ABSTRACT
It is always challenging to integrate multiple functions into one material system. However, those materials/devices will address society's critical global challenges and technological demands if achieved with innovative design strategies and engineering. Here, one such material with a broader spectrum of desired properties appropriate for seven applications is identified and explored, and a glucose-sensing-triggered energy-storage mechanism is demonstrated. To date, the Titanium (Ti)-Zinc (Zn) binary alloys are investigated only as mixed phases and for a maximum of three applications. In contrast, the novel single phase of structurally stable 50 Ti-50 Zn (Ti0.5 Zn0.5 ) is synthesized and proven suitable for seven emerging applications. Interestingly, it is thermally stable up to 750 °C and possesses excellent mechanical, tribological properties and corrosion resistance. While exceptional biocompatibility is evident even up to a concentration of 500 µg mL-1 , the antibacterial activity against E. coli is also seen. Further, rapid detection and superior selectivity for glucose, along with supercabattery behavior, unambiguously demonstrate that this novel monophase is a remarkable multifunctional material than the existing mixed-phase Ti-Zn compounds. The coin-cell supercapacitor shows outstanding stability up to 30 000 cycles with >100% retention capacity. This allows us to prototype a glucose-sensing-triggered energy-storage-device system for wearable point-of-care diagnostic applications.
ABSTRACT
Water vapor in atmosphere is ubiquitous, and it varies according to geographical locations. Various toxic and non-toxic gases co-exist with water vapor/moisture in the atmosphere. This computational study addresses the fact that how those gases interact with water vapor. We have done quantum chemical density functional theory calculations to probe the interaction of certain gases with a finite number of water molecules in gas phase with various functionals/basis sets. An ensemble of 14 gas molecules comprising various diatomic, triatomic, and polyatomic gases have been chosen for the investigations. The intermolecular interactions are understood from the interaction energy, electrostatic potential, frontier molecular orbitals, energy gap, and natural bond orbital analyses. Furthermore, quantum molecular descriptors such as electronegativity, chemical potential, chemical hardness and electrophilicity index are calculated to have deep insight on chemical nature of the gas molecules. Additionally, we have done implicit solvent modelling using PCM, and the corresponding solvation energies have been calculated. Interestingly, all the calculations and analyses have projected the similar results that Cl2, SO2, and NH3 have very high interaction with the water clusters. To mimic various altitudes (0 km, 5 km and 10 km) in the atmosphere, thermochemistry calculations have been carried out at different temperature and pressure values. The Gibbs free energies of formation suggest that the hydration of Cl2 is higher followed by O2, SO2 and NH3 at all altitudes. Remarkably, it is found that the formation of hydrated clusters of Cl2 and O2 with 4H2O are thermodynamically favourable. On the other hand, SO2 and NH3 requires 5H2O and 3H2O to form thermodynamically favourable clusters. In summary, it is anticipated that this kind of extensive computational studies facilitate to understand the structural, electronic, chemical and thermochemical properties of hydrated atmospheric gases that leads to the formation of prenucleation clusters followed by atmospheric aerosols.
