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Our recent publication in Chem. Eur. J. 2022, 28, e202104341 has inspired Prof. Peter B. Crowley (P.C.) to write a Correspondence questioning the presented concept of electrostatic self-assembly. The offered criticism is twofold: 1) the role of the cationic pillar[5]arene macrocycle to act as molecular glue in the formation of electrostatically driven protein assemblies is questioned by arguing that the pillararene is not incorporated into the frameworks. 2) Later, P.C. speculates that when the frameworks form, the role of electrostatic interactions is not firmly established and cation-pi bonding is the more plausible interaction. In this response, the raised comments are addressed. We present direct experimental NMR evidence showing that the pillar[5]arene is incorporated into the frameworks. Furthermore, we discuss the electrostatic self-assembly and our ferritin-related research line more broadly and clarify the role of key experiments.
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http://dx.doi.org/10.1002/chem.202202022 | DOI Listing |
J Colloid Interface Sci
September 2025
Ministry-of-Education Key Laboratory for the Green Preparation and Application of Functional Materials, Hubei Key Laboratory of Polymer Materials, School of Materials Science & Engineering, Hubei University, Wuhan 430062, PR China. Electronic address:
Effective removal of ethylene (CH) during fruit and vegetables storage and transport remains a critical challenge for post-harvest preservation. Although S-scheme heterojunctions can improve charge separation and redox capacity for ethylene degradation, their efficiency is still restricted by limited carrier transfer and sluggish oxygen activation. Here, we rationally designed a novel 2D/2D SnNbO/BiMoO monolayer S-scheme heterojunction integrated with Pt co-catalyst to address these limitations.
View Article and Find Full Text PDFLangmuir
September 2025
School of Light Industry Science and Engineering, Beijing Technology and Business University, Beijing 100048, People's Republic of China.
The study of the self-assembly of surfactants in aqueous solutions, though a traditional field, remains fascinating and full of novelty. In this article, the anionic perfluorodecanoic acid surfactant (PFA) is separately complexed with three hydroxyalkylamines (monoethanolamine (MEA), diethylamine (DEA), and triethanolamine (TEA)) in aqueous solutions. The transformation of aggregate morphologies from spherical unilamellar to nanotubes and then to spherical bilamellar is observed at room temperature, which is confirmed by cryo-transmission electron microscopy (cryo-TEM).
View Article and Find Full Text PDFJ Colloid Interface Sci
September 2025
College of Chemistry & Chemical Engineering, Yan'an University, Shaanxi Key Laboratory of Chemical Reaction Engineering, Yan'an 716000, China. Electronic address:
Hydrogen evolution reaction (HER) driven by solar energy has attracted considerable attention due to its outstanding efficiency, environmental compatibility, and sustainability. Regrettably, the sluggish progress of the HER and the limitations in charge separation efficiency impede its practical photocatalysis. Herein, a two-step electrostatic self-assembly approach is adopted to construct NiO/CdMnS/TiCT (NO/CMS/TCT) ternary heterojunction with bidirectional carrier channels for boost photogenerated separation and oriented carrier accumulation.
View Article and Find Full Text PDFAdv Colloid Interface Sci
August 2025
Institute of Mechanics, Moscow State University, Moscow 119192, Russia.
CO₂ geological utilization and storage involve complex multiphase interfacial behaviors that significantly influence the overall efficiency. Recently, bio-based materials have attracted increasing attention as promising candidates for interfacial regulation owing to their structural diversity, abundance, and environmental compatibility. This review summarizes recent advances in utilizing biomass-derived materials to regulate interfacial behaviors in subsurface multiphase systems.
View Article and Find Full Text PDFProc Natl Acad Sci U S A
September 2025
Department of Chemical and Biomolecular Engineering, Samueli School of Engineering, University of California, Irvine, CA 92697.
Charge and energy transport within living systems are fundamental processes that enable the autonomous function of excitable cells and tissues. To date, localized control of these transport processes has been enabled by genetic modification approaches to render light sensitivity to cells. Here, we present peptidic nanoassemblies as constituents of a cardiac biomaterial platform that leverages complementary sequence interactions to direct photoinduced energy transport at the cellular interface.
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