The term photonic crystals appears because of the analogy between electron waves in crystals and the light waves in artificial periodic dielectric structures. During the recent years the investigation of one-, two-and three-dimensional periodic structures has attracted a widespread attention of the world optics community because of great potentiality of such structures in advanced applied optical fields. The interest in periodic structures has been stimulated by the fast development of semiconductor technology that now allows the fabrication of artificial structures, whose period is comparable with the wavelength of light in the visible and infrared ranges.

http://ieeexplore.ieee.org/iel5/6354/16969/00781867.pdf

Photonic crystals

Science and technologies based on terahertz frequency electromagnetic radiation (100 GHz–30 THz) have developed rapidly over the last 30 years. For most of the 20th Century, terahertz radiation, then referred to as sub-millimeter wave or far-infrared radiation, was mainly utilized by astronomers and some spectroscopists. Following the development of laser based terahertz time-domain spectroscopy in the 1980s and 1990s the field of THz science and technology expanded rapidly, to the extent that it now touches many areas from fundamental science to 'real world' applications. For example THz radiation is being used to optimize materials for new solar cells, and may also be a key technology for the next generation of airport security scanners. While the field was emerging it was possible to keep track of all new developments, however now the field has grown so much that it is increasingly difficult to follow the diverse range of new discoveries and applications that are appearing. At this point in time, when the field of THz science and technology is moving from an emerging to a more established and interdisciplinary field, it is apt to present a roadmap to help identify the breadth and future directions of the field. The aim of this roadmap is to present a snapshot of the present state of THz science and technology in 2017, and provide an opinion on the challenges and opportunities that the future holds. To be able to achieve this aim, we have invited a group of international experts to write 18 sections that cover most of the key areas of THz science and technology. We hope that The 2017 Roadmap on THz science and technology will prove to be a useful resource by providing a wide ranging introduction to the capabilities of THz radiation for those outside or just entering the field as well as providing perspective and breadth for those who are well established. We also feel that this review should serve as a useful guide for government and funding agencies.

https://iopscience.iop.org/article/10.1088/1361-6463/50/4/043001/pdf

The 2017 terahertz science and technology roadmap

Organic (opto)electronic materials have received considerable attention due to their applications in thin-film-transistors, light-emitting diodes, solar cells, sensors, photorefractive devices, and many others. The technological promises include low cost of these materials and the possibility of their room-temperature deposition from solution on large-area and/or flexible substrates. The article reviews the current understanding of the physical mechanisms that determine the (opto)electronic properties of high-performance organic materials. The focus of the review is on photoinduced processes and on electronic properties important for optoelectronic applications relying on charge carrier photogeneration. Additionally, it highlights the capabilities of various experimental techniques for characterization of these materials, summarizes top-of-the-line device performance, and outlines recent trends in the further development of the field. The properties of materials based both on small molecules and on conjug...

Organic Optoelectronic Materials: Mechanisms and Applications

Terahertz waveforms with peak fields of 72 MV cm−1 and a central frequency of 30 THz drive interband polarization in bulk GaSe off-resonantly and accelerate excited electron–hole pairs, inducing dynamical Bloch oscillations. This results in the emission of phase-stable, high-harmonic transients over the whole frequency range of 0.1–675 THz.

Sub-cycle control of terahertz high-harmonic generation by dynamical Bloch oscillations

The 2016 terahertz science and technology roadmap

Ultrafast studies1,2 of excitations on the nanometre scale are essential for guiding applications in nanotechnology. Efforts to integrate femtosecond lasers with scanning tunnelling microscopes (STMs)3 have yielded a number of ultrafast STM techniques4,5,6,7,8,9,10,11,12,13,14, but the basic ability to directly modulate the STM junction bias while maintaining nanometre spatial resolution has been limited to ∼10 ps (refs 7,8) and has required specialized probe or sample structures. Here, without any modification to the STM design, we modulate the STM junction bias by coupling terahertz pulses to the scanning probe tip of an STM and demonstrate terahertz-pulse-induced tunnelling in an STM. The terahertz STM (THz-STM) provides simultaneous subpicosecond (<500 fs) time resolution and nanometre (2 nm) imaging resolution under ambient laboratory conditions, and can directly image ultrafast carrier capture into a single InAs nanodot. The THz-STM accesses an ultrafast tunnelling regime that opens the door to subpicosecond scanning probe microscopy of materials with atomic resolution. An ultrafast terahertz (THz) scanning tunnelling microscope (STM) with subpicosecond time resolution and nanometre spatial resolution has been developed. THz pulses are coupled to the metal tip of a commercial STM and THz-pulse-induced tunnelling is observed in the STM. The THz-STM can directly image ultrafast carrier capture by a single InAs nanodot.

An ultrafast terahertz scanning tunnelling microscope

The syntheses of colloidal silicon nanocrystals (Si-NCs) with dimensions in the 3–4 nm size regime as well as effective methodologies for their functionalization with alkyl, amine, phosphine, and acetal functional groups are reported. Through rational variation in the surface moieties we demonstrate that the photoluminescence of Si-NCs can be effectively tuned across the entire visible spectral region without changing particle size. The surface-state dependent emission exhibited short-lived excited-states and higher relative photoluminescence quantum yields compared to Si-NCs of equivalent size exhibiting emission originating from the band gap transition. The Si-NCs were exhaustively characterized using transmission electron microscopy (TEM), X-ray photoelectron spectroscopy (XPS), and Fourier transformed infrared spectroscopy (FTIR), and their optical properties were thoroughly investigated using fluorescence spectroscopy, excited-state lifetime measurements, photobleaching experiments, and solvatochromi...

Size vs surface: tuning the photoluminescence of freestanding silicon nanocrystals across the visible spectrum via surface groups.

The role of surface species in the optical properties of silicon nanocrystals (SiNCs) is the subject of intense debate. Changes in photoluminescence (PL) energy following hydrosilylation of SiNCs with alkyl-terminated surfaces are most often ascribed to enhanced quantum confinement in the smaller cores of oxidized NCs or to oxygen-induced defect emission. We have investigated the PL properties of alkyl-functionalized SiNCs prepared using two related methods: thermal and photochemical hydrosilylation. Photochemically functionalized SiNCs exhibit higher emission energies than the thermally functionalized equivalent. While microsecond lifetime emission attributed to carrier recombination within the NC core was observed from all samples, much faster, size-independent nanosecond lifetime components were only observed in samples prepared using photochemical hydrosilylation that possessed substantial surface oxidation. In addition, photochemically modified SiNCs exhibit higher absolute photoluminescent quantum y...

Evolution of the Ultrafast Photoluminescence of Colloidal Silicon Nanocrystals with Changing Surface Chemistry

One-pot syntheses of surface functionalized germanium nanocrystals (GeNCs) based upon traditional hot injection and microwave-assisted heating of a Ge(II) dihydride single source precursor have been developed. The reported procedures offer in situ hydrogermylation-based covalent attachment of alkene/alkyne derived surface moieties that give access to hydrophobic or hydrophilic GeNCs.

One-pot synthesis of functionalized germanium nanocrystals from a single source precursor

We explore the dynamics of blue emission from dodecylamine and ammonia functionalized silicon nanocrystals (Si NCs) with average diameters of ∼3 and ∼6 nm using time-resolved photoluminescence (TRPL) spectroscopy. The Si NCs exhibit nanosecond PL decay dynamics that is independent of NC size and uniform across the emission spectrum. The TRPL measurements reveal complete quenching of core state emission by a charge transfer state that is responsible for the blue PL with a radiative recombination rate of ∼5 × 10^7 s^(−1). A detailed picture of the charge transfer state emission dynamics in these functionalized Si NCs is proposed.

/pdf/charge-transfer-state-emission-dynamics-in-blue-emitting-iaqbcewr7f.pdf

Glenda De Los Reyes

Papers

An ultrafast terahertz scanning tunnelling microscope

Size vs surface: tuning the photoluminescence of freestanding silicon nanocrystals across the visible spectrum via surface groups.

Evolution of the Ultrafast Photoluminescence of Colloidal Silicon Nanocrystals with Changing Surface Chemistry

One-pot synthesis of functionalized germanium nanocrystals from a single source precursor

Charge transfer state emission dynamics in blue-emitting functionalized silicon nanocrystals