Utilize este identificador para referenciar este registo: https://hdl.handle.net/1822/24485

TítuloStrong light-matter interactions in heterostructures of atomically thin films
Autor(es)Britnell, Líam
Ribeiro, R. M.
Eckmann, A.
Jalil, R.
Belle, B. D.
Mishchenko, A.
Kim, Y.-J.
Gorbachev, R. V.
Georgiou, T.
Morozov, S. V.
Grigorenko, A. N.
Geim, A. K.
Casiraghi, C.
Castro Neto, A. H.
Novoselov, K. S.
Data13-Jun-2013
EditoraAmerican Association for the Advancement of Science
RevistaScience
CitaçãoScience 340, 1311 (2013)
Resumo(s)The isolation of various two-dimensional (2D) materials, and the possibility to combine them in vertical stacks, has created a new paradigm in materials science: heterostructures based on 2D crystals. Such a concept has already proven fruitful for a number of electronic applications in the area of ultrathin and flexible devices. Here we expand the range of such structures to photoactive ones by utilizing semiconducting transition metal dichalcogenides (TMDC)/graphene stacks. Van Hove singularities in the electronic density of states of TMDC guarantees enhanced light-matter interactions, leading to enhanced photon absorption and electron-hole creation (which are collected in transparent graphene electrodes). This allows development of extremely efficient flexible photovoltaic devices with photo-responsivity above 0.1 A/W (corresponding to an external quantum efficiency of above 30%).
TipoArtigo
URIhttps://hdl.handle.net/1822/24485
DOI10.1126/science.1235547
ISSN0036-8075
Versão da editorahttp://www.sciencemag.org/content/340/6138/1311.full.html
Arbitragem científicayes
AcessoAcesso aberto
Aparece nas coleções:CDF - CEP - Artigos/Papers (with refereeing)

Ficheiros deste registo:
Ficheiro Descrição TamanhoFormato 
Science_130426.docDocumento principal5,17 MBMicrosoft WordVer/Abrir

Partilhe no FacebookPartilhe no TwitterPartilhe no DeliciousPartilhe no LinkedInPartilhe no DiggAdicionar ao Google BookmarksPartilhe no MySpacePartilhe no Orkut
Exporte no formato BibTex mendeley Exporte no formato Endnote Adicione ao seu ORCID