Abstract
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.
Cite
CITATION STYLE
Liu, S., Yang, Y., Huang, H., Zheng, J., Liu, G., Ho To, T., & Huang, B. (2022). Giant and bidirectionally tunable thermopower in nonaqueous ionogels enabled by selective ion doping. Science Advances, 8(1). https://doi.org/10.1126/sciadv.abj3019
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