塞贝克系数
材料科学
热电效应
电阻率和电导率
聚合物
离子键合
电导率
化学物理
联轴节(管道)
热电材料
离子电导率
共轭体系
纳米技术
离子
金属
电极
热导率
导电聚合物
光电子学
氢
凝聚态物理
化学工程
谐振器耦合系数
过渡金属
作者
Jeong Gye Lee,Hojun Ji,Eunsol Ok,Hyunji Lee,Giwon Lee,Sungjun Park,Daegun Kim,Kilwon Cho
出处
期刊:Small
[Wiley]
日期:2025-12-15
卷期号:22 (7): e11108-e11108
被引量:2
标识
DOI:10.1002/smll.202511108
摘要
Abstract The thermoelectric (TE) properties of the n‐type conjugated polymer (CP) polybenzodifuran‐dione (PBFDO) are systematically modulated via counter‐ion exchange, in which protons initially present as the counter‐ion are replaced with various cations of increasing ionic radius. Ion exchange varied polaron‐cation coupling, macroscopic conducting network, and macroscopic structural order, enabling purpose‐oriented TE properties control, depending on the cation. In potassium‐exchanged PBFDO film, a weakened polaron‐cation coupling and improved structural order facilitated a transition from hopping to band‐like transport, doubling electrical conductivity to realize an electrode‐suitable material. Meanwhile, ammonium exchange not only increased the electrical conductivity but also maintained a high Seebeck coefficient through hydrogen bonding, yielding a record‐high power factor of 225 µW m −1 K −2 for n‐type CPs, demonstrating a strategic tuning of TE properties in PBFDO. The ammonium‐exchanged PBFDO film thereby achieved a high TE figure‐of‐merit, ZT of 0.13, which is the highest reported for n‐type CPs exhibiting metallic conductivity.
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