Yin Qingyang, Liu Qian, Liu Yatao, Qu Zhibin, Sun Fei, Wang Chongzhen, Yuan Xintong, Li Yuzhang, Shen Li, Zhang Chi, Lu Yunfeng
Department of Chemical and Biomolecular Engineering, University of California, Los Angeles, CA, 90095, USA.
School of Chemical Science and Engineering, Institute for Advanced Studies, Tongji University, Shanghai, 200092, China.
Adv Mater. 2024 Jul;36(30):e2404689. doi: 10.1002/adma.202404689. Epub 2024 May 20.
Revitalizing metal anodes for rechargeable batteries confronts challenges such as dendrite formation, limited cyclicity, and suboptimal energy density. Despite various efforts, a practical fabrication method for dendrite-free metal anodes remains unavailable. Herein, focusing on Li as exemplar, a general strategy is reported to enhance reversibility of the metal anodes by forming alloyed metals, which is achieved by induction heating of 3D substrate, lithiophilic metals, and Li within tens of seconds. It is demonstrated that preferred alloying interactions between substrates and lithiophilic metals created a lithiophilic metal-rich region adjacent to the substrate, serving as ultrastable lithiophilic host to guide dendrite-free deposition, particularly during prolonged high-capacity cycling. Simultaneously, an alloying between lithiophilic metals and Li creates a Li-rich region adjacent to electrolyte that reduces nucleation overpotential and constitutes favorable electrolyte-Li interface. The resultant composite Li anodes paired with high areal loading LiNiCoMnO cathodes achieve superior cycling stability and remarkable energy density above 1200 Wh L (excluding packaging). Furthermore, this approach shows broader applicability to other metal anodes plagued by dendrite-related challenges, such as Na and Zn. Overall, this work paves the way for development of commercially viable metal-based batteries that offer a combination of safety, high energy density, and durability.
为可充电电池重振金属阳极面临着诸如枝晶形成、循环寿命有限和能量密度不理想等挑战。尽管做出了各种努力,但仍未找到一种实用的无枝晶金属阳极制造方法。在此,以锂为例,报道了一种通过形成合金金属来提高金属阳极可逆性的通用策略,这是通过在几十秒内对3D基底、亲锂金属和锂进行感应加热来实现的。结果表明,基底与亲锂金属之间优选的合金化相互作用在基底附近形成了一个富含亲锂金属的区域,作为超稳定的亲锂主体来引导无枝晶沉积,特别是在长时间高容量循环期间。同时,亲锂金属与锂之间的合金化在靠近电解质的地方形成了一个富锂区域,该区域降低了成核过电位并构成了有利的电解质-锂界面。由此产生的复合锂阳极与高面载量的LiNiCoMnO阴极配对,实现了卓越的循环稳定性和超过1200 Wh L(不包括包装)的显著能量密度。此外,这种方法对其他受枝晶相关挑战困扰的金属阳极(如钠和锌)具有更广泛的适用性。总体而言,这项工作为开发兼具安全性、高能量密度和耐用性的商业可行的金属基电池铺平了道路。