材料科学
锚固
氧化还原
电极
阳离子聚合
离子键合
热电效应
纳米技术
化学工程
离子
高分子化学
物理化学
化学
有机化学
热力学
结构工程
物理
工程类
冶金
作者
Xinyuan Li,Jianchao Jia,Yongqiang Dai,Xuanshuo Zhang,Lifeng Guan,Dehui� Zhang,Fred Wang,Qianming Wang,Wei Zeng
标识
DOI:10.1002/aenm.202500584
摘要
Abstract The design of high‐performance n‐type ionic thermoelectric cells (i‐TE cells) tailored for harvesting low‐grade thermal energy presents significant challenges. In this study, an n‐type i‐TE cell exhibiting substantial negative thermopower and a high output energy density is developed by leveraging the synergistic interplay between thermal diffusion within an ionic hydrogel electrolyte and redox reactions at the electrode interface. Specifically, a gel network featuring dual positive groups is synthesized by cross‐linking quaternized chitosan and guanidine molecules via glutaraldehyde, with thermal diffusion further enhanced by incorporating crown ether for complexation. Additionally, NiCo(CO 3 )(OH) 2 , a material known for its high hydrophilicity, is utilized as the anode to facilitate rapid ion and electron transfer at the electrode interface. The integration of optimized thermal diffusion within polycationic electrolytes with electrode interface‐enhanced ion/electron transport mechanisms significantly improves the sustained output performance and thermoelectric conversion efficiency of the i‐TE cell. Notably, the thermopower (Seebeck coefficient) of this n‐type i‐TE cell achieves a value of −26.04 mV K −1 , and its 2 h output energy density reached 1301.61 J m −2 under a temperature difference (ΔT) of 15 K. These findings offer a novel design paradigm for high‐performance n‐type i‐TE cell.
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