Simultaneously Suppressing Charge Recombination and Decomposition of Perovskite Solar Cells by Conjugated Covalent Organic Frameworks. Issue 33 (19th July 2022)

• Record Type: Journal Article
• Authors: Nie, Riming; Chu, Weicun; Li, Zhongping; Li, He; Chen, Shanshan; Chen, Yaqing; Zhang, Zhuhua; Liu, Xiaoming; Guo, Wanlin; Seok, Sang Il
• Is Part Of: Advanced energy materials. Volume 12:Issue 33(2022)
• Page Start: n/a
• Page End: n/a
• Publication Date: 2022-07-19
• Subjects: better crystallization -- covalent organic frameworks -- humidity and thermal stabilities -- perovskite solar cells; Energy harvesting -- Materials -- Periodicals; Energy conversion -- Materials -- Periodicals; Energy storage -- Materials -- Periodicals; Photovoltaics -- Periodicals; Fuel cells -- Periodicals; Thermoelectric materials -- Periodicals; 621.31
• DOI: 10.1002/aenm.202200480
• Languages: English
• ISSNs: 1614-6832

Abstract

Abstract: The power conversion efficiency (PCE) of perovskite solar cells (PSCs) has rapidly increased over the past 10 years. However, along with further efficiency improvements, it is necessary to improve the long‐term stability of perovskite materials, which limits the commercialization of PSCs. Therefore, it is urgent to find ways to simultaneously suppress charge recombination and degradation of perovskite materials. Here, two covalent organic frameworks (COFs) are synthesized by reacting thieno[3, 2‐b]thiophene‐2, 5‐dicarbaldehyde (TTDA) with 1, 3, 5‐tris(4‐aminophenyl)benzene (TAPB) or 2, 4, 6‐tris(4‐aminophenyl)‐1, 3, 5‐triazine (TTA). The addition of these two COFs to the perovskite layer allows for more efficient charge separation through spatially separated frontier orbitals, and can also inhibit the degradation of the FAPbI3 layer and the formation of δ‐FAPbI3 . The PSCs with TTDA‐TTA‐COF exhibit higher efficiency and open‐circuit voltage than those with TTDA‐TAPB‐COF. This is attributed to the better crystallization of perovskites induced by stronger well‐conjugated properties and π–π interactions in TTDA‐TTA‐COF. The champion PSC with TTDA‐TTA‐COF exhibits a PCE of 23.35% and excellent long‐term stability. To the best of one's knowledge, this is the highest efficiency among PSCs fabricated using crystalline organic frameworks as additives. This work provides a new route to fabricate efficient and stable PSCs by incorporating proper COFs. Abstract : 2D conjugated covalent organic frameworks, TTDA‐TAPB‐COF and TTDA‐TTA‐COF, are designed to simultaneously suppress charge recombination and decomposition of perovskite materials. The champion perovskite solar cell with TTDA‐TTA‐COF exhibits a power conversion efficiency of 23.35% and excellent long‐term stability. To the best of one's knowledge, this is the highest efficiency in perovskite solar cells using the strategy of crystalline organic frameworks.