High Thermopower of Agarose‐Based Ionic Thermoelectric Gel Through Micellization Effect Decoupling the Cation/Anion Thermodiffusion

Author:

Li Qikai12ORCID,Yu Dangkai13,Wang Shuaihua13,Zhang Xinbo13,Li Yuchen13,Feng Shien‐Ping24,Liu Weishu13

Affiliation:

1. Department of Materials Science and Engineering Southern University of Science and Technology Shenzhen Guangdong 518055 P. R. China

2. Department of Mechanical Engineering The University of Hong Kong Pokfulam Road Hong Kong 999077 P. R. China

3. Shenzhen Engineering Research Center for Novel Electronic Information Materials and Devices Southern University of Science and Technology Shenzhen 518055 China

4. Department of Advanced Design and Systems Engineering City University of Hong Kong Kowloon Hong Kong 999077 P. R. China

Abstract

AbstractIonic 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.

Publisher

Wiley

Subject

Electrochemistry,Condensed Matter Physics,Biomaterials,Electronic, Optical and Magnetic Materials

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