ABSTRACT
At the ultrathin scale, nanomaterials exhibit interesting chemical and physical properties, like flexibility, and polymer-like rheology. However, to limit the dimensions of composite nanomaterials at the ultrathin level is still a challenging task. Herein, by adopting a new low temperature single step and single pot wet chemical approach, we have successfully fabricated two dimensional (2D) mixed oxide ZnO-Fe2O3 dendritic nanosheets (FZDNSs). Various control experimental outcomes demonstrate that precursor salts of both the metals are crucial for the formation of stable 2D FZDNSs. The obtained FZDNSs not only exhibit the best photoreduction performance but also much enhanced electrocatalytic performance. This work will provide a promising avenue for the synthesis of cost effective transition metal mixed oxide based 2D nanosheets having wide ranging applications.
ABSTRACT
Eco-friendly, efficient, and durable electrocatalysts from earth-abundant materials are crucial for water splitting through hydrogen and oxygen generation. However, available methods to fabricate electrocatalysts are either hazardous and time-consuming or require expensive equipment, hindering the large-scale, eco-friendly production of artificial fuels. Here, we present a rapid, single-step method for producing MoSx/NiF electrocatalysts with controlled sulfur-vacancies via electric-field-assisted pulsed laser ablation (EF-PLA) in liquid and in-situ deposition on nickel foam, enabling efficient water splitting. Electric-field parameters efficiently control S-vacancy active sites in electrocatalysts. Higher electric fields yield a MoSx/NiF electrocatalyst with a larger density of S-vacancy sites, suited for HER due to lower Gibbs free energy for H∗ adsorption, while lower electric fields produce an electrocatalyst with lower S-vacancy sites, better suited for OER, as shown by both experimental and theoretical results. The present work opens a horizon in designing high-efficiency catalysts, for a wide range of chemical reactions.
ABSTRACT
Laser-induced thermocapillary deformation of liquid surfaces has emerged as a promising tool to precisely characterize the thermophysical properties of pure fluids. However, challenges arise for nanofluid (NF) and soft bio-fluid systems where the direct interaction of the laser generates an intriguing interplay between heating, momentum, and scattering forces which can even damage soft biofluids. Here, we report a versatile, pump-probe-based, rapid, and non-contact interferometric technique that resolves interface dynamics of complex fluids with the precision of ~1 nm in thick-film and 150 pm in thin-film regimes below the thermal limit without the use of lock-in or modulated beams. We characterize the thermophysical properties of complex NF in three exclusively different types of configurations. First, when the NF is heated from the bottom through an opaque substrate, we demonstrate that our methodology permits the measurement of thermophysical properties (viscosity, surface tension, and diffusivity) of complex NF and biofluids. Second, in a top illumination configuration, we show a precise characterization of NF by quantitively isolating the competing forces, taking advantage of the different time scales of these forces. Third, we show the measurement of NF confined in a metal cavity, in which the transient thermoelastic deformation of the metal surface provides the properties of the NF as well as thermo-mechanical properties of the metal. Our results reveal how the dissipative nature of the heatwave allows us to investigate thick-film dynamics in the thin-film regime, thereby suggesting a general approach for precision measurements of complex NFs, biofluids, and optofluidic devices.
ABSTRACT
Owing to technological advancements and the ever-increasing population, the search for renewable energy resources has increased. One such attempt at finding effective renewable energy is recycling of lithium-ion batteries and using the recycled material as an electrocatalyst for the oxygen evolution reaction (OER) step in water splitting reactions. In electrocatalysis, the OER plays a crucial role and several electrocatalysts have been investigated to improve the efficiency of O2 gas evolution. Present research involves the use of citric acid coupled with lemon peel extracts for efficient recovery of lithium cobaltate from waste lithium-ion batteries and subsequent use of the recovered cathode material for OER in water splitting. Optimum recovery was achieved at 90 °C within 3 h of treatment with 1.5 M citric acid and 1.5% extract volume. The consequent electrode materials were calcined at 600, 700 and 800 °C and compared to the untreated waste material calcined at 600 °C for OER activity. The treated material recovered and calcined at 600 °C was the best among all of the samples for OER activity. Its average particle size was estimated to be within the 20-100 nm range and required a low overpotential of 0.55 V vs. RHE for the current density to reach 10 mA/cm2 with a Tafel value of 128 mV/dec.
ABSTRACT
Hybrid organic-inorganic perovskite solar cells (HOIPs), especially CH3NH3PbI3 (MAPbI3), have received tremendous attention due to their excellent power conversion efficiency (25.2%). However, two fundamental hurdles, long-term stability and lead (Pb) toxicity, prevent HOIPs from practical applications in the solar industry. To overcome these issues, compositional engineering has been used to modify cations at A- and B-sites and anions at the X-site in the general form ABX3. In this work, we used the density functional theory (DFT) to incorporate Rb, Cs, and FA at the A-site to minimize the volatile nature of MA, while the highly stable Ca2+ and Sr2+ were mixed with the less stable Ge2+ and Sn2+ at the B-site to obtain a Pb-free perovskite. To further enhance the stability, we mixed the X-site anions (I/Br). Through this approach, we introduced 20 new perovskite species to the lead-free perovskite family and 7 to the lead-containing perovskite family. The molecular dynamic (MD) simulations, enthalpy formation, and tolerance and octahedral factor study confirm that all of the perovskite alloys we introduced here are as stable as pristine MAPbI3. All Pb-free perovskites have suitable and direct band gaps (1.42-1.77 eV) at the Γ-point, which are highly desirable for solar cell applications. Most of our Pb-free perovskites have smaller effective masses and exciton binding energies. Finally, we show that the introduced perovskites have high absorption coefficients (105 cm-1) and strong absorption efficiencies (above 90%) in a wide spectral range (300-1200 nm), reinforcing their significant potential applications. This study provides a new way of searching for stable lead-free perovskites for sustainable and green energy applications.
