Ecofriendly Hydroxyalkyl Cellulose Additives for Efficient and Stable MAPbI3‐Based Inverted Perovskite Solar Cells

能量转换效率 纤维素 钝化 钙钛矿(结构) 化学工程 可再生能源 材料科学 纳米技术 光电子学 电气工程 图层(电子) 工程类
作者
Xue‐Feng Zhu,Rui Lin,Hao Gu,Hui‐Chao Hu,Zheng Liu,Guichuan Xing,Yibing Wu,Xinhua Ouyang
出处
期刊:Energy & environmental materials [Wiley]
卷期号:6 (5) 被引量:16
标识
DOI:10.1002/eem2.12426
摘要

Perovskite solar cells (PSCs) have been demonstrated to be one of the most promising technologies in the field of renewable energy. However, the presence of the defects in the perovskite films greatly limits the efficiency and the stability of the PSCs. The additive engineering is one of the most effective approaches to overcome this problem. Most of the successful additives are extracted from the petroleum‐based materials, while the research on the biomass‐based additives is still lagging behind. In this paper, two ecofriendly hydroxyalkyl cellulose additives, i.e., hydroxyethyl cellulose (HEC) and hydroxylpropyl cellulose (HPC), are investigated on the performance of the MAPbI 3 ‐based inverted PSCs. Due to the strong interaction between the hydroxyl groups of the cellulose and the divalent cations of the perovskite, these additives enhance the crystal grain orientation and significantly repair the defects of the perovskite films. Working as the additives, these two cellulose derivatives show a strong passivation ability, which significantly reduces the trap density and improves the optoelectronic feature of the PSCs. Compared with the average power conversion efficiency (PCE) of the control device (19.19%), an enhancement of ~10% is achieved after the addition of HEC. The optimized device (PCE = 21.25%) with a long‐term stability (10:80 h, PCE = 20.93%) is achieved by the incorporation of the HEC additives into the precursor solution. It is the best performance among the PSCs with the cellulose additives up to now. This research provides a novel choice to develop a cost‐effective and renewable additive for the PSCs with high efficiency and excellent long‐term stability.
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