Energy harvesting: an integrated view of materials, devices and applications.

Energy harvesting refers to the set of processes by which useful energy is captured from waste, environmental, or mechanical sources and is converted into a usable form. The discipline of energy harvesting is a broad topic that includes established methods and materials such as photovoltaics and thermoelectrics, as well as more recent technologies that convert mechanical energy, magnetic energy and waste heat to electricity. This article will review various state-of-the-art materials and devices for direct energy conversion and in particular will include multistep energy conversion approaches. The article will highlight the nano-materials science underlying energy harvesting principles and devices, but also include more traditional bulk processes and devices as appropriate and synergistic. Emphasis is placed on device-design innovations that lead to higher efficiency energy harvesting or conversion technologies ranging from the cm/mm-scale down to MEMS/NEMS (micro- and nano-electromechanical systems) devices. Theoretical studies are reviewed, which address transport properties, crystal chemistry, thermodynamic analysis, energy transfer, system efficiency and device operation. New developments in experimental methods; device design and fabrication; nanostructured materials fabrication; materials properties; and device performance measurement techniques are discussed.

Precision shock tuning on the national ignition facility.

Ignition implosions on the National Ignition Facility [J. D. Lindl et al., Phys. Plasmas 11, 339 (2004)] are underway with the goal of compressing deuterium-tritium fuel to a sufficiently high areal density (ρR) to sustain a self-propagating burn wave required for fusion power gain greater than unity. These implosions are driven with a very carefully tailored sequence of four shock waves that must be timed to very high precision to keep the fuel entropy and adiabat low and ρR high. The first series of precision tuning experiments on the National Ignition Facility, which use optical diagnostics to directly measure the strength and timing of all four shocks inside a hohlraum-driven, cryogenic liquid-deuterium-filled capsule interior have now been performed. The results of these experiments are presented demonstrating a significant decrease in adiabat over previously untuned implosions. The impact of the improved shock timing is confirmed in related deuterium-tritium layered capsule implosions, which show the highest fuel compression (ρR~1.0 g/cm(2)) measured to date, exceeding the previous record [V. Goncharov et al., Phys. Rev. Lett. 104, 165001 (2010)] by more than a factor of 3. The experiments also clearly reveal an issue with the 4th shock velocity, which is observed to be 20% slower than predictions from numerical simulation.

Radiation produced by femtosecond laser-plasma interaction during dielectric breakdown.

Optical breakdown by femtosecond and nanosecond laser pulses in transparent dielectrics produces an ionized region of dense plasma confined within the bulk of the material. This ionized region is responsible for broadband radiation that accompanies the breakdown process. Spectroscopic measurements of the accompanying light have been used to show that, depending on the laser parameters, the spectra may originate from plasma-induced second-harmonic generation, supercontinuum generation, or thermal emission by the plasma. By monitoring the emission from the ionized region, one can ascertain the predominant breakdown mechanism and the morphology of the damage region.

Multiwavelength investigation of laser-damage performance in potassium dihydrogen phosphate after laser annealing.

The laser-induced damage performance of potassium dihydrogen phosphate and deuterated potassium dihydrogen phosphate nonlinear optical crystals after pre-exposure to lower-energy laser pulses (laser annealing, also known as laser conditioning) is investigated as a function of wavelength for both the damaging and conditioning pulses. We obtain a quantitative evaluation of the bulk damage performance of these materials by measuring the density of damage events as a function of laser parameters. This new method allows for a detailed assessment of the improvement of material performance from laser conditioning and reveals the key parameters for optimizing performance depending on the operational wavelength.

Localized dynamics during laser-induced damage in optical materials.

Laser-induced damage in wide band-gap optical materials is the result of material modifications arising from extreme conditions occurring during this process. The material absorbs energy from the laser pulse and produces an ionized region that gives rise to broadband emission. By performing a time-resolved investigation of this emission, we demonstrate both that it is blackbody in nature and that it provides the first direct measurement of the localized temperature of the material during and following laser damage initiation for various optical materials. For excitation using nanosecond laser pulses, the plasma, when confined in the bulk, is in thermal equilibrium with the lattice. These results allow for a detailed characterization of temperature, pressure, and electron densities occurring during laser-induced damage.

Wavelength dependence of laser-induced damage: determining the damage initiation mechanisms.

A novel experimental approach is employed to understand the mechanisms of laser induced damage. Using an OPO (optical parametric oscillator) laser, we have measured the damage thresholds of deuterated potassium dihydrogen phosphate (DKDP) from the near ultraviolet into the visible. Distinct steps, whose width is of the order of k(B)T, are observed in the damage threshold at photon energies associated with the number of photons (3-->2 or 4-->3) needed to promote a ground state electron across the energy gap. The wavelength dependence of the damage threshold suggests that a primary mechanism for damage initiation in DKDP is a multiphoton process in which the order is reduced through excited defect state absorption.

Electron- or hole-assisted reactions of H defects in hydrogen-bonded KDP.

We present an ab initio study of the stability and defect reactions of neutral and charged H interstitial (H(i)) and H vacancy (H(v)) in KH2PO4 (KDP). We find that while there is no interaction between the neutral H(i) and the host, the addition of an electron leads to the ejection of a H host atom and the subsequent formation of an interstitial H2 molecule and a H(v). In sharp contrast, the addition of a hole results in the formation of a hydroxyl bond. Thus, H(i) in both charged states severs the H-bonded network. For the H(v), the addition of a hole leads to the formation of a peroxyl bridge. The neutral H(i) and the positively charged H(v) induce states in the gap. The results elucidate the underlying atomic mechanism for the defect reactions suggested by experiment.

Imaging of laser-induced reactions of individual defect nanoclusters.

The response of individual defect nanoclusters located in the bulk of a dielectric material following exposure to 355-nm, 3-ns high-power laser irradiation is investigated by use of microscopic fluorescence imaging. Experiments were carried out on KH(2)PO(4) crystals. We provide direct imaging of the reaction to an external stimulus of individual defect clusters and demonstrate a novel method of studying the dynamic behavior of bulk defects.

Microscopic fluorescence imaging of bulk defect clusters in KH(2)PO(4) crystals.

A microscopic fluorescence imaging system is used to detect optically active centers located inside a transparent dielectric crystal. Defect centers in the bulk of KH(2)PO(4) crystals are imaged based on their near-infrared emission following photoexcitation. The spatial resolution of the system is 1mum in the image plane and 25mum in depth. The experimental results indicate the presence of a large number of optically active defect clusters in different KH(2)PO(4) crystals, whereas the concentration of these clusters depends on the crystal sector and growth method.

The nature of the interior of uranus based on studies of planetary ices at high dynamic pressure.

Data from the Voyager II spacecraft showed that Uranus has a large magnetic field with geometry similar to an offset tilted dipole. To interpret the origin of the magnetic field, measurements were made of electrical conductivity and equation-of-state data of the planetary "ices" ammonia, methane, and "synthetic Uranus" at shock pressures and temperatures up to 75 gigapascals and 5000 K. These pressures and temperatures correspond to conditions at the depths at which the surface magnetic field is generated. Above 40 gigapascals the conductivities of synthetic Uranus, water, and ammonia plateau at about 20(ohm-cm)(-1), providing an upper limit for the electrical conductivity used in kinematic or dynamo calculations. The nature of materials at the extreme conditions in the interior is discussed.