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The Institute of Problems of Chemical P... Publications | LitMetric

6 results match your criteria: "The Institute of Problems of Chemical Physics RAS[Affiliation]"

This work demonstrates an easy and cost-effective synthesis of PANI-PPY conducting nanoflakes (NFs) with a self-healing capability. Scanning electron microscopic (SEM) analysis shows the minimum width of NFs as 30 nm, while HRTEM analysis confirms the shape, size, and semi-crystalline nature of the polymer. These PANI-PPY NFs were used to fabricate a contact separation mode triboelectric nanogenerator (TENG) based self-powered photosensor which gave the maximum output voltage (149 V), maximum output current (16 µA), current density 0.

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Triboelectric nanogenerators (TENGs) as a revolutionary system for harvesting mechanical energy have demonstrated high vitality and great advantage, which open up great prospects for their application in various areas of the society of the future. The past few years have seen exponential growth in many new classes of self-healing polymers (SHPs) for TENGs. This review presents and evaluates the SHP range for TENGs, and also attempts to assess the impact of modern polymer chemistry on the development of advanced materials for TENGs.

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Self-healing and shape memory metallopolymers: state-of-the-art and future perspectives.

Dalton Trans

March 2020

Laboratory of Metallopolymers, The Institute of Problems of Chemical Physics RAS, Academician Semenov avenue 1, Chernogolovka, Moscow Region, 142432 Russian Federation.

Metallopolymers (MPs) or metal-containing polymers have shown great potential as self-healing and shape memory materials due to their unique characteristics, including universal architectures, composition, properties and surface chemistry. Over the past few decades, the exponential growth of many new classes of MPs that deal with these issues has been demonstrated. This review presents and assesses the latest achievements and problems associated with the use of MPs as self-healing and shape memory materials.

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Solvation of anions in acetonitrile solutions: FTIR and quantum chemical study for Br, ClO, AsF, and CFSO.

Spectrochim Acta A Mol Biomol Spectrosc

March 2020

Institute of Solid State Chemistry UB RAS, Pervomaiskaya st., 91, Ekaterinburg 620990, Russia; NTI Competence Center for New and Mobile Power Sources Technologies of the Institute of Problems of Chemical Physics RAS, Academician Semenov av. 1, Chernogolovka, Moscow region 142432, Russia. Electronic address:

Anion solvation in acetonitrile solutions was comparatively studied using FTIR spectroscopy and quantum chemical calculations at the RTF + MP2/6-311G** level of theory with solvation model density (SMD) corrections. Infrared spectra for all stable anionic complexes X(CHCN) (where X = Br (monatomic halide), ClO (polyatomic tetrahedral), AsF (polyatomic octahedral), CFSO (polyatomic ethane-like) and n = 1-8) were calculated and subsequently used in the analysis of the FTIR spectra of (BuN)X and LiX acetonitrile solutions across a wide range of concentrations. Spectroscopic manifestations of solvation were established for all X examined.

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Metallopolymers (MPs) or metal-containing polymers have shown great potential as new drug delivery systems (DDSs) due to their unique properties, including universal architectures, composition, properties and surface chemistry. Over the past few decades, the exponential growth of many new classes of MPs that deal with these issues has been demonstrated. This review presents and assesses the recent advances and challenges associated with using MPs as DDSs.

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Synthetic methodologies and spatial organization of metal chelate dendrimers and star and hyperbranched polymers.

Dalton Trans

August 2017

Laboratory of Metallopolymers, The Institute of Problems of Chemical Physics RAS, Academician Semenov avenue 1, Chernogolovka, Moscow Region, 142432 Russian Federation.

The synthetic methodologies, physico-chemical peculiarities, properties, and structure of metal chelate dendrimers and star and hyperbranched polymers are considered. These compounds are subdivided into molecular, intracomplex, and macrocyclic types which in turn are classified depending on the nature of the donor atoms (N,N-, N,O-, N,S-, O,O-, O,S-, S,S-, P,P-chelates, etc.).

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