Ionic Liquid Electrolyte for Lithium Metal Batteries: Physical, Electrochemical, and Interfacial Studies of N-Methyl-N-butylmorpholinium Bis(fluorosulfonyl)imide
The ionic liquid (IL) N-methyl-N-butylmorpholinium bis(fluorosulfonyl)imide (C4mmor FSI) is examined from physical and electrochemical perspectives. Pulsed field gradient NMR spectroscopy shows that ion diffusivities are low compared with similar, non-ethereal ILs. Ionicity values indicate that abov...
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Veröffentlicht in: | Journal of physical chemistry. C 2010-12, Vol.114 (49), p.21775-21785 |
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creator | Lane, George H Bayley, Paul M Clare, Bronya R Best, Adam S MacFarlane, Douglas R Forsyth, Maria Hollenkamp, Anthony F |
description | The ionic liquid (IL) N-methyl-N-butylmorpholinium bis(fluorosulfonyl)imide (C4mmor FSI) is examined from physical and electrochemical perspectives. Pulsed field gradient NMR spectroscopy shows that ion diffusivities are low compared with similar, non-ethereal ILs. Ionicity values indicate that above room temperature, less than 50% of ions contribute to conductivity. Lithium cycling in symmetrical cells using a C4mmor FSI-based electrolyte is best demonstrated at elevated temperatures. Specific capacities of 130 mAh g−1 are achieved in a Li−LiFePO4 battery at 85 °C. FT-IR spectroscopic investigations of lithium electrodes suggest the presence of alkoxide species in the solid electrolyte interphase (SEI), implying a ring-opening reaction of C4mmor with lithium metal. In contrast, the SEI derived from N-methyl-N-propylpiperidinium FSI lacks the alkoxide signature but shows signs of alkyl unsaturation, and the activation energy for Li+ transport through this SEI is slightly lower than that for the C4mmor-derived SEI. Our detailed findings give insight into the capabilities and limitations of rechargeable lithium metal batteries utilizing a C4mmor FSI electrolyte. |
doi_str_mv | 10.1021/jp1054809 |
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Pulsed field gradient NMR spectroscopy shows that ion diffusivities are low compared with similar, non-ethereal ILs. Ionicity values indicate that above room temperature, less than 50% of ions contribute to conductivity. Lithium cycling in symmetrical cells using a C4mmor FSI-based electrolyte is best demonstrated at elevated temperatures. Specific capacities of 130 mAh g−1 are achieved in a Li−LiFePO4 battery at 85 °C. FT-IR spectroscopic investigations of lithium electrodes suggest the presence of alkoxide species in the solid electrolyte interphase (SEI), implying a ring-opening reaction of C4mmor with lithium metal. In contrast, the SEI derived from N-methyl-N-propylpiperidinium FSI lacks the alkoxide signature but shows signs of alkyl unsaturation, and the activation energy for Li+ transport through this SEI is slightly lower than that for the C4mmor-derived SEI. Our detailed findings give insight into the capabilities and limitations of rechargeable lithium metal batteries utilizing a C4mmor FSI electrolyte.</description><identifier>ISSN: 1932-7447</identifier><identifier>EISSN: 1932-7455</identifier><identifier>DOI: 10.1021/jp1054809</identifier><language>eng</language><publisher>American Chemical Society</publisher><subject>C: Energy Conversion and Storage</subject><ispartof>Journal of physical chemistry. 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In contrast, the SEI derived from N-methyl-N-propylpiperidinium FSI lacks the alkoxide signature but shows signs of alkyl unsaturation, and the activation energy for Li+ transport through this SEI is slightly lower than that for the C4mmor-derived SEI. Our detailed findings give insight into the capabilities and limitations of rechargeable lithium metal batteries utilizing a C4mmor FSI electrolyte.</description><subject>C: Energy Conversion and Storage</subject><issn>1932-7447</issn><issn>1932-7455</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2010</creationdate><recordtype>article</recordtype><recordid>eNptkM1OwzAQhC0EEqVw4A18QaISAf_EacKNVgUqlYIEnCPHsRVXTlxs55DH4U1xVeiJ065W38yOBoBLjG4xIvhus8WIpTkqjsAIF5Qk05Sx48OeTk_BmfcbhBhFmI7A99J2WsCV_up1DRdGiuCsGYKEyrp4Do3uW_giAzdwxkOQTkt_D9-awWvBzc2fRDSy3R94V8NlF0HFhY6q99DXUQOtguskGjWDSdZJ1YfBtNZtG2t0t_sx0_5amd4663ujbDeYiW51Lc_BieLGy4vfOQafj4uP-XOyen1azh9WCaeEhUQQInGq8ikjvCpqzJjADFVIYkEUzpgSaqpIlWdUFYhXsk7zIitwTjgtBKUZHYPJ3lfEBN5JVW6dbrkbSozKXbflodvIXu1ZLny5sb3rYrJ_uB_BPXs-</recordid><startdate>20101216</startdate><enddate>20101216</enddate><creator>Lane, George H</creator><creator>Bayley, Paul M</creator><creator>Clare, Bronya R</creator><creator>Best, Adam S</creator><creator>MacFarlane, Douglas R</creator><creator>Forsyth, Maria</creator><creator>Hollenkamp, Anthony F</creator><general>American Chemical Society</general><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>20101216</creationdate><title>Ionic Liquid Electrolyte for Lithium Metal Batteries: Physical, Electrochemical, and Interfacial Studies of N-Methyl-N-butylmorpholinium Bis(fluorosulfonyl)imide</title><author>Lane, George H ; Bayley, Paul M ; Clare, Bronya R ; Best, Adam S ; MacFarlane, Douglas R ; Forsyth, Maria ; Hollenkamp, Anthony F</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-a325t-c22e14f8752ab9d155c150b0e1c2f165fcf7f2b863f90abed48969182a39c3363</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2010</creationdate><topic>C: Energy Conversion and Storage</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Lane, George H</creatorcontrib><creatorcontrib>Bayley, Paul M</creatorcontrib><creatorcontrib>Clare, Bronya R</creatorcontrib><creatorcontrib>Best, Adam S</creatorcontrib><creatorcontrib>MacFarlane, Douglas R</creatorcontrib><creatorcontrib>Forsyth, Maria</creatorcontrib><creatorcontrib>Hollenkamp, Anthony F</creatorcontrib><collection>CrossRef</collection><jtitle>Journal of physical chemistry. C</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Lane, George H</au><au>Bayley, Paul M</au><au>Clare, Bronya R</au><au>Best, Adam S</au><au>MacFarlane, Douglas R</au><au>Forsyth, Maria</au><au>Hollenkamp, Anthony F</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Ionic Liquid Electrolyte for Lithium Metal Batteries: Physical, Electrochemical, and Interfacial Studies of N-Methyl-N-butylmorpholinium Bis(fluorosulfonyl)imide</atitle><jtitle>Journal of physical chemistry. C</jtitle><addtitle>J. Phys. Chem. C</addtitle><date>2010-12-16</date><risdate>2010</risdate><volume>114</volume><issue>49</issue><spage>21775</spage><epage>21785</epage><pages>21775-21785</pages><issn>1932-7447</issn><eissn>1932-7455</eissn><abstract>The ionic liquid (IL) N-methyl-N-butylmorpholinium bis(fluorosulfonyl)imide (C4mmor FSI) is examined from physical and electrochemical perspectives. Pulsed field gradient NMR spectroscopy shows that ion diffusivities are low compared with similar, non-ethereal ILs. Ionicity values indicate that above room temperature, less than 50% of ions contribute to conductivity. Lithium cycling in symmetrical cells using a C4mmor FSI-based electrolyte is best demonstrated at elevated temperatures. Specific capacities of 130 mAh g−1 are achieved in a Li−LiFePO4 battery at 85 °C. FT-IR spectroscopic investigations of lithium electrodes suggest the presence of alkoxide species in the solid electrolyte interphase (SEI), implying a ring-opening reaction of C4mmor with lithium metal. In contrast, the SEI derived from N-methyl-N-propylpiperidinium FSI lacks the alkoxide signature but shows signs of alkyl unsaturation, and the activation energy for Li+ transport through this SEI is slightly lower than that for the C4mmor-derived SEI. Our detailed findings give insight into the capabilities and limitations of rechargeable lithium metal batteries utilizing a C4mmor FSI electrolyte.</abstract><pub>American Chemical Society</pub><doi>10.1021/jp1054809</doi><tpages>11</tpages></addata></record> |
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subjects | C: Energy Conversion and Storage |
title | Ionic Liquid Electrolyte for Lithium Metal Batteries: Physical, Electrochemical, and Interfacial Studies of N-Methyl-N-butylmorpholinium Bis(fluorosulfonyl)imide |
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