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具有吸收互补给体和受体的9.73%效率非富勒烯全有机小分子太阳能电池。

9.73% Efficiency Nonfullerene All Organic Small Molecule Solar Cells with Absorption-Complementary Donor and Acceptor.

作者信息

Bin Haijun, Yang Yankang, Zhang Zhi-Guo, Ye Long, Ghasemi Masoud, Chen Shanshan, Zhang Yindong, Zhang Chunfeng, Sun Chenkai, Xue Lingwei, Yang Changduk, Ade Harald, Li Yongfang

机构信息

Beijing National Laboratory for Molecular Sciences, CAS Key Laboratory of Organic Solids, CAS Research/Education Center for Excellence in Molecular Sciences, Institute of Chemistry, Chinese Academy of Sciences , Beijing 100190, China.

School of Chemistry and Chemical Engineering, University of Chinese Academy of Sciences , Beijing 100049, China.

出版信息

J Am Chem Soc. 2017 Apr 12;139(14):5085-5094. doi: 10.1021/jacs.6b12826. Epub 2017 Mar 29.

Abstract

In the last two years, polymer solar cells (PSCs) developed quickly with n-type organic semiconductor (n-OSs) as acceptor. In contrast, the research progress of nonfullerene organic solar cells (OSCs) with organic small molecule as donor and the n-OS as acceptor lags behind. Here, we synthesized a D-A structured medium bandgap organic small molecule H11 with bithienyl-benzodithiophene (BDTT) as central donor unit and fluorobenzotriazole as acceptor unit, and achieved a power conversion efficiency (PCE) of 9.73% for the all organic small molecules OSCs with H11 as donor and a low bandgap n-OS IDIC as acceptor. A control molecule H12 without thiophene conjugated side chains on the BDT unit was also synthesized for investigating the effect of the thiophene conjugated side chains on the photovoltaic performance of the p-type organic semiconductors (p-OSs). Compared with H12, the 2D-conjugated H11 with thiophene conjugated side chains shows intense absorption, low-lying HOMO energy level, higher hole mobility and ordered bimodal crystallite packing in the blend films. Moreover, a larger interaction parameter (χ) was observed in the H11 blends calculated from Hansen solubility parameters and differential scanning calorimetry measurements. These special features combined with the complementary absorption of H11 donor and IDIC acceptor resulted in the best PCE of 9.73% for nonfullerene all small molecule OSCs up to date. Our results indicate that fluorobenzotriazole based 2D conjugated p-OSs are promising medium bandgap donors in the nonfullerene OSCs.

摘要

在过去两年中,以n型有机半导体(n-OSs)作为受体的聚合物太阳能电池(PSC)发展迅速。相比之下,以有机小分子作为供体、n-OS作为受体的非富勒烯有机太阳能电池(OSC)的研究进展较为滞后。在此,我们合成了一种D-A结构的中带隙有机小分子H11,其以联噻吩-苯并二噻吩(BDTT)作为中心供体单元,氟苯并三唑作为受体单元,并以H11作为供体、低带隙n-OS IDIC作为受体,实现了全有机小分子OSC 9.73%的功率转换效率(PCE)。还合成了一种在BDT单元上没有噻吩共轭侧链的对照分子H12,用于研究噻吩共轭侧链对p型有机半导体(p-OSs)光伏性能的影响。与H12相比,具有噻吩共轭侧链的二维共轭H11在共混膜中表现出强烈的吸收、较低的HOMO能级、更高的空穴迁移率和有序的双峰微晶堆积。此外,通过汉森溶解度参数和差示扫描量热法测量计算得出,在H11共混物中观察到了更大的相互作用参数(χ)。这些特殊特性与H11供体和IDIC受体的互补吸收相结合,使得非富勒烯全小分子OSC的PCE达到了目前最好的9.73%。我们的结果表明,基于氟苯并三唑的二维共轭p-OSs是用于非富勒烯OSC的有前景的中带隙供体。

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