This paper reviews the recent advances in experiment and theory of the induction of chiroptical effects, primarily circular dichroism (CD), at the plasmonic and excitonic resonances of achiral inorganic nanocrystals (NCs) capped and/or formed with chiral molecules. It also addresses stronger chiroptical effects obtained in intrinsically chiral inorganic nanostructures obtained from growing enantiomeric excess of intrinsically chiral NCs or arranging achiral plasmonic particles in chiral configurations. The accumulated experimental data and theory on various CD induction mechanisms provide an extended set of tools to properly analyze and understand the electromagnetic influence of chiral molecules on inorganic particles and obtain new general insights into the interaction of capping molecules with inorganic NCs. Among the field-induced CD mechanisms developed recently one can name the Coulomb (near-field, dipolar) mechanism for nanostructures much smaller than the wavelength, and for larger nanostructures, the electromagnetic (effective chiral medium), and intrinsically chiral plasmonic mechanisms.

A large number of inorganic materials form crystals with chiral symmetry groups. Enantioselectively synthesizing nanostructures of such materials should lead to interesting optical activity effects. Here we report the synthesis of colloidal tellurium and selenium nanostructures using thiolated chiral biomolecules. The synthesis conditions are tuned to obtain tellurium nanostructures with chiral shapes and large optical activity. These nanostructures exhibit visible optical and chiroptical responses that shift with size and are successfully simulated by an electromagnetic model. The model shows that they behave as chiral optical resonators. The chiral tellurium nanostructures are transformed into chiral gold and silver telluride nanostructures with very large chiroptical activity, demonstrating a simple colloidal chemistry path to chiral plasmonic and semiconductor metamaterials. These materials are natural candidates for studies related to interactions of chiral (bio)molecules with chiral inorganic surfaces, with relevance to asymmetric catalysis, chiral crystallization and the evolution of homochirality in biomolecules.

Circular dichroism (CD) induced at exciton transitions by chiral ligands attached to single component and core/shell colloidal quantum dots (QDs) was used to study the interactions between QDs and their capping ligands. Analysis of the CD line shapes of CdSe and CdS QDs capped with l-cysteine reveals that all of the features in the complex spectra can be assigned to the different excitonic transitions. It is shown that each transition is accompanied by a derivative line shape in the CD response, indicating that the chiral ligand can split the exciton level into two new sublevels, with opposite angular momentum, even in the absence of an external magnetic field. The role of electrons and holes in this effect could be separated by experiments on various types of core/shell QDs, and it was concluded that the induced CD is likely related to interactions of the highest occupied molecular orbitals of the ligands with the holes. Hence, CD was useful for the analysis of hole level–ligand interactions in quantum semiconductor heterostructures, with promising outlook toward better general understanding the properties of the surface of such systems.

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The synthesis of chiral penicillamine-capped CdS and CdSe quantum dots (QDs) was adjusted to control the size of the nanoparticles. This, together with size separation, allowed for simultaneous tuning of absorption, circular dichroism (CD), and fluorescence on a wide wavelength range. Band edge transitions were accompanied by circular dichroism peaks which red-shifted together with the increase in particle size. The clear correlation between absorption and CD bands as well as between absorption bands and size in semiconductor QDs was used to derive an experimental scaling law for optical activity. The decrease in the intensity of circular dichroism-to-absorption ratio (dissymmetry) with the increase in particle size was stronger than linear, probably exponential. In addition, strong material type dependence was observed. The CD line shape appeared to be sensitive to the nature of the transition and may thus serve as a tool for sorting out the electronic states of the QDs. Fluorescence-detected circular dichroism (FDCD) was introduced as a new probe of optically active fluorescent nanoparticles. The analysis of the size and material dependence of the chiroptical induction effect leads to the conclusion that it is primarily an electronic interaction effect between the adsorbed chiral molecules and the electron-hole states.

Chiroptical effects are routinely observed in three dimensional objects lacking mirror symmetry or quasi-two-dimensional thin films lacking in-plane mirror symmetry. Here we show that symmetric plasmonic planar arrays of circular nanoholes produced strong chiroptical responses at visible wavelengths on tilting them with respect to the incident light beam due to the collective asymmetric nature of their surface plasmon excitations. This extrinsic chiroptical effect can be stronger than the local chiroptical response in arrays of intrinsically chiral nanoholes and may be useful for chiral sensing and negative refraction.

Colloidal hollow silver nanoparticles were produced by a fast chemical reduction of silver oxide nanoparticles capped with glutathione. These hollow silver particles were surprisingly single crystalline and had almost perfect spherical shells. The reaction was further tested for the transformation of silver oxide nanoparticles to hollow silver sulfide nanoparticles by a reaction with sulfide ions. Analysis of the dimensions of the precursor Ag 2 O nanoparticles and product hollow Ag nanoparticles as well as the sensitivity of the reduction process to the nature of reducing agent and its concentration hints that the reaction had to proceed through inward diffusion of reducing agent versus fast outward diffusion/dissolution of silver ions. We believe that this type of reactions resembles transformation reactions that have been associated with the nanoscale Kirkendall effect in its broader sense.

Despite persistent and extensive observations of crystals with chiral shapes, the mechanisms underlying their formation are not well understood. Although past studies suggest that chiral shapes can form because of crystallization in the presence of chiral additives, or because of an intrinsic tendency that stems from the crystal structure, there are many cases in which these explanations are not suitable or have not been tested. Here, an investigation of model tellurium nanocrystals provides insights into the chain of chirality transfer between crystal structure and shape. We show that this transfer is mediated by screw dislocations, and shape chirality is not an outcome of the chiral crystal structure or ligands.