Yu Zefeng, Wang Luyao, Mu Xijiao, Chen Chun-Chao, Wu Yiying, Cao Jing, Tang Yu
State Key Laboratory of Applied Organic Chemistry, Key Laboratory of Nonferrous Metal Chemistry and Resources Utilization of Gansu Province, College of Chemistry and Chemical Engineering, Lanzhou University, Lanzhou, 730000, P. R. China.
School of Materials Science and Engineering, Shanghai Jiao Tong University, Shanghai, 200240, P. R. China.
Angew Chem Int Ed Engl. 2021 Mar 15;60(12):6294-6299. doi: 10.1002/anie.202016087. Epub 2021 Feb 12.
Low conductivity and hole mobility in the pristine metal phthalocyanines greatly limit their application in perovskite solar cells (PSCs) as the hole-transporting materials (HTMs). Here, we prepare a Ni phthalocyanine (NiPc) decorated by four methoxyethoxy units as HTMs. In NiPc, the two oxygen atoms in peripheral substituent have a modified effect on the dipole direction, while the central Ni atom contributes more electron to phthalocyanine ring, thus efficiently increasing the intramolecular dipole. Calculation analyses reveal the extracted holes within NiPc are mainly concentrated on the phthalocyanine core induced by the intramolecular electric field, and further to be transferred by π-π stacking space channel between NiPc molecules. Finally, the best efficiency of PSCs with NiPc as dopant-free HTMs realizes a record value of 21.23 % (certified 21.03 %). The PSCs also exhibit the good moisture, heating and light stabilities. This work provides a novel way to improve the performance of PSCs with free-doped metal phthalocyanines as HTMs.
原始金属酞菁的低电导率和空穴迁移率极大地限制了它们作为空穴传输材料(HTM)在钙钛矿太阳能电池(PSC)中的应用。在此,我们制备了一种由四个甲氧基乙氧基单元修饰的镍酞菁(NiPc)作为HTM。在NiPc中,外围取代基中的两个氧原子对偶极方向有修饰作用,而中心Ni原子向酞菁环贡献更多电子,从而有效增加了分子内偶极。计算分析表明,NiPc内提取的空穴主要集中在由分子内电场诱导的酞菁核上,并通过NiPc分子间的π-π堆积空间通道进一步转移。最终,以NiPc作为无掺杂HTM的PSC的最佳效率实现了21.23%的创纪录值(认证值为21.03%)。这些PSC还表现出良好的耐湿性、耐热性和耐光性。这项工作为提高以无掺杂金属酞菁作为HTM的PSC的性能提供了一种新方法。