RESUMEN
The increasing demand for wearable electronics calls for advanced energy storage solutions that integrate high electrochemical performances and mechanical robustness. Ionogel is a promising candidate due to its stretchability combined with high ionic conductivity. However, simultaneously optimizing both the electrochemical and mechanical performance of ionogels remains a challenge. This paper reports a tough and highly ion-conductive ionogel through ion impregnation and solvent exchange. The fabricated ionogel consists of double interpenetrating networks of long polymer chains that provide high stretchability. The polymer chains are crosslinked by hydrogen bonds that induce large energy dissipation for enhanced toughness. The resultant ionogel possesses mechanical stretchability of 26, tensile strength of 1.34 MPa, and fracture toughness of 4175 J m-2. Meanwhile, due to the high ion concentrations and ion mobility in the gel, a high ionic conductivity of 3.18 S m-1 at room temperature is achieved. A supercapacitor of this ionogel sandwiched with porous fiber electrodes provides remarkable areal capacitance (615 mF cm-2 at 1 mA cm-2), energy density (341.7 µWh cm-2 at 1 mA cm-2), and power density (20 mW cm-2 at 10 mA cm-2), offering significant advantages in applications where high efficiency, compact size, and rapid energy delivery are crucial, such as flexible and wearable electronics.
RESUMEN
Anode-free all-solid-state lithium metal batteries (ASLMBs) promise high energy density and safety but suffer from a low initial Coulombic efficiency and rapid capacity decay, especially at high cathode loadings. Using operando techniques, we concluded these issues were related to interfacial contact loss during lithium stripping. To address this, we introduce a conductive carbon felt elastic layer that self-adjusts the pressure at the anode side, ensuring consistent lithium-solid electrolyte contact. This layer simultaneously provides electronic conduction and releases the plating pressure. Consequently, the first Coulombic efficiency dramatically increases from 58.4% to 83.7% along with a >10-fold improvement in cycling stability. Overall, this study reveals an approach for enhancing anode-free ASLMB performance and longevity by mitigating lithium stripping inefficiency through self-adjusting interfacial pressure enabled by a conductive elastic interlayer.
RESUMEN
Methylammonium lead iodide (CH3NH3PbI3), with the organic-inorganic hybrid perovskite (OIHP) structure, has gained tremendous research interest due to its excellent photo-electron conversion ability in the application of photovoltaics. Despite its solution processed polycrystalline thin film form in solar cells, the single crystalline counterpart may offer some incredibly novel optoelectronic functionalities. In this work, a sizable (>5 mm) and high quality CH3NH3PbI3 single crystal has been synthesized by the inverse temperature crystallization method, and a white-light photodetector of the structure glass/ITO/Ga/ CH3NH3PbI3/Au was fabricated. Overbroad photo-excitation intensities ranging from 0.1 mW/cm2 to 100 mW/cm2 using a sun-light simulator, the on-off ratio is tunable in a wide-range from 65 to 2250 at zero bias voltage. The responsivity (R) and detectivity (D*) are 36.2 mA/W and 2.68×1011 Jones respectively at a weak white-light intensity such as 0.1 mW/cm2. Both the photodetective parameters decrease with the increase of the illumination intensity. Based on impedance spectra obtained at working condition and light intensity dependent Jsc measurements, the surface trap-assist recombination may play a dominating role. The corresponding lifetime (τsurf) and resistance (Rsurf_trap) exhibit fast decays at higher illumination intensities. This fundamental study may pave the way for exploring the contribution of the surface trap-assist recombination in the CH3NH3PbI3 single crystal based photodetector. We believe it is applicable for integration in micro-photonics for sensitive and weak white-light photo-detection.