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Organic solar cell (OSC) development continues to demonstrate impressive device efficiency improvements. However, the materials synthetic simplicity essential to industrialization remains seriously lacking attention, imparting inferior performance records in low‐cost devices. Hence, low bandgap and completely non‐fused electron acceptors (CNFEAs) having simple molecular structures are investigated herein. In contrast to typically explored fused‐ring acceptors with smaller backbone conformational variations, minimizing the interface recombination sites through a greater extent of localized domains is identified as more critical in CNFEAs, leading to remarkable fill factors (FFs) approaching 75%, among the highest currently realized for low‐cost systems. However, this comes with diminishing charge generation efficiency. The general ternary blend optimization strategy modifying the morphology of host components is limited in preserving such remarkably high FFs. To suppress the trade‐off while keeping notable FFs, a new perspective of constructing functionally bridged components based on optical, electronic, and thermodynamic properties is introduced here. Specifically, charge generation is unrestrained from the host acceptor localized domains through the introduction of a "bridge" component while also taking advantage of the configuration to channel polarons toward the efficient transport moieties of the host components. Accordingly, this work incubates understanding‐guided optimizations toward the advancement of more practical devices. [ABSTRACT FROM AUTHOR]

Rapid population growth and widespread industrialization are the main contributing factors to the increasing contamination of the world's diminishing freshwater resources. This work investigates Fe/TiO2 as an efficient and sustainable photocatalyst for treating organic micropollutants in water. The photocatalysts prepared by these mechanochemical methods used a high-energy ball milling technique to manipulate Fe/TiO2's structural, optical, and catalytic properties for the photo-oxidation of 2,4-Dichlorophenol (2,4-DCP). Doping with iron effectively reduced the band gap of rutile TiO2 from 3 to 2.22 eV. By reducing the ball/powder ratio from 34 to 7, the removal efficiency of 2,4-DCP increased from 65.2 to 84.7%. Measuring the TOC indicated 63.5 and 49.4% mineralization by Fe/TiO2-7 and rutile TiO2, respectively, after 24 h. The energy yields for the Fe/TiO2 and rutile TiO2 were 0.13 and 0.06 g 2,4-DCP/kW h, respectively. [ABSTRACT FROM AUTHOR]

Indoor exposure to volatile organic compounds (VOCs) is detrimental to the health of the occupants, and their removal is crucial in maintaining good air quality. Novel adsorbents prepared by modifying Metal-Organic Frameworks (MOFs), MIL101 (Cr), UiO-66, and UiO-66-NH 2 with [BMIM][CH 3 COO] ionic liquid, were characterized and tested for toluene adsorption. [BMIM][CH 3 COO]/MIL101 performed best with a fast sorption rate, large sorption capacity, and good regenerability. It displays synergistic interactions between the IL and MOF. Adding one weight percent [BMIM][CH 3 COO] to UiO-66 and UiO-66-NH 2 has a synergistic effect with respective 14% and 5% enhancements sorption over calculated values. The strong interactions between IL and UiO-66 and UiO-66-NH 2 , as observed in their thermogravimetric data, results in poor toluene sorption for 10 wt% [BMIM][CH 3 COO] loadings. This work provides a basis for IL modification of MOFs for enhanced sorption of VOCs for air treatment., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2022 Elsevier Inc. All rights reserved.)