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用于柔性固态超级电容器的具有高离子电导率和大电压窗口的电极不可渗透和可交联的聚(环氧乙烷)-聚(环氧丙烷)-聚(环氧乙烷)三嵌段聚合物电解质。

Electrode-Impregnable and Cross-Linkable Poly(ethylene oxide)-Poly(propylene oxide)-Poly(ethylene oxide) Triblock Polymer Electrolytes with High Ionic Conductivity and a Large Voltage Window for Flexible Solid-State Supercapacitors.

机构信息

Center for Membranes, Korea Research Institute of Chemical Technology , 141 Gajeong-ro, Yuseong-gu, Daejeon 305-600, Republic of Korea.

Department of Chemical Engineering, Hanyang University , 17 Haengdang-dong, Seongdong-gu, Seoul 133-791, Republic of Korea.

出版信息

ACS Appl Mater Interfaces. 2017 Oct 4;9(39):33913-33924. doi: 10.1021/acsami.7b09909. Epub 2017 Sep 25.

Abstract

We present cross-linkable precursor-type gel polymer electrolytes (GPEs) that have large ionic liquid uptake capability, can easily penetrate electrodes, have high ion conductivity, and are mechanically strong as high-performance, flexible all-solid-state supercapacitors (SC). Our polymer precursors feature a hydrophilic-hydrophobic poly(ethylene oxide)-poly(propylene oxide)-poly(ethylene oxide) (PEO-PPO-PEO) triblock main-chain structure and trifunctional silane end groups that can be multi-cross-linked with each other through a sol-gel process. The cross-linked solid-state electrolyte film with moderate IL content (200 wt %) shows a well-balanced combination of excellent ionic conductivity (5.0 × 10 S cm) and good mechanical stability (maximum strain = 194%). Moreover, our polymer electrolytes have various advantages including high thermal stability (decomposition temperature > 330 °C) and the capability to impregnate electrodes to form an excellent electrode-electrolyte interface due to the very low viscosity of the precursors. By assembling our GPE-impregnated electrodes and solid-state GPE film, we demonstrate an all-solid-state SC that can operate at 3 V and provides an improved specific capacitance (112.3 F g at 0.1 A g), better rate capability (64% capacity retention until 20 A g), and excellent cycle stability (95% capacitance decay over 10 000 charge/discharge cycles) compared with those of a reference SC using a conventional PEO electrolyte. Finally, flexible SCs with a high energy density (22.6 W h kg at 1 A g) and an excellent flexibility (>93% capacitance retention after 5000 bending cycles) can successfully be obtained.

摘要

我们提出了可交联的前驱体型凝胶聚合物电解质(GPE),它具有大的离子液体吸收能力,容易渗透电极,具有高离子电导率,并且作为高性能、柔性全固态超级电容器(SC)具有机械强度。我们的聚合物前体具有亲水性-疏水性聚(环氧乙烷)-聚(环氧丙烷)-聚(环氧乙烷)(PEO-PPO-PEO)三嵌段主链结构和三官能硅烷端基,可以通过溶胶-凝胶过程彼此多交联。具有中等 IL 含量(200wt%)的交联固态电解质膜具有优异的离子电导率(5.0×10 S cm)和良好的机械稳定性(最大应变=194%)的良好平衡组合。此外,我们的聚合物电解质具有多种优点,包括高耐热性(分解温度>330°C)和由于前体的低粘度而能够浸渍电极形成优异的电极-电解质界面的能力。通过组装我们的 GPE 浸渍电极和固态 GPE 膜,我们展示了一种全固态 SC,它可以在 3V 下运行,并提供改进的比电容(在 0.1Ag 时为 112.3F g),更好的倍率性能(直到 20Ag 时保持 64%的容量),以及优异的循环稳定性(10000 次充放电循环后电容衰减 95%),与使用传统 PEO 电解质的参考 SC 相比。最后,成功获得了具有高能量密度(在 1Ag 时为 22.6Wh kg)和出色柔韧性(在 5000 次弯曲循环后保持>93%的电容)的柔性 SC。

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