HMGB1 promotes neutrophil PD-L1 expression through TLR2 and mediates T cell apoptosis leading to immunosuppression in sepsis.

Neutrophils and T lymphocytes are closely related to occurrence of immunosuppression in sepsis. Studies have shown that neutrophil apoptosis decreases and T lymphocyte apoptosis increases in sepsis immunosuppression, but the specific mechanism involved remains unclear. In the present study, we found Toll-like Receptor 2 (TLR2) and programmed death-ligand 1 (PD-L1) were significantly activated in bone marrow neutrophils of wild-type mice after LPS treatment and that they were attenuated by treatment with C29, an inhibitor of TLR2. PD-L1 activation inhibits neutrophil apoptosis, whereas programmed death protein 1 (PD-1)activation promotes apoptosis of T lymphocytes, which leads to immunosuppression. Mechanistically, when sepsis occurs, pro-inflammatory factors and High mobility group box-1 protein (HMGB1) passively released from dead cells cause the up-regulation of PD-L1 through TLR2 on neutrophils. The binding of PD-L1 and PD-1 on T lymphocytes leads to increased apoptosis of T lymphocytes and immune dysfunction, eventually resulting in the occurrence of sepsis immunosuppression. In vivo experiments showed that the HMGB1 inhibitor glycyrrhizic acid (GA) and the TLR2 inhibitor C29 could inhibit the HMGB1/TLR2/PD-L1 pathway, and improving sepsis-induced lung injury. In summary, this study shows that HMGB1 regulates PD-L1 and PD-1 signaling pathways through TLR2, which leads to immunosuppression.

Low-cost BPO4 In Situ Synthetic Li3PO4 Coating and B/P-Doping to Boost 4.8 V Cyclability for Sulfide-Based All-Solid-State Lithium Batteries.

Structural damage of Ni-rich layered oxide cathodes such as LiNi0.8Co0.1Mn0.1O2 (NCM811) and serious interfacial side reactions and physical contact failures with sulfide electrolytes (SEs) are the main obstacles restricting ≥4.6 V high-voltage cyclability of all-solid-state lithium batteries (ASSLBs). To tackle this constraint, here, a modified NCM811 with Li3PO4 coating and B/P co-doping using inexpensive BPO4 as raw materials via the one-step in situ synthesis process is presented. Phosphates have good electrochemical stability and contain the same anion (O2-) and cation (P5+) as in cathode and SEs, respectively, thus Li3PO4 coating precludes interfacial anion exchange, lessening side reactivity. Based on the high bond energy of B─O and P─O, the lattice O and crystal texture of NCM811 can be stabilized by B3+/P5+ co-doping, thereby suppressing microcracks during high-voltage cycling. Therefore, when tested in combination with Li─In anode and Li6PS5Cl solid electrolytes (LPSCl), the modified NCM811 exhibits extraordinary performance, with 200.36 mAh g-1 initial discharge capacity (4.6 V), cycling 2300 cycles with decay rate as low as 0.01% per cycle (1C), and 208.26 mAh g-1 initial discharge capacity (4.8 V), cycling 1986 cycles with 0.02% per cycle decay rate. Simultaneously, it also has remarkable electrochemical abilities at both -20 °C and 60 °C.

Progressive activation of porous vanadium nitride microspheres with intercalation-conversion reactions toward high performance over a wide temperature range for zinc-ion batteries.

Rechargeable aqueous zinc-ion batteries have great promise for becoming next-generation storage systems, although the irreversible intercalation of Zn2+ and sluggish reaction kinetics impede their wide application. Therefore, it is urgent to develop highly reversible zinc-ion batteries. In this work, we modulate the morphology of vanadium nitride (VN) with different molar amounts of cetyltrimethylammonium bromide (CTAB). The optimal electrode has porous architecture and excellent electrical conductivity, which can alleviate volume expansion/contraction and allow for fast ion transmission during the Zn2+ storage process. Furthermore, the CTAB-modified VN cathode undergoes a phase transition that provides a better framework for vanadium oxide (VOx). With the same mass of VN and VOx, VN provides more active material after phase conversion due to the molar mass of the N atom being less than that of the O atom, thus increasing the capacity. As expected, the cathode displays an excellent electrochemical performance of 272 mAh g-1 at 5 A g-1, high cycling stability up to 7000 cycles, and excellent performance over a wide temperature range. This discovery creates new possibilities for the development of high-performance multivalent ion aqueous cathodes with rapid reaction mechanisms.

Mo-Pre-Intercalated MnO2 Cathode with Highly Stable Layered Structure and Expanded Interlayer Spacing for Aqueous Zn-Ion Batteries.

Although manganese-based oxides possess high voltage and low cost, the sluggish reaction kinetics and poor structural stability hinder their applications in aqueous rechargeable Zn-ion batteries (ZIBs). Herein, a molybdenum (Mo) pre-intercalation strategy is proposed to solve the above issues of δ-MnO2. The pre-intercalated Mo dopants, acting as the interlayer pillars, can not only expand the interlayer spacing but also reinforce the layered structure of δ-MnO2, finally achieving enhanced reaction kinetics and superb cycling stability during carrier (de)intercalation. Moreover, oxygen defects, introduced due to Mo-pre-intercalation, play a critical role in the fast reaction kinetics and capacity improvement of the Mo-pre-intercalated δ-MnO2 (Mo-MnO2) cathode. Therefore, the Mo-MnO2 cathode displays a high energy density of 451 Wh kg-1 (based on cathode mass), excellent rate capability, and admirable long-term cycling performance with a high capacity of 159 mAhg-1 at 1.0 A g-1 after 1000 cycles. In addition, the energy storage mechanism of Zn2+/H+ stepwise reversible (de)intercalation is also revealed by ex situ experiments. This work provides an insightful guide for boosting the electrochemical performance of Mn-based oxide cathodes for ZIBs.

Nitrogen-doped carbon encapsulated zinc vanadate polyhedron engineered from a metal-organic framework as a stable anode for alkali ion batteries.

In this work, we fabricated vanadium/zinc metal-organic frameworks (V/Zn-MOFs) derived from self-assembled metal organic frameworks, to further disperse ultrasmall Zn2VO4 nanoparticles and encapsulate them in a nitrogen-doped nanocarbon network (ZVO/NC) under in situ pyrolysis. When employed as an anode for lithium-ion batteries, ZVO/NC delivers a high reversible capacity (807 mAh g-1 at 0.5 A g-1) and excellent rate performance (372 mAh g-1 at 8.0 A g-1). Meanwhile, when used in sodium-ion batteries, it exhibits long-term cycling stability (7000 cycles with 145 mAh g-1 at 2.0 A g-1). Additionally, when employed in potassium-ion batteries, it also shows outstanding electrochemical performance with reversible capacities of 264 mAh g-1 at 0.1 A g-1 and 140 mAh g-1 at 0.5 A g-1 for 1000 cycles. The mechanism by which the pseudocapacitive behaviour of ZVO/NC enhances battery performance under a suitable electrolyte was probed, which offers useful enlightenment for the potential development of anodes of alkali-ion batteries. The performance of Zn2VO4 as an anode for SIBs/PIBs was investigated for the first time. This work provides a new horizon in the design ZVO/NC as a promising anode material owing to the intrinsically synergic effects of mixed metal species and the multiple valence states of V.

Facile Synthesis of Ultra-Small Few-Layer Nanostructured MoSe2 Embedded on N, P Co-Doped Bio-Carbon for High-Performance Half/Full Sodium-Ion and Potassium-Ion Batteries.

Sodium/potassium-ion batteries (SIBs/PIBs) arouse intensive interest on account of the natural abundance of sodium/potassium resources, the competitive cost and appropriate redox potential. Nevertheless, the huge challenge for SIBs/PIBs lies in the scarcity of an anode material with high capacity and stable structure, which are capable of accommodating large-size ions during cycling. Furthermore, using sustainable natural biomass to fabricate electrodes for energy storage applications is a hot topic. Herein, an ultra-small few-layer nanostructured MoSe2 embedded on N, P co-doped bio-carbon is reported, which is synthesized by using chlorella as the adsorbent and precursor. As a consequence, the MoSe2 /NP-C-2 composite represents exceedingly impressive electrochemical performance for both sodium-ion batteries (SIBs) and potassium-ion batteries (PIBs). It displays a promising reversible capacity (523 mAh g-1 at 100 mA g-1 after 100 cycles) and impressive long-term cycling performance (192 mAh g-1 at 5 A g-1 even after 1000 cycles) in SIBs, which are some of the best properties of MoSe2 -based anode materials for SIBs to date. To further probe the great potential applications, full SIBs pairing the MoSe2 /NP-C-2 composite anode with a Na3 V2 (PO4 )3 cathode also exhibits a satisfactory capacity of 215 mAh g-1 at 500 mA g-1 after 100 cycles. Moreover, it also delivers a decent reversible capacity of 131 mAh g-1 at 1 A g-1 even after 250 cycles for PIBs.

Electrospun VSe1.5/CNF composite with excellent performance for alkali metal ion batteries.

Exploring advanced anode materials with excellent electrochemical performance for rechargeable batteries, including lithium-ion batteries (LIBs), sodium-ion batteries (SIBs) and potassium-ion batteries (PIBs), has attracted great attention. However, low electronic conductivity, severe particle agglomeration and lack of effective synthesis methods have still greatly hampered their rapid development. Herein, we initially fabricate a novel VSe1.5/CNF composite through a facile electrospinning method followed by selenization. The electrochemical measurements show that VSe1.5/CNFs can enable the rapid and durable storage of Li+, Na+, and K+ ions. When used as an anode material for LIBs, the VSe1.5/CNF composite delivers a high capacity of 932 mA h g-1 after 400 cycles at a high current density of 1 A g-1. In addition, for SIBs, the VSe1.5/CNF composite manifests a high reversible capacity of 668 mA h g-1 after 50 cycles and an excellent capacity of 265 mA h g-1 at 2 A g-1 even after an ultra-long 6000 cycles. This is one of the best performances of vanadium-based anode materials for SIBs reported so far. Most remarkably, the VSe1.5/CNF composite also demonstrates a satisfactory reversible K+ storage performance. The simple synthetic route and excellent ion storage properties make the VSe1.5/CNF composite a great prospect for application as an anode material for alkali metal ion batteries.

Rational design of few-layer MoSe2 confined within ZnSe-C hollow porous spheres for high-performance lithium-ion and sodium-ion batteries.

Rechargeable battery systems, including Li-ion batteries and Na-ion batteries, have attracted great interest in energy storage because of their high energy density, low cost, efficient energy storage and suitable redox potential. Nevertheless, their rapid development is still greatly hampered by some typical constraints including low coulombic efficiency, large volume changes and severe particle agglomeration and pulverization during the charge-discharge process. Here, we fabricate a few-layer MoSe2 confined within a ZnSe-C hollow porous sphere nanocomposite through a simple self-assembly strategy followed by selenization, which efficiently circumvents these problems. The fabricated ZnSe/MoSe2@C electrode demonstrates diverse advantages, including the existence of a few-layer structure, an in situ porous carbon matrix, multicomponent coordination and excellent pseudocapacitive behavior. When used as an anode material, it displays extraordinarily attractive electrochemical performance for both lithium-ion batteries (LIBs) and sodium-ion batteries (SIBs). The reversible capacity of ZnSe/MoSe2@C for LIBs reaches as high as 1051 mA h g-1 at 0.2 A g-1 (150 cycles). A long-term high-rate cycling test reveals an excellent stability of 524 mA h g-1 at 4 A g-1 after 600 cycles. In addition, for SIBs, ZnSe/MoSe2@C also manifests a high initial coulombic efficiency of 89% at 0.2 A g-1 and a remarkable reversible capacity of 381 mA h g-1 at a high current density of 4 A g-1 even after 250 cycles with negligible capacity loss. This is one of the best performances of ZnSe-based anode materials for SIBs reported so far. The regulation strategy reported in the present work is expected to offer new insights into the fabrication of high performance anode materials for SIBs.

Facile synthesis of hierarchical lychee-like Zn3V3O8@C/rGO nanospheres as high-performance anodes for lithium ion batteries.

In the present work, the hierarchical Zn3V3O8@C/rGO composite with a unique lychee-like architecture was fabricated by a simple one-pot ethanol thermal reduction strategy. When used as an anode material, it exhibited outstanding electrochemical performance for lithium-ion batteries (LIBs). For instance, the Zn3V3O8@C/rGO composite delivers high reversible capacities (1012 mAh g-1 at 0.1 A g-1 after 200 cycles) and high rate stability (448 mAh g-1 at 4 A g-1 after 1000 cycles). This outstanding performance can be attributed to the synergistic effect of the diverse structural virtues, effective interface and dual-spatially hybrid carbon network. Significantly, this one-pot simple strategy can be extended to fabricating highly stable and high rate performance of vanadates or other anode materials for LIBs.