpenAlex topics: Advancements in Battery Materials · Advanced Battery Materials and Technologies · Advanced Battery Technologies Research

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

Affiliations

CSIR-Network of Institutes for Solar Energy and CSIR-National Chemical Laboratory, Dr. Homi Bhabha Road, Pune 411008, Maharashtra, India

Funding

Department of Science and Technology, Ministry of Science and Technology · Council of Scientific and Industrial Research

References (46)

Show source-provided references
1. Armand M. · Nature · 2008 · 451 · 65210.1038/451652a ↗
2. Choi N.-S. · Angew. Chem., Int. Ed. · 2012 · 51 · 999410.1002/anie.201201429 ↗
3. Novak P. · Chem. Rev. · 1997 · 97 · 20710.1021/cr941181o ↗
4. Luo C. · Nano Lett. · 2014 · 14 · 159610.1021/nl500026j ↗
5. Wu H. · Nat. Commun. · 2013 · 4 · 194310.1038/ncomms2941 ↗
6. Zhou W. · J. Am. Chem. Soc. · 2013 · 135 · 1673610.1021/ja409508q ↗
7. Suga T. · Adv. Mater. · 2009 · 21 · 162710.1002/adma.200803073 ↗
8. Fu Y. Z. · Chem. Mater. · 2012 · 24 · 308110.1021/cm301661y ↗
9. Yang Y. · ACS Nano · 2011 · 5 · 918710.1021/nn203436j ↗
10. Huang W. · Angew. Chem., Int. Ed. · 2013 · 52 · 916210.1002/anie.201302586 ↗
11. Genorio B. · Angew. Chem., Int. Ed. · 2010 · 49 · 722210.1002/anie.201001539 ↗
12. Walker W. · J. Am. Chem. Soc. · 2010 · 132 · 651710.1021/ja1012849 ↗
13. Liang Y. L. · Chem. Sci. · 2013 · 4 · 133010.1039/c3sc22093a ↗
14. Song Z. · Chem. Commun. · 2009 · 44810.1039/B814515F ↗
15. Armand M. · Nat. Mater. · 2009 · 8 · 12010.1038/nmat2372 ↗
16. Liang Y. L. · Adv. Energy Mater. · 2013 · 3 · 60010.1002/aenm.201200947 ↗
17. Song Z. · Energy Environ. Sci. · 2014 · 10 · 1039
18. Renault S. · Chem. Commun. · 2011 · 47 · 241410.1039/C0CC04440G ↗
19. Geng J. · Energy Environ. Sci. · 2010 · 3 · 192910.1039/c0ee00126k ↗
20. Wu H. · J. Mater. Chem. A · 2013 · 1 · 636610.1039/c3ta10473g ↗
21. Vadehra, G. S.; Maloney, R. P.; Garcia-Garibay, M. A.; Dunn, B.Chem. Mater.ASAP.
22. Morita Y. · Nat. Mater. · 2011 · 10 · 94710.1038/nmat3142 ↗
23. Shin J.-Y. · Angew. Chem., Int. Ed. · 2014 · 53 · 309610.1002/anie.201310374 ↗
24. Sakaushi K. · Angew. Chem., Int. Ed. · 2012 · 51 · 785010.1002/anie.201202476 ↗
25. Hanyu Y. · Sci. Rep. · 2012 · 2 · 45310.1038/srep00453 ↗
26. Chen H. · ChemSusChem · 2008 · 1 · 34810.1002/cssc.200700161 ↗
27. Wang S. · Nano Lett. · 2013 · 13 · 440410.1021/nl402239p ↗
28. Gottis S. · ACS Appl. Mater. Interfaces · 2014 · 6 · 1087010.1021/am405470p ↗
29. Song Z. · Angew. Chem., Int. Ed. · 2010 · 49 · 844410.1002/anie.201002439 ↗
30. Han X. · Adv. Mater. · 2007 · 19 · 161610.1002/adma.200602584 ↗
31. Sharma P. · J. Phys. Chem. Lett. · 2013 · 4 · 319210.1021/jz4017359 ↗
32. Song Z. · Nano Lett. · 2012 · 12 · 220510.1021/nl2039666 ↗
33. Wu H. · Adv. Mater. · 2014 · 26 · 333810.1002/adma.201305452 ↗
34. Nokami T. · J. Am. Chem. Soc. · 2012 · 134 · 1969410.1021/ja306663g ↗
35. Shimizu A. · J. Power Sources · 2014 · 260 · 21110.1016/j.jpowsour.2014.03.027 ↗
36. Xu X. H. · J. Appl. Polym. Sci. · 2010 · 116 · 45510.1002/app.31485 ↗
37. Che Y. · J. Am. Chem. Soc. · 2007 · 129 · 635410.1021/ja070164g ↗
38. Balakrishnan K. · J. Am. Chem. Soc. · 2005 · 127 · 1049610.1021/ja052940v ↗
39. Yagai S. · Angew. Chem., Int. Ed. · 2008 · 47 · 336710.1002/anie.200705385 ↗
40. Van Herrikhuyzen J. · J. Am. Chem. Soc. · 2004 · 126 · 1002110.1021/ja048819q ↗
41. Ustinov A. · J. Am. Chem. Soc. · 2011 · 133 · 1620110.1021/ja2066225 ↗
42. Briseno A. L. · Nano Lett. · 2007 · 7 · 284710.1021/nl071495u ↗
43. Pisula W. · Adv. Mater. · 2010 · 22 · 363410.1002/adma.201000585 ↗
44. Arulkashmir A. · Chem. Commun. · 2014 · 50 · 32610.1039/C3CC45391J ↗
45. Wu Z.-S. · Nat. Commun. · 2013 · 4 · 3487
46. Lee S. W. · Nat. Nanotechnol. · 2010 · 5 · 53110.1038/nnano.2010.116 ↗