Multicarrier Dynamics in Quantum Dots.

Multicarrier dynamics play an essential role in quantum dot photophysics and photochemistry, and they are primarily governed by nonradiative Auger processes. Auger recombination affects the performance of lasers, light-emitting diodes, and photodetectors, and it has been implicated in fluorescence intermittency phenomena which are relevant in microscopy and biological tagging. Auger cooling is an important mechanism of rapid electron thermalization. Inverse Auger recombination, known as impact ionization, results in carrier multiplication which can enhance the efficiencies of solar cells. This article first reviews the physical picture, theoretical framework and experimental data for Auger processes in bulk crystalline semiconductors. With this context these aspects are then reexamined for nanocrystal quantum dots, and we first consider fundamental features of Auger recombination in these systems. Methods for the chemical control of Auger recombination and Auger cooling are then discussed in the context of how they illuminate the underlying mechanisms, and we also examine the current understanding of carrier multiplication in quantum dots. Manifestations of Auger recombination in quantum dot devices are finally considered, and we conclude the article with a perspective on remaining unknowns in quantum dot multicarrier physics.

Bright, Modular, and Switchable Near-Infrared II Emission from Compact Tetrathiafulvalene-Based Diradicaloid Complexes.

Near-infrared (NIR)-emitting molecules are promising candidates for biological sensing and imaging applications; however, many NIR dyes are large conjugated systems which frequently have issues with stability, solubility, and tunability. Here, we report a novel class of compact and tunable fluorescent diradicaloid complexes which are air-, water-, light-, and temperature-stable. These properties arise from a compressed π manifold which promotes an intense ligand-centered π-π transition in the NIR II (1000-1700 nm) region and which subsequently emits at ∼1200 nm. This emission is among the brightest known for monomolecular lumiphores with deep NIR II (>1100 nm) emission, nearly an order of magnitude brighter than the commercially available NIR II dye IR 26. Furthermore, this fluorescence is electrochemically sensitive, with efficient switching upon addition of redox agents. The brightness, stability, and modularity of this system distinguish it as a promising candidate for the development of new technologies built around NIR emission.

Toward Bright Mid-Infrared Emitters: Thick-Shell n-Type HgSe/CdS Nanocrystals.

A procedure is developed for the growth of thick, conformal CdS shells that preserve the optical properties of 5 nm HgSe cores. The n-doping of the HgSe/CdS core/shell particles is quantitatively tuned through a simple postsynthetic Cd treatment, while the doping is monitored via the intraband optical absorption at 5 µm wavelength. Photoluminescence lifetime and quantum yield measurements show that the CdS shell greatly increases the intraband emission intensity. This indicates that decoupling the excitation from the environment reduces the nonradiative recombination. We find that weakly n-type HgSe/CdS are the brightest solution-phase mid-infrared chromophores reported to date at room temperature, achieving intraband photoluminescence quantum yields of 2%. Such photoluminescence corresponds to intraband lifetimes in excess of 10 ns, raising important questions about the fundamental limits to achievable slow intraband relaxation in quantum dots.

Direct Imprinting of Quasi-3D Nanophotonic Structures into Colloidal Quantum-Dot Devices.

Three-dimensional (3D) subwavelength nanostructures have emerged and triggered tremendous excitement because of their advantages over the two-dimensional (2D) counterparts in fields of plasmonics, photonic crystals, and metamaterials. However, the fabrication and integration of 3D nanophotonic structures with colloidal quantum dots (CQDs) faces several technological obstacles, as conventional lithographic and etching techniques may affect the surface chemistry of colloidal nanomaterials. Here, the direct fabrication of functional quasi-3D nanophotonic structures into CQD films is demonstrated by one-step imprinting with well-controlled precision in both vertical and lateral directions. To showcase the potential of this technique, diffraction gratings, bilayer wire-grid polarizers, and resonant metal mesh long-pass filters are imprinted on CQD films without degrading the optical and electrical properties of CQD. Furthermore, a dual-diode CQD detector into an unprecedented mid-wave infrared two-channel polarization detector is functionalized by embedding an imprinted bilayer wire-grid polarizer within the CQDs. The results show that this approach offers a feasible pathway to combine quasi-3D nanostructures with colloidal materials-based optoelectronics and access a new level of light manipulation.

Auger Suppression in n-Type HgSe Colloidal Quantum Dots.

Transient infrared photoluminescence upconversion is used to study the exciton dynamics in small-gap HgSe colloidal quantum dots in the 2000-6500 cm-1 (0.25-0.80 eV) range. The intraband mid-infrared photoluminescence decays show absent or greatly reduced Auger relaxation of biexcitons, proposed as a generic feature of weakly n-type quantum dots due to the sparse density of states in the conduction band. The nonradiative relaxation of the intraband carriers is instead consistent with near-field energy transfer to molecular vibrations of the surface ligands. In contrast, the interband near-infrared photoluminescence decays exhibit the typical distinct exciton and biexciton lifetimes with Auger coefficients comparable to other similarly sized quantum dots. Also observed are spectral and dynamical evidence of fine structure in the intraband transitions consistent with spin-orbit splitting of the electron P levels, and the emergence of plasmonic resonances in large particles.

Slow Auger Relaxation in HgTe Colloidal Quantum Dots.

The biexciton lifetimes in HgTe colloidal quantum dots are measured as a function of particle size. Samples produced by two synthetic methods, leading to partially aggregated or well-dispersed particles, exhibit markedly different dynamics. The relaxation characteristics of partially aggregated HgTe inhibit reliable determinations of the Auger lifetime. In well-dispersed HgTe quantum dots, the biexciton lifetime increases approximately linearly with particle volume, confirming trends observed in other systems. The extracted Auger coefficient is three orders of magnitude smaller than that for bulk HgCdTe materials with similar energy gaps. We discuss these findings in the context of understanding Auger relaxation in quantum-confined systems and their relevance to mid-infrared optoelectronic devices based on HgTe colloidal quantum dots.