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Factors and governing mechanisms influencing the open circuit voltage – a key determinant for improving the device performance efficiency.

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The organic solar cell (OSC) is a promising emerging low‐cost thin film photovoltaics technology. The power conversion efficiency (PCE) of OSCs has overpassed 16% for single junction and 17% for organic–organic tandem solar cells with the development of low bandgap organic materials synthesis and device processing technology. The main barrier of commercial use of OSCs is the poor stability of devices. Herein, the factors limiting the stability of OSCs are summarized. The limiting stability factors are oxygen, water, irradiation, heating, metastable morphology, diffusion of electrodes and buffer layers materials, and mechanical stress. The recent progress in strategies to increase the stability of OSCs is surveyed, such as material design, device engineering of active layers, employing inverted geometry, optimizing buffer layers, using stable electrodes and encapsulation materials. The International Summit on Organic Photovoltaic Stability guidelines are also discussed. The potential research strategies to achieve the required device stability and efficiency are highlighted, rendering possible pathways to facilitate the viable commercialization of OSCs.

Photovoltaic is one of the promising renewable sources of power to meet the future challenge of energy need. Organic and perovskite thin film solar cells are an emerging cost-effective photovoltaic technology because of low-cost manufacturing processing and their light weight. The main barrier of commercial use of organic and perovskite solar cells is the poor stability of devices. Encapsulation of these photovoltaic devices is one of the best ways to address this stability issue and enhance the device lifetime by employing materials and structures that possess high barrier performance for oxygen and moisture. The aim of this review paper is to find different encapsulation materials and techniques for perovskite and organic solar cells according to the present understanding of reliability issues. It discusses the available encapsulate materials and their utility in limiting chemicals, such as water vapour and oxygen penetration. It also covers the mechanisms of mechanical degradation within the individual layers and solar cell as a whole, and possible obstacles to their application in both organic and perovskite solar cells. The contemporary understanding of these degradation mechanisms, their interplay, and their initiating factors (both internal and external) are also discussed.

Organic solar cells possess multiple desirable traits, such as low cost, flexibility, and semitransparency, which opens up potential avenues unavailable to other solar technologies, a prime example of this being window applications. For this specific application, a delicate balance between the transmission of light through the device and power conversion efficiency (PCE), dependent on the amount of light absorbed, must be optimized. Here, we report a high-efficiency semitransparent device based on a novel fullerene-free material system. Using an active layer based on the material system PBDB-T:ITIC, optimized devices exhibited PCEs exceeding 7% while also achieving an average visible transmittance (AVT) of 25%. The concurrent demonstration of high efficiency with an AVT of 25% represents a notable step forward for semitransparent organic solar cells. Additionally, the influence of the active layer thickness on the color rendering properties of these cells was studied. Optimization of the active layer thickness can lead to high-efficiency cells, with high visible transmission as well as the ability to display an image accurately.

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Tin oxide (SnO 2 ) has been reported as a promising electron transport layer (ETL) for planar heterojunction perovskite solar cells (PSCs). This work reports a low temperature solution-processed bilayer SnO 2 as an efficient ETL in gas-quenched planar-heterojunction methylammonium lead iodide (MAPbI 3 ) perovskite solar cells. SnO 2 nanoparticles were employed to fill the pin-holes of sol−gel SnO 2 layer and form a smooth and compact bilayer structure. The PCE of bilayer devices has increased by 30% compared with sol− gel reference device and the J sc , V oc , and FF has been improved simultaneously. The superior performance of bilayer SnO 2 is attributed to the reduced current leakage, enhanced electron extraction characteristics, and mitigated the trapassisted interfacial recombination via X-ray photoelectron spectroscopy (XPS), electrochemical impedance spectroscopy (EIS), and space-charge limited current−voltage (SCLC) analysis.