Molecular Design of Hole Transport Materials to Immobilize Ion Motion for Photostable Perovskite Solar Cells.
Angew Chem Int Ed Engl
; : e202412042, 2024 Aug 16.
Article
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| MEDLINE
| ID: mdl-39149940
ABSTRACT
Poor operational stability is a crucial factor limiting the further application of perovskite solar cells (PSCs). Organic semiconductor layers can be a powerful means for reinforcing interfaces and inhibiting ion migration. Herein, two hole-transporting molecules, pDPA-SFX and mDPA-SFX, are synthesized with tuned substituent connection sites. The meta-substituted mDPA-SFX results in a larger dipole moment, more ordered packing, and better charge mobility than pDPA-SFX, accompany with strong interface bonding on perovskite surfaces and suppressed ion motion as well. Importantly, mDPA-SFX-based PSCs exhibit an efficiency that has significantly increased from 22.5% to 24.8% and a module-based efficiency of 19.26% with an active area of 12.95 cm2. The corresponding cell retain 94.8% of its initial efficiency at maximum power point tracking (MPPT) after 1,000 h (T95 = 1,000 h). The MPPT T80 lifetime is as long as 2,238 h. This work illustrates that a small degree of structural variation in organic compounds leaves considerable room for developing new HTMs for light stable PSCs.
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MEDLINE
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En
Revista:
Angew Chem Int Ed Engl
Año:
2024
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Article
País de afiliación:
China