Energy Level Tuning in CsPbBr 3 Perovskite Solar Cells through In Situ-Polymerized PEDOT Hole Transport Layer

作者：Anling Tong, Xuanheng Chen, Yang Wang, Yuhong Wang, Qingshui Zheng, Ruowei He, Zhihang Jin, Weihai Sun, Yunlong Li, Jihuai Wu · 发表于：ACS Applied Materials & Interfaces · 年份：2024 · DOI：10.1021/acsami.4c08526 · 被引用次数：13 · 研究领域：Perovskite Materials and Applications、Conducting polymers and applications、Solid-state spectroscopy and crystallography

The all-inorganic CsPbBr 3 perovskite solar cells exhibit excellent stability against humidity and thermal conditions as well as relatively low production cost, rendering them a gradually emerging research hot spot in the field of photovoltaics. However, the absence of a hole transport layer (HTL) in its common structure and the substantial energy level difference of up to 0.6 eV between the highest occupied molecular orbital (HOMO) level of CsPbBr 3 and the work function of the carbon electrode have emerged as the primary factor limiting the improvement of its power conversion efficiency (PCE). In this work, the monomer 2,5-dibromo-3,4-ethylenedioxythiophene (DBEDOT) is spin-coated onto the surface of the CsPbBr 3 film directly and then subjected to annealing; DBEDOT undergoes in situ polymerization to form poly(3,4-ethylenedioxythiophene) (PEDOT), which aims to ameliorate the issue of excessive energy level difference between CsPbBr 3 and the carbon electrode, and to facilitate the extraction and transport efficiency of holes between the CsPbBr 3 perovskite and the carbon electrode. Compared to the pristine device, the PCE of the device based on in situ polymerization is enhanced and achieves a maximum efficiency of 9.81%. Furthermore, the unencapsulated devices based on in situ polymerization maintain 95.9% of their original efficiency after 40 days of stability testing.