Solution-processed, binder-free pristine Ti3C2Tx MXene electrodes enabled by MAI passivation for high-performance, scalable perovskite solar cells
Issued Date
2025-08-01
Resource Type
eISSN
26665239
Scopus ID
2-s2.0-105010950853
Journal Title
Applied Surface Science Advances
Volume
28
Rights Holder(s)
SCOPUS
Bibliographic Citation
Applied Surface Science Advances Vol.28 (2025)
Suggested Citation
Chunlim H., Depijan M., Srisawad K., Meekati T., Wongratanaphisan D., Ruankham P., Kanjanaboos P., Pakawatpanurut P. Solution-processed, binder-free pristine Ti3C2Tx MXene electrodes enabled by MAI passivation for high-performance, scalable perovskite solar cells. Applied Surface Science Advances Vol.28 (2025). doi:10.1016/j.apsadv.2025.100803 Retrieved from: https://repository.li.mahidol.ac.th/handle/123456789/111360
Title
Solution-processed, binder-free pristine Ti3C2Tx MXene electrodes enabled by MAI passivation for high-performance, scalable perovskite solar cells
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Abstract
While carbon electrodes offer a cost-effective option for perovskite solar cells (PSCs), their efficiency is often compromised by the insulating polymer binders required. Addressing this limitation, we demonstrate a polymer binder-free electrode using pristine Ti<inf>3</inf>C<inf>2</inf>T<inf>x</inf> MXene, applied directly onto the perovskite via a simple solution-processing technique. A major obstacle emerged: the direct interface between untreated, hydrophilic Ti<inf>3</inf>C<inf>2</inf>T<inf>x</inf> and the perovskite proved unstable, causing rapid degradation. We resolved this critical issue by introducing a novel methylammonium iodide (MAI) surface treatment for Ti<inf>3</inf>C<inf>2</inf>T<inf>x</inf> prior to deposition. This passivation strategy proved essential, stabilizing the interface by neutralizing reactive surface groups. PSCs utilizing these MAI-treated, binder-free Ti<inf>3</inf>C<inf>2</inf>T<inf>x</inf> electrodes achieved 13.8 % power conversion efficiency, substantially exceeding carbon controls (10.7 %), primarily due to a significantly enhanced fill factor (75.2 % vs 58.2 %) and low sheet resistance. Furthermore, demonstrating practical potential, these MXene electrodes maintain performance better than carbon when the active area is scaled up. Although encapsulation is required to protect the hydrophilic MXene and ensure long-term stability (>360 h) in ambient conditions, this work charts an effective course for developing highly conductive, scalable, binder-free electrodes for advanced PSCs.