Lowering the dielectric mismatch for efficient inverted perovskite solar cells through incorporating cyano-functionalized fullerene additive
Fullerene derivatives especially [1,1]-phenyl-C 61 -butyric-acid-methyl-ester (PC 61 BM) have been commonly used as electron transport layers and additives of inverted (p-i-n) perovskite solar cells (PVKSCs); however the dielectric constant (the ε r ) of PC 61 BM (3.8) is much smaller than those of...
Gespeichert in:
Veröffentlicht in: | Science China materials 2023-06, Vol.66 (6), p.2146-2158 |
---|---|
Hauptverfasser: | , , , , , , , , , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
Zusammenfassung: | Fullerene derivatives especially [1,1]-phenyl-C
61
-butyric-acid-methyl-ester (PC
61
BM) have been commonly used as electron transport layers and additives of inverted (p-i-n) perovskite solar cells (PVKSCs); however the dielectric constant (the
ε
r
) of PC
61
BM (3.8) is much smaller than those of organolead halide hybrid perovskites (6.5 for CH
3
NH
3
PbI
3
[MAPbI
3
]), resulting in unfavorable exciton dissociation and impeded interfacial charge transport and consequently undesirable nonradiative recombination. Herein, a novel cyanofunctionalized fullerene in which two cyano groups are incorporated
via
a rhodanine moiety (abbreviated C
60
-Rhd-CN) was synthesized and introduced into the MAPbI
3
active layer to construct inverted PVKSCs
via
an anti-solvent method. The involvement of two electron-withdrawing cyano groups within C
60
-Rhd-CN obviously increases the
ε
r
value (5.1) relative to PC
61
BM (3.8), hence lowering the dielectric mismatch between MAPbI
3
and fullerene. Besides, the cyano groups enable strong coordination interactions with the Pb
2+
ions of MAP-bI
3
, rendering efficient defect passivation of perovskite. As a result, C
60
-Rhd-CN incorporation facilitates exciton dissociation and interfacial charge transport and suppresses the nonradiative recombination, affording dramatic power conversion efficiency (PCE) enhancement of inverted PVKSC devices from 18.43% to 20.81%. Furthermore, C
60
-Rhd-CN incorporation helps to improve the ambient and thermal stabilities of PVKSC devices. To elucidate the critical role of cyano groups in increasing the the
ε
r
value and efficiency enhancement, another analogous novel rhodanine-functionalized fullerene with the two cyano groups substituted by a sulfur atom (abbreviated C
60
-Rhd-S) was also synthesized, which delivered a lower PCE of 19.45% than C
60
-Rhd-CN-incorporated devices due mainly to its lower the
ε
r
value (4.0). |
---|---|
ISSN: | 2095-8226 2199-4501 |
DOI: | 10.1007/s40843-022-2365-3 |