材料科学
三元运算
热电材料
离子
离子液体
热电效应
兴奋剂
纳米技术
塞贝克系数
光电子学
离子键合
化学
热导率
计算机科学
热力学
物理
催化作用
复合材料
有机化学
程序设计语言
生物化学
作者
Sijing Liu,Yuewang Yang,He Huang,Jiongzhi Zheng,Gongze Liu,Tsz Ho To,Baoling Huang
出处
期刊:Science Advances
[American Association for the Advancement of Science (AAAS)]
日期:2022-01-05
卷期号:8 (1)
被引量:52
标识
DOI:10.1126/sciadv.abj3019
摘要
Ionic thermoelectrics show great potential in thermal sensing owing to their ultrahigh thermopower, low cost, and ease in production. However, the lack of effective n-type ionic thermoelectric materials seriously hinders their applications. Here, we report giant and bidirectionally tunable thermopowers within an ultrawide range from −15 to +17 mV K−1 in solid ionic liquid–based ionogels. Particularly, a record high negative thermopower of −15 mV K−1 is achieved in the ternary ionogel, rendering it among the best n-type ionic thermoelectric materials under the same condition. A thermopower regulation strategy through ion doping to selectively induce ion aggregates to enhance ion-ion interactions is proposed. These selective ion interactions are found to be decisive in modulating the sign and magnitude of the thermopower in the ionogels. A prototype wearable device integrated with 12 p-n pairs is demonstrated with a total thermopower of 0.358 V K−1, showing promise for ultrasensitive thermal detection.
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