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Tetrabutylammonium Hydroxide-Functionalized Ti3C2T MXene for Significantly Improving the Photovoltaic Performance of
Wei Huang1, Ling Ding1, Dianhui Wang1
1Guangxi Key Laboratory of Information Materials, School of Materials Science and Engineering, Guilin University of Electronic Technology, Guilin 541004, China.
Abstract:
An appropriate electron transport layer (ETL) or cathode buffer layer (CBL) is critical for high-performance perovskite solar cells (PVSCs). In this work, tetrabutylammonium hydroxide (TBAOH)-functionalized Ti3C2T MXene (TBAOH-Ti3C2T) is developed to improve the photovoltaic performance of PVSCs. TBAOH-Ti3C2T is synthesized by HF etching and then TBAOH intercalation, and TBAOH can effectively attach to the Ti3C2T surface during the intercalation process. In hole transport material (HTM)-free carbon-based PVSCs with the structure of ITO/ETL/MAPbI3/carbon, the SnO2 doped by TBAOH-Ti3C2T (SnO2:TBAOH-Ti3C2T) as ETL shows decreased WF and increased conductivity and improves the growth of the perovskite film with a larger grain and significantly reduced defects, which synergistically facilitate charge transport and extraction and reduce charge recombination. The HTM-free carbon-based PVSC with SnO2:TBAOH-Ti3C2T ETL exhibits a significantly higher PCE of 14.93% with enhanced device stability compared to the control device with pristine SnO2 ETL (11.95%) and also outperforms most of the HTM-free carbon-based PVSCs with MAPbI3 perovskite reported so far. In traditional inverted PVSCs with the structure of ITO/PTAA/MAPbI3/PCBM/CBL/Ag, the TBAOH-Ti3C2T is utilized as a CBL to significantly enhance device performance with a high PCE of 21.16%, which is obviously superior than that (16.26%) of the control device without CBL. The impressive results indicate that tetrabutylammonium hydroxide-functionalized Ti3C2T MXene possesses great application potential in different functional layers for high-performance PVSCs.
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