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In recent years, perovskite solar cells (PSCs) have attracted significant attention due to their excellent photoelectric properties. However, several key performance parameters of these devices still fall short of their theoretical limits. Among these parameters, the regulation of open‐circuit voltage (VOC) has been a focal point of intensive research efforts, playing a pivotal role in advancing the efficiency of PSCs. This review first provides an overview of the generation and loss mechanism of VOC. It then discusses the significance of interface engineering in VOC regulation. Recent developments in high‐efficiency PSCs realized via interface engineering have been summarized and categorized into three key areas: surface modification, interface structure optimization, and surface dimensional engineering. Finally, a comprehensive summary of past research in this domain and offered insights into the future prospects of enhancing VOC in PSCs is provided. [ABSTRACT FROM AUTHOR]

Luminescent solar concentrators (LSCs) have recently emerged as promising candidates due to their advantages in effectively collecting solar energy through large-area photovoltaic windows for reducing the cost of solar cells. Colloidal quantum dots (QDs) have been demonstrated as the preferred choice of fluorophore materials for high-performance LSCs thanks to their exceptional optical properties. Nonetheless, the use of toxic heavy metals in QDs and expensive preparation technology impede their commercialization. Herein, we demonstrate a series of quaternary ammonium-type manganese halide hybrids featuring non-toxic and highly luminescent properties, and manipulate their optical properties by varying the Mn⋯Mn distance. The optimal (BTMA)2MnBr4 (BTMA+ = benzyl trimethylammonium) material exhibits the highest photoluminescence quantum yield (PLQY) nearing 100%. In addition, the interaction between (BTMA)2MnBr4 and polyethylene oxide (PEO) enables the obtained film to display bright green light emission and exceptional transparency. Furthermore, the prepared (BTMA)2MnBr4@PEO film is constructed on the LSC (20 mm × 20 mm × 2 mm) surface as a fluorescent layer, realizing a photovoltaic conversion efficiency of 2.06% and an internal quantum efficiency of 45.33% under 1 sun AM 1.5G illumination. These results indicate the significant promise of manganese halide hybrids for large-area, efficient, and ecofriendly LSCs. [ABSTRACT FROM AUTHOR]

Polymers play a crucial role in promoting the progress of high‐performance inverted perovskite solar cells (PSCs). However, few polymers have simultaneously achieved defect passivation and device encapsulation in PSCs. Herein, a telechelic silicone polymer (poly(dimethylsiloxane‐co‐methylsiloxane acrylate) [PDMA]) is introduced, which possesses crosslinking capability to enable structure regulation through a condensation reaction. By leveraging the advantages of the polymers before and after crosslinking, a synergistic strategy of defect healing and device encapsulation for PSCs is developed via the application of the targeted polymer. PDMA as additives anchors tightly at the grain boundaries (GBs) and bridges the perovskite grains, achieving defect passivation and GBs crosslinking, increasing the efficiency of inverted PSCs from 22.32% to 24.41%. Crosslinked PDMA (CPDMA) is used as an encapsulant to encapsulate the entire device, enabling non‐destructive encapsulation at room temperature and inhibiting perovskite degradation under photothermal aging. Remarkably, the PDMA‐modified device with CPDMA encapsulation maintains 98% of its initial efficiency after 1200 h under continuous illumination at 55 ± 5 °C and retains 95% of its original efficiency after 1000 h of damp heat testing, meeting one of the IEC61215:2016 standards. [ABSTRACT FROM AUTHOR]

Radio‐photovoltaic cell is a micro nuclear battery for devices operating in extreme environments, which converts the decay energy of a radioisotope into electric energy by using a phosphor and a photovoltaic converter. Many phosphors with high light yield and good environmental stability have been developed, but the performance of radio‐photovoltaic cells remains far behind expectations in terms of power density and power conversion efficiency, because of the poor photoelectric conversion efficiency of traditional photovoltaic converters under low‐light conditions. This paper reports an radio‐photovoltaic cell based on an intrinsically stable formamidinium‐cesium perovskite photovoltaic converter exhibiting a wide light wavelength response from 300 to 800 nm, high open‐circuit voltage (VOC), and remarkable efficiency at low‐light intensity. When a He ions accelerator is adopted as a mimicked α radioisotope source with an equivalent activity of 0.83 mCi cm−2, the formamidinium‐cesium perovskite radio‐photovoltaic cell achieves a VOC of 0.498 V, a short‐circuit current (JSC) of 423.94 nA cm−2, and a remarkable power conversion efficiency of 0.886%, which is 6.6 times that of the Si reference radio‐photovoltaic cell, as well as the highest among all radio‐photovoltaic cells reported so far. This work provides a theoretical basis for enhancing the performance of radio‐photovoltaic cells. [ABSTRACT FROM AUTHOR]

Hepatocellular carcinoma (HCC) is one of the most common malignant tumors in China, accounting for the majority of primary liver cancer cases. Liver resection is the preferred curative method for early-stage HCC. However, up to 80–85% of patients have already missed the opportunity of radical surgery due to tumor advances at the time of consultation. Conversion therapies are a series of medications and treatments for initially inoperable patients. For early-stage unresectable HCC (uHCC) patients, conversion therapies are designed to meet surgical requirements by increasing the volume of the residual liver. Meanwhile, for advanced cases, conversion therapies strive for tumor shrinkage and down-staging, creating the opportunity for liver resection or liver transplantation. This review summarizes the latest advances in conversion therapies and highlights their potential for improving the survival benefit of patients with uHCC. [ABSTRACT FROM AUTHOR]

Inorganic-organic hybrid lead halide perovskites are emerging optoelectronic materials for solar cell application. However, the toxicity concerns and poor stability largely hamper their practical applications. For these reasons, the search for "perovskite-inspired" alternatives, having the same advantages but overcoming the drawbacks of the lead-based one, has become an important sector in the field. Among the candidates, Bi3+ and Sb3+ containing materials are of great interest, due to their electronic structures resembling the Pb2+. Bismuth/antimony chalcohalides have been known for a long time as the potential absorber in photovoltaics, even if their performances are still low. Interestingly, pnictogen chalcohalides can be the stepping stone toward numerous quaternary compounds, including some perovskite structures. The understanding of the fundamental properties and the current limitations of both the starting ternary compounds and the final quaternary materials can allow the achievement of improved photovoltaic absorbers, stable, and efficient. In this review, the fundamental properties and device performances of many ternary pnictogen chalcohalides and the derived quaternary compounds are summarized, focusing on the different preparation strategies. [ABSTRACT FROM AUTHOR]

The performance of perovskite solar cells (PSCs) is negatively affected by iodine (I2) impurities generated from the oxidation of iodide ions in the perovskite precursor powder, solution, and perovskite films. In this study, the use of potassium formate (HCOOK) as a reductant to minimize the presence of detrimental I2 impurities is presented. It is demonstrated that HCOOK can effectively reduce I2 back to I− in the precursor solution as well as in the devices under external conditions. Furthermore, the introduced formate anion (HCOO−) and alkali metal cation (K+) can reduce the defect density within the perovskite film by modulating perovskite growth and passivating electronic defects, significantly prolonging the carrier lifetime and reducing the J–V hysteresis. Consequently, the maximum efficiency of the HCOOK‐doped planar n–i–p PSCs reaches 23.8%. After 1000 h of operation at maximum power point tracking under continuous 1 sun illumination, the corresponding encapsulated devices retain 94% of their initial efficiency. [ABSTRACT FROM AUTHOR]

The most employed strategies for adjusting the electrocatalytic activity and selectivity of covalent organic frameworks (COFs) in the oxygen reduction reaction involve modifying the number and placement of heteroatoms, degree of asymmetry, and molecular configuration of the building units. However, the utilization of linkage conversion, which can induce huge local structure change, has been rarely explored for achieving such goals. In this work, we present the successful conversion of imine linkages into nonsubstituted quinoline within thiazolo-[5,4-d]thiazole-based COFs via a Rh-catalyzed C–H activation strategy. This conversion resulted in improved performance in the oxygen reduction reaction, specifically the production of hydrogen peroxide with a selectivity of 61–69% in acid solution (pH = 3.1), a high production rate (106.3 mg L−1 in 100 min), and good durability. Control experiments and theoretical calculations were conducted to investigate the underlying mechanisms, indicating that the active sites could be the quinoline nitrogen and thiazole nitrogen. Furthermore, an analysis of the electronic structure revealed that the enhanced performance following linkage conversion was attributed to an increase in in-plane π electron delocalization. This delocalization induced charge redistribution around the active sites, optimizing the adsorption of oxygen intermediates. Overall, the work paves novel pathways to fine-tune the oxygen reduction reaction performance of COFs linked by imine bonds. [ABSTRACT FROM AUTHOR]