Ajou University repository

Large-area metal surface plasmon–polymer coupled nanocomposite thin film at air–liquid interface for low voltage operated high-performance photodetector
  • Singh, Manish Kumar ;
  • Mishra, Richa ;
  • Prakash, Rajiv ;
  • Yi, Junsin ;
  • Heo, Junseok ;
  • Pandey, Rajiv Kumar
Citations

SCOPUS

8

Citation Export

DC Field Value Language
dc.contributor.authorSingh, Manish Kumar-
dc.contributor.authorMishra, Richa-
dc.contributor.authorPrakash, Rajiv-
dc.contributor.authorYi, Junsin-
dc.contributor.authorHeo, Junseok-
dc.contributor.authorPandey, Rajiv Kumar-
dc.date.issued2023-01-01-
dc.identifier.issn0300-9440-
dc.identifier.urihttps://dspace.ajou.ac.kr/dev/handle/2018.oak/32981-
dc.description.abstractCoupling of metal surface plasmon resonance (SPR) with organic molecules and successive fabrication of large-area films is an effective approach for enhancing photogenerated excitons while retaining their optical thickness. In this regard, we present the facile synthesis of a silver nanoparticle (Ag NP) SPR–polymer coupled large-area nanocomposite thin film (8 ± 0.5-cm-diameter circular film) at the air–liquid interface and the fabrication of a high-performance visible-region photodetector (PD). The formation of nanocomposite films was investigated via multiple techniques, which revealed the formation of an SPR/organic molecule unified system. The photoresponse of the nanocomposite film was examined by fabricating a sandwich-structure ITO/PQT-12-Ag NP/Al Schottky device PD and measuring the photocurrent; responsivity R(λ), which was 9.624 × 104, 3.384 × 104, and 2.372 × 104 mA/W; external quantum efficiency, which was 19.03 × 103, 8.92 × 103, and 5.54 × 103; and detectivity (D), which was 1.06 × 1013, 3.70 × 1012, and 2.60 × 1012 Jones, at a bias voltage of −1.5 V for 627-nm (red), 470-nm (blue), and 530-nm (green) light, respectively. The high performance of the PDs in the visible region was discussed according to the spectral, KPFM, morphological, and energy band diagram results.-
dc.description.sponsorshipThis work was supported by the Industrial Strategic Technology Development Program ( 20000300 ) funded by the Ministry of Trade, Industry and Energy (MOTIE, Korea). This work was also supported by a grant from the Korea Institute of Energy Technology Evaluation and Planning (KETEP) funded by the Korean government ( MOTIE ) ( 20218520010100 , International Joint Research on Silicon/III-V tandem solar cell to achieve over 40 % efficiency) and ( 20214000000640 the Advanced Energy Research Center for Tandem Solar Cells Based on Silicon (AERC-TSC)).-
dc.language.isoeng-
dc.publisherElsevier B.V.-
dc.subject.meshAir liquid interfaces-
dc.subject.meshLarge area film-
dc.subject.meshMargonian flow-
dc.subject.meshMetal surfaces-
dc.subject.meshNanocomposite thin films-
dc.subject.meshOrganic exciton-
dc.subject.meshOrganics-
dc.subject.meshPerformance-
dc.subject.meshSERS-
dc.subject.meshSurface-plasmon resonance-
dc.titleLarge-area metal surface plasmon–polymer coupled nanocomposite thin film at air–liquid interface for low voltage operated high-performance photodetector-
dc.typeArticle-
dc.citation.titleProgress in Organic Coatings-
dc.citation.volume174-
dc.identifier.bibliographicCitationProgress in Organic Coatings, Vol.174-
dc.identifier.doi10.1016/j.porgcoat.2022.107231-
dc.identifier.scopusid2-s2.0-85139591457-
dc.identifier.urlwww.elsevier.com/locate/porgcoat-
dc.subject.keywordLarge area film-
dc.subject.keywordMargonian flow-
dc.subject.keywordOrganic excitons-
dc.subject.keywordPhotocurrent-
dc.subject.keywordSERS-
dc.description.isoafalse-
dc.subject.subareaChemical Engineering (all)-
dc.subject.subareaSurfaces, Coatings and Films-
dc.subject.subareaOrganic Chemistry-
dc.subject.subareaMaterials Chemistry-
Show simple item record

Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.

Related Researcher

 Heo, Junseok Image
Heo, Junseok허준석
Department of Intelligence Semiconductor Engineering
Read More

Total Views & Downloads

File Download

  • There are no files associated with this item.