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The capacity of transition metal oxide cathode for Li-ion batteries can be further enhanced by increasing the charging potential. However, these high voltage cathodes suffer from fast capacity decay because the large volume change of cathode breaks the active materials and cathode-electrolyte interphase (CEI), resulting in electrolyte penetration into broken active materials and continuous side reactions between cathode and electrolytes. Herein, a robust LiF-rich CEI was formed by potentiostatic reduction of fluorinated electrolyte at a low potential of 1.7 V. By taking LiCoO 2 as a model cathode, we demonstrate that the LiF-rich CEI maintains the structural integrity and suppresses electrolyte penetration at a high cut-off potential of 4.6 V. The LiCoO 2 with LiF-rich CEI exhibited a capacity of 198 mAh g À 1 at 0.5C and an enhanced capacity retention of 63.5 % over 400 cycles as compared to the LiF-free LiCoO 2 with only 17.4 % of capacity retention.

Single‐crystalline cathode materials have attracted intensive interest in offering greater capacity retention than their polycrystalline counterparts by reducing material surfaces and phase boundaries. However, the single‐crystalline LiCoO2 suffers severe structural instability and capacity fading when charged to high voltages (4.6 V) due to Co element dissolution and O loss, crack formation, and subsequent electrolyte penetration. Herein, by forming a robust cathode electrolyte interphase (CEI) in an all‐fluorinated electrolyte, reversible planar gliding along the (003) plane in a single‐crystalline LiCoO2 cathode is protected due to the prevention of element dissolution and electrolyte penetration. The robust CEI effectively controls the performance fading issue of the single‐crystalline cathode at a high operating voltage of 4.6 V, providing new insights for improved electrolyte design of high‐energy‐density battery cathode materials.

Bistable display has been a long-awaited goal due to its zero energy cost when maintaining colored or colorless state and electrochromic material has been highly considered as a potential way to achieve bistable display due to its simple structure and possible manipulation. However, it is extremely challenging with insurmountable technical barriers related to traditional electrochromic mechanisms. Herein a prototype for bistable electronic billboard and reader with high energy efficiency is demonstrated with excellent bistability (decay 7% in an hour), reversibility (10 4 cycles), coloration efficiency (430 cm 2 C −1 ) and very short voltage stimulation time (2 ms) for color switching, which greatly outperforms current products. This is achieved by stabilization of redox molecule via intermolecular ion transfer to the supramolecular bonded colorant and further stabilization of the electrochromic molecules in semi-solid media. This promising approach for ultra-energy-efficient display will promote the development of switching molecules, devices and applications in various fields of driving/navigation/industry as display to save energy.

Ink‐free printing based on rewritable paper is an efficient and environmental friendly way to reuse paper, protect resources, and save energy for sustainable development of human society. Among various kinds of rewritable media, light responsive rewritable paper (LRP) is one of the most popular research areas due to its clean and favorable noncontact writing. Visible light is more suitable for LRP for its superior penetration and much less damages to organic molecules than UV light. However, visible‐light‐responsive rewritable paper (VLRP) has only limited successes so far. Herein, a VLRP is newly designed and fabricated based on photoinduced proton transfer (PPT) between photoacid and pH‐sensitive dyes. Success of it is highly benefited from systematical investigation and in‐depth understanding on the key influence factors, such as concentration‐induced undesired isomerization, temperature, humidity, and light intensity, on the PPT and its inverse process. As‐prepared VLRP shows long‐awaited properties, such as, high color contrast and resolution, appropriate legible time of prints, excellent reversibility (>100 cycles), easiness to achieve multicolor prints, and agreeing well with environmental concept of green printing. In addition, study of influence factors on PPT in this work, to some extent, may also help people understand complex photocycle process in biosystem.

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Autophagy is a housekeeping lysosomal degradation pathway important for cellular survival, homeostasis and function. Various disease models have shown that upregulation of autophagy may be beneficial to combat disease pathogenesis. However, despite several recently reported small-molecule screens for synthetic autophagy inducers, natural chemicals of diverse structures and functions have not been included in the synthetic libraries, and characterization of their roles in autophagy has been lacking. To discover novel autophagy-regulating compounds and study their therapeutic mechanisms, we used analytic chemistry approaches to isolate natural phytochemicals from a reservoir of medicinal plants used in traditional remedies. From this pilot plant metabolite library, we identified several novel autophagy-inducing phytochemicals, including Rg2. Rg2 is a steroid glycoside chemical that activates autophagy in an AMPK-ULK1-dependent and MTOR-independent manner. Induction of autophagy by Rg2 enhances the clearance of protein aggregates in a cell-based model, improves cognitive behaviors in a mouse model of Alzheimer disease, and prevents high-fat diet-induced insulin resistance. Thus, we discovered a series of autophagy-inducing phytochemicals from medicinal plants, and found that one of the compounds Rg2 mediates metabolic and neurotrophic effects dependent on activation of the autophagy pathway. These findings may help explain how medicinal plants exert the therapeutic functions against metabolic diseases.

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