Template-assisted strategies are widely used to fabricate nanostructured materials. By taking these strategies a step forward, herein we report the design of two chiral plasmonic nanostructures based on Au nanoparticle (NP) assemblies organized in clockwise and anticlockwise directions, having opposite response to circularly polarized light. The chiral plasmonic nanostructures are obtained by growing Au NPs on chiral templates based on d- and l-forms of alanine functionalized phenyleneethynylenes. Interestingly, Au NP assemblies show mirror symmetrical electronic circular dichroism (ECD) bands at their surface plasmon frequency originating through their asymmetric organization. Upon increasing the temperature, the chiral templates dissociate as evident from the disappearance of their ECD signal. The profound advantage of the thermoresponsive nature of the templates is employed to obtain free-standing chiral plasmonic nanostructures. The tilt angle high-resolution transmission electron microscopic measurements indicate that the NP assemblies, grown on a template based on the d-isomer, organize in clockwise direction ( P-form) and on l-isomer in anticlockwise direction ( M-form). The inherent chirality prevailing on the surface of the template drives the helical growth of the Au NPs in opposite directions. Experimental results are rationalized by a model which accounts for the large polarizability of Au NPs. The large polarizability leads to large oscillating dipole moments whose effects become prominent when interparticle distances are comparable to the particle size.

Chiral Plasmons: Au Nanoparticle Assemblies on Thermoresponsive Organic Templates / George, Jino; Kar, Sabnam; Anupriya, Edappalil Satheesan; Somasundaran, Sanoop Mambully; Das, Anjali Devi; Sissa, Cristina; Painelli, Anna; Thomas, K George. - In: ACS NANO. - ISSN 1936-0851. - (2019). [10.1021/acsnano.8b09624]

Chiral Plasmons: Au Nanoparticle Assemblies on Thermoresponsive Organic Templates

Das, Anjali Devi;Sissa, Cristina;Painelli, Anna
;
2019

Abstract

Template-assisted strategies are widely used to fabricate nanostructured materials. By taking these strategies a step forward, herein we report the design of two chiral plasmonic nanostructures based on Au nanoparticle (NP) assemblies organized in clockwise and anticlockwise directions, having opposite response to circularly polarized light. The chiral plasmonic nanostructures are obtained by growing Au NPs on chiral templates based on d- and l-forms of alanine functionalized phenyleneethynylenes. Interestingly, Au NP assemblies show mirror symmetrical electronic circular dichroism (ECD) bands at their surface plasmon frequency originating through their asymmetric organization. Upon increasing the temperature, the chiral templates dissociate as evident from the disappearance of their ECD signal. The profound advantage of the thermoresponsive nature of the templates is employed to obtain free-standing chiral plasmonic nanostructures. The tilt angle high-resolution transmission electron microscopic measurements indicate that the NP assemblies, grown on a template based on the d-isomer, organize in clockwise direction ( P-form) and on l-isomer in anticlockwise direction ( M-form). The inherent chirality prevailing on the surface of the template drives the helical growth of the Au NPs in opposite directions. Experimental results are rationalized by a model which accounts for the large polarizability of Au NPs. The large polarizability leads to large oscillating dipole moments whose effects become prominent when interparticle distances are comparable to the particle size.
Chiral Plasmons: Au Nanoparticle Assemblies on Thermoresponsive Organic Templates / George, Jino; Kar, Sabnam; Anupriya, Edappalil Satheesan; Somasundaran, Sanoop Mambully; Das, Anjali Devi; Sissa, Cristina; Painelli, Anna; Thomas, K George. - In: ACS NANO. - ISSN 1936-0851. - (2019). [10.1021/acsnano.8b09624]
File in questo prodotto:
File Dimensione Formato  
ACS Nano .pdf

accesso aperto

Tipologia: Documento in Pre-print
Licenza: Creative commons
Dimensione 1.68 MB
Formato Adobe PDF
1.68 MB Adobe PDF Visualizza/Apri

I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.

Utilizza questo identificativo per citare o creare un link a questo documento: http://hdl.handle.net/11381/2857831
Citazioni
  • ???jsp.display-item.citation.pmc??? ND
  • Scopus 23
  • ???jsp.display-item.citation.isi??? 24
social impact