Ultrathick electrode design is a promising strategy to enhance the specific energy of Li‐ion batteries (LIBs) without changing the underlying materials chemistry. However, the low Li‐ion conductivity ...caused by ultralong Li‐ion transport pathway in traditional random microstructured electrode heavily deteriorates the rate performance of ultrathick electrodes. Herein, inspired by the vertical microchannels in natural wood as the highway for water transport, the microstructures of wood are successfully duplicated into ultrathick bulk LiCoO2 (LCO) cathode via a sol–gel process to achieve the high areal capacity and excellent rate capability. The X‐ray‐based microtomography demonstrates that the uniform microchannels are built up throughout the whole wood‐templated LCO cathode bringing in 1.5 times lower of tortuosity and ≈2 times higher of Li‐ion conductivity compared to that of random structured LCO cathode. The fabricated wood‐inspired LCO cathode delivers high areal capacity up to 22.7 mAh cm−2 (five times of the existing electrode) and achieves the dynamic stress test at such high areal capacity for the first time. The reported wood‐inspired design will open a new avenue to adopt natural hierarchical structures to improve the performance of LIBs.
Inspired by the vertical microchannels in natural wood as the highway for water transport, an ultra‐thick bulk LiCoO2 (LCO) cathode with vertical channels is fabricated to enhance the transport of Li+. Remarkably, the fabricated LCO cathode shows low tortuosity and high Li‐ion conductivity, and can deliver high areal capacity up to 22.7 mAh cm−2.
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BFBNIB, FZAB, GIS, IJS, KILJ, NLZOH, NUK, OILJ, SAZU, SBCE, SBMB, UL, UM, UPUK
Fast charging of lithium ion batteries is essential for next‐generation energy‐storage systems. However, the poor ionic and electronic transport of anodes with its rather high mass loading limits the ...practical applications of this technology. Herein, a multiscale design from niobium titanium oxide anode material to electrode structure is proposed for fast charging lithium ion batteries with a practical level of areal capacity (3 mAh cm−2). At the atomic scale, the introduction of oxygen vacancy and surface carbon coating enables niobium titanium oxide (TiNb2O7−x@C) to possess excellent ionic and electronic conductivity. For the microscopic electrode structure, 1D TiNb2O7−x@C fibers are tightly assembled to form a high‐speed transport network of ions and electrons throughout the electrode. As a result, the obtained TiNb2O7−x@C electrode shows excellent rate capability (1.83 mAh cm−2 at 1 C) and cycling stability under an areal capacity of 3 mAh cm−2 (2.35 mAh cm−2 after 100 cycles at 0.5 C) in half‐cells. Significantly, a full‐cell coupled with practical level mass loading of lithium cobalt oxide cathode is demonstrated to deliver 1.55 mAh cm−2 at 3 C for the first time.
A multiscale electrode design strategy is reported to achieve fast ionic and electronic transport for improving the electrochemical performance of TiNb2O7 electrodes at high mass loading (>11 mg cm−2). Moreover, a TiNb2O7–x@C/LiCoO2 full‐cell with practical level mass loading is fabricated, which displays excellent fast‐charging performance.
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BFBNIB, FZAB, GIS, IJS, KILJ, NLZOH, NUK, OILJ, SAZU, SBCE, SBMB, UL, UM, UPUK
Peroxisomes account for ~35% of total H2O2 generation in mammalian tissues. Peroxisomal ACOX1 (acyl‐CoA oxidase 1) is the first and rate‐limiting enzyme in fatty acid β‐oxidation and a major producer ...of H2O2. ACOX1 dysfunction is linked to peroxisomal disorders and hepatocarcinogenesis. Here, we show that the deacetylase sirtuin 5 (SIRT5) is present in peroxisomes and that ACOX1 is a physiological substrate of SIRT5. Mechanistically, SIRT5‐mediated desuccinylation inhibits ACOX1 activity by suppressing its active dimer formation in both cultured cells and mouse livers. Deletion of SIRT5 increases H2O2 production and oxidative DNA damage, which can be alleviated by ACOX1 knockdown. We show that SIRT5 downregulation is associated with increased succinylation and activity of ACOX1 and oxidative DNA damage response in hepatocellular carcinoma (HCC). Our study reveals a novel role of SIRT5 in inhibiting peroxisome‐induced oxidative stress, in liver protection, and in suppressing HCC development.
Synopsis
This study reveals a role for SIRT5 in regulating peroxisomal H2O2 and ROS homeostasis and indicates its potential function in liver protection and hepatocellular carcinoma suppression.
SIRT5 is localized in peroxisomes where it controls H2O2 metabolism.
SIRT5‐mediated desuccinylation inhibits ACOX1 activity by suppressing its active dimer formation.
SIRT5 downregulation increases ACOX1 activity and oxidative DNA damage response in HCC.
This study reveals a role for SIRT5 in regulating peroxisomal H2O2 and ROS homeostasis and indicates its potential function in liver protection and hepatocellular carcinoma suppression.
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FZAB, GIS, IJS, KILJ, NLZOH, NUK, OILJ, SAZU, SBCE, SBMB, UL, UM, UPUK
The commercial ceramic nanoparticle coated microporous polyolefin separators used in lithium batteries are still vulnerable under external impact, which may cause short circuits and consequently ...severe safety threats, because the protective ceramic nanoparticle coating layers on the separators are intrinsically brittle. Here, a nacre‐inspired coating on the separator to improve the impact tolerance of lithium batteries is reported. Instead of a random structured ceramic nanoparticle layer, ion‐conductive porous multilayers consisting of highly oriented aragonite platelets are coated on the separator. The nacre‐inspired coating can sustain external impact by turning the violent localized stress into lower and more uniform stress due to the platelet sliding. A lithium‐metal pouch cell using the aragonite platelet coated separator exhibits good cycling stability under external shock, which is in sharp contrast to the fast short circuit of a lithium‐metal pouch cell using a commercial ceramic nanoparticle coated separator.
A nacre‐inspired coating is fabricated to improve the impact tolerance of the separator in a lithium battery via efficient energy dissipation. Remarkably, the pouch cell using the nacre‐inspired porous aragonite platelet coated separator performs with much lower instantaneous open‐circuit voltage change and faster voltage recovery than the cell using the commercial ceramic nanoparticle coated separator under external impaction.
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BFBNIB, FZAB, GIS, IJS, KILJ, NLZOH, NUK, OILJ, SAZU, SBCE, SBMB, UL, UM, UPUK
The absence of tumor antigens leads to a low response rate, which represents a major challenge in immune checkpoint blockade (ICB) therapy. Pyroptosis, which releases tumor antigens and ...damage‐associated molecular patterns (DAMPs) that induce antitumor immunity and boost ICB efficiency, potentially leads to injury when occurring in normal tissues. Therefore, a strategy and highly efficient agent to induce tumor‐specific pyroptosis but reduce pyroptosis in normal tissues is urgently required. Here, a smart tumor microenvironmental reactive oxygen species (ROS)/glutathione (GSH) dual‐responsive nano‐prodrug (denoted as MCPP) with high paclitaxel (PTX) and photosensitizer purpurin 18 (P18) loading is rationally designed. The ROS/GSH dual‐responsive system facilitates the nano‐prodrug response to high ROS/GSH in the tumor microenvironment and achieves optimal drug release in tumors. ROS generated by P18 after laser irradiation achieves controlled release and induces tumor cell pyroptosis with PTX by chemo‐photodynamic therapy. Pyroptotic tumor cells release DAMPs, thus initiating adaptive immunity, boosting ICB efficiency, achieving tumor regression, generating immunological memory, and preventing tumor recurrence. Mechanistically, chemo‐photodynamic therapy and control‐release PTX synergistically induce gasdermin E (GSDME)‐related pyroptosis. It is speculated that inspired chemo‐photodynamic therapy using the presented nano‐prodrug strategy can be a smart strategy to trigger pyroptosis and augment ICB efficiency.
A smart tumor microenvironmental reactive oxygen species/glutathione dual‐responsive nano‐prodrug (denoted as MCPP) with high paclitaxel and photosensitizer purpurin 18 loading is designed. Chemo‐photodynamic therapy using the presented nano‐prodrug strategy can be a smart strategy to trigger pyroptosis and augment the efficiency of immune checkpoint blockade therapy.
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FZAB, GIS, IJS, KILJ, NLZOH, NUK, OILJ, SAZU, SBCE, SBMB, UL, UM, UPUK
Natural polymer nanofibers are attractive sustainable raw materials to fabricate separators for high‐performance lithium ion batteries (LIBs). Unfortunately, complicated pore‐forming processes, low ...ionic conductivity, and relatively low mechanical strength of previously reported natural polymer nanofiber‐based separators severely limit their performances and applications. Here, a chemical modification strategy to endow high performance to natural polymer nanofiber‐based separators is demonstrated by grafting cyanoethyl groups on the surface of chitin nanofibers. The fabricated cyanoethyl‐chitin nanofiber (CCN) separators not only exhibit much higher ionic conductivity but also retain excellent mechanical strength in comparison to unmodified chitin nanofiber separators. Through density function theory calculations, the mechanism of high Li+ ion transport in the CCN separator is unraveled as weakening of the binding of Li+ ions over that of PF6− ions with chitin, via the cyanoethyl modification. The LiFePO4/Li4Ti5O12 full cells using CCN separators show much better rate capability and enhanced capacity retention compared to the cell using commercial polypropylene (PP) separators. Beyond this, the CCN separator can work very well even at an elevated temperature of 120 °C in the LiFePO4/Li cell. The proposed strategy chemical modification of natural polymer nanofibers will open a new avenue to fabricate sustainable separators for LIBs with superior performance.
A dense chitin nanofiber‐based separator with a high lithium ion transference number is achieved by a facile surface chemical modification method. This is a new type of separator that falls in between a traditional separator and gel electrolyte, and thus shows good comprehensive performance when compared with the liquid electrolyte‐based polyolefin separator and gel electrolyte.
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BFBNIB, FZAB, GIS, IJS, KILJ, NLZOH, NUK, OILJ, SAZU, SBCE, SBMB, UL, UM, UPUK
Nanoparticle‐based tumor immunotherapy has emerged to show great potential for simultaneously regulating the immunosuppressive tumor microenvironment, reducing the unpleasant side effects, and ...activating tumor immunity. Herein, an excipient‐free glutathione/pH dual‐responsive prodrug nanoplatform is reported for immunotherapy, simply by sequentially liberating 5‐aminolevulinic acid and immunogenically inducing doxorubicin drug molecules, which can leverage the acidity and reverse tumor microenvironment. The obtained nanoplatform effectively boosts the immune system by promoting dendritic cell maturation and reducing the number of immune suppressive immune cells, which shows the enhanced adjunctive effect of anti‐programmed cell death protein 1 therapy. Overall, the prodrug‐based immunotherapy nanoplatform may offer a reliable strategy for improving synergistic antitumor efficacy.
A prodrug‐based versatile nanomedicine featured with rational size, high drug loading, and well‐controlled release is reported for enhancing cancer immunotherapy by effectively boosting the immune system by promoting dendritic cell maturation and reducing immune suppressive immune cells, producing a reliable strategy for lighting the corner of cancer immunotherapy.
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BFBNIB, FZAB, GIS, IJS, KILJ, NLZOH, NUK, OILJ, SAZU, SBCE, SBMB, UL, UM, UPUK
High‐voltage spinel cobalt‐free LiNi0.5Mn1.5O4 (LNMO) is one of the most promising cathode candidates for next‐generation lithium‐ion batteries (LIBs) due to its high specific capacity, high ...operating voltage, and low cost. However, inferior electronic conductivity, transition metal dissolution, and fast capacity degradation of LNMO, especially in high mass loading for high areal capacity, are the critical material challenges for its practical application. Herein, trace multiple Cr‐Fe‐Cu elements doping of LiNi0.45Cr0.0167Fe0.0167Cu0.0167Mn1.5O4 (CFC0.5‐LNMO) cathode is achieved by a blow‐spinning strategy to exhibit very stable cycling at a practical level of areal capacity up to 3 mAh cm–2. It is demonstrated that the Cu, Fe, and Cr doping into the LNMO lattice can suspend the Mn dissolution and improve the Li ion diffusivity and electronic conductivity of the LNMO host. As a result, the obtained CFC0.5‐LNMO cathode exhibits an excellent rate performance (1.75 mAh cm–2 at 1C) and long cycling stability under an areal capacity of 3 mAh cm–2 (78% capacity retention over 300 cycles at 0.5C).
A trace multiple Cr‐Fe‐Cu co‐doping strategy in the high voltage LiNi0.5Mn1.5O4 (LNMO) cathode via a blow‐spinning technique is reported. The co‐modified LNMO can be charged to a high voltage of 4.95 V without structural collapse, exhibiting good rate capability and stable cycling performance under the areal capacity of 3.04 mAh cm−2 (78.2% capacity retention after 300 cycles at 0.5 C).
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BFBNIB, FZAB, GIS, IJS, KILJ, NLZOH, NUK, OILJ, SAZU, SBCE, SBMB, UL, UM, UPUK
For the first time, organic semiconducting polymer dots (Pdots) based on poly(9,9′‐dioctylfluorenyl‐2,7‐diyl)‐co‐(1,4‐benzo‐{2,1′,3} thiadiazole) (PFBT) and polystyrene grafting with ...carboxyl‐group‐functionalized ethylene oxide (PS‐PEG‐COOH) are introduced as a photocatalyst towards visible‐light‐driven hydrogen generation in a completely organic solvent‐free system. With these organic Pdots as the photocatalyst, an impressive initial rate constant of 8.3 mmol h−1 g−1 was obtained for visible‐light‐driven hydrogen production, which is 5‐orders of magnitude higher than that of pristine PFBT polymer under the same catalytic conditions. Detailed kinetics studies suggest that the productive electron transfer quench of the excited state of Pdots by an electron donor is about 40 %. More importantly, we also found that the Pdots can tolerate oxygen during catalysis, which is crucial for further application of this material for light‐driven water splitting.
Organic polymer dots were used as a photocatalyst for visible‐light‐driven hydrogen generation for the first time and showed impressive activity with an initial hydrogen generation rate of 8.3 mmol h−1 g−1 without the assistance of any co‐catalysts. Do=donor.
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BFBNIB, FZAB, GIS, IJS, KILJ, NLZOH, NUK, OILJ, SAZU, SBCE, SBMB, UL, UM, UPUK
Mare volcanics on the Moon are the key record of thermo-chemical evolution throughout most of lunar history
. Young mare basalts-mainly distributed in a region rich in potassium, rare-earth elements ...and phosphorus (KREEP) in Oceanus Procellarum, called the Procellarum KREEP Terrane (PKT)
-were thought to be formed from KREEP-rich sources at depth
. However, this hypothesis has not been tested with young basalts from the PKT. Here we present a petrological and geochemical study of the basalt clasts from the PKT returned by the Chang'e-5 mission
. These two-billion-year-old basalts are the youngest lunar samples reported so far
. Bulk rock compositions have moderate titanium and high iron contents with KREEP-like rare-earth-element and high thorium concentrations. However, strontium-neodymium isotopes indicate that these basalts were derived from a non-KREEP mantle source. To produce the high abundances of rare-earth elements and thorium, low-degree partial melting and extensive fractional crystallization are required. Our results indicate that the KREEP association may not be a prerequisite for young mare volcanism. Absolving the need to invoke heat-producing elements in their source implies a more sustained cooling history of the lunar interior to generate the Moon's youngest melts.
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GEOZS, IJS, IMTLJ, KISLJ, NLZOH, NUK, OILJ, PNG, SAZU, SBCE, SBMB, UL, UM, UPUK, ZAGLJ
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