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In this study, a membraneless photofuel cell, namely, μ-DropFC, was designed and developed to harvest chemical and solar energies simultaneously. The prototypes can also perform environmental remediation to demonstrate their multitasking potential as a sustainable hybrid device in a single embodiment. A hydrogen peroxide (H2O2) microdroplet at optimal pH and salt loading was utilized as a fuel integrated with Al as an anode and zinc phthalocyanine (ZnPC)-coated Cu as a cathode. The presence of n-type semiconductor ZnPC in between the electrolyte and metal enabled the formation of a photo-active Schottky junction suitable for power generation under light. Concurrently, the oxidation and reduction of H2O2 on the electrodes helped in the conversion of chemical energy into the electrical one in the same membraneless setup. The suspension of Au nanoparticles (Au NPs) in the droplet helped in enhancing the overall power density under photonic illumination through the effects of localized surface plasmon resonance (LSPR). Furthermore, the presence of photo-active n-type CdS NPs enabled the catalytic photo-degradation of dyes under light in the same embodiment. A 40 μL μ-DropFC could show a significantly high open circuit potential of ∼0.58 V along with a power density of 0.72 mW cm−2. Under the same condition, the integration of ten such μ-DropFCs could produce a power density of ∼7 mW cm−2 at an efficiency of 3.4%, showing the potential of the prototype for a very large scale integration (VLSI). The μ-DropFC could also degrade ∼85% of an industrial pollutant, rhodamine 6G, in 1 h while generating a power density of ∼0.6 mW cm−2. The performance parameters of μ-DropFCs were found to be either comparable or superior to the existing prototypes. In a way, the affordable, portable, membraneless, and high-performance μ-DropFC could harvest energy from multiple resources while engaging in environmental remediation.

The aggregation and deposition of neurotoxic Aβ fibrils are key in the etiology of Alzheimer's disease (AD). It has been clinically recognized as a major form of dementia across the globe. Finding and testing various natural compounds to target Aβ fibrils to disrupt their stable structures seems to be a promising and attractive therapeutic strategy. The destabilization effects of caffeine on Aβ fibrils are investigated via in silico studies, where a series of molecular dynamics (MD) simulations, each of 100 ns, was conducted. The simulation outcomes obtained henceforth clearly indicated the drift of the terminal chains from the protofibrils, leading to disorganization of the characteristically organized cross-β structures of Aβ fibrils. The structural instability of Aβ17-42 protofibrils is explained through enhanced fluctuations in the RMSD, radius of gyration and RMSF values in the presence of caffeine. The key interactions providing stability, comprising D23-K28 salt bridges, intra- and inter-chain hydrogen bonding and hydrophobic interactions involving interchain A21-V36 and F19-G38 and intrachain L34-V36, were found to be disrupted due to increases in the distances between the participating components. The loss of β-sheet structure with the introduction of turns and α-helices in terminal chains may further inhibit the formation of higher order aggregates, which is necessary to stop the progression of the disease. The atomistic details obtained via MD studies relating to the mechanism behind the underlying destabilization of Aβ17-42 protofibrils by caffeine encourage further investigations exploring the potency of natural compounds to treat AD via disrupting preformed neurotoxic Aβ protofibrils.

Liquid droplets loaded with paramagnetic or diamagnetic salts, namely liquibots, showed controlled migration inside a fluid medium and on slippery solid surfaces under remote magnetic guidance. The water or oilbots of size ranging from a millimetre to a few microns showed facile attraction, repulsion, division, and coalescence when guided by a magnetic field. The speed of the liquibots could be tuned by varying the size, salt-loading, and magnetic field strength. While the paramagnetic liquibot migrated towards a magnet with a velocity as high as ∼8 body length per s, the diamagnetic one migrated away from the field with a maximum velocity of ∼1 body length per s. The liquibots transported and delivered commercially available drugs to targeted locations showing their potential as drug-delivery vehicles. Remarkably, the experiments showed the utility of the liquibots in digital microfluidics because they moved easily on slippery solid surfaces. For example, a waterbot was split into many droplets on an oil coated solid surface before forming the patterns resembling polygons under magnetic guidance. Further, the liquibot based Packman™ game could also be played with the help of magnetic guidance. The extent of control demonstrated on the motions of the remotely guided liquibots could be useful in diverse futuristic applications including drug-transport, digital-microfluidics, and droplet-electronics.