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We report a facile but general method to prepare highly water-soluble and biocompatible photoinitiators for digital light processing (DLP)-based 3D printing of high-resolution hydrogel structures. Through a simple and straightforward one-pot procedure, we can synthesize a metal-phenyl(2,4,6-trimethylbenzoyl)phosphinates (M-TMPP)-based photoinitiator with excellent water solubility (up to ∼50 g/L), which is much higher than that of previously reported water-soluble photoinitiators. The M-TMPP aqueous solutions show excellent biocompatibility, which meets the prerequisite for biomedical applications. Moreover, we used M-TMPP to prepare visible light (405 nm)-curable hydrogel precursor solutions for 3D printing hydrogel structures with a high water content (80 wt %), high resolution (∼7 μm), high deformability (more than 80% compression), and complex geometry. The printed hydrogel structures demonstrate great potential in flexible electronic sensors due to the fast mechanical response and high stability under cyclic loadings.

Since first developed, the conducting materials in wireless communication and electromagnetic interference (EMI) shielding devices have been primarily made of metal-based structures. Here, we present a highly conductive and corrosion-resistant graphene assembled film (GAF) that can be used to fabricate multi-band 5G wireless communication electronics and EMI protection at frequencies ranging from tens of MHz to THz to demonstrate its potential in metal replacement in practical electronics. The GAF based antennas (dipole antenna, ultra-wideband antenna and 5G wireless communication antenna array) are comparable with metal-based antennas in terms of performance and device complexity. The EMI shielding effectiveness of GAF can reach up to 127 dB in the frequency range of 2.6 GHz - 0.32 THz, and a maximum shielding effectiveness per unit thickness is of 6966 dB/mm. Furthermore, the GAF metamaterials exhibit promising frequency selection characteristics and angular stability as flexible frequency selective surfaces that can work at 3.5 GHz and 60 GHz respectively.

Despite the large number of experimental works divulging the use of carbonaceous materials in LIB anodes, there are very few reports modeling the relationships between the characteristics of the electrode active materials and their lithium storage capacity. In this work, it is aimed to model the influence of the size and shape of carbon nano-spheres (carbon dots) on their lithium storage capacity. This study divides lithium storage of carbon nano-spheres into two segregate surface- and bulk-related mechanisms and calculates the capacity as the summation of these two components. Accordingly, a novel model employing a new factor called normalized volume, to accurately add the contribution of the surface lithium storage component to the bulk one, is introduced. The model also considers the size and morphology of the carbonaceous nano-particles simultaneously to estimate the specific capacity of the LIB anodes. The model revealed the fact that the decrease in the size of carbon nano-spheres below 20 nm dramatically results in the enhancement of the lithium storage capacity. The comparison of the estimated values with the experimental data of the literature confirmed the satisfactory consistency of the measured and predicted capacities. More importantly, this model is capable of being utilized as a fundamental tool to predict the specific lithium storage capacity of various carbon nano-structures considering their shape and dimension.

Electrochemical capacitors, also called supercapacitors (SCs), have been gaining a more significant position as electrochemical energy storage devices in recent years. They are energy storage devices with a considerable power density, a satisfactory energy density and a long-life cycle, suitable for a large number of applications. The further development of these devices relies on providing suitable, low-cost, environmentally friendly, and abundant materials for use as the active materials in the electrodes. Among the current materials used, activated carbons have a superior performance. Their excellent electrochemical performance, high specific surface area, high adsorption, tunable surface chemistry, fast ion/electron transport, abundant functional moieties, low cost, and abundance have made them promising candidates as SC electrodes. These advantages can be enhanced if the activated carbons are prepared from biomass precursors. Recently, scientists have focused on biomass because it is abundant and renewable, low cost, simply processed, and environmentally friendly. The fundamentals of SCs as an electrochemical energy storage device are discussed and biomass from various sources is categorized and introduced. Finally, the activation techniques for these biomass precursors and their use as electrode materials for SCs are discussed.