Design of an Innovative Graphite Exchanger for Adsorption Heat Pumps and Chillers

Abstract In this work, an innovative adsorber for application in adsorption heat pumps and chillers is presented. The adsorber consists of several assembled graphite plates and the flow path of heat transfer fluid. Each plate consists of a process side (where zeolite is deposited onto) and a heat transfer fluid (HTF) side where liquid water flows. The resulting adsorbent heat exchanger is able to deliver about 0.5-1 kW cooling power and possesses attractive thermo physical properties, especially in term of low weight, volume and thermal capacity. Experimental testing of the full-scale adsorber by a testing station available at CNR ITAE is currently ongoing

Water Splitting with Enhanced Efficiency Using a Nickel-Based Co-Catalyst at a Cupric Oxide Photocathode

Homemade non-critical raw materials such as Ni or NiCu co-catalysts were added at the photocathode of a tandem cell, constituted by photoelectrodes made of earth-abundant materials, to generate green solar hydrogen from photoelectrochemical water splitting. Oxygen evolving at the Ti-and-P-doped hematite/TCO-based photoanode and hydrogen at the cupric oxide/GDL-based photocathode are separated by an anion exchange polymer electrolyte membrane placed between them. The effect of the aforementioned co-catalysts was studied in a complete PEC cell in the presence of the ionomer dispersion and the anionic membrane to evaluate their impact under practical conditions. Notably, different amounts of Ni or NiCu co-catalysts were used to improve the hydrogen evolution reaction (HER) kinetics and the overall solar-to-hydrogen (STH) efficiency of the photoelectrochemical cells. At −0.6 V, in the bias-assisted region, the photocurrent density reaches about 2 mA cm−2 for a cell with 12 µg cm−2 of Ni loading, followed by 1.75 mA cm−2 for the cell configuration based on 8 µg cm−2 of NiCu. For the best-performing cell, enthalpy efficiency at −0.4 V reaches a first maximum value of 2.03%. In contrast, the throughput efficiency, which is a ratio between the power output and the total power input (solar + electric) provided by an external source, calculated at −1.225 V, reaches a maximum of 10.75%. This value is approximately three times higher than the best results obtained in our previous studies without the use of co-catalysts at the photocathode.The authors gratefully acknowledge funding from the European Union’s Horizon 2020 research and innovation program under grant agreement no. 760930 (FotoH2 project)

Unravelling the Influence of Binder Typology during the Additive Manufacturing of Hybrid Multi-Channel Cylinders for Catalytic Purposes

In this work, a 3D printing methodology based on the robocasting of catalytic ink pastes was applied to obtain structured matrix-like cylinders as innovative materials for an effective utilization of carbon dioxide. The influence of three different binders (i.e., PEI, HPMC and MC) on the physio-chemical, mechanical and catalytic properties of multi-channel monoliths was studied against a reference binder-free powdered system in order to envisage the effectiveness of the printing procedure in realizing hybrid advanced materials at a higher control and reproducibility than from traditional preparation techniques. In terms of textural and structural properties, the micro-extruded 3D cylinders only evidenced a slight difference in terms of relative crystallinity, with minor effects on the surface area exposure in relation to the specific binder used during the direct ink writing process. More importantly, the typology of binder significantly affected the rheological properties of the catalytic ink, with the need of a controlled viscosity to ensure a suitable thixotropic behaviour of the extrudable pastes, finally determining an optimal mechanical resistance of the final 3D monolith. The experimental validation of the hybrid multi-channel cylinders under conditions of CO2 hydrogenation demonstrated the great potential of additive manufacturing in the realization of catalyst architectures characterized by unique features and fidelity scarcely reproducible via conventional synthetic techniques

Numerical 3D Model of a Novel Photoelectrolysis Tandem Cell with Solid Electrolyte for Green Hydrogen Production

The only strategy for reducing fossil fuel-based energy sources is to increase the use of sustainable ones. Among renewable energy sources, solar energy can significantly contribute to a sustainable energy future, but its discontinuous nature requires a large storage capacity. Due to its ability to be produced from primary energy sources and transformed, without greenhouse gas emissions, into mechanical, thermal, and electrical energy, emitting only water as a by-product, hydrogen is an effective carrier and means of energy storage. Technologies for hydrogen production from methane, methanol, hydrocarbons, and water electrolysis using non-renewable electrical power generate CO2. Conversely, employing photoelectrochemistry to harvest hydrogen is a sustainable technique for sunlight-direct energy storage. Research on photoelectrolysis is addressed to materials, prototypes, and simulation studies. From the latter point of view, models have mainly been implemented for aqueous-electrolyte cells, with only one semiconductor-based electrode and a metal-based counter electrode. In this study, a novel cell architecture was numerically modelled. A numerical model of a tandem cell with anode and cathode based on metal oxide semiconductors and a polymeric membrane as an electrolyte was implemented and investigated. Numerical results of 11% solar to hydrogen conversion demonstrate the feasibility of the proposed novel concept

Scalability and Investigation of the Geometrical Features and Shapes of a Tandem Photo-Electrolysis Cell Based on Non-Critical Raw Materials

Tandem photoelectrochemical cells (PECs) are devices useful for water splitting (WS) with the production of oxygen at the photoanode (PA) and hydrogen at the photocathode (PC) by adsorbing more than 75% of the solar irradiation; a portion of the UV/Vis direct solar irradiation is captured by the PA and a diffused or transmitted IR/Vis portion by the PC. Herein, Ti-doped hematite (PA) and CuO (PC) were employed as abundant and non-critical raw semiconductors characterised by proper band gap and band edge banding for the photoelectrochemical WS and absorption of sunlight. The investigation of inexpensive PEC was focused on the scalability of an active area from 0.25 cm2 to 40 cm2 with a rectangular or square shape. For the first time, this study introduces the novel concept of a glass electrode membrane assembly (GEMA), which was developed with an ionomeric glue to improve the interfacial contact between the membrane and photoelectrodes. On a large scale, the electron–hole recombination and the non-optimal photoelectrodes/electrolyte interface were optimized by inserting a glass support at the photocathode and drilled fluorine tin oxide (FTO) at the photoanode to ensure the flow of reagents and products. Rectangular 40 cm2 PEC showed a larger maximum enthalpy efficiency of 0.6% compared to the square PEC, which had a value of 0.37% at a low bias-assisted voltage (−0.6 V). Furthermore, throughput efficiency reached a maximum value of 1.2% and 0.8%, demonstrating either an important effect of the PEC geometries or a non-significant variation of the photocurrent within the scalability

Numerical 3D Model of a Novel Photoelectrolysis Tandem Cell with Solid Electrolyte for Green Hydrogen Production

The only strategy for reducing fossil fuel-based energy sources is to increase the use of sustainable ones. Among renewable energy sources, solar energy can significantly contribute to a sustainable energy future, but its discontinuous nature requires a large storage capacity. Due to its ability to be produced from primary energy sources and transformed, without greenhouse gas emissions, into mechanical, thermal, and electrical energy, emitting only water as a by-product, hydrogen is an effective carrier and means of energy storage. Technologies for hydrogen production from methane, methanol, hydrocarbons, and water electrolysis using non-renewable electrical power generate CO2. Conversely, employing photoelectrochemistry to harvest hydrogen is a sustainable technique for sunlight-direct energy storage. Research on photoelectrolysis is addressed to materials, prototypes, and simulation studies. From the latter point of view, models have mainly been implemented for aqueous-electrolyte cells, with only one semiconductor-based electrode and a metal-based counter electrode. In this study, a novel cell architecture was numerically modelled. A numerical model of a tandem cell with anode and cathode based on metal oxide semiconductors and a polymeric membrane as an electrolyte was implemented and investigated. Numerical results of 11% solar to hydrogen conversion demonstrate the feasibility of the proposed novel concept.This research was funded by the European Union’s Horizon 2020 research and innovation program under grant agreement ID 760930 (FotoH2 project)