材料科学
塞贝克系数
离子键合
热电效应
琼脂糖
胶束
离子
化学工程
烷基
水溶液
物理化学
有机化学
色谱法
热力学
复合材料
化学
热导率
物理
工程类
作者
Qikai Li,Dangkai Yu,Shuai‐Hua Wang,Xinbo Zhang,Yuchen Li,Shien‐Ping Feng,Weishu Liu
标识
DOI:10.1002/adfm.202305835
摘要
Abstract Ionic thermoelectric (i‐TE) gels can have a high thermopower, if the thermodiffusion of mobile cation/anion is decoupled, attracting increasing attentions. Herein, it is shown a high p‐type i‐TE thermopower of 41.8 mV K −1 in agarose‐based ionic thermoelectric gels of AG‐ x Na:DBS (AG: agarose, Na:DBS: sodium dodecyl benzene sulfonate). The exclusively high thermopower is relative to the successfully decoupling the thermodiffusion of cation Na + and anion DBS − . A unique porous structure is formed due to the micellization of the amphiphilic DBS − with the hydrophilic benzenesulfonic group attached to the hydrous agarose gel chains, while the hydrophobic alkyl chain point to the pore centers. As a result, the DBS − micelles are almost immobile as compared with Na + , which can be reconsidered as a part of the gel matrix. The work shines a light on decoupling of cation/anion thermodiffusion through tailoring the microstructure of the quasi‐solid i‐TE materials.
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