Choi Seung Ho, Baek Chang Hoon, Oh Jihoon, Lee Geung-Jong, Kim Minsoo, Lee Hyesu, Yoo Dong-Joo, Jung Yoon Seok, Kim KyungSu, Yu Ji-Sang, Cho Woosuk, Park Haesun, Choi Jang Wook
Advanced Batteries Research Center, Korea Electronics Technology Institute, Seongnam, Republic of Korea.
Department of Chemical and Biomolecular Engineering, Yonsei University, Seoul, Republic of Korea.
Nat Commun. 2025 Jul 1;16(1):5871. doi: 10.1038/s41467-025-61074-9.
Achieving stable cyclability in initially anode-free all-solid-state batteries is challenging due to non-uniform Li (de)plating, especially under practical operating conditions. Here, we introduce a bilayer comprising a silver(Ag)-doped Li-argyrodite electrolyte layer in contact with the undoped Li-argyrodite electrolyte. During charging, electrochemical exsolution of Ag from the silver-doped Li argyrodite forms nanoscale, lithiophilic silver seeds along grain boundaries and in pores where they are accessible for electron transfer. These silver seeds alloy with Li to induce uniform Li plating underneath and return to the electrolyte layer upon Li stripping to enhance the reversibility during cycling. With silver exsolution, a pouch-type full-cell with a volumetric energy density of 1312 Wh L (excluding the packaging materials) and areal discharge capacity of 7.0 mAh cm at 0.7 mA cm, demonstrated stable cycling at a practical stack pressure of 2.0 MPa. This study highlights that Ag diffusion in the Li-argyrodite solid electrolyte and its electrochemical exsolution are an effective strategy for robust, high-energy-density initially anode-free all-solid-state batteries.
在初始无阳极全固态电池中实现稳定的循环性能具有挑战性,这是由于锂(脱)镀不均匀,特别是在实际操作条件下。在此,我们引入了一种双层结构,其由与未掺杂的锂硫银锗矿电解质接触的银(Ag)掺杂的锂硫银锗矿电解质层组成。在充电过程中,银从掺杂银的锂硫银锗矿中发生电化学析出,沿着晶界和孔隙形成纳米级的亲锂银籽晶,在这些地方它们可用于电子转移。这些银籽晶与锂形成合金,在其下方诱导均匀的锂镀层,并在锂剥离时回到电解质层,以增强循环过程中的可逆性。通过银析出,一种软包型全电池在0.7 mA/cm²下具有1312 Wh/L的体积能量密度(不包括包装材料)和7.0 mAh/cm²的面积放电容量,在2.0 MPa的实际堆叠压力下表现出稳定的循环性能。这项研究突出表明,银在锂硫银锗矿固体电解质中的扩散及其电化学析出是实现坚固、高能量密度的初始无阳极全固态电池的有效策略。