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- Aerogel cathodes for electrochemical CO2 reduction [Comunicação oral]Publication . Messias, Sofia; Fialho, Maria T.; Paninho, A. B.; Branco, Luis C; Nunes, A. V. M.; Martins, Rodrigo; Mendes, Manuel Joao; Nunes, D.; Rangel, C. M.; Machado, AnaABSTRACT: Electrochemical reduction of carbon dioxide powered by renewable energy to produce fuels and chemicals is a technology with potential to contribute to an economy based on a carbon neutral cycle. The development of cost effective, highly active and stable catalysts for CO2 electroreduction is being intensively researched. This work addresses the development of aerogel supported copper-zinc bimetallic catalysts[1]. Aerogels are substances with exceptional properties with many current and potential applications [2-3]. Due to their high surface area, stability in corresponding gaseous or liquid phases, transport through large meso and macropores they are especially suited as catalysts and carrier materials for catalysis and, when electric conductive for electro-catalysis. Aerogels prepared by the sol gel method and impregnated with metallic particles will be tested as cathodes for the co-electrolysis of CO2 and water to produce syngas at temperatures near room temperature and high-pressure. In this way this process can be directly coupled to other high pressure processes, such as Fischer-Tropsch that use high pressure syngas as raw material. Productivities and faradaic efficiencies will be evaluated. The characterization of the aerogel-based cathodes will be undertaken by surface analysis techniques. BET surface areas will be determined. The catalytic cathodes will be tested in an ionic liquid-based electrolyte as a way to increase current densities, due to the high CO2 solubilities exhibited by some ionic liquid families.
- Tuning cathode porosity for electrochemical reduction of CO2 at high pressure [Resumo]Publication . Messias, Sofia; Fialho, Maria T.; Paninho, A. B.; Nunes, A. V. M.; Branco, Luis C; Nunes, D.; Martins, Rodrigo; Mendes, Manuel Joao; Rangel, C. M.; Machado, AnaABSTRACT: The development of active and stable catalytic cathodes is critical for advancing electrochemical carbon dioxide reduction into fuels and chemicals from Lab to market. This is a technology with a high potential to contribute to combat climate changes by using captured CO2, water and renewable energy [1]. The use of pressures higher than atmospheric pressure to carry out the co-electrolysis of CO2 and water has been recognized as an important process intensification parameter to increase productivities and energy efficiency [2]. Ongoing work addresses the preparation of aerogels by the sol gel method and impregnation with zinc and copper metallic particles to be used as cathodes for the co-electrolysis of CO2 and water to produce syngas at temperatures near room temperature and high-pressure. Ionic liquid-based electrolytes are used to increase CO2 concentration at the surface of the electrode and consequently productivities, as some ionic liquid families are known to solubilize high amounts of CO2. Aerogels have been investigated for many different applications including as catalyst supports, due to their high surface area, stability in gaseous or liquid phases, and efficient transport through large meso and macropores. The present work reports a strategy to tune the pore sizes of the catalytic electrodes by the use of reticulating agents and supercritical CO2 drying. Productivities and faradaic efficiencies of the porous materials with the different reticulating agents are compared and interpreted in respect to their surface characterization e.g. BET surface areas and morphologies determined by SEM. The potential of new aerogel-based catalytic cathodes on the efficiency of the electrochemical CO2 reduction will be discussed and its impact in fostering supercritical fluids technology through its use in processes for the mitigation of climate changes.
- Prediction of sunlight-driven CO2 conversion: producing methane from photovoltaics, and full system design for single-house applicationPublication . Vieira, F.; Sarmento, B.; Machado, Ana; Facão, Jorge; Carvalho, Maria João; Mendes, Manuel Joao; Fortunato, Elvira; Martins, RodrigoABSTRACT: CO2 capture and utilization (CCU) technologies are being immensely researched as means to close the anthropogenic carbon cycle. One approach known as artificial photosynthesis uses solar energy from photovoltaics (PV), carbon dioxide and water to generate hydrocarbon fuels, being methane (CH4) a preferential target due to the already in place infrastructures for its storage, distribution and consumption. Here, a model is developed to simulate a direct (1-step) solar methane production approach, which is studied in two scenarios: first, we compare it against a more conventional 2-step methane production route, and second, we apply it to address the energetic needs of concept buildings with usual space and domestic hot water heating requirements. The analysed 2-step process consists in the PV-powered synthesis of an intermediate fuel - syngas - followed by its conversion to CH4 via a Fischer -Tropsch (methanation) process. It was found that the 1-step route could be adequate to a domestic, small scale use, potentially providing energy for a single-family house, whilst the 2-step can be used in both small and large scale applications, from domestic to industrial uses. In terms of overall solar-to-CH4 energy efficiency, the 2-step method reaches 13.26% against the 9.18% reached by the 1-step method. Next, the application of the direct solar methane technology is analysed for domestic buildings, in different European locations, equipped with a combination of solar thermal collectors (STCs) and PV panels, in which the heating needs that cannot be fulfilled by the STCs are satisfied by the combustion of methane synthesized by the PV-powered electrolyzers. Various combinations of situations for a whole year were studied and it was found that this auxiliary system can produce, per m(2) of PV area, in the worst case scenario 23.6 g/day (0.328 kWh/day) of methane in Stockholm, and in the best case scenario 47.4 g/day (0.658 kWh/day) in Lisbon.