Recently, in combination with seed-mediated growth, thiolated chiral molecule-guided growth has shown great promise in obtaining chiral plasmonic nanostructures. Previously, with the assistance of chiral cysteines (Cys), we realized helical growth of plasmonic shells on gold nanorod (AuNR) seeds dispersed in cetyltrimethylammonium bromide (CTAB) solution. Herein, we further studied the roles of non-chiral cationic surfactants in tuning the helical growth. Both the counter anion and the hydrocarbon chain length of the surfactants were found to affect the formation of helical shells greatly. In particular, we exhibited surfactant-modulated conversion of the chiral shell deposition mode between layer growth and island growth. By optimizing growth conditions, an obvious plasmonic circular dichroism (PCD) response could be achieved for the island helical shell. Our findings demonstrated promising potential of nanochemical synthesis in fabricating chiral plasmonic nanostructures with small structural sizes.
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http://dx.doi.org/10.1039/d3nr01371e | DOI Listing |
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December 2024
State Key Laboratory of Heavy Oil Processing, College of Chemistry and Chemical Engineering, China University of Petroleum (East China), Qingdao, 266580, China.
Chiral plasmonic nanomaterials have attracted significant awareness due to their applications in chiral catalysis, biosensing, photonics, and separation. Constructing plasmonic core-shell nanomaterials with geometric chirality and desirable optical chirality is a crucial yet challenging task for extending the range of chiral plasmonic nanomaterials. Here, a two-step method is reported for the synthesis of Gold (Au) branches wrapped silver (Ag) nanocubes (L/DBAg@Au) with strong and tunable circular dichroism (CD) signals under the regulation of L/D-cysteine (L/D-Cys).
View Article and Find Full Text PDFAdv Sci (Weinh)
December 2024
Henan Key Laboratory of Crystalline Molecular Functional Materials, College of Chemistry and Pingyuan Laboratory, Zhengzhou University, Zhengzhou, 450001, China.
Curvature-induced interfacial electric field effects and local strain engineering offer a powerful approach for optimizing the intrinsic catalytic activity of single-atom catalysts (SACs). Investigations into the surface curvature on SACs are still ongoing, and the impact of the concave surface is often overlooked. In this work, theoretical calculations indicate that curved surfaces, particularly those with concavity, can optimize the electronic structures of single Fe sites and facilitate the reductive release of *OH.
View Article and Find Full Text PDFJ Environ Manage
December 2024
Department of Chemistry, Soongsil University, Seoul, 06978, South Korea. Electronic address:
Chiral Au@Pt nanoparticles (NPs) with optically plasmonic and catalytic active surfaces were sustainably prepared to serve as label-free surface enhanced Raman scattering (SERS) platform to distinguish D- and L-enantiomers of alanine and tartaric acid. Surface morphologies were characterized by high-angle annular dark-field imaging-scanning transmission electron microscopy (HADDF-STEM) and selected area energy diffraction (SAED) patterns. The amounts of Pt on chiral Au NPs were estimated by the inductively coupled plasma-optical emission spectrometer (ICP-OES) and X-ray diffraction (XRD).
View Article and Find Full Text PDFPhys Chem Chem Phys
December 2024
School of Civil Engineering and Transportation, South China University of Technology, Guangzhou, 510640, People's Republic of China.
Due to the multi-factor coupling effect, the rule of interlayer friction in low-dimensional homogeneous thin-wall shell structures is still unclear. Double walled carbon nanotubes (DWCNTs) having a typical low-dimensional homogeneous thin-wall shell structure are selected for this study. The interlayer friction of numerous chiral DWCNTs is investigated using molecular dynamics simulations to systematically analyze and understand the coupling mechanisms of various factors in interlayer friction.
View Article and Find Full Text PDFNanoscale
December 2024
MOLTECH-Anjou, UMR 6200, CNRS, UNIV Angers, 2 bd Lavoisier, 49045 ANGERS Cedex, France.
Monoanionic and neutral nickel(II) and platinum(II) bis(dithiolene) complexes based on the 5,6-diethyl-5,6-dihydro-1,4-dithiin-2,3-dithiolate (de-dddt) chiral ligand have been prepared in racemic and enantiopure forms. Neutral closed-shell species have been generated from monoanionic precursors upon electrocrystallization. The racemic anionic (TBA)[Ni(,-de-dddt)(,-de-dddt)] complex crystallized in the centrosymmetric space group 2/, while the neutral complexes crystallized in the enantiomorphic tetragonal space group 422 or 422.
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