Abstract:Ceramics-based solid-state batteries with lithium metal anode show great potential to realize a battery revolution because of their features of nonflammability and higher energy density. Among the inorganic electrolytes, garnet-type...
“…In comparison, in this work, the Li/1LiF-LLZTO/LFP full cell exhibits an extended lifespan and higher capacity retention at a high current density than other reported full cells utilizing LLZO electrolyte, lithium metal anode, and LFP cathode (Fig. 10(f)) [17,20,[42][43][44][45][46][52][53][54][55][56][57][58][59][60][61]. Additionally, the charge/discharge profiles for the 1st, 100th, 200th, 300th, 400th, and 500th cycles are shown in Fig.…”
Li 7 La 3 Zr 2 O 12 (LLZO) is considered as a promising solid-state electrolyte due to its high ionic conductivity, wide electrochemical window, and excellent electrochemical stability. However, its application in solid-state lithium metal batteries (SSLMBs) is impeded by the growth of lithium dendrites in LLZO due to some reasons such as its high electronic conductivity. In this study, lithium fluoride (LiF) was introduced into Ta-doped LLZO (LLZTO) to modify its grain boundaries to enhance the performance of SSLMBs. A nanoscale LiF layer was uniformly coated on the LLZTO grains, creating a threedimensional continuous electron-blocking network at the grain boundaries. Benefiting from the electronic insulator LiF and the special structure of the modified LLZTO, the symmetric cells based on LLZO achieved a high critical current density (CCD) of 1.1 mA•cm −2 (in capacity-constant mode) and maintained stability over 2000 h at 0.3 mA•cm −2 . Moreover, the full cells combined with a LiFePO 4 (LFP) cathode, demonstrated excellent cycling performance, retaining 97.1% of capacity retention after 500 cycles at 0.5 C. Therefore, this work provides a facile and effective approach for preparing a modified electrolyte suitable for high-performance SSLMBs.
“…In comparison, in this work, the Li/1LiF-LLZTO/LFP full cell exhibits an extended lifespan and higher capacity retention at a high current density than other reported full cells utilizing LLZO electrolyte, lithium metal anode, and LFP cathode (Fig. 10(f)) [17,20,[42][43][44][45][46][52][53][54][55][56][57][58][59][60][61]. Additionally, the charge/discharge profiles for the 1st, 100th, 200th, 300th, 400th, and 500th cycles are shown in Fig.…”
Li 7 La 3 Zr 2 O 12 (LLZO) is considered as a promising solid-state electrolyte due to its high ionic conductivity, wide electrochemical window, and excellent electrochemical stability. However, its application in solid-state lithium metal batteries (SSLMBs) is impeded by the growth of lithium dendrites in LLZO due to some reasons such as its high electronic conductivity. In this study, lithium fluoride (LiF) was introduced into Ta-doped LLZO (LLZTO) to modify its grain boundaries to enhance the performance of SSLMBs. A nanoscale LiF layer was uniformly coated on the LLZTO grains, creating a threedimensional continuous electron-blocking network at the grain boundaries. Benefiting from the electronic insulator LiF and the special structure of the modified LLZTO, the symmetric cells based on LLZO achieved a high critical current density (CCD) of 1.1 mA•cm −2 (in capacity-constant mode) and maintained stability over 2000 h at 0.3 mA•cm −2 . Moreover, the full cells combined with a LiFePO 4 (LFP) cathode, demonstrated excellent cycling performance, retaining 97.1% of capacity retention after 500 cycles at 0.5 C. Therefore, this work provides a facile and effective approach for preparing a modified electrolyte suitable for high-performance SSLMBs.
“…4c), which indicates the dendrite-suppressing ability of the LSi15 electrode and superior interface stability during Li cycling. In comparison, the control cell with the pristine Li electrode, reported in our previous work, 41 shows a noisy potential with large voltage polarization and serious voltage fluctuations upon cycling. The cell fails to cycle in a few hours owing to the lithium dendrite-induced short-circuit, as confirmed by the post-morphological observation on the cross section of the LLZTO pellet (Fig.…”
Section: Resultsmentioning
confidence: 75%
“…As shown in Fig. 4a, the symmetric cell with pure Li electrodes shows a much higher area specific resistance (ASR) of 273.1 Ω cm 2 (referring to the one-sided electrode–electrolyte interface), 41 while a considerable impedance decrease is observed for the Li–Li 4.4 Si|LLZTO|Li–Li 4.4 Si symmetric cells, which is mainly attributed to the better interface connection between the Li–Li 4.4 Si composites and the LLZTO pellet. Specifically, as the mass ratio of Si addition increases, the arc impedance displays an initially decreasing and then increasing trend.…”
Section: Resultsmentioning
confidence: 99%
“…). 18,35–41 Among the strategies mentioned above, tuning the wettability of molten Li by constructing an alloy anode shows great promise because of its easy operability and manufacturing scalability. Benefitting from the improved wettability of molten Li with LLZO, an intimate interface contact and thus a much reduced interfacial resistance is achieved.…”
Section: Introductionmentioning
confidence: 99%
“…), [24][25][26][27][28][29][30][31] adding a so polymer/gel buffer layer, [32][33][34] or compositing the Li anode with a lithiophilic phase to adjust surface energy of molten Li (Li@graphite, Li@Na, Li@Si 3 N 4 , Li@g-C 3 N 4 , Li@Mg 3 N 2 , Li@Zn, Li@Sn, Li@S, etc.). 18,[35][36][37][38][39][40][41] Among the strategies mentioned above, tuning the wettability of molten Li by constructing an alloy anode shows great promise because of its easy operability and manufacturing scalability. Benetting from the improved wettability of molten Li with LLZO, an intimate interface contact and thus a much reduced interfacial resistance is achieved.…”
The application of ceramic garnet-type Li7La3Zr2O12 electrolytes is restricted by the challenge of poor contact with metallic lithium, which results in high interfacial resistance, uneven current distribution, and severe lithium...
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