TY - JOUR
T1 - N-type organic thermoelectrics
T2 - demonstration of ZT > 0.3
AU - Liu, Jian
AU - van der Zee, Bas
AU - Alessandri, Riccardo
AU - Sami, Selim
AU - Dong, Jingjin
AU - Nugraha, Mohamad I.
AU - Barker, Alex J.
AU - Rousseva, Sylvia
AU - Qiu, Li
AU - Qiu, Xinkai
AU - Klasen, Nathalie
AU - Chiechi, Ryan C.
AU - Baran, Derya
AU - Caironi, Mario
AU - Anthopoulos, Thomas D.
AU - Portale, Giuseppe
AU - Havenith, Remco W. A.
AU - Marrink, Siewert J.
AU - Hummelen, Jan C.
AU - Koster, L. Jan Anton
PY - 2020/11/10
Y1 - 2020/11/10
N2 - The ‘phonon-glass electron-crystal’ concept has triggered most of the progress that has been achieved in inorganic thermoelectrics in the past two decades. Organic thermoelectric materials, unlike their inorganic counterparts, exhibit molecular diversity, flexible mechanical properties and easy fabrication, and are mostly ‘phonon glasses’. However, the thermoelectric performances of these organic materials are largely limited by low molecular order and they are therefore far from being ‘electron crystals’. Here, we report a molecularly n-doped fullerene derivative with meticulous design of the side chain that approaches an organic ‘PGEC’ thermoelectric material. This thermoelectric material exhibits an excellent electrical conductivity of >10 S cm
−1 and an ultralow thermal conductivity of <0.1 Wm
−1K
−1, leading to the best figure of merit ZT = 0.34 (at 120 °C) among all reported single-host n-type organic thermoelectric materials. The key factor to achieving the record performance is to use ‘arm-shaped’ double-triethylene-glycol-type side chains, which not only offer excellent doping efficiency (~60%) but also induce a disorder-to-order transition upon thermal annealing. This study illustrates the vast potential of organic semiconductors as thermoelectric materials.
AB - The ‘phonon-glass electron-crystal’ concept has triggered most of the progress that has been achieved in inorganic thermoelectrics in the past two decades. Organic thermoelectric materials, unlike their inorganic counterparts, exhibit molecular diversity, flexible mechanical properties and easy fabrication, and are mostly ‘phonon glasses’. However, the thermoelectric performances of these organic materials are largely limited by low molecular order and they are therefore far from being ‘electron crystals’. Here, we report a molecularly n-doped fullerene derivative with meticulous design of the side chain that approaches an organic ‘PGEC’ thermoelectric material. This thermoelectric material exhibits an excellent electrical conductivity of >10 S cm
−1 and an ultralow thermal conductivity of <0.1 Wm
−1K
−1, leading to the best figure of merit ZT = 0.34 (at 120 °C) among all reported single-host n-type organic thermoelectric materials. The key factor to achieving the record performance is to use ‘arm-shaped’ double-triethylene-glycol-type side chains, which not only offer excellent doping efficiency (~60%) but also induce a disorder-to-order transition upon thermal annealing. This study illustrates the vast potential of organic semiconductors as thermoelectric materials.
KW - THERMAL-CONDUCTIVITY
KW - NANOSTRUCTURED THERMOELECTRICS
KW - ELECTRONIC-STRUCTURE
KW - POLYMER
KW - EFFICIENCY
KW - MOBILITY
KW - DESIGN
KW - DOPANT
KW - POWER
KW - HEAT
U2 - 10.1038/s41467-020-19537-8
DO - 10.1038/s41467-020-19537-8
M3 - Article
C2 - 33173050
SN - 2041-1723
VL - 11
JO - Nature Communications
JF - Nature Communications
IS - 1
M1 - 5694
ER -