材料科学
电压
功率密度
离子键合
电势能
热电效应
光电子学
温度梯度
能量密度
电流密度
导电体
能量(信号处理)
活化能
电气工程
纳米技术
能量转换
离子电导率
储能
工程物理
工作(物理)
电位梯度
塞贝克系数
盐度
化学工程
消散
工作产出
扩散
联轴节(管道)
功率(物理)
电解质
比能量
热能
微流控
机械能
作者
Hao Yang,Q-Y Huang,Wei Fang,Yifan Wang,Yaru Yue,Hao Wang,LI Zhe,Qin Gao,Pengchi Zhang,Xinzhe Li,Mingyu Song,Chuanyu Li,Xudong Cai,Chen Li,Jing Li,Kuan Sun
标识
DOI:10.1002/admt.202501775
摘要
ABSTRACT Ionic thermoelectric (i‐TE) materials are characterized by their flexibility, non‐toxicity, and high thermopower, rendering them highly promising for powering wearable electronic devices. However, their current energy density remains relatively low, peaking at merely 12.4 J m −2 K −2 , insufficient to meet the energy demands of modern electrical devices. Here we present a novel strategy to enhance the energy density of i‐TE materials through the implementation of an asymmetric device configuration. In this approach, a polyelectrolyte, polydimethyl diallyl ammonium chloride (PDDAC), is deposited on one side of a polyvinyl alcohol (PVA) hydrogel, significantly boosting power output by leveraging the salinity gradient energy derived from a nonthermally driven diffusion process. Consequently, we achieved an impressive energy density of 52.5 ± 4.5 J m −2 K −2 , marking the highest value reported in this field to date. This substantial improvement is attributed to the synergistic coupling of salinity gradient energy with ionic thermoelectricity, which enhances the overall voltage and energy output by adding a voltage contribution from the salinity gradient to the ionic thermovoltage.
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