Silver nanoparticles (Ag NPs) have accumulated significant interest due to their exceptional physicochemical properties and remarkable applications in biomedicine, electronics, and catalysis sensing. This comprehensive review provides an in-depth study of synthetic approaches such as biological synthesis, chemical synthesis, and physical synthesis with a detailed overview of their sub-methodologies, highlighting advantages and disadvantages. Additionally, structural properties affected by synthesis methods are discussed in detail by examining the dimensions and surface morphology. The review explores the distinctive properties of Ag NPs, including optical, electrical, catalytic, and antimicrobial properties, which render them beneficial for a range of applications. Furthermore, this review describes the diverse applications in several fields, such as medicine, environmental science, electronics, and optoelectronics. However, with numerous applications, several kinds of issues still exist. Future attempts need to address difficulties regarding synthetic techniques, environmental friendliness, and affordability. In order to ensure the secure utilization of Ag NPs, it is necessary to establish sustainability in synthetic techniques and eco-friendly production methods. This review aims to give a comprehensive overview of the synthesis, structural analysis, properties, and multifaceted applications of Ag NPs.

While traditional three‐layer structure supercapacitors are under mechanical manipulations, the high‐stress region concentrates, inevitably causing persistent structural problems including interlayer slippage, crease formation, and delamination of the electrode–electrolyte interface. Toward this, an all‐polymeric, all‐elastic and non‐laminated supercapacitor with high mechanical reliability and excellent electrochemical performance is developed. Specifically, a polypyrrole electrode layer is in situ integrated into a silk fibroin‐based elastic supramolecular hydrogel film with extensive hydrogen and covalent bonds, where a non‐laminate device is realized with structural elasticity at the device level. The non‐laminate configuration can avoid slippage and delamination, while the elasticity can preclude crease formation. Furthermore, under more severe mechanical damage, the supercapacitors can restore the electrochemical performance through non‐autonomous self‐healing capabilities, where the supramolecular design of host–guest interactions in the hydrogel matrix results in a superior self‐healing efficiency approaching ≈95.8% even after 30 cutting/healing cycles. The all‐elastic supercapacitor delivers an areal capacitance of 0.37 F cm⁻² and a volumetric energy density of 0.082 mW h cm⁻³, which can well‐maintain the specific capacitance even at −20 °C with over 85.2% retention after five cut/healing cycles.

Flexible piezoelectric nanogenerators are emerging as a promising solution for powering next-generation flexible electronics by converting mechanical energy into electrical energy. However, traditional ferroelectric ceramics, despite their excellent piezoelectric properties, lack flexibility; while piezoelectric polymers, although highly flexible, have low piezoelectricity. The quest to develop materials that combine high piezoelectricity with exceptional flexibility has thus become a research focus. Herein, we present a breakthrough in this field with the fabrication of freestanding (111)-oriented PbZr_0.52Ti_0.48O₃ single crystalline thin films, which exhibit remarkable flexibility and a high converse piezoelectric coefficient (~585 pm/V). This is achieved through water-soluble sacrificial layer to relieve substrate clamping and controlling the crystal orientation to further enhance the piezoelectric response. Our nanogenerators, constructed using these freestanding nanoscale membranes, demonstrate a record-high output power density (~63.5 mW/cm³), excellent flexibility (with a strain tolerance >3.4%), and superior mechanical stability in cycling tests (>60,000 cycles). These advancements pave the way for high-performance, flexible electronic devices utilizing ferroelectric oxide thin films.

High porosity (40% to 60%) 316L stainless steel containing well-interconnected open-cell porous structures with pore openness index of 0.87 to 1 were successfully fabricated by binder jetting and subsequent sintering processes coupled with a powder space holder technique. Mono-sized (30 µm) and 30% (by volume) spherically shaped poly(methyl methacrylate) (PMMA) powder was used as the space holder material. The effects of processing conditions such as: (1) binder saturation rates (55%, 100% and 150%), and (2) isothermal sintering temperatures (1000 ^○C to 1200 ^○C) on the porosity of 316L stainless steel parts were studied. By varying the processing conditions, porosity of 40% to 45% were achieved. To further increase the porosity values of 316L stainless steel parts, 30 vol. % (or 6 wt. %) of PMMA space holder particles were added to the 3D printing feedstock and porosity values of 57% to 61% were achieved. Mercury porosimetry results indicated pore sizes less than 40 µm for all the binder jetting processed 316L stainless steel parts. Anisotropy in linear shrinkage after the sintering process was observed for the SS316L parts with the largest linear shrinkage in the Z direction. The Young’s modulus and compression properties of 316L stainless steel parts decreased with increasing porosity and low Young’s modulus values in the range of 2 GPa to 29 GPa were able to be achieved. The parts fabricated by using pure 316L stainless steel feedstock sintered at 1200 ^○C with porosity of ~40% exhibited the maximum overall compressive properties with 0.2% compressive yield strength of 52.7 MPa, ultimate compressive strength of 520 MPa, fracture strain of 36.4%, and energy absorption of 116.7 MJ/m³, respectively. The Young’s modulus and compression properties of the binder jetting processed 316L stainless steel parts were found to be on par with that of the conventionally processed porous 316L stainless steel parts and even surpassed those having similar porosities, and matched to that of the cancellous bone types.