• Energy Research

Due to the increasing trend of using renewable energy, the development of an energy storage system (ESS) attracts great research interest. A zinc–air battery (ZAB) is a promising ESS due to its high capacity, low cost and high potential to support circular economy principles. However, despite ZABs' technological advancements, a generic dynamic model for a ZAB, which is a key component for effective battery management and monitoring, is still lacking. ZABs show nonlinear behaviour where the steady-state gain is strongly dependent on operating conditions. The present study aims to develop a dynamic model, being capable of predicting the nonlinear dynamic behaviour of a refuellable ZAB, using a linear parameter-varying (LPV) technique. The LPV model is constructed from a family of linear time-invariant models, where the discharge current level is used as a scheduling parameter. The developed LPV model is benchmarked against linear and nonlinear model counterparts. Herein, the LPV model performs remarkably well in capturing the nonlinear behaviour of a ZAB. It significantly outperforms the linear model. Overall, the LPV approach provides a systematic way to construct a robust dynamic model which well represents the nonlinear behaviour of a ZAB.

Light induced fullerene dimerization is controlled by both the fullerene and polymer morphology of organic solar cells.

Aluminum–air batteries (AABs) have recently received extensive attention because of their high energy density and low cost. Nevertheless, a critical issue limiting their practical application is corrosion of aluminum (Al) anode in an alkaline aqueous electrolyte, which results from hydrogen evolution reaction (HER). To effectively solve the corrosion issue, dissolution of Al anode should be carried out in a nonaqueous electrolyte. However, the main cathodic reaction, known as oxygen reduction reaction (ORR), is sluggish in such a nonaqueous electrolyte. A dual-electrolyte configuration with an anion exchange membrane separator allows AABs to implement a nonaqueous anolyte along with an aqueous catholyte. Thus, this work addresses the issue of anode corrosion in an alkaline Al–air flow battery via a dual-electrolyte system. The battery configuration consisted of an Al anode | anolyte | anion exchange membrane | catholyte | air cathode. The anolytes were methanol solutions containing 3 M potassium hydroxide (KOH) with different ratios of water. An aqueous polymer gel electrolyte was used as the catholyte. The corrosion of Al in the anolytes was duly investigated. The increase of water content in the anolyte reduced overpotential and exhibited faster anodic dissolution kinetics. This led to higher HER, along with a greater corrosion rate. The performance of the battery was also examined. At a discharge current density of 10 mA·cm−2, the battery using the anolyte without water exhibited the highest specific capacity of 2328 mAh/gAl, producing 78% utilization of Al. At a higher content of water, a higher discharge voltage was attained. However, due to greater HER, the specific capacity of the battery decreased. Besides, the circulation rate of the anolyte affected the performance of the battery. For instance, at a higher circulation rate, a higher discharge voltage was attained. Overall, the dual-electrolyte system proved to be an effective approach for suppressing anodic corrosion in an alkaline Al–air flow battery and enhancing discharge capacity.

AbstractNowadays, due to global warming stemming from excessive use of fossil fuel, there is considerable interest in promoting renewable energy sources. However, because of the intermittent nature of these energy sources, efficient energy storage systems are needed. In this regard, zinc-air flow batteries (ZAFBs) are seen as having the capability to fulfill this function. In flow batteries, the electrolyte is stored in external tanks and circulated through the cell. This study provides the requisite experimental data for parameter estimation as well as model validation of ZAFBs. Each data set includes: current (mA), voltage (V), capacity (mAh), specific capacity (mAh/g), energy (Wh), specific energy (mWh/g) and discharge time (h:min:s.ms). Discharge data involved forty experiments with discharge current in the range of 100–200 mA, and electrolyte flow rates in the range of 0–140 ml/min. Such data are crucial for the modelling and theoretical/experimental analysis of ZAFBs.

AbstractImproving the long-term stability of perovskite solar cells is critical to the deployment of this technology. Despite the great emphasis laid on stability-related investigations, publications lack consistency in experimental procedures and parameters reported. It is therefore challenging to reproduce and compare results and thereby develop a deep understanding of degradation mechanisms. Here, we report a consensus between researchers in the field on procedures for testing perovskite solar cell stability, which are based on the International Summit on Organic Photovoltaic Stability (ISOS) protocols. We propose additional procedures to account for properties specific to PSCs such as ion redistribution under electric fields, reversible degradation and to distinguish ambient-induced degradation from other stress factors. These protocols are not intended as a replacement of the existing qualification standards, but rather they aim to unify the stability assessment and to understand failure modes. Finally, we identify key procedural information which we suggest reporting in publications to improve reproducibility and enable large data set analysis.