Understanding Hot-Electron Generation and Plasmon Relaxation in Metal Nanocrystals: Quantum and Classical Mechanisms

Generation of energetic (hot) electrons is an intrinsic property of any plasmonic nanostructure under illumination. Simultaneously, a striking advantage of metal nanocrystals over semiconductors lies in their very large absorption cross sections. Therefore, metal nanostructures with strong and tailored plasmonic resonances are very attractive for photocatalytic applications. However, the central questions regarding plasmonic hot electrons are how to quantify and extract the optically-excited energetic electrons in a nanocrystal. We develop a theory describing the generation rates and the energy-distributions of hot electrons in nanocrystals with various geometries. In our theory, hot electrons are generated owing to surfaces and hot spots. The formalism predicts that large optically-excited nanocrystals show the excitation of mostly low-energy Drude electrons, whereas plasmons in small nanocrystals involve mostly hot electrons. The energy distributions of electrons in an optically-excited nanocrystal show how the quantum many-body state in small particles evolves towards the classical state described by the Drude model when increasing nanocrystal size. We show that the rate of surface decay of plasmons in nanocrystals is directly related to the rate of generation of hot electrons. Based on a detailed many-body theory involving kinetic coefficients, we formulate a simple scheme describing the plasmon's dephasing. In most nanocrystals, the main decay mechanism of a plasmon is the Drude friction-like process and the secondary path comes from generation of hot electrons due to surfaces and electromagnetic hot spots. This latter path strongly depends on the size, shape and material of the nanocrystal, correspondingly affecting its efficiency of hot-electron production. The results in the paper can be used to guide the design of plasmonic nanomaterials for photochemistry and photodetectors.Comment: 90 pages, 21 figures, including Supplementary Informatio

What's so Hot about Electrons in Metal Nanoparticles?

Metal nanoparticles are excellent light absorbers. The absorption processes create highly excited electron-hole pairs and recently there has been interest in harnessing these hot charge carriers for photocatalysis and solar energy conversion applications. The goal of this Perspectives article is to describe the dynamics and energy distribution of the charge carriers produced by photon absorption, and the implications for the photocatalysis mechanism. We will also discuss how spectroscopy can be used to provide insight into the coupling between plasmons and molecular resonances. In particular, the analysis shows that the choice of material and shape of the nanocrystal can play a crucial role in hot electron generation and coupling between plasmons and molecular transitions. The detection and even calculation of many-body hot-electron processes in the plasmonic systems with continuous spectra of electrons and short lifetimes are challenging, but at the same time very interesting from the point of view of both potential applications and fundamental physics. We propose that developing an understanding of these processes will provide a pathway for improving the efficiency of plasmon-induced photocatalysis.Comment: To be published in ACS Energy. 41 pages and 8 figures, including Supplementary Informatio

Temporal plasmonics: Fano and Rabi regimes in the time domain in metal nanostructures

The Fano and Rabi models represent remarkably common effects in optics. Here we study the coherent time dynamics of plasmonic systems exhibiting Fano and Rabi resonances. We demonstrate that these systems show fundamentally different dynamics. A system with a Fano resonance displays at most one temporal beat under pulsed excitation, whereas a system in the Rabi regime may have any number of beats. Remarkably, the Fano-like systems show time dynamics with very characteristic coherent tails despite the strong decoherence that is intrinsic for such systems. The coherent Fano and Rabi dynamics that we predicted can be observed in plasmonic nanocrystal dimers in time-resolved experiments. Our study demonstrates that such coherent temporal plasmonics includes nontrivial and characteristic relaxation behaviors and presents an interesting direction to develop with further research.Comment: 31 pages [main text (4 figures) + supplemental (12 figures)

Aluminum Nanoparticles with Hot Spots for Plasmon-Induced Circular Dichroism of Chiral Molecules in the UV Spectral Interval

Plasmonic nanocrystals with hot spots are able to localize optical energy in small spaces. In such physical systems, near-field interactions between molecules and plasmons can become especially strong. This paper considers the case of a nanoparticle dimer and a chiral biomolecule. In our model, a chiral molecule is placed in the gap between two plasmonic nanoparticles, where the electromagnetic hot spot occurs. Since many important biomolecules have optical transitions in the UV, we consider the case of Aluminum nanoparticles, as they offer strong electromagnetic enhancements in the blue and UV spectral intervals. Our calculations show that the complex composed of a chiral molecule and an Al-dimer exhibits strong CD signals in the plasmonic spectral region. In contrast to the standard Au- and Ag-nanocrystals, the Al system may have a much better spectral overlap between the typical biomolecule's optical transitions and the nanocrystals' plasmonic band. Overall, we found that Al nanocrystals used as CD antennas exhibit unique properties as compared to other commonly studied plasmonic and dielectric materials. The plasmonic systems investigated in this study can be potentially used for sensing chirality of biomolecules, which is of interest in applications such as drug development.Comment: 31 pages, 7 figure

Universal imprinting of chirality with chiral light by employing plasmonic metastructures

Chirality, either of light or matter, has proved to be very practical in biosensing and nanophotonics. However, the fundamental understanding of its temporal dynamics still needs to be discovered. A realistic setup for this are the so-called metastructures, since they are optically active and are built massively, hence rendering an immediate potential candidate. Here we propose and study the electromagnetic-optical mechanism leading to chiral optical imprinting on metastructures. Induced photothermal responses create anisotropic permittivity modulations, different for left or right circularly polarized light, leading to temporal-dependent chiral imprinting of hot-spots, namely imprinting of chirality. The above effect has not been observed yet, but it is within reach of modern experimental approaches. The proposed nonlinear chiroptical effect is general and should appear in any anisotropic material; however, we need to design a particular geometry for this effect to be strong. These new chiral time-dependent metastructures may lead to a plethora of applications.Comment: Main (29 pages, 6 figures) and supplemental (46 pages, 35 figures