Developing Y-Branched Polymer Acceptor with 3D Architecture to Reconcile Between Crystallinity and Miscibility Yielding >15% Efficient All-Polymer Solar Cells

被引:26
作者
Ji, Jingjing [1 ]
Zhu, Lei [2 ,3 ]
Xiong, Xia [4 ]
Liu, Feng [2 ,3 ]
Liang, Ziqi [1 ]
机构
[1] Fudan Univ, Dept Mat Sci, Shanghai 200433, Peoples R China
[2] Shanghai Jiao Tong Univ, Frontiers Sci Ctr Transformat Mol, Sch Chem & Chem Engn, Situ Ctr Phys Sci, Shanghai 200240, Peoples R China
[3] Shanghai Jiao Tong Univ, Ctr Hydrogen Sci, Shanghai 200240, Peoples R China
[4] Shanghai Inst Technol, Sch Chem & Environm Engn, Shanghai 201418, Peoples R China
基金
中国国家自然科学基金;
关键词
all-polymer solar cells; crystallinity; miscibility; polymer acceptor; Y-branched; HYPERBRANCHED POLYMERS; MOLECULAR-WEIGHT;
D O I
10.1002/advs.202200864
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
In all-polymer solar cells (all-PSCs), there remains such a dilemma that obtains good miscibility and crystallinity simultaneously. Herein a new family of Y-shape polymer acceptor, namely PYTT is developed, which is copolymerized from Y6 and benzotrithiophene units in three-way directions. Benefiting from its high-density end-chains and extended pi-conjugation thanks to highly-branched 3D architecture, PYTT displays better organic solubility despite much higher molecular weights, larger crystallinity, and tighter pi-stacking than the linear counterpart-PYT comprising Y6 and thiophene moieties, while showing identical optical absorption yet threefold higher photoluminescence intensity. In PYTT blend film with PM6 polymer donor, the interpenetrating nano-fibrillar structures are formed with well-intermixed polymeric domain sizes close to the exciton diffusion length, which is greatly conducive to exciton dissociation and charge transport in device. Consequently, PYTT-based all-PSCs exhibit all increased photovoltaic parameters, yielding a decent power conversion efficiency of 15.60%, which is approximate to 20% enhancement over PYT-based device, along with low nonradiative loss of 0.221 meV.
引用
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页数:9
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