材料科学
钙钛矿(结构)
图层(电子)
平面的
原子层沉积
等离子体
电子
钙钛矿太阳能电池
化学物理
化学工程
纳米技术
计算机科学
量子力学
物理
计算机图形学(图像)
工程类
作者
Yinghuan Kuang,Valerio Zardetto,Roderick van Gils,Saurabh Karwal,Dibyashree Koushik,Marcel A. Verheijen,Lachlan E. Black,Christ H. L. Weijtens,Sjoerd C. Veenstra,Ronn Andriessen,W. M. M. Kessels,Mariadriana Creatore
标识
DOI:10.1021/acsami.8b09515
摘要
Abstract In this work, we present an extensive characterization of plasma-assisted atomic-layer-deposited SnO2 layers, with the aim of identifying key material properties of SnO2 to serve as an efficient electron transport layer in perovskite solar cells (PSCs). Electrically resistive SnO2 films are fabricated at 50 °C, while a SnO2 film with a low electrical resistivity of 1.8 × 10–3 Ω cm, a carrier density of 9.6 × 1019 cm–3, and a high mobility of 36.0 cm2/V s is deposited at 200 °C. Ultraviolet photoelectron spectroscopy indicates a conduction band offset of ∼0.69 eV at the 50 °C SnO2/Cs0.05(MA0.17FA0.83)0.95Pb(I2.7Br0.3) interface. In contrast, a negligible conduction band offset is found between the 200 °C SnO2 and the perovskite. Surprisingly, comparable initial power conversion efficiencies (PCEs) of 17.5 and 17.8% are demonstrated for the champion cells using 15 nm thick SnO2 deposited at 50 and 200 °C, respectively. The latter gains in fill factor but loses in open-circuit voltage. Markedly, PSCs using the 200 °C compact SnO2 retain their initial performance at the maximum power point over 16 h under continuous one-sun illumination in inert atmosphere. Instead, the cell with the 50 °C SnO2 shows a decrease in PCE of approximately 50%.
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