Renewable energy commercialization

Résumé

Renewable energy commercialization involves the deployment of three generations of renewable energy technologies dating back more than 100 years. First-generation technologies, which are already mature and economically competitive, include biomass, hydroelectricity, geothermal power and heat. Second-generation technologies are market-ready and are being deployed at the present time; they include solar heating, photovoltaics, wind power, solar thermal power stations, and modern forms of bioenergy. Third-generation technologies require continued R&D efforts in order to make large contributions on a global scale and include advanced biomass gasification, hot-dry-rock geothermal power, and ocean energy. As of 2012, renewable energy accounts for about half of new nameplate electrical capacity installed and costs are continuing to fall. Public policy and political leadership helps to "level the playing field" and drive the wider acceptance of renewable energy technol

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https://en.wikipedia.org/wiki/Renewable_energy_commercialization

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The emergence of concentrator photovoltaics for perovskite solar cells

Mohammad Khaja Nazeeruddin, Anurag Roy

The emergence of high-efficiency photovoltaic research is undergoing intense study and is technologically desirable to meet sustainable energy and environmental demand. However, every single solar cell has a theoretical power conversion efficiency limit, and, thus, without compromising the cost, the power conversion efficiency enhancement of a solar cell is highly challenging. As a convenient solution, concentrating photovoltaics can focus sunlight onto an extremely high-efficiency solar cell integrating various optics. Concentrating photovoltaics use optical devices that collect and redirect the light toward the smaller photovoltaic cell and reduce the demand for the mined elements required for the solar cell fabrication. The research interest from the photovoltaic community has concentrated on organic-inorganic hybrid halide perovskite absorbers, and nowadays, perovskite solar cells manifest their outstanding contribution among the low-cost photovoltaic technologies. Inevitably, large-area perovskite solar cells suffer a lot with their poor stability, hindering their commercialization pace. Thus, the implementation of concentrating photovoltaic technology in perovskite solar cells demonstrates an inherent advantage using a smaller size solar cell. This review provides an overview of concentrating photovoltaic technology implementation, including their recent research and development portfolio, their economic benefits in combination with inexpensive optical elements and tracking systems, limitations, challenges, and relative scope of the future study, focusing on the emerging perovskite solar cell technology.

AIP Publishing2021

Chargement

Energy demand and economic development are intrinsically linked. Earlier economic development came at the price of serious environmental pollution, posing a risk to life on earth. Thus, a transition from fossil to renewable energy is needed. Among the renewable energy technologies, gasification of biomass promises high process efficiency and flexibility concerning the feedstock and products. In such a process, gas contaminants have to be removed to protect downstream equipment and the environment. Finding an optimal configuration of process steps in gas cleanup chains, offering reliability, availability and high efficiency at low operating and capital costs is still a challenge and one of the major hurdles for commercial deployment of biomass gasification processes. This thesis aimed to investigate the gas cleanup chain as part of gasification processes. Two aspects, the analysis of gas contaminants and their elimination, were examined. At first, three analytical methods, aimed at the detection of sulphur containing hydrocarbons, tars and trace elements, were developed. In the next step, these analytical tools were employed to investigate the performance of gas cleanup units, intended for the removal of the sulphur containing hydrocarbon thiophene, tars and the trace element Se. The removal of thiophene by activated carbons (AC) was explored experimentally and theoretically. Experiments were performed in a packed bed column between 100-200°C. The adsorption process was described by a 1D approach, including mass transfer phenomena and axial dispersion. Experimental validation showed good agreement between measured and predicted breakthrough times and capacities. A global sensitivity analysis (GSA) was performed to rank the importance of model input factors and gain further process insight. The work showed that ACs are a promising option for thiophene removal and provided a generic approach for the application of GSA to adsorption models. In this context, the analysis demonstrated that the selection of common model assumptions deserves as much attention as the model parameters. Further work chapter aimed at understanding the effect of H2O, H2 and H2S on the decomposition of thiophene over CaO. Experiments were performed in a fixed bed reactor at 810°C. The factors were varied as part of a full factorial design at two levels. Results were fitted to a linear model with interactions. Analysis showed that H2O and H2S had a major effect on thiophene conversion, while that of H2 was less pronounced. Interactions between varied factors were found to be negligible. A UV-Vis method was developed to obtain online information on tar compound concentrations in real process gases in the low ppmv region. Spectra were analysed for their tar composition by two chemometric approaches. Applied to two case studies, the developed tool proved to be a rapid, sensitive tool, applicable to qualitative process monitoring with the added benefit of quantification in gases with a limited number of tar compounds. An ICP-MS was employed as a tool for the online detection of trace elements. The low detection limits (< 2 ppbv for H2Se, PH3; < 0.1 ppbv for AsH3; < 0.01 ppbv for Hg) and the high temporal resolution render this method a quick and robust tool for the performance evaluation of sorbent materials. A case study investigated the capture of H2Se by a Zn/Al2O3 sorbent between 150-350°C.

EPFL2017

Chargement

Decreasing the Stability of Borohydride with Ionic Liquids for Hydrogen Storage and Carbon Dioxide Conversion

Loris Giovanni Lombardo

The world needs to move from a fossil fuel to a renewable energy based society. With the increasing electricity production from wind and PV, short and long term energy storage are becoming one of challenge of the 21st century. While batteries are the preferred method for short term storage, another technology is required for seasonal storage. Hydrogen is a valuable energy carrier owning its high energy density (122 kJ/g). However, compact and safe storage of H2 is challenging. The current solution is to compress hydrogen up to 700 bar for mobile application (fuel cell cars), and metal hydrides for stationary application. Material-based H2 storage avoids using high-pressure cylinder. Complex hydrides are especially attractive for solid-state H2 storage due to their high gravimetric and volumetric hydrogen density. Sodium borohydride (NaBH4) contains 10.6 mass% of H2, but high temperatures are needed to release H2 (505 Â°C) and the reaction is not reversible under moderate conditions. To apply complex hydrides in real applications, they must be modified to improve the kinetics and thermodynamics of H2 desorption. Several possibilities exist such as confinement into scaffolds, catalyst addition, or combination of several hydrides to modify the dehydrogenation pathway. The stability of complex hydrides is determined by the localization of the charge on the central atom of the complex. Therefore, in this thesis the interaction of highly polar or ionic compounds with complex hydrides were investigated. We combine NaBH4 with a special class of organic salts: ionic liquids (IL). Considering their chemical and thermal stability, IL are attractive additive. Using organic additives instead of expensive metal catalysts is another advantage. Two different techniques were employed to combine the IL and NaBH4. The first one consists of mechanochemically milling them to create an interaction between BH4- and IL. The second one is to directly synthesized IL borohydrides ([IL][BH4]) by metathesis reaction. Different ILs, such as vinylbenzyltrimethylammonium chloride ([VBTMA][Cl]), 1-butyl-3-methylimidazolium chloride ([bmim][Cl]), and 1-ethyl-1-methylpyrrolidinium bromide ([EMPY][Br]) were tested. [bmim][BH4] was able to release H2 below 100 Â°C. The hydrogen content ranges between 2.4 mass% and 2.9 mass%. The second challenge of this century is the CO2 problematic. Atmospheric CO2 concentration linearly increases, leading to greenhouse effect. Carbon capture and sequestration (CCS) and utilization (CCU) are primordial research topic to stabilize the CO2 emission. Hydrides are primary reducing agents, thus reduction of CO2 can be accomplished with them. Direct CO2 reduction at ambient conditions is challenging for classical borohydrides. With our [IL][BH4], gaseous CO2 can be captured and reduced under ambient conditions (1 bar, RT). Three CO2 bounds with boron to give triformatoborohydride ([HB(OCHO)3]â. Dilute CO2 (6 vol%) can be used as well. The reaction was followed in real time with a magnetic suspended balance (MSB). Further, CO2 reduction happened when air is used as a carbon dioxide source. Formic acid can be obtained by adding HCl. Thus, ionic liquid borohydrides have great potential as a CO2 absorber and reducer to alternative fuels. In short, we applied ionic liquid to destabilized borohydrides. The resulting materials exhibited potential for solid-state hydrogen storage, as well as CO2 capture and transformation.

EPFL2021

Chargement

EPFL2017

Decreasing the Stability of Borohydride with Ionic Liquids for Hydrogen Storage and Carbon Dioxide Conversion

Loris Giovanni Lombardo

EPFL2021