An official website of the United States government
Electronically doped metal oxide nanocrystals exhibit tunable infrared localized surface plasmon resonances (LSPRs). Despite the many benefits of IR resonant LSPRs in solution processable nanocrystals, the ways in which the electronic structure of the host semiconductor material impact metal oxide LSPRs are still being investigated. Semiconductors provide an alternative dielectric environment than metallically bonded solids, such as noble metals, which can impact how these materials undergo electronic relaxation following photoexcitation. Understanding these differences is key to developing applications that take advantage of the unique optical and electronic properties offered by plasmonic metal oxide NCs. Here, we use the two-temperature model in conjunction with femtosecond transient absorption experiments to describe how the internal temperature of two representative metal oxide nanocrystal systems, cubic WO 3−x and bixbyite Sn-doped In 2 O 3 , change following LSPR excitation. We find that the low free carrier concentrations of metal oxide NCs lead to less efficient heat generation as compared to metallic nanocrystals such as Ag. This suggests that metal oxide NCs may be ideal for applications wherein untoward heat generation may disrupt the application's overall performance, such as solar energy conversion and photonic gating.
more »
« less
This content will become publicly available on May 15, 2026
Plasmonic catalysis with bi-resonant noble metal – CuFeS2 chalcopyrite hybrid structures
Both noble metal nanoparticles (NPs) and chalcopyrite (CuFeS2) nanocrystals (NCs) provide resonant absorption in the visible, albeit through different mechanisms. Coherent oscillations of free conduction band electrons give rise to localized plasmons in noble metal NPs, whereas collective oscillations of bound electrons are responsible for quasistatic resonances in CuFeS2 NCs. This manuscript reviews the photophysical and photocatalytic properties of both noble metal and chalcopyrite nanostructures as well as direct and indirect charge and energy transfer processes in hybrid structures containing noble metal NPs and either semiconductor NCs or molecular photosensitizers or photocatalysts. CuFeS2 NCs share structural similarities with conventional semiconductor NCs, but the availability of collective charge oscillations in the visible facilitates a resonant coupling to localized plasmons in NPs. Hybrid nanostructures containing both metal and chalcopyrite building blocks are examined as a platform for wavelength-dependent charge and energy transfer and bifunctional reactivity for enhanced plasmonic photocatalysis.
more »
« less
- Award ID(s):
- 2403854
- PAR ID:
- 10591171
- Publisher / Repository:
- Institute of Physics Publishing
- Date Published:
- Journal Name:
- Nanotechnology
- ISSN:
- 0957-4484
- Format(s):
- Medium: X
- Sponsoring Org:
- National Science Foundation
More Like this
-
-
Plasmonic nanostructures and metasurfaces are appealing hosts for investigation of novel optical devices and exploration of new frontiers in physical/optical processes and materials research. Recent studies have shown that these structures hold the promise of greater control over the optical and electronic properties of quantum emitters, offering a unique horizon for ultra-fast spin-controlled optical devices, quantum computation, laser systems, and sensitive photodetectors. In this Perspective, we discuss how heterostructures consisting of metal oxides, metallic nanoantennas, and dielectrics can offer a material platform wherein one can use the decay of plasmons and their near fields to passivate the defect sites of semiconductor quantum dots while enhancing their radiative decay rates. Such a platform, called functional metal-oxide plasmonic metasubstrates (FMOPs), relies on formation of two junctions at very close vicinity of each other. These include an Au/Si Schottky junction and an Si/Al oxide charge barrier. Such a double junction allows one to use hot electrons to generate a field-passivation effect, preventing migration of photo-excited electrons from quantum dots to the defect sites. Prospects of FMOP, including impact of enhancement exciton–plasmon coupling, collective transport of excitation energy, and suppression of quantum dot fluorescence blinking, are discussed.more » « less
-
Metal–semiconductor hybrid nanomaterials (HNMs) exhibit unique properties that are distinct from individual nanostructures, leading to promising applications in optical technologies. The interfacial linkage of semiconductor and metal nanoparticles (NPs) via cogelation is an effective strategy to produce HNMs that show strong plasmon‐exciton coupling and improved physical properties. However, optical properties of these hybrids show little to no tunability. Herein, CdSe/Ag hybrid aerogels that show tunable absorption and photoluminescence (PL) are produced by cogelation of CdSe nanorods (NRs) or NPs with Ag hollow NPs. Hybrid electronic states are created by overlapping the excitonic absorption of CdSe NRs or NPs with the plasmonic absorption of Ag NPs. Physical characterization of the hybrids reveals an interconnected network of hexagonal CdSe and cubic Ag NPs, linked by Ag+and Se2−surface species, without intervening ligands. PL spectra exhibit maxima at 640 and 720 nm for the CdSe NPs/Ag and CdSe NRs/Ag hybrids, respectively, corresponding to new radiative decay mechanisms. Time‐resolved PL data support the emergence of new radiative pathways, kinetically and energetically distinct from the excitonic and plasmonic properties of primary NPs. This new approach of metal–semiconductor hybrid formation through cogelation is intriguing for the design of high‐efficiency HNMs without detrimental PL quenching.more » « less
-
Abstract Nanostructures made of metallic materials support collective oscillations of their conduction electrons, commonly known as surface plasmons. These modes, whose characteristics are determined by the material and morphology of the nanostructure, couple strongly to light and confine it into subwavelength volumes. Of particular interest are metallic nanostructures for which the size along one dimension approaches the nanometer or even the subnanometer scale, since such morphologies can lead to stronger light–matter interactions and higher degrees of confinement than regular three‐dimensional nanostructures. Here, the plasmonic response of metallic nanodisks of varying thicknesses and aspect ratios is investigated under far‐ and near‐field excitation conditions. It is found that, for far‐field excitation, the strength of the plasmonic response of the nanodisk increases with its thickness, as expected from the increase in the number of conduction electrons in the system. However, for near‐field excitation, the plasmonic response becomes stronger as the thickness of the nanodisk is reduced. This behavior is attributed to the higher efficiency with which a near‐field source couples to the plasmons supported by thinner nanodisks. The results of this work advance the understanding of the plasmonic response of thin metallic nanostructures, thus increasing their potential for the development of novel applications.more » « less
-
Controlling matter at the level of electrons using ultrafast laser sources represents an important challenge for science and technology. Recently, we introduced a general laser control scheme (the Stark control of electrons at interfaces or SCELI) based on the Stark effect that uses the subcycle structure of light to manipulate electron dynamics at semiconductor interfaces [A. Garzón-Ramírez and I. Franco, Phys. Rev. B 98, 121305 (2018)]. Here, we demonstrate that SCELI is also of general applicability in molecule–semiconductor interfaces. We do so by following the quantum dynamics induced by non-resonant few-cycle laser pulses of intermediate intensity (non-perturbative but non-ionizing) across model molecule–semiconductor interfaces of varying level alignments. We show that SCELI induces interfacial charge transfer regardless of the energy level alignment of the interface and even in situations where charge exchange is forbidden via resonant photoexcitation. We further show that the SCELI rate of charge transfer is faster than those offered by resonant photoexcitation routes as it is controlled by the subcycle structure of light. The results underscore the general applicability of SCELI to manipulate electron dynamics at interfaces on ultrafast timescales.more » « less
