December 1 - 6, 2024
Boston, Massachusetts
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2024 MRS Fall Meeting & Exhibit
EN09.11.17

Organic Thermoelectric Device Utilizing Charge Transfer Interface as the Charge Generation by Harvesting Thermal Energy

When and Where

Dec 5, 2024
8:00pm - 10:00pm
Hynes, Level 1, Hall A

Presenter(s)

Co-Author(s)

Mana Kameyama1,Shun Kondo1,Kentaro Imaoka1,Yoko Shimoi2,Fabrice Mathevet3,Takashi Fujihara4,Hiroshi Goto4,Hajime Nakanotani1,5,Masayuki Yahiro2,Chihaya Adachi1,5

Kyushu University1,ISIT2,Sorbonne Université3,GCE Institute4,Kyushu university I2CNER5

Abstract

Mana Kameyama1,Shun Kondo1,Kentaro Imaoka1,Yoko Shimoi2,Fabrice Mathevet3,Takashi Fujihara4,Hiroshi Goto4,Hajime Nakanotani1,5,Masayuki Yahiro2,Chihaya Adachi1,5

Kyushu University1,ISIT2,Sorbonne Université3,GCE Institute4,Kyushu university I2CNER5
Currently, environmental power generation technologies that convert not only sunlight but also heat, vibration, and other micro-energies around us into electric power have been attracting attention around the world. Thermoelectric devices using waste heat have been put to practical use, but their use is limited due to the problems of using the high cost of materials and the limited installation space required to form a temperature difference. In this study, we propose organic thermoelectric devices based on a new mechanism by utilizing the charge-transfer (CT) complexes that cause carrier separation with thermal energy as low as room temperature and the charge diffusion ability in organic thin films.<br/>As CT forming materials, CuPc (Copper (II) phthalocyanine) and F<sub>16</sub>CuPc (Copper (II) 1,2,3,4,8,9,10,11,15,16,17,18,22,23,24,25-hexadecafluoro-29H,31H-phthalocyanine) were used as a donor and an acceptor, respectively. In addition, C<sub>60</sub> (fullerene) and BCP (2,9-dimethyl-4,7-diphenyl-1,10-phenanthroline) were inserted as the electron transport layers. In Device A, which utilizes CuPc (30 nm)/F<sub>16</sub>CuPc (20 nm)/C<sub>60</sub> (40 nm)/BCP (20 nm), we confirmed power generation with the value of V<sub>oc</sub>=180 mV, J<sub>SC</sub>=20 nA cm<sup>-2</sup>, and P<sub>max</sub>=0.9 nWcm<sup>-2</sup> in a completely dark environment at room temperature. Further, when the F<sub>16</sub>CuPc film thickness was changed from 100 nm to 200 nm (Device B), the power generation efficiency improved with increasing F<sub>16</sub>CuPc film thickness. This can be ascribed to the improvement of diffusion force in the thicker F<sub>16</sub>CuPc film, resulting in suppressed carrier recombination. When the C<sub>60</sub> film thickness was changed from 40 nm to 20 nm (Device C), we observed the thinner C<sub>60</sub> film leads to higher efficiency. Further, when the BCP film thickness was changed from 20 nm to 5 nm (Device D), the efficiency increased with decreasing BCP film thickness, while the devices without BCP showed lower efficiency. Based on these results, we fabricated an optimized CuPc (300 nm)/F<sub>16</sub>CuPc (200 nm)/C<sub>60</sub> (3 nm)/BCP (5 nm) device and obtained the value of V<sub>oc</sub>=462 mV, J<sub>SC</sub>=3.94 μA cm<sup>-2</sup>, and P<sub>max</sub>=394 nWcm<sup>-2</sup>, demonstrating the proposed devices have high potential as a new power generation mechanism.

Keywords

electrical properties | organic

Symposium Organizers

Ana Claudia Arias, University of California, Berkeley
Derya Baran, King Abdullah University of Science and Technology
Francisco Molina-Lopez, KU Leuven
Luisa Petti, Free University of Bozen Bolzano

Symposium Support

Bronze
1-Material Inc.
Journal on Flexible Electronics
Nextron Corporation
Sciprios GmbH

Session Chairs

Ana Claudia Arias
Luisa Petti

In this Session