ジャーナル論文 Covalent functionalization of transition metal dichalcogenides with perylene for light harvesting devices
Ruben Canton-Vitoria (author) (この著者で検索)
;
Yuki Matsunaga (author) (この著者で検索)
;
Shaochun Zhang (author) (この著者で検索)
;
Mengsong Xue (author) (この著者で検索)
;
Minoru Osada (author) (この著者で検索)
ORCID https://orcid.org/0000-0002-6439-8068 (unauthenticated)
National Institute for Materials Science
ORCID ;
Ryo Kitaura (author) (この著者で検索)
ORCID SAMURAI
コレクション

引用
Ruben Canton-Vitoria, Yuki Matsunaga, Shaochun Zhang, Mengsong Xue, Minoru Osada, Ryo Kitaura. Covalent functionalization of transition metal dichalcogenides with perylene for light harvesting devices. Nanoscale. 2025, 17 (13), 8084-8100. https://doi.org/10.1039/d4nr05364h

説明:

(abstract)

This study examines the optical and electronic properties of eight 2D transition metal chalcogenides (TMDs) covalently functionalized with perylene, forming hybrid materials. Characterization was performed using XPS, Raman, EDX, TEM, and AFM, while UV-Vis-NIR absorption and photoluminescence spectroscopy assessed optical properties. Electronic properties were analyzed via cyclic voltammetry and FET devices. The results showed that perylene’s spectroscopic features dominate, with WSe₂ and MoSe₂ exhibiting a new near-IR band and MoTe₂ showing enhanced conductivity. Perylene also boosted absorption (400–600 nm), improving photoresponse, with responsivities over 2 × 10⁵ % and 2 × 10⁴ mA W⁻¹. These hybrids rival top non-covalent functionalization methods, emphasizing covalent functionalization’s potential for tuning 2D materials.

権利情報:

キーワード: 2D materials

刊行年月日: 2025-02-27

出版者: Royal Society of Chemistry (RSC)

掲載誌:

  • Nanoscale (ISSN: 20403372) vol. 17 issue. 13 p. 8084-8100

研究助成金:

  • Japan Society for the Promotion of Science P19368
  • Ministry of Education, Culture, Sports, Science and Technology

原稿種別: 著者最終稿 (Accepted manuscript)

MDR DOI: https://doi.org/10.48505/nims.5436

公開URL: https://doi.org/10.1039/d4nr05364h

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更新時刻: 2025-04-20 17:34:24 +0900

MDRでの公開時刻: 2025-04-20 17:17:36 +0900

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