Variable renewable energy | EPFL Graph Search

Variable renewable energy (VRE) or intermittent renewable energy sources (IRES) are renewable energy sources that are not dispatchable due to their fluctuating nature, such as wind power and solar power, as opposed to controllable renewable energy sources, such as dammed hydroelectricity or biomass, or relatively constant sources, such as geothermal power. The use of small amounts of intermittent power has little effect on grid operations. Using larger amounts of intermittent power may require upgrades or even a redesign of the grid infrastructure. Options to absorb large shares of variable energy into the grid include using storage, improved interconnection between different variable sources to smooth out supply, using dispatchable energy sources such as hydroelectricity and having overcapacity, so that sufficient energy is produced even when weather is less favourable. More connections between the energy sector and the building, transport and industrial sectors may also help.

Triple-mode grid-balancing plants via biomass gasification and reversible solid-oxide cell stack: Concept and thermodynamic performance

Chengzhou Li, Tzu-En Lin, François Maréchal, Maria del Mar Perez Fortes, Jan Van Herle, Ligang Wang, Yumeng Zhang

Biomass-to-electricity or -chemical via power-to-x can be potential flexibility means for future electrical grid with high penetration of variable renewable power. However, biomass-to-electricity will not be dispatched frequently and becomes less economically-beneficial due to low annual operating hours. This issue can be addressed by integrating biomass-to-electricity and -chemical via ‘‘reversible’’ solid-oxide cell stacks to form a triple-mode grid-balancing plant, which could flexibly switch among power generation, power storage and power neutral (with chemical production) modes. This paper investigates the optimal designs of such a plantconcept with a multi-time heat and mass integration platform considering different technology combinationsand multiple objective functions to obtain a variety of design alternatives. The results show that increasing plant efficiencies will increase the total cell area needed for a given biomass feed. The efficiency difference among different technology combinations with the same gasifier type is less than 5% points. The efficiency reaches up to 50%–60% for power generation mode, 72%–76% for power storage mode and 47%–55% for power neutral mode. When penalizing the syngas not converted in the stacks, the optimal plant designs interact with the electrical and gas grids in a limited range. Steam turbine network can recover 0.21–0.24 kW electricity per kW dry biomass energy (lower heating value), corresponding to an efficiency enhancement of up to 20%points. The difference in the amounts of heat transferred in different modes challenges the design of a common heat exchange network.

2020

Interfacial engineering for competitive Dye-Sensitized Solar Cells production

Natalie Flores Diaz

Renewable energy deployment and implementation of a circular economy will play a crucial role in decreasing CO2 emissions to meet the target from the Paris agreement. Dye-sensitized solar cells (DSSCs) can be designed in various colors and transparency for building-integrated photovoltaics (BIPV). This emerging technology has gained significant attention for its remarkably high power conversion efficiency (PCE) under indoor lighting up to 34%. To improve the performance of DSSCs, various approaches to study and reduce the interfacial electron recombination from the conduction band of the semiconductor to the electrolyte were implemented in this thesis. One of the approaches was the design of a tandem electrolyte containing two redox species, the radical AZADO (AZ+/0) and the [Co(bpy)3]2+/3+ complex. DSSCs with tandem electrolytes showed increased open-circuit voltage (VOC) up to 1009 mV and enhanced PCE of 9.15%. The VOC enhancement was determined to result from the higher redox potential of (AZ+/0) and the slower electron recombination rate. These findings demonstrate the advantages of employing tandem electrolytes to improve the VOC and overall performance of DSSCs. To decrease the solvent's volatility and the interfacial electron recombination in cobalt-based electrolytes, hyperbranched networks (HB) were designed through a click thiol-ene reaction between a thiol-siloxane and an acrylate monomer. The formed polymers were denoted HB1 (thiol-siloxane and PEGMA) and HB2 (thiol-siloxane and PEGMA). The addition of 20% of HB polymers to a cobalt-based electrolyte retained up to 98% of their initial weight until 150°C. The devices employing 10%(v/v) of HB1 attained the highest PCE under AM1.5 of 8.52%, comparable to 9.36% for the cobalt reference electrolyte. All the HB-electrolytes presented higher VOC values than the cobalt reference due to an upward shift in the CB of TiO2 and longer electron lifetimes. It was determined that the HB-polymers reduce the electron recombination and enhance the photovoltaic performance under low light intensity leading to a PCE of 23.19% under 1000 lux compared to 20.37% for the Co-reference. We then developed a new dye, R7, with a strong electron-donating PAH core and BPT2 as the central building block and a bulkier HF donor to decrease electron recombination at the interface TiO2/electrolyte. We found that in the presence of a copper electrolyte, the dye R7 outperformed devices with R6. EIS revealed that the bulky HF-donor introduction effectively suppressed the electron recombination between the TiO2 surface and the redox shuttle. Additionally, we employed a co-sensitized system of R7+Y123 to reach the outstanding parameters of JSC of 16.15 mAcm-2, VOC of 1035 mV, FF of 0.76 to achieve a top PCE of 12.7%. To the best of our knowledge, this is the highest for copper-based DSSCs using a blue photosensitizer. Lastly, the interfacial phenomena in DSSCs with carbon counter electrodes (CCEs) and copper-based electrolytes were studied to determine the feasibility of the production of monolithic DSSCs with copper-based hole-transporting materials. It was found that the electron transport in devices with CCEs is in the same order of magnitude as those with PEDOT. However, the devices with CCEs presented a decrease of 2 orders of magnitude in the recombination resistance, resulting in decreased VOC and JSC, leading to a PCE of 17% compared to 24.5% for PEDOT devices under 1000 lux illumination.

EPFL2021

Metal-organic framework derived copper catalysts for CO2 to ethylene conversion

Jun Li, Ning Wang

The electrochemical reduction of CO2 to ethylene provides a carbon-neutral avenue for the conversion of CO2 to value-added fuels and feedstocks, so contributing to the storage of intermittent renewable electricity. The exploration of efficient electrocatalysts with high ethylene selectivity and productivity is highly desirable but remains challenging. Here, we present a Cu-based catalyst derived from a metal-organic framework (Cu-MOF) which shows enhanced performance due to its porous morphology, complex oxidation states and strong lattice strain. X-ray diffraction, X-ray photoelectron spectroscopy, and X-ray absorption spectroscopy are utilized to track the evolution of the crystal structure and oxidation states during the reaction, and the results reveal that Cu2+ ions are rapidly reduced to Cu+ and then slowly to Cu-0, resulting in a Cu@CuxO core@shell structure. The tensile strain caused by the distorted grain is beneficial for the activation of CO2. Cu+/Cu-0 interfaces formed through stabilized Cu+ facilitate *CO-CO dimerization, promoting conversion to C2+ products and suppressing conversion to C-1 products. The optimized catalyst exhibits a 51% Faraday efficiency (FE) for ethylene and a 70% FE for C2+ products, with 20 h operational stability in an H-cell configuration, and a partial ethylene current density of 150mA cm(-2) in a flow-cell configuration.

ROYAL SOC CHEMISTRY2020

Interfacial engineering for competitive Dye-Sensitized Solar Cells production

Natalie Flores Diaz

EPFL2021