1990
DOI: 10.1016/0167-2738(90)90062-v
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Dimensionally stable Li-alloy electrodes for secondary batteries

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Cited by 121 publications
(54 citation statements)
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“…The formation of a rough surface and the creation of voids within the electrode could be due to the lattice expansion that occurs during the lithiation of aluminum to form the LiAl alloy. Going from metallic aluminum to the LiAl alloy results in a 97% expansion in the lattice [42]. However, this is significantly less than the lattice expansion during the lithiation of Si to Li22Si5 and Sn to Li22Sn5 which are 323% and 300% [43] respectively.…”
Section: Resultsmentioning
confidence: 90%
“…The formation of a rough surface and the creation of voids within the electrode could be due to the lattice expansion that occurs during the lithiation of aluminum to form the LiAl alloy. Going from metallic aluminum to the LiAl alloy results in a 97% expansion in the lattice [42]. However, this is significantly less than the lattice expansion during the lithiation of Si to Li22Si5 and Sn to Li22Sn5 which are 323% and 300% [43] respectively.…”
Section: Resultsmentioning
confidence: 90%
“…[268,337,338] A similar concept of supporting small particles of electroactive Li alloys with less active or non-active matrices was introduced in 1981. [333] The matrix material can be a conductive polymer, [348,349] a porous membrane, [350] an inert metal-like copper, [327] or another mixed conductor. [289,291,333,334] [351,352] or silver [353±356] show good cycling behavior.…”
Section: Lithium Alloys As Negative Insertion Electrode Materialsmentioning
confidence: 99%
“…Due to the significant changes in the volume of these materials associated with the lithiation and delithiation processes, much work is presently carried out to study how to circumvent this problem [3] using for instance, metal oxides [3][4][5][6][7][8][9][10] where the oxide serves as a buffering matrix during the lithiation process, or by utilising nanoparticles to minimize the effects of the volume changes [11][12][13]. Other approaches involve embedding the active electrode material in a composite matrix [14][15][16], the use of amorphous alloys [17][18][19], or intermetallic systems (A x B y ) which have a strong structural relationship to that of their lithiated products [20][21][22]. In these materials, both metals can either be active with respect to lithium (see e.g.…”
Section: Introductionmentioning
confidence: 99%