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The heat effect of nonthermal plasma significantly enhanced the synergy between the plasma and the catalytically active sites. Consequently, nearly 100% NH₃decomposition was achieved over the low-loading Ru/Al₂O₃catalyst under adiabatic conditions. 

This work demonstrates a series of functionalization methods to enhance the utility of thermoplastic-elastomer derived ordered mesoporous carbons, including chemical activation, heteroatom doping, and the introduction of nanoparticles. 

Degradable epoxy-amine thermosets derived from cyclic-ketal monomers offer robust performance and facile end-of-use processing, enabling recovery of diketone building blocks and pristine carbon fiber from fiber reinforced polymer composites. 

Abstract Dimethylammonium lead iodide (DMAPbI_x) has the potential to address the phase stability issue of inorganic perovskite solar cells (PSCs). In this study, the crystallinity, phase structure, defect states, and crystal growth habits of DMAPbI_xare controlled by adjusting thexvalue during synthesis, where N,N‐dimethylacetamide (DMAC) is used as the solvent to regulate perovskite film growth. Furthermore, large‐area CsPbI_2.85Br_0.15perovskite films with preferred oriented growth are achieved using the optimizedxvalue in DMAPbI_xthrough the slot‐die coating method. The inorganic PSCs, with a n‐i‐p structure and the active area of 0.04 cm², achieve a champion power conversion efficiency (PCE) of 19.82%, with an open‐circuit voltage (V_oc) of 1.16 V based on perovskite films formed by slot‐die coating. This work provides important insights into the DMAPbI_x‐based method for fabricating high‐quality inorganic perovskite films, and paves the way for large‐area inorganic PSCs fabrication for practical applications. 

Abstract The optimal selection of alkyl chains and halogen ions in ammonium salts for addressing specific defect types in perovskite films remains unclear, although ammonium salts emerged as a promising strategy to enhance the performance of perovskite solar cells (PSCs). Herein, four ammonium salts are introduced with different alkyl chain types and halogen ions to passivate perovskite films. Branched‐alkyl chain ammonium salts exhibited superior passivation effects compared to linear‐alkyl chain salts, with the alkyl chain structure having a more significant impact on device performance than the halogen ion component. In addition, DFT calculations are performed to investigate which defect types in perovskite films are most effectively passivated by different alkyl chain types and halogen ions in ammonium salts. Branched‐alkyl chain ammonium salts demonstrated superior passivation effects on V_Pband V_FAdefects in perovskite films compared to linear‐alkyl chain salts, while exhibiting similar passivation effects for V_Idefects. PSCs passivated with tert‐OAI achieved an impressive efficiency of 25.49%, with a V_ocof 1.19 V, a J_scof 25.40 mA cm⁻², and an FF of 84.34%. This work highlights a targeted ammonium salt passivation strategy tailored to address different defect types in perovskite films, accounting for variations in perovskite composition and fabrication environments.