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
解耦(概率)
烷基
水溶液
有机化学
色谱法
热力学
复合材料
化学
热导率
物理
工程类
控制工程
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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