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Ярославцев Андрей Борисович

Базовая кафедра неорганической химии и материаловедения Института общей и неорганической химии им. Н.С. Курнакова РАН

Профиль на hse.ru ↗ тел.: 23530
Публикаций
90
Языков
1
Наград
8
Конференций
1
Профиль Публикации (90) Курсы (6)

Профессиональные интересы

мембраныИонная проводимость

Должности

  • Заведующий кафедрой — Базовая кафедра неорганической химии и материаловедения Института общей и неорганической химии им. Н.С. Курнакова РАН
  • Профессор — Базовая кафедра неорганической химии и материаловедения Института общей и неорганической химии им. Н.С. Курнакова РАН
  • Академический директор — Аспирантская школа по химии

Био

  • · Начал работать в НИУ ВШЭ в 2009 году.
  • · Научно-педагогический стаж: 33 года.

Образование

  • 2006 · Член-корреспондент РАН
  • 1995 · Ученое звание: Профессор
  • 1995 · Доктор наук
  • 1978 · Специалитет: Московский государственный университет им. М.В. Ломоносова, специальность «Химия», квалификация «Химик»

Опыт работы

  • · 1994-2018: Институт общей и неорганической химии РАН им. Н.С. Курнакова:
  • · Ведущий научный сотрудник, Заведующий сектором, Заведующий лабораторией, Главный научный сотрудник
  • · 2010-2018: Институт нефтехимического синтеза РАН им. А.В. Топчиева:
  • · Заведующий лабораторией
  • · 1997-2009: Российский фонд фундаментальных исследований:
  • · Начальник отдела, Ответственный секретарь
  • · 1994-2018: Российский химико-технологический университет им. Д.И.Менделеева:
  • · Профессор
  • · 2009-2018: Московский государственный университет им. М.В.Ломоносова:
  • · Младший научный сотрудник, ассистент, доцент, профессор

Награды и поощрения

  • · Почетная грамота НИУ ВШЭ (март 2026)
  • · Благодарность НИУ ВШЭ (март 2024)
  • · Медаль Ордена "За заслуги перед Отечеством" II степени (февраль 2024)
  • · Благодарность Факультета химии НИУ ВШЭ (февраль 2023)
  • · Благодарственное письмо проректора НИУ ВШЭ (ноябрь 2021)
  • · Надбавка за публикацию в журнале из Списка А (и приравненном к нему научном издании) (2025–2026, 2024–2025, 2023–2024)
  • · Надбавка за публикацию в международном рецензируемом научном издании (2022–2023, 2021–2022, 2019–2020)
  • · Лучший преподаватель — 2025

Гранты и проекты

  • — · на соискание учёной степени кандидата наук

Конференции (1)

Показать все
  • · 2018: 14th International Conference “Fundamental problems of solid state ionics” (Черноголовка). Доклад: Ion transport in composite membranes based on polybenzimidazoles and silica with modified surface

Идентификаторы исследователя

  • ORCID: 0000-0001-8446-6198
  • ResearcherID: C-2070-2013
  • SPIN РИНЦ: 8429-8844
  • Scopus AuthorID: 7005239278

Публикации (90)

Perfluorosulfonic acid polymer membrane with increased chemical stability for hydrogen-air fuel cell

2025 · ARTICLE · en

One of the key tasks of hydrogen energy development is to obtain chemically stable proton exchange polymer membranes with high proton conductivity. This article presents the results on the investigation of the stabilization of proton-conducting membranes with a Nafion®-type structure using modification by fluorine. The membranes examined in this study exhibited high thermal stability and mechanical properties that are comparable to those of commercial membranes. The water uptake and proton conductivity of the recast perfluorosulfonic acid membranes exceed those of the commercial Nafion®212 membrane. The conductivity of the obtained membranes was found to be 4.25 mS/cm at a relative humidity (RH) of 50 % at 30 °C. The maximum power density of membrane-electrode assemblies based on the obtained membranes is 20 % higher than that based on Nafion®212. The results of this study demonstrate that fluorination can significantly improve the stability of the proton-conducting membranes under hydrogen-air fuel cell operating conditions.

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Composite cathodes containing g-sulfur and reduced graphene oxide for lithium–sulfur batteries

2025 · ARTICLE · en

A sulfur–reduced graphene oxide (rGO) composite was investigated as a cathode material for lithium–sulfur batteries. The cathode material containing both monoclinic (g-S) and orthorhombic (a-S) sulfur and rGO exhibits excellent electrochemical performance. The discharge capacity of (a+g)S@rGO in Li–S battery at C/8 is 950 and 620 mAh g−1 for cycles 1 and 20, respectively. © 2025 Mendeleev Communications.

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Effect of Composition of Low-Molecular-Weight Plasticizers on the Properties of Gel Polymer Electrolytes for Lithium Metal Batteries Based on Composite Membrane Nafion and Sulfonated Zirconia

2025 · ARTICLE · en

Modern studies in the field of lithium metal batteries focus on the development of safe and stable electrolytes with high ionic conductivity and electrochemical stability. In this context, promising materials are gel polymer electrolytes based on perfluorosulfonic acid cation-exchange membranes modified with inorganic fillers and solvated with aprotic solvents. This study addresses Nafion® composite membranes containing surface-sulfonated zirconia (sZrO2) and solvated with binary mixtures of ethylene carbonate (EC) with dimethylacetamide (DMAc), dimethylformamide (DMF), and dimethyl sulfoxide (DMSO) at a 1 : 1 ratio by volume. The presented systems demonstrate the dependence of ionic conductivity on the nature of the solvent, following the series: EC–DMAc > EC–DMF > EC–DMSO, with the maximum conductivity (2.2 mS/cm at 25°C) being achieved for the Nafion@sZrO2–EC–DMAc composition. The resulting electrolytes are electrochemically stable up to 4.2 V (vs. to Li+/Li), which makes them compatible with cathode materials such as LiFePO4 (LFP). However, DMSO slowly interacts with lithium metal to form a low-conductivity SEI layer, whereas EC–DMAc and EC–DMF systems provide stable operation of Li|Li cells for >1000 h at a current density of 0.1 mA/cm2. Cyclic tests of Li|LFP cells with Nafion@sZrO2–EC–DMAc and Nafion@sZrO2–EC–DMF electrolytes show an initial discharge capacity of ∼155 mA h/g (0.1C) and high stability—capacity loss after 50 cycles at 0.5C is 4.7 and 2.0%, respectively. The obtained results confirm the potential of using Nafion®-based composite gel polymer electrolytes solvated with amide solvents in new generation lithium metal batteries.

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Anion-Exchange Membranes Based on Cardo Polybenzimidazole and Zinc Ions for Selective Extraction of Monovalent Ions by Electrodialysis

2025 · ARTICLE · en

Abstract: Anion-exchange membranes based on cardo polybenzimidazole and zinc(II) ions with various molar ratios of metal ions (0, 0.05, 0.25, 0.50, and 1.00) were prepared by casting solutions of metal–polymer complexes. The introduction of zinc(II) ions into the structure of cardo polybenzimidazole is accompanied by the formation of a cross-linked polymer matrix due to the coordination of metal ions to the pyridine nitrogen atoms of the monomer unit (–N=) and the appearance of anion-conducting properties. Increasing the metal content leads to an increase in the ionic conductivity of the membranes in the nitrate form from 1.8 × 10–8 to 8.3 × 10–6 S/cm. It is shown that the obtained materials demonstrate preferential transfer of monovalent anions (chloride, fluoride, nitrate) compared to divalent anions (sulfate) during electrodialysis. The selectivity coefficients reach 9.7 and 14 for chloride–sulfate and nitrate–sulfate pairs, and 5.7 and 9.1 for chloride–fluoride and nitrate–fluoride pairs, respectively. The obtained selectivity coefficient values exceed the corresponding values for the commercial Neosepta AMX anion-exchange membrane. At the same time, long-term cycling of the obtained membranes in galvanostatic mode leads to their degradation with leaching of zinc ions.

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High-Voltage LiCoPO4 Cathode Material for Lithium-Ion Batteries (A Review)

2025 · ARTICLE · en

The state-of-the-art in investigations in the field of cathode materials based on lithium–cobalt double phosphate for lithium-ion rechargeable batteries is surveyed. The specific features of the LiCoPO4 crystal structure, the transfer rate of charge carriers, the main synthetic methods of preparation, and the electrochemical characteristics of LiCoPO4-based cathodes such as discharge capacity, charge–discharge rate, and cyclability are considered. The electrochemical characteristics of lithium-ion batteries based on LiCoPO4 can be considerably improved by using nanosized and composite materials, doping with different cations, and using electrolytes stable at high potentials. The average working potential of LiCoPO4 is ~4.8 V vs. Li/Li+, the discharge capacity at 0.1 С approaches its theoretical value (167 mAh/g).

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An unexpected imidazole-induced porphyrinylphosphonate-based MOF-to-HOF structural transformation leading to the enhancement of proton conductivity

2024 · ARTICLE · en

Post-synthetic modification of proton-conducting metal–organic frameworks (MOFs) by loading small molecules capable of generating protons into pores is an efficient approach for developing a new type of material with improved ionic conductivity. Herein, the synthesis, characterization and proton conductivity of a novel electroneutral MOF based on palladium(II) meso-tetrakis(4-(phosphonatophenyl))porphyrinate, IPCE-1Pd, are reported. The exposure of the obtained framework to imidazole by the diffusion vapor method has surprisingly led to its complete crystal-to-crystal MOF-to-HOF transformation, resulting in the formation of a novel hydrogen-bonded organic framework (HOF) IPCE-1Pd_Im, which is the first example of such kind of structural change among all known MOFs. This modification has led to an almost 25-fold increase in the proton conductivity in comparison with the pristine MOF, reaching up to 6.54 × 10−3 S cm−1 at 85 °C and 95% relative humidity, which is one of the highest values among all known porphyrin-based HOFs.

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Layered P2-type Na2/3Ni1/3Mn2/3O2: conductivity and electrochemical characteristics

2024 · ARTICLE · en

The cathode material of Na2/3Ni1/3Mn2/3O2 composition (NNMO) was obtained by the carbonate coprecipitation followed by solid-phase reaction and characterized by XRD analysis, ICP-MS, electron and impedance spectroscopy. NNMO crystallizes in a P2-type layered hexagonal structure (sp. gr. P63/mmc), consists of spherical agglomerates of ~1 - 3 microns in size, formed from the plate-like primary grains. The particles have the smallest size in the direction of the crystallographic "c" axis. The NNMO ionic conductivity value at room temperature was 1.8*10−4 and 1.3*10−4 S cm−1 when measured perpendicularly and parallel to the compression axis, respectively. The activation energy determined from impedance spectroscopy data was equal to the value of ~21 kJ mol−1. The estimated in dc mode values of electronic conductivity were by 2-3 orders of magnitude less than ionic conductivity. The obtained materials were tested as cathodes in sodium-ion battery cells versus sodium metal. The discharge capacity of NNMO was 160 mAh g−1 and 86 mAh g−1 in the potential range of 1.5-4.0 V and 2.3-4.0 V, respectively (20 mA g−1). NNMO was shown to be stable under cycling in the potential range of 2.3-4.0 V.

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Composite cathode material based on sulfur and microporous carbon for Li–S batteries

2024 · ARTICLE · en

In this work, a new cathode material for lithium-sulfur (Li-S) batteries was developed. Microporous carbon (with predominant pore size ≤1.2 nm) served as both a matrix for sulfur retention and conductive additive. The obtained S/C composite was investigated by X-ray diffraction, low-temperature nitrogen adsorption, scanning electron microscopy, Raman and impedance spectroscopy and tested as cathode in the Li-S battery. Microporous carbon was shown to be capable of adsorbing lithium polysulfides thereby suppressing their migration toward lithium anode. The discharge capacity of the S/C composite at the 1st and 20th cycles in Li-S battery operation was 513 and 421 mAh∙g-1 at a scan rate of 0.1 mV s-1.

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On the analysis of monovalent-ion selectivity of anion-exchange membranes

2024 · ARTICLE · en

The scientific community has shown great interest in the selectivity of anion-exchange membranes (AEMs), particularly regarding their ability to monovalent-ions selective transport. In this work, we have studied the selectivity of an original anion-exchange membrane and a layer-by-layer (LbL) surface-modified membrane in the electrodialysis (ED) desalination of sodium chloride and sodium sulfate mixture in a lab-scale cell. The effect of various experimental factors on the desalination process and the selectivity of the separation of ions with different charges, such as the composition of the concentrate compartment, electrolyte concentrations in the concentrate and diluate compartments (0.004–0.5 M), the specific current value (0.82–9.0 mA/cm2), the desalination time, and the stirring of solution were considered. To explain the observed patterns, diffusion experiments and numerical simulations using the COMSOL® software package were carried out. Our findings demonstrate that the method chosen for conducting the benchmark desalination of a mixture of chlorides and sulfates can significantly affect the values of the selectivity coefficients and the accuracy of their determination for both standard and surface-modified membranes. For the latter, varying the desalination conditions leads to improved P(Cl/SO4) due to modification of up to 40 %.

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Mechanisms of formation and shape control of pentagonal Pd-nanostars and their unique properties in electrocatalytic methanol oxidation and membrane separation of high-purity hydrogen

2024 · ARTICLE · en

Membranes on palladium alloy basis with surface modified by nanoparticles with high catalytic activity are useful in deep hydrogen purification and single-stage process of high-purity hydrogen production. This paper reports the development and improvement of methods for synthesis of Pd-based pentatwinned nanoparticles of strictly specified morphology with certain shapes, facets and composition. The competing effect of surfactants and optimization of the halide ions ratio in solution make it possible to direct a particle growth towards formation of pentatwinned Pd-nanostars. Pd–23%Ag coatings synthesized on the surface showed uniquely high peak current density of up to 238 mA cm−2 in alkaline methanol oxidation reaction. This is due to both increased surface area and greater catalytic activity of nanostars’ facets. A record increase in hydrogen permeability of up to 12.5 mmol s−1 m−2 at 100 °C has been achieved for palladium-silver membranes with modified surface. This indicates an acceleration of sorption/desorption stages. The developed method for controlling morphology of nanoscale coatings opens the way to the production of membrane hydrogen filters, which operate at room temperature.

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Курсы (6)