Reactivity with Water and Bulk Ruthenium Redox of Lithium Ruthenate in Basic Solutions

The reactivity of water with Li-rich layered Li₂RuO₃ and partial exchange of Li₂O with H₂O within the structure is studied under aqueous (electro)chemical conditions. Upon slow delithiation in water over long time periods, micron-sized Li₂RuO₃ particles structurally transform from an O3 structure to an O1 structure with a corresponding loss of 1.25 Li ions per formula unit. The O1 stacking of the honeycomb Ru layers is imaged using high-resolution high-angle annular dark-field scanning transmission electron microscopy, and the resulting structure is solved by X-ray powder diffraction and electron diffraction. In situ X-ray absorption spectroscopy suggests that reversible oxidation/reduction of bulk Ru sites is realized on potential cycling between 0.4 and 1.25 V_RHE in basic solutions. In addition to surface redox pseudocapacitance, the partially delithiated phase of Li₂RuO₃ shows high capacity, which can be attributed to bulk Ru redox in the structure. This work demonstrates that the interaction of aqueous electrolytes with Li-rich layered oxides can result in the formation of new phases with (electro)chemical properties that are distinct from the parent material. This understanding is important for the design of aqueous batteries, electrochemical capacitors, and chemically stable cathode materials for Li-ion batteries.     

Charge Photogeneration in Non-Fullerene Organic Solar Cells: Influence of Excess Energy and Electrostatic Interactions

In organic solar cells, photogenerated singlet excitons form charge transfer (CT) complexes, which subsequently split into free charge carriers. Here, the contributions of excess energy and molecular quadrupole moments to the charge separation process are considered. The charge photogeneration in two separate bulk heterojunction systems consisting of the polymer donor PTB7-Th and two non-fullerene acceptors, ITIC and h-ITIC, is investigated. CT state dissociation in these donor–acceptor systems is monitored by charge density decay dynamics obtained from transient absorption experiments. The electric field dependence of charge carrier generation is studied at different excitation energies by time delayed collection field (TDCF) and sensitive steady-state photocurrent measurements. Upon excitation below the optical gap, free charge carrier generation becomes less field dependent with increasing photon energy, which challenges the view of charge photogeneration proceeding through energetically lowest CT states. The average distance between electron–hole pairs at the donor–acceptor interface is determined from empirical fits to the TDCF data. The delocalization of CT states is larger in PTB7-Th:ITIC, the system with larger molecular quadrupole moment, indicating the sizeable effect of the electrostatic potential at the donor–acceptor interface on the dissociation of CT complexes.     

Tissue Regeneration through Cyber-Physical Systems and Microbots

Tissue engineering is a systematic approach of assembling cells onto a 3D scaffold to form a functional tissue in the presence of critical growth factors. The scaffolding system guides stem cells through topological, physiochemical, and mechanical cues to differentiate and integrate to form a functional tissue. However, cellular communication during tissue formation taking place in a reactor needs to be understood properly to enable appropriate positioning of the cells in a 3D environment. Hence, sensors and actuators integrated with cyber-physical system (CPS) may be able to sense the tissue microenvironment and direct cells/cellular aggregates to an appropriate position, respectively. This can facilitate better cell-to-cell communication and cell–extracellular matrix communication for proper tissue morphogenesis. Advancements are made in the field of smart scaffolds that can morph cells/cellular aggregates after sensing the cellular microenvironment in a desired 3D architecture by providing appropriate cues. Recent scientific developments in the additive manufacturing technology have enabled the fabrication of smart scaffolds to create structural and functional tissue constructs. Sensors/actuators, cyber-systems, smart materials, and additive manufacturing put together is expected to lead to improved tissue-engineered medical products. The present review aims to highlight the possibilities of advancement of BioCPS for tissue engineering and regenerative medicine.     

Identification of chemical species created during γ-irradiation of antioxidant used in polyethylene and polyethylene-co-vinyl acetate multilayer film

With the increasing use of γ-irradiated containers made of multilayer polymeric flexible films for food and biopharmaceutical applications, the possible migration of degradation products of the polymers and their additives is becoming a topic of concern. This article aims at highly reliably identifying the degradation products generated after gamma irradiation and their origin to later on assess their potential harmfulness in single-use containers. In this study, GC–MS is used to identify by-products created by γ-irradiation of primary and secondary antioxidants usually present in polyolefin-based biotechnological single-use materials and to confirm identification relevancy based on the literature survey or standard when available. Degradation pathways are proposed to account for the formation of by-products identified during the study and to list intermediates and other by-products present in too small amounts to be detected and identified accurately in all extractable studies.