Scientific publications

Herein, a rapid electrochemical approach for testing of yeast cells damage using hydrogen peroxide spiking and Pd-NPs-based electrodes was proposed. The approach is based on the analyzing of electrochemical interactions between the droplets of yeast suspension spiked with hydrogen peroxide solutions (H2O2) and the surface of screen printed electrode modified by palladium nanoparticles (Pd-NPs). For the intact cells the characteristic anodic electrochemical signal recorded at 0.28 – 0.3 V remains at a constant level due to self-regulation processes regardless the spiked amount of hydrogen peroxide. In contrast, the increase of the anodic current corresponding to the added H2O2 concentration reflects the damage of yeast cells. Significantly, by introduction of peroxide-sensitive oxidoreductase in the design of Pd-NPs, which led to the formation of hybrid oxidoreductase-Pd-NPs electrodes, it was possible to modify the electrochemical read-out of the proposed approach.

Lithium-ion batteries are constantly developing as the demands for power and energy storage increase. One promising approach to designing high-performance lithium-ion batteries is using conversion/alloying materials, such as SnO2. This class of materials does, in fact, present excellent performance and ease of preparation; however, it suffers from mechanical instabilities during cycling that impair its use. One way to overcome these problems is to prepare composites with bi-dimensional materials that stabilize them. Thus, over the past 10 years, two-dimensional materials with excellent transport properties (graphene, MXenes) have been developed that can be used synergistically with conversion materials to exploit both advantages. In this work, a 50/50 (by mass) SnO2/Ti3C2Tz nanocomposite is prepared and optimized as a negative electrode for lithium-ion batteries. The nanocomposite delivers over 500 mAh g−1 for 700 cycles at 0.1 A g−1 and demonstrates excellent rate capability, with 340 mAh g−1 at 8 A g−1. These results are due to the synergistic behavior of the two components of the nanocomposite, as demonstrated by ex situ chemical, structural, and morphological analyses. This knowledge allows, for the first time, to formulate a reaction mechanism with lithium-ions that provides partial reversibility of the conversion reaction with the formation of SnO.

High-performance electrochemical applications have expedited the research in high-power devices. As such, supercapacitors, including electrical double-layer capacitors (EDLCs) and pseudocapacitors, have gained significant attention due to their high power density, long cycle life, and fast charging capabilities. Yet, no device lasts forever. It is essential to understand the mechanisms behind performance degradation and aging so that these bottlenecks can be addressed and tailored solutions can be developed. Herein, the factors contributing to the aging and degradation of supercapacitors, including electrode materials, electrolytes, and other aspects of the system, such as pore blocking, electrode compositions, functional groups, and corrosion of current collectors are examined. The monitoring and characterizing of the performance degradation of supercapacitors, including electrochemical methods, in situ, and ex situ techniques are explored. In addition, the degradation mechanisms of different types of electrolytes and electrode materials and the effects of aging from an industrial application standpoint are analyzed. Next, how electrode degradations and electrolyte decompositions can lead to failure, and pore blocking, electrode composition, and other factors that affect the device's lifespan are examined. Finally, the future directions and challenges for reducing supercapacitors' performance degradation, including developing new materials and methods for characterizing and monitoring the devices are summarized.

Solvent engineering is a powerful and versatile method to tune colloidal stability. Here, we link the molecular structure of apolar ligand shells on gold nanoparticles with their colloidal stability in solvent mixtures. The agglomeration temperature of the particles was measured with small-angle X-ray scattering. It depended on solvent composition and changed linearly for hexane–hexadecane mixtures, but nonlinearly for cyclohexane–hexadecane and hexanol–hexadecane mixtures. Molecular dynamics (MD) simulations indicate that agglomeration is dominated by temperature-dependent ligand order in the alkane mixtures and that the temperature at which the ligand shell orders depends on the solvent composition near the ligands, which can differ substantially from the bulk composition. Small-angle neutron scattering confirmed that, at intermediate solvent compositions above the agglomeration temperature, the fraction of cyclohexane near the ligands was larger than in the bulk. The enrichment of cyclohexane near the ligands stabilized their disordered state, which, consequently, led to the experimentally observed nonlinear trend of the agglomeration temperature. In contrast, hexanol was depleted from the ligand shell at all temperatures. This again stabilized the disordered state. Furthermore, we found that agglomeration at high hexanol fractions was driven by a solvophobic effect that exceeded the influence of ligand order. The results show that strong nonlinearities in the colloidal stability of nanoparticle dispersions in solvent mixtures are directly linked to the molecular details of ligand–solvent and solvent–solvent interactions, which can be used to precisely tune stability.

Supercapacitors are highly valued energy storage devices with high power density, fast charging ability, and exceptional cycling stability. A profound understanding of their charging mechanisms is crucial for continuous performance enhancement. Electrochemical quartz crystal microbalance (EQCM), a detection means that provides in situ mass change information during charging–discharging processes at the nanogram level, has received greatly significant attention during the past decade due to its high sensitivity, non-destructiveness and low cost. Since being used to track ionic fluxes in porous carbons in 2009, EQCM has played a pivotal role in understanding the charging mechanisms of supercapacitors. Herein, we review the critical progress of EQCM hitherto, including theory fundamentals and applications in supercapacitors. Finally, we discuss the fundamental effects of ion desolvation and transport on the performance of supercapacitors. The advantages and defects of applying EQCM in supercapacitors are thoroughly examined, and future directions are proposed.

Additive manufacturing enables the fabrication of bio-inspired materials possessing intricate architectures across broad length scales leading to systems that are simultaneously stiff, tough, and lightweight. A digital light processing (DLP) strategy was used to additively manufacture polymer foams with controlled porosity through the incorporation of thermally expandable microspheres. Following initial photopolymerization, a subsequent thermal processing step reproducibly allows access to a broad range of foam densities. Using uniaxial compression, we investigated how foaming impacts the mechanics of the composite material, including modulus, Poisson’s ratio, and energy dissipation. It was observed that the 3D-printed foams are remarkably resilient under cyclic loading, with sustained values of both modulus and energy dissipation under repeated loading at large deformations.

Actin-based motility is a complex process in which the actin-polymerization is the primary force-generating motor machinery. It can produce protrusive forces through actin filaments polymerization and cross-link during lamellipodia protrusion in migrating cells and it is responsible for the intracellular motion of certain pathogens in infected host cells. We propose a multi-physics model for actin-based motility, stemming from continuity equations that account for the actin chemical kinetics. Thermodynamic restrictions are identified, moving from the multiplicative decomposition of the deformation gradient into chemical and elastic parts. Constitutive theory and chemical kinetics are prescribed to finally write governing equations for the multi-physics problem. The field equations are solved numerically with the finite element method. As a proof of concept, a one-dimensional model for actin-based motility of bacteria pathogens is studied.

Current environmental challenges and the shrinking fossil-fuel feedstock are important criteria for the next generation of polymer materials. In this context, we present a fully bio-based material, which shows promise as a thermoplastic elastomer (TPE). Due to the use of β-farnesene and L-lactide as monomers, bio-based feedstocks, namely sugar cane and corn, can be used. A bifunctional initiator for the carbanionic polymerization was employed, to permit an efficient synthesis of ABA-type block structures. In addition, the “green” solvent MTBE (methyl tert-butyl ether) was used for the anionic polymerisation, enabling excellent solubility of the bifunctional anionic initiator. This afforded low dispersity (Đ=1.07 to 1.10) and telechelic polyfarnesene macroinitiators. These were employed for lactide polymerization to obtain H-shaped triblock copolymers. TEM and SAXS revealed clearly phase-separated morphologies, and tensile tests demonstrated elastic mechanical properties. The materials featured two glass transition temperatures, at – 66 °C and 51 °C as well as gyroid or cylindrical morphologies, resulting in soft elastic materials at room temperature.

There are no targeted therapies for patients with triple-negative breast cancer (TNBC). TNBC is enriched in breast cancer stem cells (BCSC), which play a key role in metastasis, chemoresistance, relapse, and mortality. γδ T cells hold great potential in immunotherapy against cancer and might provide an approach to therapeutically target TNBC. γδ T cells are commonly observed to infiltrate solid tumors and have an extensive repertoire of tumor-sensing mechanisms, recognizing stress-induced molecules and phosphoantigens (pAgs) on transformed cells. Herein, we show that patient-derived triple-negative BCSCs are efficiently recognized and killed by ex vivo expanded γδ T cells from healthy donors. Orthotopically xenografted BCSCs, however, were refractory to γδ T-cell immunotherapy. We unraveled concerted differentiation and immune escape mechanisms: xenografted BCSCs lost stemness, expression of γδ T-cell ligands, adhesion molecules, and pAgs, thereby evading immune recognition by γδ T cells. Indeed, neither promigratory engineered γδ T cells, nor anti–PD-1 checkpoint blockade, significantly prolonged overall survival of tumor-bearing mice. BCSC immune escape was independent of the immune pressure exerted by the γδ T cells and could be pharmacologically reverted by zoledronate or IFNα treatment. These results pave the way for novel combinatorial immunotherapies for TNBC.

The cathode material NaFePO of sodium-ion batteries exhibits complex phase segregation thermodynamics with the existence of an intermediate phase, and large volume change during (dis)charging. A virtual multiscale modeling chain is established to construct a 3D anisotropic electro-chemo-mechanical phase-field model based on first-principles calculations for NaFePO, which considers phase changes, electrochemical reactions, anisotropic diffusion, anisotropic misfit strain, and anisotropic elasticity, as well as the concentration-dependence of the elasticity tensor. The elastic properties of NaFePO are determined by first-principles for the first time. We investigate how surface reaction kinetics and crystal anisotropy influence the full 3D microstructure evolution, with results that include phase evolution, interface morphology, and stress evolution in NaFePO particles. We find that the existence of 1D Na diffusion channels leads to a kinetically arrested state of single wave propagation along [010]. Furthermore, defect-actuated in-plane diffusion induces low-energy single wave propagation along [100] controlled by the concentration dependent anisotropic elasticity tensor. In addition, the morphology of the double wave propagation along [010] is more prone to particle cracking and mechanical degradation. Beyond NaFePO, the findings of this work point towards opportunities to engineer desired phase behavior with better mechanical stability by defect-actuated out-of-1D diffusion of an intercalation electrode material.