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Subject: membrane ×

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    Ultrathin positively charged electrode skin for durable anion-intercalation battery chemistries
    ([London] : Nature Publishing Group UK, 2023) Sabaghi, Davood; Wang, Zhiyong; Bhauriyal, Preeti; Lu, Qiongqiong; Morag, Ahiud; Mikhailovia, Daria; Hashemi, Payam; Li, Dongqi; Neumann, Christof; Liao, Zhongquan; Dominic, Anna Maria; Nia, Ali Shaygan; Dong, Renhao; Zschech, Ehrenfried; Turchanin, Andrey; Heine, Thomas; Yu, Minghao; Feng, Xinliang
    The anion-intercalation chemistries of graphite have the potential to construct batteries with promising energy and power breakthroughs. Here, we report the use of an ultrathin, positively charged two-dimensional poly(pyridinium salt) membrane (C2DP) as the graphite electrode skin to overcome the critical durability problem. Large-area C2DP enables the conformal coating on the graphite electrode, remarkably alleviating the electrolyte. Meanwhile, the dense face-on oriented single crystals with ultrathin thickness and cationic backbones allow C2DP with high anion-transport capability and selectivity. Such desirable anion-transport properties of C2DP prevent the cation/solvent co-intercalation into the graphite electrode and suppress the consequent structure collapse. An impressive PF6−-intercalation durability is demonstrated for the C2DP-covered graphite electrode, with capacity retention of 92.8% after 1000 cycles at 1 C and Coulombic efficiencies of > 99%. The feasibility of constructing artificial ion-regulating electrode skins with precisely customized two-dimensional polymers offers viable means to promote problematic battery chemistries.
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    Fluorescence Microscopy of the HIV-1 Envelope
    (Basel : MDPI, 2020) Carravilla, Pablo; Nieva, José L.; Eggeling, Christian
    Human immunodeficiency virus (HIV) infection constitutes a major health and social issue worldwide. HIV infects cells by fusing its envelope with the target cell plasma membrane. This process is mediated by the viral Env glycoprotein and depends on the envelope lipid composition. Fluorescent microscopy has been employed to investigate the envelope properties, and the processes of viral assembly and fusion, but the application of this technique to the study of HIV is still limited by a number of factors, such as the small size of HIV virions or the difficulty to label the envelope components. Here, we review fluorescence imaging studies of the envelope lipids and proteins, focusing on labelling strategies and model systems.