Metal‐halide perovskites have emerged as versatile materials for various electronic and optoelectronic devices such as diodes, solar cells, photodetectors, and sensors due to their interesting properties of high absorption coefficient in the visible regime, tunable bandgap, and high power conversion efficiency. Recently, metal‐free organic perovskites have also emerged as a particular class of perovskites materials for piezoelectric applications. This broadens the chemical variety of perovskite structures with good mechanical adaptability, light‐weight, and low‐cost processability. Despite these achievements, the fundamental understanding of the underlying phenomenon of piezoelectricity in metal‐free perovskites is still lacking. Therefore, this perspective emphasizes the overview of piezoelectric properties of metal‐halide, metal‐free perovskites, and their recent progress which may encourage material designs to enhance their applicability towards practical applications. Finally, challenges and outlooks of piezoelectric metal‐free perovskites are highlighted for their future developments.
Smart fabrics that can harvest ambient energy and provide diverse sensing functionality via triboelectric effects have evoked great interest for next‐generation healthcare electronics. Herein, a novel borophene/ecoflex nanocomposite is developed as a promising triboelectric material with tailorability, durability, mechanical stability, and flexibility. The addition of borophene nanosheets enables the borophene/ecoflex nanocomposite to exhibit tunable surface triboelectricity investigated by Kelvin probe force microscopy. The borophene/ecoflex nanocomposite is further fabricated into a fabric‐based triboelectric nanogenerator (B‐TENG) for mechanical energy harvesting, medical assistive system, and wound healing applications. The durability of B‐TENG provides consistent output performance even after severe deformation treatments, such as folding, stretching, twisting, and washing procedures. Moreover, the B‐TENG is integrated into a smart keyboard configuration combined with a robotic system to perform an upper‐limb medical assistive interface. Furthermore, the B‐TENG is also applied as an active gait phase sensing system for instantaneous lower‐limb gait phase visualization. Most importantly, the B‐TENG can be regarded as a self‐powered in vitro electrical stimulation device to conduct continuous wound monitoring and therapy. The as‐designed B‐TENG not only demonstrates great potential for multifunctional self‐powered healthcare sensors, but also for the promising advancements toward wearable medical assistive and therapeutic systems.
This work deals with first-principles and in silico studies of graphene oxide-based whole-cell selective aptamers for cancer diagnostics utilising a tunable-surface strategy. Herein, graphene oxide (GO) was constructed as a surface-based model with poly( N -isopropylacrylamide) (PNIPAM) covalently grafted as an “on/off”-switch in triggering interactions with the cancer-cell protein around its lower critical solution temperature. The atomic building blocks of the aptamer and the PNIPAM adsorbed onto the GO was investigated at the density functional theory (DFT) level. The presence of the monomer of PNIPAM stabilised the system’s π-π interaction between GO and its nucleobases as confirmed by higher bandgap energy, satisfying the eigenvalues of the single-point energy observed rather than the nucleobase and the GO complex independently. The unaltered geometrical structures of the surface emphasise the physisorption type interaction between the nucleobase and the GO/NIPAM surface. The docking result for the aptamer and the protein, highlighted the behavior of the PNIPAM- graft -GO is exhibiting globular and extended conformations, further supported by molecular dynamics (MD) simulations. These studies enabled a better understanding of the thermal responsive behavior of the polymer-enhanced GO complex for whole-cell protein interactions through computational methods.
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