An Amino Acid-Enabled Separator for Effective Stabilization of Li Anodes
Source abstract
Abstract
Fundamentally suppressing Li dendrite growth is known to be critical for realizing the potential high energy density for Li-metal batteries (LMBs). Inspired by the ionic transport function of proteins, we previously discovered that utilizing natural proteins was able to stabilize the Li anode but have not demonstrated how a specific amino acid of the protein enabled the function. In this study, we decorate the separator with Leucine ( Leu ) amino acid assisted by poly(acrylic acid) (PAA) for effectively stabilizing the Li-metal anode, so as to dramatically improve the cycling performance of LMBs. The decorated separator improves electrolyte wettability and effectively suppresses Li dendrite growth. As a result, the amino acid-enabled separator prolongs the cycle life of the symmetrical Li|Li cells, exhibits higher Coulombic efficiency in the Li|Cu cells, and improves the cycling performance in LMBs with the LiFePO 4 cathode. This work is an initial study on applying a specific amino acid of proteins to enhance the performance of batteries, providing a new strategy on guiding Li + deposition, and laying an important foundation for functional separator design of high-energy-density batteries.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Advanced Battery Materials and Technologies · Advancements in Battery Materials · Advanced Battery Technologies Research
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
School of Mechanical and Materials Engineering, Washington State University, Pullman, Washington 99164, United States
Funding
National Institute of Food and Agriculture · Division of Chemical, Bioengineering, Environmental, and Transport Systems · Extreme Science and Engineering Discovery Environment
References (31)
Show source-provided references
1. 10.1038/s41560-019-0338-x10.1038/s41560-019-0338-x ↗
2. 10.1016/j.joule.2020.06.01610.1016/j.joule.2020.06.016 ↗
3. 10.3390/nano708019610.3390/nano7080196 ↗
4. 10.1021/acsnano.1c0027010.1021/acsnano.1c00270 ↗
5. 10.1021/acsenergylett.0c0020710.1021/acsenergylett.0c00207 ↗
6. 10.1039/C7SC00668C10.1039/C7SC00668C ↗
7. 10.1016/j.matt.2019.05.01610.1016/j.matt.2019.05.016 ↗
8. 10.1021/acsami.2c1066710.1021/acsami.2c10667 ↗
9. 10.1016/j.jechem.2022.06.01710.1016/j.jechem.2022.06.017 ↗
10. 10.1016/j.ensm.2019.02.02610.1016/j.ensm.2019.02.026 ↗
11. 10.1016/j.cej.2022.13528310.1016/j.cej.2022.135283 ↗
12. 10.1021/acs.chemrev.1c0083810.1021/acs.chemrev.1c00838 ↗
13. 10.1016/j.ensm.2021.06.03310.1016/j.ensm.2021.06.033 ↗
14. 10.1021/acsami.8b1752110.1021/acsami.8b17521 ↗
15. 10.1038/nenergy.2016.1010.1038/nenergy.2016.10 ↗
16. 10.1002/aenm.20170256110.1002/aenm.201702561 ↗
17. 10.1016/j.ccr.2017.03.01910.1016/j.ccr.2017.03.019 ↗
18. 10.1142/1361010.1142/13610 ↗
19. 10.1016/j.jechem.2021.05.01410.1016/j.jechem.2021.05.014 ↗
20. 10.1016/j.seppur.2021.11957010.1016/j.seppur.2021.119570 ↗
21. 10.1016/j.electacta.2023.14186010.1016/j.electacta.2023.141860 ↗
22. 10.1088/0953-8984/21/39/39550210.1088/0953-8984/21/39/395502 ↗
23. 10.1103/PhysRevLett.77.386510.1103/PhysRevLett.77.3865 ↗
24. 10.1038/s41524-018-0127-210.1038/s41524-018-0127-2 ↗
25. 10.1093/imamat/6.3.22210.1093/imamat/6.3.222 ↗
26. 10.1002/admt.20220187510.1002/admt.202201875 ↗
27. 10.1002/jcc.2049510.1002/jcc.20495 ↗
28. 10.3109/1040923950908514010.3109/10409239509085140 ↗
29. 10.3168/jds.S0022-0302(84)81628-810.3168/jds.S0022-0302(84)81628-8 ↗
30. 10.1002/jrs.433510.1002/jrs.4335 ↗
31. 10.1038/s41560-020-0648-z10.1038/s41560-020-0648-z ↗