In:
Energy & Environmental Science, Royal Society of Chemistry (RSC), Vol. 16, No. 4 ( 2023), p. 1597-1609
Abstract:
State-of-the-art n–i–p perovskite solar cells (PSCs) suffer from stability issues due to ionic interdiffusion. Herein, by enlarging the indacenodithiophene π-bridge donor (D′) to combine with the methoxy triphenylamine donor (D) and benzothiadiazole acceptor (A), three linear molecules termed L1, L2 and L3 with a D–A–D′–A–D structure are developed as dopant-free hole transport materials (HTMs). The π-bridge extension with active sites for coordination leverages the intramolecular dipole effect and intermolecular packing effect, resulting in a conformally bonded ultrathin interface with compact and uniform coverage (∼60 nm) to retard iodine migration and protect the buried perovskite. The unencapsulated L3-PSC (ITO/SnO 2 /perovskite/L3/MoO 3 /Au) achieved an impressive PCE of 22.61% (certified 21.79%, 0.0525 cm 2 ). Ultrafast laser spectroscopy reveals that L-series molecules have a sequential reduction of photoexcited energy disorder to illustrate the structure–performance–stability relationship. L3-PSC maintains over 85% of the initial efficiency after 500 h at 85 °C maximum power point tracking (MPP) and enables the possibility of using small molecules to stabilize n–i–p PSCs.
Type of Medium:
Online Resource
ISSN:
1754-5692
,
1754-5706
Language:
English
Publisher:
Royal Society of Chemistry (RSC)
Publication Date:
2023
detail.hit.zdb_id:
2439879-2
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