Copper-coordinated cellulose ion conductors for solid-state batteries

材料科学 导电体 离子 阴极 阳极 离子电导率 聚合物 电导率 导电聚合物 导线 快离子导体 化学物理 电解质 纳米技术 电极 化学工程 复合材料 化学 有机化学 工程类 物理化学 冶金
作者
Chunpeng Yang,Qisheng Wu,Weiqi Xie,Xin Zhang,Alexandra H. Brozena,Jin Zheng,Mounesha N. Garaga,Byung Hee Ko,Yimin Mao,Shuaiming He,Yue Gao,Pengbo Wang,Madhusudan Tyagi,Feng Jiao,Robert M. Briber,Paul Albertus,Chunsheng Wang,Steve Greenbaum,Yan‐Yan Hu,Akira Isogai,Martin Winter,Kang Xu,Yue Qi,Liangbing Hu
出处
期刊:Nature [Springer Nature]
卷期号:598 (7882): 590-596 被引量:408
标识
DOI:10.1038/s41586-021-03885-6
摘要

Although solid-state lithium (Li)-metal batteries promise both high energy density and safety, existing solid ion conductors fail to satisfy the rigorous requirements of battery operations. Inorganic ion conductors allow fast ion transport, but their rigid and brittle nature prevents good interfacial contact with electrodes. Conversely, polymer ion conductors that are Li-metal-stable usually provide better interfacial compatibility and mechanical tolerance, but typically suffer from inferior ionic conductivity owing to the coupling of the ion transport with the motion of the polymer chains1–3. Here we report a general strategy for achieving high-performance solid polymer ion conductors by engineering of molecular channels. Through the coordination of copper ions (Cu2+) with one-dimensional cellulose nanofibrils, we show that the opening of molecular channels within the normally ion-insulating cellulose enables rapid transport of Li+ ions along the polymer chains. In addition to high Li+ conductivity (1.5 × 10−3 siemens per centimetre at room temperature along the molecular chain direction), the Cu2+-coordinated cellulose ion conductor also exhibits a high transference number (0.78, compared with 0.2–0.5 in other polymers2) and a wide window of electrochemical stability (0–4.5 volts) that can accommodate both the Li-metal anode and high-voltage cathodes. This one-dimensional ion conductor also allows ion percolation in thick LiFePO4 solid-state cathodes for application in batteries with a high energy density. Furthermore, we have verified the universality of this molecular-channel engineering approach with other polymers and cations, achieving similarly high conductivities, with implications that could go beyond safe, high-performance solid-state batteries. By coordinating copper ions with the oxygen-containing groups of cellulose nanofibrils, the molecular spacing in the nanofibrils is increased, allowing fast transport of lithium ions and offering hopes for solid-state batteries.
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