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Register a new userSolar Thermoradiative-Photovoltaic Energy Conversion
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We propose a solar thermal energy conversion system consisting of a solar absorber, a thermoradiative cell or negative illumination photodiode, and a photovoltaic cell. Because it is a heat engine, this system can also be paired with thermal storage to provide reliable electricity generation. Heat from the solar absorber drives radiative recombination current in the thermoradiative cell, and its emitted light is absorbed by the photovoltaic cell to provide an additional photocurrent. Based on the principle of detailed balance, we calculate a limiting solar conversion efficiency of 85% for fully concentrated sunlight and 45% for one sun with an absorber and single-junction cells of equal areas. Ideal and nonideal solar thermoradiative-photovoltaic systems outperform solar thermophotovoltaic converters for low bandgaps and practical absorber temperatures. Their performance enhancement results from a high tolerance to nonradiative generation/recombination and an ability to minimize radiative heat losses. We show that a realistic device with all major losses could achieve increases in solar conversion efficiency by up to 7.9% (absolute) compared to a solar thermophotovoltaic device under low optical concentration. Our results indicate that these converters could serve as efficient heat engines for low cost single axis tracking systems.
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Detection and direct power conversion of high energy and high intensity ionizing radiation could be a key element in next generation nuclear reactor safety systems and space-born devices. For example, the Fukushima catastrophe in 2011 could have been largely prevented if 1% of the reactors remnant radiation ($gamma$-rays of the nuclear fission) were directly converted within the reactor to electricity to power the water cooling circuit. It is reported here that the hybrid halide perovskite methylammonium lead triiodide could perfectly play the role of a converter. Single crystals were irradiated by a typical shut-down $gamma$-spectrum of a nuclear reactor with 7.61E14 Bq activity exhibit a high-efficiency of $gamma$-ray to free charge carrier conversion with radiation hardening. The power density of 0.3 mW/kg of methylammonium lead triiodide at 50 Sv/h means a four times higher efficiency than that for silicon-based cells. The material was stable to the limits of the experiment without changing its performance up to 100 Sv/h dose rate and 57 Sv H*(10) ambient total $gamma$-dose. Moreover, the {gamma}-shielding performance of methylammonium lead triiodide was found to be superior to both ordinary and barite concrete.
Current approaches for electric power generation from nanoscale conducting or semi-conducting layers in contact with moving aqueous droplets are promising as they show efficiencies of around 30 percent, yet, even the most successful ones pose challenges regarding fabrication and scaling. Here, we report stable, all-inorganic single-element structures synthesized in a single step that generate electrical current when alternating salinity gradients flow along its surface in a liquid flow cell. 10 nm to 30 nm thin nanolayers of iron, vanadium, or nickel produce several tens of mV and several microA cm^-2 at aqueous flow velocities of just a few cm s^-1. The principle of operation is strongly sensitive to charge-carrier motion in the thermal oxide nano-overlayer that forms spontaneously in air and then self terminates. Indeed, experiments suggest a role for intra-oxide electron transfer for Fe, V, and Ni nanolayers, as their thermal oxides contain several metal oxidation states, whereas controls using Al or Cr nanolayers, which self-terminate with oxides that are redox inactive under the experimental conditions, exhibit dramatically diminished performance. The nanolayers are shown to generate electrical current in various modes of application with moving liquids, including sliding liquid droplets, salinity gradients in a flowing liquid, and in the oscillatory motion of a liquid without a salinity gradient.
However, their electrocatalytic activity is still poorly understood. This work deciphers the origin of the catalytic activity of counter-electrodes (CEs)/current collectors made of self-standing carbon nanotubes fibers (CNTfs) using Co$^(+2)$/Co$^(+3)$ redox couple electrolytes. This is based on comprehensive electrochemical and spectroscopic characterizations of fresh and used electrodes applied to symmetric electrochemical cells using platinum-based CEs as a reference. As the most relevant findings, two straight relationships were established: i) the limiting current and stability increase rapidly with surface concentration of oxygen-containing functional groups, and ii) the catalytic potential is inversily related to the amount of residual metallic Fe catalyst nanoparticles interspersed in the CNTf network. Finally, the fine tune of the metallic nanoparticle content and the degree of functionalization enabled fabrication of efficient and stable dye-sensitized solar cells with cobalt electrolytes and CNTf-CE outperforming those with reference Pt-CEs.
Energy harvesting from sun and outer space using thermoradiative devices (TRD), despite being promising renewable energy sources, are limited only to daytime and nighttime period, respectively. A system with 24-hour continuous energy generation remains an open question thus far. Here, we propose a TRD-based power generator that harvests solar energy via concentrated solar irradiation during daytime and via thermal infrared emission towards the outer space at nighttime, thus achieving the much sought-after 24-hour electrical power generation. We develop a rigorous thermodynamical model to investigate the performance characteristics, parametric optimum design, and the role of various energy loss mechanisms. Our model predicts that the TRD-based system yields a peak efficiency of 12.6% at daytime and a maximum power density of 10.8 Wm$^{-2}$ at nighttime, thus significantly outperforming the state-of-art record-setting thermoelectric generator. These findings reveal the potential of TRD towards 24-hour electricity generation and future renewable energy technology.
A galvanic displacement reaction-based, room-temperature dip-and-dry technique is demonstrated for fabricating selectively solar-absorbing plasmonic nanostructure-coated foils (PNFs). The technique, which allows for facile tuning of the PNFs spectral reflectance to suit different radiative and thermal environments, yields PNFs which exhibit excellent, wide-angle solar absorptance (0.96 at 15{deg}, to 0.97 at 35{deg}, to 0.79 at 80{deg}) and low hemispherical thermal emittance (0.10) without the aid of antireflection coatings. The thermal emittance is on par with those of notable selective solar absorbers (SSAs) in the literature, while the wide-angle solar absorptance surpasses those of previously reported SSAs with comparable optical selectivities. In addition, the PNFs show promising mechanical and thermal stabilities at temperatures of up to 200{deg}C. Along with the performance of the PNFs, the simplicity, inexpensiveness and environment-friendliness of the dip-and-dry technique makes it an appealing alternative to current methods for fabricating selective solar absorbers.
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