Dipole-field-assisted charge extraction in metal-perovskite-metal back-contact solar cells

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作者
Xiongfeng Lin
Askhat N. Jumabekov
Niraj N. Lal
Alexander R. Pascoe
Daniel E. Gómez
Noel W. Duffy
Anthony S. R. Chesman
Kallista Sears
Maxime Fournier
Yupeng Zhang
Qiaoliang Bao
Yi-Bing Cheng
Leone Spiccia
Udo Bach
机构
[1] Monash University,Department of Materials Science & Engineering
[2] CSIRO Manufacturing,Plasmonics & Photochemistry Laboratory
[3] RMIT University,ARC Centre of Excellence in Exciton Science
[4] CSIRO Energy,School of Chemistry and ARC Centre of Excellence in Electromaterials Science
[5] Monash University,Department of Chemical Engineering
[6] Monash University,Department of Chemical Engineering
[7] College of Electronic Science and Technology,undefined
[8] Melbourne Centre for Nanofabrication,undefined
[9] Monash University,undefined
[10] Monash University,undefined
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摘要
Hybrid organic-inorganic halide perovskites are low-cost solution-processable solar cell materials with photovoltaic properties that rival those of crystalline silicon. The perovskite films are typically sandwiched between thin layers of hole and electron transport materials, which efficiently extract photogenerated charges. This affords high-energy conversion efficiencies but results in significant performance and fabrication challenges. Herein we present a simple charge transport layer-free perovskite solar cell, comprising only a perovskite layer with two interdigitated gold back-contacts. Charge extraction is achieved via self-assembled monolayers and their associated dipole fields at the metal-perovskite interface. Photovoltages of ~600 mV generated by self-assembled molecular monolayer modified perovskite solar cells are equivalent to the built-in potential generated by individual dipole layers. Efficient charge extraction results in photocurrents of up to 12.1 mA cm−2 under simulated sunlight, despite a large electrode spacing.
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