4.8 Article

Efficient and Stable Quasi-2D Perovskite Solar Cells Enabled by Thermal-Aged Precursor Solution

Journal

ADVANCED FUNCTIONAL MATERIALS
Volume 31, Issue 52, Pages -

Publisher

WILEY-V C H VERLAG GMBH
DOI: 10.1002/adfm.202107675

Keywords

film quality; quasi-2D perovskite; solar cells; thermal-aged precursor solution; voltage loss

Funding

  1. National Natural Science Foundation of China (NSFC) [21875012, 21674006, 21773045]
  2. National Key Research and Development Program of China [2017YFA0206600]
  3. Chinese Academy of Sciences (100 Top Young Scientists Program)

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The mitigation of voltage loss in quasi-2D PSCs using thermal-aged precursor solutions (TAPSs) can boost the photovoltaic performance by producing high-quality perovskite films, leading to an enhanced PCE. This approach allows for the formation of compact morphology, preferential crystal orientation, and lowered trap density in the perovskite films, resulting in improved stability and reduced degradation of the device.
Quasi-2D perovskites have received wide attention in photovoltaics owing to their excellent materials robustness and merits in the device stability. However, the highest power conversion efficiency (PCE) reported on quasi-2D perovskite solar cells (PSCs) still lags those of the 3D counterparts, mainly caused by the relatively high voltage loss. Here, a study is presented on the mitigation of voltage loss in quasi-2D PSCs via usage of thermal-aged precursor solutions (TAPSs). Based on the (AA)(2)MA(4)Pb(5)I(16) (n = 5) quasi-2D perovskite absorber with a bandgap of approximate to 1.60 eV, a record-high open-circuit voltage of 1.24 V is obtained, resulting in boosting the PCE to 18.68%. The enhanced photovoltaic performance afforded by TAPS is attributed to the thermal-aged solution processing that triggers colloidal aggregations to reduce the nucleation sites inside the solution. As a result, formation of high-quality perovskite films featuring compact morphology, preferential crystal orientation, and lowered trap density is allowed. Of importance, with the improved film quality, the corrosion of Ag electrode induced by ion migrations is effectively restrained, which leads to a satisfactory storage stability with <2% degradation after 1200 h under nitrogen environment without encapsulation.

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