Surface passivation in perovskite solar cells can enhance device efficiency, yet incomplete interfacial functionality poses challenges to long-term reliability. Here we present a strategic interfacial engineering approach using sodium heptafluorobutyrate to fully functionalize the perovskite surface. Sodium heptafluorobutyrate acts as an ion shield that tunes the perovskite surface work function and increases the defect formation energy, resulting in an improved interface with the electron transport layer that minimizes recombination and boosts electron extraction under operation. We find that a sodium-heptafluorobutyrate-functionalized perovskite surface promotes a uniform, compact C ₆₀ layer that effectively blocks ion diffusion and stabilizes the device stack. This approach allows p–i–n perovskite solar cells to achieve a record power conversion efficiency (PCE) of 27.02% (certified 26.96% with a maximum-power-point-tracking PCE of 26.61%). Devices with an active area of 1 cm ² deliver a PCE of 25.95%. Perovskite solar cells retain 100% of their initial efficiency following 1,200 h of continuous 1-sun illumination at the maximum power point. Devices also demonstrate exceptional thermal stability, retaining 92% of the initial PCE when ageing at 85 °C for 1,800 h and 94% after 200 thermal cycles between –40 °C and +85 °C.

Fluoride‐contaminated drinking waters are known to cause severe health hazards such as fluorosis and arthritis. This paper presents the encapsulation of iron oxide nanoparticles in kaolin‐bentonite composites adsorbents (KBNPs) for the removal of fluoride from drinking water by adsorption compared with kaolin‐bentonite composite (KB). Adsorbents with an average weight of ∼200 mg and ∼7 mm diameter (granules) were prepared in the ratio of 10 : 10 : 0.1 for kaolinite, bentonite, and magnetite nanoparticles, respectively. The granules were air‐dried and calcined at 750°C and contacted with 2 mg/L sodium fluoride solution at varying time periods. The adsorbents were characterized using Fourier transform infrared spectroscopy (FTIR), scanning electron microscopy (SEM) formulation, and Brunauer–Emmett–Teller (BET), whereas the adsorption mechanism and the kinetics were explained using the Langmuir isotherm, Freundlich models, and pseudo‐first‐order and pseudo‐second‐order models. The results showed that the BET surface areas for the granules were 10 m²/g and 3 m²/g for KBNPs and KB, respectively. The SEM images for the adsorbents before and after adsorption confirm the plate‐like morphology of kaolin and bentonite. The FTIR analyses of bentonite (3550 cm⁻¹–4000 cm⁻¹) and kaolin (400–1200 cm⁻¹) correspond to the structural hydroxyl groups and water molecules in the interlayer space of bentonites and the vibrational modes of SiO₄ tetrahedron of kaolin, respectively. The KBNPs composites also recorded a fluoride removal efficiency of ∼91% after 120 minutes compared with 64% for KB composites without Fe₃O₄ nanoparticles. The adsorptions of fluoride by the KBNPs and KB granules were found to agree with the Freundlich isotherm and a pseudo‐second‐order kinetic model, respectively. The results clearly show that the impregnation of clays with magnetite nanoparticles has significant effect in the removal of fluoride, and the implication of the results has been discussed to show the impact of clay‐magnetite nanoparticles composites in the removal of fluoride from contaminated water.

The aim of the work is to improve the release properties of curcumin onto human breast cancer cell lines using coated halloysite nanotubes (HNTs) with chitosan as a polycation. A loading efficiency of 70.2% (w/w) was attained for loading 4.9 mg of the drug into 0.204 g bed volume of HNTs using the vacuum suction method. Results acquired from Brunauer-Emmett-Teller (BET), Fourier-transform infrared (FTIR) spectroscopy, transmission electron microscopy (TEM), scanning electron spectroscopy (SEM), zeta potential, and thermogravimetric analysis (TGA) indicated the presence of the drug and the biopolymer in and around the nanotubes. The release properties of drug-loaded HNTs (DLHNTs) and chitosan-coated drug-loaded HNTs (DLHNTs-CH) were evaluated. The release percentages of DLHNTs and DLHNTs-CH after 6 h were 50.7 and 37%, respectively. Based on the correlation coefficients obtained by fitting the release nature of curcumin from the two samples, the Korsmeyer-Peppas model was found to be the best-fitted model. In vitro cell viability studies were carried out on the human breast cancer cell line MCF-7, using the MTT and trypan blue exclusion assays. Prior to the Trypan blue assay, the IC₅₀ of curcumin was determined to be $~$30 µM. After 24 h of incubation, the recorded cell viability values were 94, 68, 57, and 51% for HNTs, DLHNTs-CH, DLHNTs, and curcumin, respectively. In comparison to the release studies, it could be deducted that sustained lethal doses of curcumin were released from the DLHNTs-CH within the same time. It is concluded from this work that the “burst release” of naked drugs could be slowly administered using chitosan-coated HNTs as potential drug carriers.

Stability issues could prevent lead halide perovskite solar cells (PSCs) from commercialization despite it having a comparable power conversion efficiency (PCE) to silicon solar cells. Overcoming drawbacks affecting their long‐term stability is gaining incremental importance. Excess lead iodide (PbI₂) causes perovskite degradation, although it aids in crystal growth and defect passivation. Herein, we synthesized functionalized oxo‐graphene nanosheets (Dec‐oxoG NSs) to effectively manage the excess PbI₂. Dec‐oxoG NSs provide anchoring sites to bind the excess PbI₂ and passivate perovskite grain boundaries, thereby reducing charge recombination loss and significantly boosting the extraction of free electrons. The inclusion of Dec‐oxoG NSs leads to a PCE of 23.7 % in inverted (p‐i‐n) PSCs. The devices retain 93.8 % of their initial efficiency after 1,000 hours of tracking at maximum power points under continuous one‐sun illumination and exhibit high stability under thermal and ambient conditions.

Annealing is one of the processing methods that are used for the fabrication of defect-free, photoactive perovskite films with compact grains in highly efficient and stable perovskite solar cells (PSCs). Thus, the annealing temperature is a key parameter for the control of the interdiffusion (of constituent elements) in photoactive films. In this paper, we present the results of a systematic study of the effects of annealing on the interdiffusion of constituent elements in efficient formamidinium-based PSCs. We also explore the effects of annealing-induced interdiffusion on layer microstructures, local strains, and the optoelectronic properties of perovskite films. We observe a dramatic upward diffusion of tin (Sn) and titanium (Ti) from fluorine-doped tin oxide and titanium dioxide (TiO₂) to the perovskite films. We also observe a downward diffusion of lead (Pb) and iodine (I) from the perovskite films to the mesoporous layer of the electron transporting layer (ETL), after annealing at temperatures between 100 and 150 °C. The diffused I substitutes for Ti in the ETL, which improves the optoelectronic properties of the films, for annealing temperatures between 100 and 130 °C. The annealing-induced interdiffusion that occurs at higher temperatures (between 140 and 150 °C) results in higher levels of interdiffusion, along with increased local strains that lead to the nucleation of pores and cracks. Finally, the implications of the results are discussed for the design of PSCs with improved photoconversion efficiencies and stability.