Molecular Design of Hole-Collecting Materials for Co-Deposition Processed Perovskite Solar Cells: A Tripodal Triazatruxene Derivative with Carboxylic Acid Groups

High-performance and cost-effective hole-collecting materials (HCMs) are indispensable for commercially viable perovskite solar cells (PSCs). Here, we report an anchorable HCM composed of a triazatruxene core connected with three alkyl carboxylic acid groups (<b>3CATAT-C3</b>). In contrast to the phosphonic acid-containing tripodal analog (<b>3PATAT-C3</b>), <b>3CATAT-C3</b> molecules can form a hydrophilic monolayer on a transparent conducting oxide surface, which is beneficial for subsequent perovskite film deposition in the traditional layer-by-layer fabrication process. More importantly, the larger diffusion coefficient and higher surface energy make <b>3CATAT-C3</b> suitable for the simplified, cost-effective one-step co-deposition process in which <b>3CATAT-C3</b> was directly added as part of the perovskite precursor solution. <b>3CATAT-C3</b> is predominantly located at the perovskite bottom surface after spin-coating the mixed precursor solution, facilitating charge extraction. Devices with <b>3CATAT-C3</b> fabricated by this co-deposition method exhibit superior performance with a champion power conversion efficiency of over 23%. The unencapsulated devices showed good operational stability (retaining 90% of the initial output after 100 h), thermal durability (retaining 95% of the initial value after heating at 105 °C under air), and excellent storage stability (showing no drop in performance over 8000 h). Based on the results of time-of-flight secondary-ion mass spectroscopy (ToF-SIMS) and diffusion order nuclear magnetic resonance spectroscopy (DOSY), we elucidated the effect of anchoring groups on the performance of the tripodal HCMs in PSCs as well as the mechanism of the co-deposition fabrication process. Our findings provide valuable insights for the molecular design of multifunctional hole-collecting materials, further advancing the performance of perovskite solar cells.

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Publication Details

Journal
Journal of the American Chemical Society
Published
2025-01-10
DOI
https://doi.org/10.1021/jacs.4c15857
Citations
20
Primary Topic
Perovskite Materials and Applications
Type
article
Field-Weighted Citation Impact
14.61

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article

Molecular Design of Hole-Collecting Materials for Co-Deposition Processed Perovskite Solar Cells: A Tripodal Triazatruxene Derivative with Carboxylic Acid Groups

Atsushi Wakamiya, Yoshihiko Kanemitsu, Yuta Adachi, Minh Anh Truong et al.
20 citations
Journal of the American Chemical Society
Perovskite Materials and Applications
14.61
article

Molecular Design of Hole-Collecting Materials for Co-Deposition Processed Perovskite Solar Cells: A Tripodal Triazatruxene Derivative with Carboxylic Acid Groups

Atsushi Wakamiya, Yoshihiko Kanemitsu, Yuta Adachi, Minh Anh Truong, Tiancheng Tan, Yuko Matsushige, Takumi Yamada, Yasuko Iwasaki, Aruto Akatsuka, Ryuji Kaneko, Hiroyuki K. Yoshida, Tomoya Nakamura, Tsukasa Funasaki, Shota Hira, Richard Murdey, Chizuru Asahara
article en
20 citations

Abstract

High-performance and cost-effective hole-collecting materials (HCMs) are indispensable for commercially viable perovskite solar cells (PSCs). Here, we report an anchorable HCM composed of a triazatruxene core connected with three alkyl carboxylic acid groups (<b>3CATAT-C3</b>). In contrast to the phosphonic acid-containing tripodal analog (<b>3PATAT-C3</b>), <b>3CATAT-C3</b> molecules can form a hydrophilic monolayer on a transparent conducting oxide surface, which is beneficial for subsequent perovskite film deposition in the traditional layer-by-layer fabrication process. More importantly, the larger diffusion coefficient and higher surface energy make <b>3CATAT-C3</b> suitable for the simplified, cost-effective one-step co-deposition process in which <b>3CATAT-C3</b> was directly added as part of the perovskite precursor solution. <b>3CATAT-C3</b> is predominantly located at the perovskite bottom surface after spin-coating the mixed precursor solution, facilitating charge extraction. Devices with <b>3CATAT-C3</b> fabricated by this co-deposition method exhibit superior performance with a champion power conversion efficiency of over 23%. The unencapsulated devices showed good operational stability (retaining 90% of the initial output after 100 h), thermal durability (retaining 95% of the initial value after heating at 105 °C under air), and excellent storage stability (showing no drop in performance over 8000 h). Based on the results of time-of-flight secondary-ion mass spectroscopy (ToF-SIMS) and diffusion order nuclear magnetic resonance spectroscopy (DOSY), we elucidated the effect of anchoring groups on the performance of the tripodal HCMs in PSCs as well as the mechanism of the co-deposition fabrication process. Our findings provide valuable insights for the molecular design of multifunctional hole-collecting materials, further advancing the performance of perovskite solar cells.

Journal of the American Chemical SocietyVol. 147(3)
Chiba University (JP), Kyoto University (JP), Toray Industries, Inc. (Japan) (JP), Kyoto University Institute for Chemical Research
Mazda Foundation, New Energy and Industrial Technology Development Organization, Kyoto University, Iwatani Naoji Foundation, Japan Society for the Promotion of Science, Japan Science and Technology Agency
Openalex Percentile: Top 1%
Perovskite Materials and Applications
14.61
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