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Sodium-ion batteries are commanding increasing attention owing to their promising electrochemical performance and sustainability. Organic electrode materials (OEMs) complement such technologies as they can be sourced from biomass and recycling them is environmentally friendly. Organic anodes based on sodium carboxylates have exhibited immense potential, except the limitation of current synthesis methods concerning upscaling and energy costs. In this work, a rapid and energy efficient microwave-assisted synthesis for organic anodes is presented using sodium naphthalene-2,6-dicarboxylate as a model compound. Optimizing the synthesis and electrode composition enables the compound to deliver a reversible initial capacity of ≈250 mAh g-1 at a current density of 25 mA g-1 with a high initial Coulombic efficiency (≈78%). The capacity is stable over 400 cycles and the compound also exhibits good rate performance. The successful demonstration of this rapid synthesis may facilitate the transition to preparing organic battery materials by scalable, efficient methods.Organic-inorganic halide perovskite (OIHP) solar cells hold a great promise for commercial breakthrough since their power conversion efficiency has been pushed beyond the mark of 25%, making them capable of competing with traditional crystalline silicon solar cells. The key to achieve efficient and stable perovskite solar cells is inherently related to the film morphology. The understanding of the kinetic processes of film formation and degradation opens up possibilities to tailor the film morphology via the regulation of precursor and processing parameters. In situ grazing-incidence X-ray scattering (GIXS) techniques allow for tracking the morphology evolution of thin films at different length scales and with high temporal resolution. In this review, the selected examples for application of in situ grazing-incidence wide-angle X-ray scattering and grazing-incidence small-angle X-ray scattering techniques to the growth and stability of OIHPs are summarized after a brief introduction to both techniques, highlighting particularly the morphological evolution of perovskite films over time. Then the correlated mathematical models are reviewed to give a toolbox for analyzing the mechanisms of film formation and degradation. Thus, an overview on the in situ GIXS methods is linked to the research of OIHP kinetics.An ion-exchange process is a promising approach to design advanced electrode materials for high-performance energy storage devices. Herein, a nanostructured Ni3 Sn2 S2 -CoS (NSS-CS) composite is fabricated by successive hydrothermal and ion-exchange processes. Since the incorporation of redox-rich cobalt element enables the NSS-CS composite to be more electrochemically active, its impact on the electrochemical performance is therefore extensively studied. Particularly, the NSS-CS-0.2 g electrode material delivered a high areal capacity of 830.4 µAh cm-2 at 5 mA cm-2 . Additionally, a room-temperature wet-chemical approach is employed to anchor nanosilver (nAg)-particles on the NSS-CS-0.2 g (nAg@NSS-CS-0.2 g) to further exalt its electrokinetics. Consequently, the nAg@NSS-CS-0.2 g electrode shows a higher areal capacity of 948.5 µAh cm-2 (193.5 mAh g-1 ) than that of the NSS-CS-0.2 g. Furthermore, its practicability is also examined by assembling a hybrid cell. The assembled hybrid cell delivers a high areal capacity of 969.2 µAh cm-2 (49.2 mAh g-1 ) at 7 mA cm-2 and maximum areal energies and power densities of 0.784 mWh cm-2 (40.8 Wh kg-1 ) and 45 mW cm-2 (2347.4 W kg-1 ), respectively. The efficiency of the hybrid cells is also tested by harvesting solar energy, followed by energizing electronic components. This work can pave the way for significant attraction in designing advanced electrodes for energy-related fields.Perovskite oxides with dispersed nanoparticles on their surface are considered instrumental in energy conversion and catalytic processes. Redox exsolution is an alternative method to the conventional deposition techniques for directly growing well-dispersed and anchored nanoarchitectures from the oxide support through thermochemical or electrochemical reduction. Herein, a new method for such nanoparticle nucleation through the exposure of the host perovskite to plasma is shown. The applicability of this new method is demonstrated by performing catalytic tests for CO2 hydrogenation over Ni exsolved nanoparticles prepared by either plasma or conventional H2 reduction. Compared to the conventional thermochemical H2 reduction, there are plasma conditions that lead to the exsolution of a more than ten times higher Ni amount from a lanthanum titanate perovskite, which is similar to the reported values of the electrochemical method. Unlike the electrochemical method, however, plasma does not require the integration of the material in an electrochemical cell, and is thus applicable to a wide range of microstructures and physical forms. Additionally, when N2 plasma is employed, the nitrogen species are stripping out oxygen from the perovskite lattice, generating a key chemical intermediate, such as NO, rendering this technology even more appealing.Developing highly efficient electrocatalysts for renewable energy conversion and environment purification has long been a research priority in the past 15 years. Covalent organic frameworks (COFs) have emerged as a burgeoning family of organic materials internally connected by covalent bonds and have been explored as promising candidates in electrocatalysis. The reticular geometry of COFs can provide an excellent platform for precise incorporation of the active sites in the framework, and the fine-tuning hierarchical porous architectures can enable efficient accessibility of the active sites and mass transportation. Considerable advances are made in rational design and controllable fabrication of COF-based organic-inorganic hybrids, that containing organic frameworks and inorganic electroactive species to induce novel physicochemical properties, and take advantage of the synergistic effect for targeted electrocatalysis with the hybrid system. Branches of COF-based hybrids containing a diversity form of metals, metal compounds, as well as metal-free carbons have come to the fore as highly promising electrocatalysts. PIN1 inhibitor API-1 This review aims to provide a systematic and profound understanding of the design principles behind the COF-based hybrids for electrocatalysis applications. Particularly, the structure-activity relationship and the synergistic effects in the COF-based hybrid systems are discussed to shed some light on the future design of next-generation electrocatalysts.Manipulating droplets by light in microscale allows precise control of microfluidics, liquid delivery, micromachines, and so on. Among these applications, microfluidic technology is of particular interest for miniaturization of the portable analysis systems, which require the integration of various liquid operations in one device. Here, a photodeformable microfluidic platform is constructed by combining Laplace pressure and capillary condensation to integrate the transportation, fusion, separation, and mixing of liquid slugs in one chip. The Laplace pressure, attributed to the photodeformation of the liquid crystal polymers, is generated to propel the slug. The capillary condensation is introduced by the delicate design of the fluid channels, allowing the fusion and separation of slugs without any connected microvalves. Catalytic oxidation reaction and protein detection processes are realized in the platform, which are amenable to a variety of miniaturized bio-medical applications, such as portable analysis and point of care testing.Lethal oxidative stress and ferrous ion accumulation-mediated degeneration/death in retinal pigment epithelium (RPE) exert an indispensable impact on retinal degenerative diseases with irreversible visual impairment, especially in age-related macular degeneration (AMD), but corresponding pathogenesis-oriented medical intervention remains controversial. In this study, the potent iron-binding nanoscale Prussian blue analogue KCa[FeIII (CN)6 ] (CaPB) with high biocompatibility is designed to inhibit RPE death and subsequently photoreceptor cell degeneration. In mice, CaPB effectively prevents RPE degeneration and ultimately fulfills superior therapeutic outcomes upon a single intravitreal injection significant rescue of retinal structures and visual function. Through high-throughput RNA sequencing and sophisticated biochemistry evaluations, the findings initially unveil that CaPB nanoparticles protect against RPE degradation by inhibiting ferroptotic cell fate. Together with the facile, large-scale preparations and in vivo biosafety, it is believed that the synthesized CaPB therapeutic nanoparticles are promising for future clinical treatment of diverse retinal diseases involving pathological iron-dependent ferroptosis, including AMD.The protection and regeneration of the water environment is currently one of the most critical concerns for the sustainable development of human society. To solve the water crisis, the use of capacitive deionization (CDI) technology to extract fresh-water that is suitable for human consumption from abundant surface-water is a feasible solution. In this work, a cobalt benzimidazole frameworks (ZIF-9) derived carbon composites with a unique quasi-microcubic morphology is synthesized and used the as-prepared materials as an electrode material for the CDI. Interestingly, the ZIF-9 derived carbon composites exhibit an impressive desalination capacity of 55.4 mg g-1 and can be reused. Measurements in surface-water (Beijing-Hangzhou Grand Canal, Slender West Lake, Initial rainwater, Rain water) show that this CDI technology based on ZIF-9 derived carbon composites not only has a strong adsorption effect on metal ions but also can remarkably kill microorganisms. The results show that the technology can effectively kill bacteria (Escherichia coli and Bacillus) and algae with 95% and 91.7% inhibition rates, respectively. This work provides a valuable example for the use of metal-organic framework-derived carbon composites as high-performance electrode materials of CDI and opens a new direction for promoting the application of CDI in surface-water.Potassium-ion batteries (PIBs) have attracted tremendous attention because of their high energy density and low-cost. As such, much effort has focused on developing electrode materials and electrolytes for PIBs at the material levels. This review begins with an overview of the high-performance electrode materials and electrolytes, and then evaluates their prospects and challenges for practical PIBs to penetrate the market. The current status of PIBs for safe operation, energy density, power density, cyclability, and sustainability is discussed and future studies for electrode materials, electrolytes, and electrode-electrolyte interfaces are identified. It is anticipated that this review will motivate research and development to fill existing gaps for practical potassium-based full batteries so that they may be commercialized in the near future.The ionic nature of organic trihalide perovskite leads to structural irregularity and energy disorder at the perovskite surface, which seriously affects the photovoltaic performance of perovskite solar cells. Here, the origin of the perovskite surface disorder is analyzed, and a facial ion-exchange strategy is designed to regulate the surface chemical environment. By the reconstruction of terminal irregular Pb-I bonds and random cations, the repaired surface is characteristic of the reduced band tail states, consequent to the suppression of the uplift of quasi-Fermi level splitting and photocarrier scattering. The optimized device gets a high open-circuit voltage and operational stability. These findings fully elaborate the underlying mechanism concerning perovskite surface problem, giving guidance on tailoring the energy disorder.