Plasmonic Properties of Silicon Nanocrystals Doped with Boron and Phosphorus

Degenerately doped silicon nanocrystals are appealing plasmonic materials due to silicon’s low cost and low toxicity. While surface plasmonic resonances of boron-doped and phosphorus-doped silicon nanocrystals were recently observed, there currently is poor understanding of the effect of surface conditions on their plasmonic behavior. Here, we demonstrate that phosphorus-doped silicon nanocrystals exhibit a plasmon resonance immediately after their synthesis but may lose their plasmonic response with oxidation. In contrast, boron-doped nanocrystals initially do not exhibit plasmonic response but become plasmonically active through postsynthesis oxidation or annealing. We interpret these results in terms of substitutional doping being the dominant doping mechanism for phosphorus-doped silicon nanocrystals, with oxidation-induced defects trapping free electrons. The behavior of boron-doped silicon nanocrystals is more consistent with a strong contribution of surface doping. Importantly, boron-doped silicon nanocrystals exhibit air-stable plasmonic behavior over periods of more than a year

Thermodynamic Driving Force in the Spontaneous Formation of Inorganic Nanoparticle Solutions

Nanoparticles are the bridge between the molecular and the macroscopic worlds. The growing number of commercial applications for nanoparticles spans from consumer products to new frontiers of medicine and next-generation optoelectronic technology. They are most commonly deployed in the form of a colloid, or “ink”, which are formulated with solvents, surfactants, and electrolytes to kinetically prevent the solid particulate phase from reaching the thermodynamically favored state of separate solid and liquid phases. In this work, we theoretically determine the thermodynamic requirements for forming a single-phase solution of spherical particles and engineer a model system to experimentally demonstrate the spontaneous formation of solutions composed of only solvent and bare inorganic nanoparticles. We show molecular interactions at the nanoparticle interface are the driving force in high-concentration nanoparticle solutions. The work establishes a regime where inorganic nanoparticles behave as molecular solutes as opposed to kinetically stable colloids, which has far-reaching implications for the future design and deployment of nanomaterial technologies

Tunable Band Gap Emission and Surface Passivation of Germanium Nanocrystals Synthesized in the Gas Phase

The narrow bulk band gap and large exciton Bohr radius of germanium (Ge) make it an attractive material for optoelectronics utilizing band-gap-tunable photoluminescence (PL). However, realization of PL due to quantum confinement remains scarcely reported. Instead, PL is often observed from surface trap states and is independent of nanocrystal (NC) size. Here, we demonstrate tunable band gap PL by chemically passivating the Ge NC surface. The exchange of native Ge–Cl surface groups with alkyl groups using Grignard reagents leads to the first instance of tunable band gap emission from free-standing Ge NCs synthesized in the gas phase. Ge NCs between 4.8 and 10.2 nm in diameter exhibit near-infrared emission featuring spectral line widths that are at least a factor of 2 narrower than any previous report

Thermodynamic Driving Force in the Spontaneous Formation of Inorganic Nanoparticle Solutions

Nanoparticles are the bridge between the molecular and the macroscopic worlds. The growing number of commercial applications for nanoparticles spans from consumer products to new frontiers of medicine and next-generation optoelectronic technology. They are most commonly deployed in the form of a colloid, or “ink”, which are formulated with solvents, surfactants, and electrolytes to kinetically prevent the solid particulate phase from reaching the thermodynamically favored state of separate solid and liquid phases. In this work, we theoretically determine the thermodynamic requirements for forming a single-phase solution of spherical particles and engineer a model system to experimentally demonstrate the spontaneous formation of solutions composed of only solvent and bare inorganic nanoparticles. We show molecular interactions at the nanoparticle interface are the driving force in high-concentration nanoparticle solutions. The work establishes a regime where inorganic nanoparticles behave as molecular solutes as opposed to kinetically stable colloids, which has far-reaching implications for the future design and deployment of nanomaterial technologies

Tunable Band Gap Emission and Surface Passivation of Germanium Nanocrystals Synthesized in the Gas Phase

The narrow bulk band gap and large exciton Bohr radius of germanium (Ge) make it an attractive material for optoelectronics utilizing band-gap-tunable photoluminescence (PL). However, realization of PL due to quantum confinement remains scarcely reported. Instead, PL is often observed from surface trap states and is independent of nanocrystal (NC) size. Here, we demonstrate tunable band gap PL by chemically passivating the Ge NC surface. The exchange of native Ge–Cl surface groups with alkyl groups using Grignard reagents leads to the first instance of tunable band gap emission from free-standing Ge NCs synthesized in the gas phase. Ge NCs between 4.8 and 10.2 nm in diameter exhibit near-infrared emission featuring spectral line widths that are at least a factor of 2 narrower than any previous report

Surface Structure and Silicon Nanocrystal Photoluminescence: The Role of Hypervalent Silyl Groups

We report a combined experimental and theoretical study of the relationship between the surface structure of silicon nanocrystals synthesized in a nonthermal plasma reactor and their photoluminescence (PL) yields. Upon heating to 160 °C, a significant change in the SiH stretch region of the vibrational spectrum is observed indicating a decrease in surface SiH₃ groups, which correlates with an increase in the PL yield. Effusion of SiH_<i>x</i> and Si₂H_2<i>x</i> from the material is detected by residual gas analysis upon heating to temperatures below 200 °C, suggesting a weakly bound species. Analysis of electron paramagnetic resonance spectra before and after heating points to a small reduction in the density of dangling bonds upon heating but this reduction does not correlate with the increase in PL yield. Electronic structure calculations indicate that SiH₃^– groups may hypervalently bond to fully coordinated surface silicon atoms, resulting in a relatively weak (0.70 eV) bond that is consistent with the experimentally observed effusion at low temperature. Furthermore, nonadiabatic molecular dynamics simulations indicate that such hypervalent silyl defects provide efficient pathways for nonradiative recombination via conical intersections that are energetically accessible after near-infrared excitation

Phosphorus-Doped Silicon Nanocrystals Exhibiting Mid-Infrared Localized Surface Plasmon Resonance

Localized surface plasmon resonances (LSPRs) enable tailoring of the optical response of nanomaterials through their free carrier concentration, morphology, and dielectric environment. Recent efforts to expand the spectral range of usable LSPR frequencies into the infrared successfully demonstrated LSPRs in doped semiconductor nanocrystals. Despite silicon’s importance for electronic and photonic applications, no LSPRs have been reported for doped silicon nanocrystals. Here we demonstrate doped silicon nanocrystals synthesized via a nonthermal plasma technique that exhibits tunable LSPRs in the energy range of 0.07–0.3 eV or mid-infrared wavenumbers of 600–2500 cm^–1

Nonthermal Plasma Synthesis of Core/Shell Quantum Dots: Strained Ge/Si Nanocrystals

In this work, we present an all-gas-phase approach for the synthesis of quantum-confined core/shell nanocrystals (NCs) as a promising alternative to traditional solution-based methods. Spherical quantum dots (QDs) are grown using a single-stage flow-through nonthermal plasma, yielding monodisperse NCs, with a concentric core/shell structure confirmed by electron microscopy. The in-flight negative charging of the NCs by plasma electrons keeps the NC cores separated during shell growth. The success of this gas-phase approach is demonstrated here through the study of Ge/Si core/shell QDs. We find that the epitaxial growth of a Si shell on the Ge QD core compressively strains the Ge lattice and affords the ability to manipulate the Ge band structure by modulation of the core and shell dimensions. This all-gas-phase approach to core/shell QD synthesis offers an effective method to produce high-quality heterostructured NCs with control over the core and shell dimensions

Controlled Doping of Silicon Nanocrystals Investigated by Solution-Processed Field Effect Transistors

The doping of semiconductor nanocrystals (NCs), which is vital for the optimization of NC-based devices, remains a significant challenge. While gas-phase plasma approaches have been successful in incorporating dopant atoms into NCs, little is known about their electronic activation. Here, we investigate the electronic properties of doped silicon NC thin films cast from solution by field effect transistor analysis. We find that, analogous to bulk silicon, boron and phosphorus electronically dope Si NC thin films; however, the dopant activation efficiency is only ∼10^–2–10^–4. We also show that surface doping of Si NCs is an effective way to alter the carrier concentrations in Si NC films

Near-Infrared Plasmonic Copper Nanocups Fabricated by Template-Assisted Magnetron Sputtering

In this article we experimentally and theoretically study the plasmonic properties of discrete copper nanocups fabricated by magnetron sputtering on ordered, non-close-packed colloidal templates. Wide tunability of the main plasmon resonance peak between 900 and 1500 nm, extending the typical plasmon resonance range previously reported for other copper nanostructures between 600 and 1000 nm, is achieved by varying shell thickness and particle size in the colloidal template. The nature of the plasmon resonance peaks is revealed from calculated charge maps and electromagnetic field intensity maps. Good agreements are found between experimental and calculated extinction spectra, which validates the geometry model and suggests that the nanocups have a well-defined shape. The main plasmon resonance peak exhibits a minor red-shift and attenuation after 3 days of oxidation and eventually stabilizes after 13 days. We also demonstrate that a potentially useful optical material that blocks near-infrared but transmits visible light can be constructed by mixing copper nanocups of three different sizes at appropriate ratios