Transforming Interface Chemistry throughout Garnet Electrolyte for Dendrite-Free Solid-State Batteries AITranslate
Abstract AITranslate
Solid-state batteries have great potential for future energy storage because of their high energy density and enhanced safety. However, uneven Li plating/stripping due to a poor Li/solid-state electrolyte (SSE) contact and Li infiltration within the SSE due to local electronic conductivity at grain boundaries are major obstacles. Here, the interface chemistry of garnet-based SSEs is thoroughly transformed via the impregnation of polyphosphoric acid (PPA). The nanometer PPA coating not only acts as a lithiophilic and elastic interlayer for uniform Li cycling but also forms an electron-insulating interphase at the grain boundary to prevent Li filament growth inside the garnet. The PPA-modified garnet electrolyte exhibits an improved critical current density of 1.5 mA cm–2 and highly stable cell cycling for 2000 h at 0.2 mA cm–2 and 500 h at a high current density of 1 mA cm–2. Our work points out a way to systematically regulate the electrolyte interface chemistry for solid-state batteries.
KeyWords AITranslate
Basic Information:
DOI:https://doi.org/10.1021/acsenergylett.2c02528
Chinese Library Classification Number:
Citation Information:
Solid-state batteries have great potential for future energy storage because of their high energy density and enhanced safety. However, uneven Li plating/stripping due to a poor Li/solid-state electrolyte (SSE) contact and Li infiltration within the SSE due to local electronic conductivity at grain boundaries are major obstacles. Here, the interface chemistry of garnet-based SSEs is thoroughly transformed via the impregnation of polyphosphoric acid (PPA). The nanometer PPA coating not only acts as a lithiophilic and elastic interlayer for uniform Li cycling but also forms an electron-insulating interphase at the grain boundary to prevent Li filament growth inside the garnet. The PPA-modified garnet electrolyte exhibits an improved critical current density of 1.5 mA cm–2 and highly stable cell cycling for 2000 h at 0.2 mA cm–2 and 500 h at a high current density of 1 mA cm–2. Our work points out a way to systematically regulate the electrolyte interface chemistry for solid-state batteries.
quote
| GB/T 7714-2015 | [1] BingQing Xiong, Qingshun Nian, Xin Zhao, et al. ACS Energy Letters, 2023(8). DOI:10.1021/acsenergylett.2c02528. |
| MLA | [1] BingQing Xiong, et al., ACS Energy Letters, no. 8, 2023, https://doi.org/10.1021/acsenergylett.2c02528. |
| APA | [1] BingQing Xiong, Qingshun Nian, Xin Zhao, Yawei Chen, Yecheng Li, Jinyu Jiang, Shuhong Jiao, Xiaowen Zhan, & Xiaodi Ren. (2023). ACS Energy Letters(8). https://doi.org/10.1021/acsenergylett.2c02528 |
| IEEE | [1] BingQing Xiong, Qingshun Nian, Xin Zhao, Yawei Chen, Yecheng Li, Jinyu Jiang, Shuhong Jiao, Xiaowen Zhan, and Xiaodi Ren, ACS Energy Letters, no. 8, 2023, doi: 10.1021/acsenergylett.2c02528. |
