Broadening the optical absorption of organic photovoltaic (OPV) materials by enhancing the intramolecular push-pull effect is a general and effective method to improve the power conversion efficiencies of OPV cells. However, in terms of the electron acceptors, the most common molecular design strategy of halogenation usually results in down-shifted molecular energy levels, thereby leading to decreased open-circuit voltages in the devices. Herein, we report a chlorinated non-fullerene acceptor, which exhibits an extended optical absorption and meanwhile displays a higher voltage than its fluorinated counterpart in the devices. This unexpected phenomenon can be ascribed to the reduced non-radiative energy loss (0.206 eV). Due to the simultaneously improved short-circuit current density and open-circuit voltage, a high efficiency of 16.5% is achieved. This study demonstrates that finely tuning the OPV materials to reduce the bandgap-voltage offset has great potential for boosting the efficiency. Halogenation has proved an effective strategy to improve the power conversion efficiencies of organic solar cells but it usually leads to lower open-circuit voltages. Here, Cui et al. unexpectedly obtain higher open-circuit voltages and achieve a record high PCE of 16.5% by chlorination.

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Over 16% efficiency organic photovoltaic cells enabled by a chlorinated acceptor with increased open-circuit voltages

Improving 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. Reliability of stability data for perovskite solar cells is undermined by a lack of consistency in the test conditions and reporting. This Consensus Statement outlines practices for testing and reporting stability tailoring ISOS protocols for perovskite devices.

/pdf/consensus-statement-for-stability-assessment-and-reporting-37ng2o1dmx.pdf

Consensus statement for stability assessment and reporting for perovskite photovoltaics based on ISOS procedures

INTRODUCTION Although advances in materials and processing have led to remarkable advancements in the energy conversion efficiency of perovskite solar cells (PSCs), increasing from 3.8% to 25.2% in only 10 years, these solar cells cannot become commercially viable unless their underperforming durability is improved. The instability of perovskites must be addressed if PSCs are to compete with silicon technology, which currently offers a 25-year performance warranty. Previous approaches to this problem include the use of metal oxide barrier layers and butyl rubber sealants. Here, we report a low-cost polymer/glass stack encapsulation scheme that enables PSCs to pass the demanding International Electrotechnical Commission (IEC) 61215:2016 Damp Heat and Humidity Freeze tests. These tests help to determine whether solar cell modules can withstand the effects of outdoor operating conditions by exposing them to repeated temperature cycling (–40° to 85°C) as well as 85% relative humidity. Our airtight encapsulation scheme prevented moisture ingress. It was also effective in suppressing outgassing of decomposition products, which limits decomposition reactions of organic hybrid PSCs by allowing these reactions to come to equilibrium. The gas compositions were verified by gas chromatography–mass spectrometry (GC-MS). RATIONALE In the GC-MS technique, gas chromatography separates the components in a mixture, and the chemical identity of each component is determined with mass spectrometry. We could directly identify with high specificity the decomposition products of multi-cation perovskite precursors, of unencapsulated perovskite test structures, and of encapsulated full cells at elevated temperatures. The results allowed us to identify thermal degradation pathways by determining the outgassing products of mixed-cation perovskites during heating. We then used GC-MS to evaluate the effectiveness of different packaging techniques developed for PSCs. The packaging schemes were a polyisobutylene (PIB)–based polymer blanket encapsulation, a polyolefin-based blanket encapsulation, and a PIB edge seal. These packaging layers were then capped by a glass cover. For the edge seal, the decomposition gases inside the cell were sampled with a syringe. The feasibilities of these packaging techniques were also demonstrated by IEC photovoltaic module standard Damp Heat and Humidity Freeze testing. RESULTS Signature decomposition products such as CH3I, CH3Br, and NH3 were identified and decomposition pathways were proposed for CH3NH3I (MAI), HC(NH2)2I (FAI), CH3NH3Br (MABr), and mixed-cation and mixed-halide (FAI)0.85 + (MABr)0.15 perovskite precursors, including their secondary decomposition reactions at 350°, 140°, and 85°C. The GC-MS results confirmed that the Br-containing precursor was less prone to thermal decomposition than an I-containing precursor. Also, CsFAMA cells were found to outgas one-fifth as much decomposition product as their FAMA counterparts, which indicated that the Cs-containing cells had better thermal stability. Although the decomposition of FAI is reversible, the mixing of MA with FA precursors caused decomposition products to participate in the secondary reaction that was irreversible. This finding confirmed the disadvantage of mixing of MA with FA perovskite through the reduction in chemical stability. The blanket-encapsulated PSCs sustained no efficiency degradation after 1800 hours of Damp Heat testing or 75 cycles of Humidity Freeze testing. CONCLUSION GC-MS identified signature volatile products of the decomposition of organic hybrid perovskites under thermal stress, thereby informing decomposition pathways. The findings are important for developing potential cell-stabilizing strategies, given that cells in the field typically experience high operating temperatures. In addition, results of GC-MS confirm that the low-cost pressure-tight encapsulation we developed is effective in suppressing such outgassing and therefore decomposition reactions of PSCs. This encapsulation scheme is the simplest of all for perovskite cells to pass IEC photovoltaic module standard tests. Our approach can be applied to evaluating the effectiveness of other packaging approaches, as well as testing the effectiveness of coatings and material compositions aimed at limiting light and thermal degradation.

Gas chromatography-mass spectrometry analyses of encapsulated stable perovskite solar cells.

The Future of Flexible Organic Solar Cells

We fabricate near-infrared absorbing organic photovoltaics that are highly transparent to visible light. By optimizing near-infrared optical-interference, we demonstrate power efficiencies of 1.3±0.1% with simultaneous average visible transmission of >65%. Subsequent incorporation of near-infrared distributed-Bragg-reflector mirrors leads to an increase in the efficiency to 1.7±0.1%, approaching the 2.4±0.2% efficiency of the opaque cell, while maintaining high visible-transparency of >55%. Finally, we demonstrate that a series-integrated array of these transparent cells is capable of powering electronic devices under near-ambient lighting. This architecture suggests strategies for high-efficiency power-generating windows and highlights an application uniquely benefiting from excitonic electronics.

Transparent, near-infrared organic photovoltaic solar cells for window and energy-scavenging applications

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.

https://onlinelibrary.wiley.com/doi/pdf/10.1002/advs.201903259

Progress in Stability of Organic Solar Cells

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.

https://www.mdpi.com/2079-6412/9/2/65/pdf

Encapsulation of Organic and Perovskite Solar Cells: A Review

Tin oxide (SnO2) 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 bila...

Bilayer SnO2 as Electron Transport Layer for Highly Efficient Perovskite Solar Cells

Inorganic cesium lead triiodide (CsPbI3) perovskite materials are becoming increasingly attractive for use in perovskite/silicon tandem solar cells, due to their almost ideal band gap energy (Eg) of about 1.7 eV. To be useful as photovoltaic absorbers, the CsPbI3 must form the cubic or black phase (α-CsPbI3). To do so at relatively low temperatures, hydroiodic acid (HI) is required as a solution additive. This paper demonstrates CsPbI3 perovskite solar cells with an efficiency of 6.44%, formed using a HI concentration of 36 μL/mL. This value is higher than the previous most commonly used HI additive concentration. Herein, by undertaking a systematic study of the HI concentration, we demonstrate that the structural, morphological, optical, and electrical properties of CsPbI3 solar cells, processed with this HI additive concentration, are superior.

Leiping Duan

Papers

Progress in Stability of Organic Solar Cells

Encapsulation of Organic and Perovskite Solar Cells: A Review

Bilayer SnO2 as Electron Transport Layer for Highly Efficient Perovskite Solar Cells

Effects of Hydroiodic Acid Concentration on the Properties of CsPbI3 Perovskite Solar Cells

Progress in non-fullerene acceptor based organic solar cells