A 16.4% efficiency organic photovoltaic cell enabled using two donor polymers with their side-chains oriented differently by a ternary strategy. Issue 7 (10th February 2020)

• Record Type: Journal Article
• Authors: Chang, Yuan; Lau, Tsz-Ki; Chow, Philip C. Y.; Wu, Ningning; Su, Dan; Zhang, Weichao; Meng, Huifeng; Ma, Chao; Liu, Tao; Li, Kun; Zou, Xinhui; Wong, Kam Sing; Lu, Xinhui; Yan, He; Zhan, Chuanlang
• Is Part Of: Journal of materials chemistry. Volume 8:Issue 7(2020)
• Page Start: 3676
• Page End: 3685
• Publication Date: 2020-02-10
• Subjects: Materials -- Research -- Periodicals; Chemistry, Analytic -- Periodicals; Environmental sciences -- Research -- Periodicals; 543.0284
• DOI: 10.1039/c9ta13293g
• Languages: English
• ISSNs: 2050-7488

Abstract

Abstract : A ternary material system featuring two donor polymers with identical absorption spectra and differently-oriented side-chains was used in an organic photovoltaic (OPV) cell. It is the first ternary blended OPV cell with two donor polymers with >16% efficiency. Abstract : Effective ternary material systems are usually achieved using a donor/acceptor guest that is structurally similar to the donor/acceptor host to maintain the film-morphology of the host binary blend. In this study, we report an unprecedented ternary material system, PBDB-TF:PBDB-T-SF:Y6, in which PBDB-T-SF is selected as the donor polymer guest of the PBDB-TF:Y6 binary blend. The absorption spectra of both polymers are almost overlapped and their energy levels are similar. However, the side-chains between the host (PBDB-TF) and the guest (PBDB-T-SF) are oriented differently, which modulates the morphology of the polymer phases from nanoscale (10–20 nm) fine fibrils in the host binary blend to an interpenetrating mesoscale polymer-crowd (>100 nm) with reduced phase crystallinity in the ternary blend. As a result, the electrical properties of the active layer are greatly improved: the hole mobility increases more than the electron mobility, resulting in balanced hole and electron mobilities; the monomolecular and bimolecular recombinations are both reduced; the charge carrier extraction is faster and the trap-assisted recombination is reduced, resulting in a longer recombination lifetime of charge carriers (0.19 μs vs. 0.15/0.11 μs). All of these contribute to the concurrently increased device fill-factor and short-circuit current-density, and finally improved efficiency (16.4%). Solid-state 19 F magic angle spinning nuclear magnetic microscopy is conducted to probe interaction between the host and guest donor polymers. This study demonstrates that mesoscale morphology such as the polymer-crowd induced by differently oriented side chains of the host–guest polymers can be a morphological feature of active layer toward high-efficiency organic photovoltaic cells.