Enhancing performance and stability of perovskite solar cells through defect passivation with a polyamide derivative obtained from benzoxazine-isocyanide chemistry

• Published in: Chemical engineering journal (Lausanne, Switzerland : 1996) Switzerland : 1996), 2022-03, Vol.431, p.133951, Article 133951
• Main Authors: Li, Lihua, Tu, Silong, You, Guofeng, Cao, Jiabing, Wu, Daogui, Yao, Lu, Zhou, Zhonggao, Shi, Wei, Wang, Wen, Zhen, Hongyu, Ling, Qidan
• Format: Article
• Language: English
• Subjects: Benzoxazine-isocyanide chemistry; Defect passivation; Dopant-free hole-transporting polymers; Perovskite solar cells; Polymer passivation
• ISSN: 1385-8947; 1873-3212
• DOI: 10.1016/j.cej.2021.133951

[Display omitted] •A phenolic hydroxyl-substituted polyamide derivative PAB serves as an passivating agent.•Hole transport polymer PM6-T10 is used in perovskite solar cells for the first time.•Three kinds of polar groups linked by flexible backbone provide effective passivation.•Devices PAB-0.15 display better device performances than the reference devices PAB-0. Owing to the presence of amounts of defects in organic/inorganic hybrid perovskite, defect passivation is considered as a significant way to improve the efficiency and stability of perovskite solar cells (PVSCs). Herein, for the first time, a phenolic hydroxyl-substituted polyamide derivative (PAB), which was prepared by benzoxazine-isocyanide chemistry (BIC) and simultaneously contained hydroxyl, secondary amine, and carboxyl functional segments, was selected as the precursor additive to passivate perovskite active layer. Different passivation groups attached in the chain of a polymer are vital for the defect passivation of perovskite containing various defects. Hydroxyl and carboxyl can act as Lewis bases to passivate the undercoordinated lead defects, and secondary amine can coordinate with iodide ion. These passivation groups linked by the flexible polymer chains provide effective interaction with trap states on the surfaces and grain boundaries of perovskite, suppressing the trap-assisted non-radiative charge carrier recombination thus. As a result, these positive effects increased the efficiency of PVSCs from 19.45% to 21.13%, and maintained 95% initial efficiency after 32 days in ambient air (humidity around 50%, room temperature). This work opens a viable avenue to develop efficient passivating polymers via benzoxazine-isocyanide chemistry.