Guobang Zhang, Jingbo Xu, Yifeng Cheng, Wenhao Ding, Mingyu Yang, Xiangjie Guo, Jingwen Sun, Pengcheng Yao, Junwu Zhu, Yongsheng Fu
High sulfur loading is essential for the practical application of lithium-sulfur (Li-S) batteries but is limited by severe polysulfide shuttling, large electrode volume changes, and sluggish Li+ transport. Herein, a dual-crosslinked binder (DCB) is constructed through hydrogen-bonding and ionic-pair interactions between quaternized soy protein isolate (QSPI) and poly (acrylic acid)-based LA133. The 3D crosslinked network enhances electrode mechanical integrity and adhesion, effectively alleviating structural degradation and volume variation during cycling. Meanwhile, abundant polar functional groups provide continuous Li+ coordination sites, and theoretical calculations reveal a hopping-mediated Li+ transport pathway between adjacent coordination sites, thereby promoting polysulfide conversion. As a result, the DCB simultaneously improves electrode stability and reaction kinetics. A 1.1 Ah Li-S pouch cell employing the DCB achieves a high energy density of 348 Wh kg-1 and stable cycling over 60 cycles under practical conditions with a low electrolyte/sulfur ratio of 4 µL mgs -1 and a low N/P ratio of 1.5. This work offers an effective dual-crosslinking strategy for regulating Li+ transport and enhancing electrode stability toward practical high-sulfur-loading Li-S batteries.