Serine synthesis controls mitochondrial biogenesis in macrophages.

Mitochondrial dysfunction is the pivotal driving factor of multiple inflammatory diseases, and targeting mitochondrial biogenesis represents an efficacious approach to ameliorate such dysfunction in inflammatory diseases. Here, we demonstrated that phosphoglycerate dehydrogenase (PHGDH) deficiency promotes mitochondrial biogenesis in inflammatory macrophages. Mechanistically, PHGDH deficiency boosts mitochondrial reactive oxygen species (mtROS) by suppressing cytoplasmic glutathione synthesis. mtROS provokes hypoxia-inducible factor-1α signaling to direct nuclear specificity protein 1 and nuclear respiratory factor 1 transcription. Moreover, myeloid Phgdh deficiency reverses diet-induced obesity. Collectively, this study reveals that a mechanism involving de novo serine synthesis orchestrates mitochondrial biogenesis via mitochondrial-to-nuclear communication, and provides a potential therapeutic target for tackling inflammatory diseases and mitochondria-mediated diseases.

Targeting methionine metabolism in cancer: opportunities and challenges.

Reprogramming of methionine metabolism is a conserved hallmark of tumorigenesis. Recent studies have revealed mechanisms regulating methionine metabolism within the tumor microenvironment (TME) that drive both cancer development and antitumor immunity evasion. In this review article we summarize advancements in our understanding of tumor regulation of methionine metabolism and therapies in development that target tumor methionine metabolism. We also delineate the challenges of methionine blockade therapies in cancer and discuss emerging strategies to address them.

Serine synthesis sustains macrophage IL-1ß production via NAD+-dependent protein acetylation.

Serine metabolism is involved in the fate decisions of immune cells; however, whether and how de novo serine synthesis shapes innate immune cell function remain unknown. Here, we first demonstrated that inflammatory macrophages have high expression of phosphoglycerate dehydrogenase (PHGDH, the rate-limiting enzyme of de novo serine synthesis) via nuclear factor κB signaling. Notably, the pharmacological inhibition or genetic modulation of PHGDH limits macrophage interleukin (IL)-1ß production through NAD+ accumulation and subsequent NAD+-dependent SIRT1 and SIRT3 expression and activity. Mechanistically, PHGDH not only sustains IL-1ß expression through H3K9/27 acetylation-mediated transcriptional activation of Toll-like receptor 4 but also supports IL-1ß maturation via NLRP3-K21/22/24/ASC-K21/22/24 acetylation-mediated activation of the NLRP3 inflammasome. Moreover, mice with myeloid-specific depletion of Phgdh show alleviated inflammatory responses in lipopolysaccharide-induced systemic inflammation. This study reveals a network by which a metabolic enzyme, involved in de novo serine synthesis, mediates post-translational modifications and epigenetic regulation to orchestrate IL-1ß production, providing a potential inflammatory disease target.

High-Performance Lithium-Sulfur Batteries via Molecular Complexation.

Beyond lithium-ion technologies, lithium-sulfur batteries stand out because of their multielectron redox reactions and high theoretical specific energy (2500 Wh kg-1). However, the intrinsic irreversible transformation of soluble lithium polysulfides to solid short-chain sulfur species (Li2S2 and Li2S) and the associated large volume change of electrode materials significantly impair the long-term stability of the battery. Here we present a liquid sulfur electrode consisting of lithium thiophosphate complexes dissolved in organic solvents that enable the bonding and storage of discharge reaction products without precipitation. Insights garnered from coupled spectroscopic and density functional theory studies guide the complex molecular design, complexation mechanism, and associated electrochemical reaction mechanism. With the novel complexes as cathode materials, high specific capacity (1425 mAh g-1 at 0.2 C) and excellent cycling stability (80% retention after 400 cycles at 0.5 C) are achieved at room temperature. Moreover, the highly reversible all-liquid electrochemical conversion enables excellent low-temperature battery operability (>400 mAh g-1 at -40 °C and >200 mAh g-1 at -60 °C). This work opens new avenues to design and tailor the sulfur electrode for enhanced electrochemical performance across a wide operating temperature range.

Dietary trace mineral pattern influences gut microbiota and intestinal health of broilers.

Dietary trace minerals can impact gut flora, which can further affect intestinal health. However, the dietary balance pattern of trace minerals for the intestinal health of broilers needs to be explored. The present study was conducted to investigate the effect of the dietary pattern of Cu, Fe, Mn, Zn, and Se on the intestinal morphology, microbiota, short-chain fatty acid concentrations, antioxidant status, and the expression of tight junction proteins in broilers. A total of 240 1-d-old Arbor Acres male broilers were randomly assigned to one of five treatments with six replicate cages of eight birds per cage for each treatment. The birds were fed the corn-soybean meal basal diet supplemented with five combination patterns of trace minerals for 42 d. The dietary treatments were as follows: the inorganic sources were added to the diet based on the recommendations of the current National Research Council (NRC, T1) and Ministry of Agriculture of P.R. China (MAP) (T2) for broiler chicks, respectively; the inorganic sources were added to the diet at the levels based on our previous results of inorganic trace mineral requirements for broilers (T3); the organic sources were added to the diet at the levels considering the bioavailabilities of organic trace minerals for broilers described in our previous studies (T4); and the organic sources were added to the diet based on the recommendations of the current MAP for broiler chicks (T5). The results showed that broilers from T1 had lower (P < 0.05) crypt depth (CD), and a higher (P < 0.05) villus height: CD in duodenum on day 21 and lower CD (P < 0.05) in jejunum on day 42 than those from T3 and T4. Broilers from T1, T3, and T5 had a higher (P < 0.05) Shannon index in cecum on day 21 than those from T4. Broilers from T1 had a higher (P < 0.05) abundance of Lactobacillus in ileum on day 21 than those from T2 and T3. Broilers from T1, T2, and T5 had a higher (P < 0.05) valeric acid concentrations in cecum on day 42 than those from T3 and T4. In addition, Birds from T2 had higher (P < 0.05) Claudin-1 mRNA levels in jejunum on day 42 than those from T3 and T4. And birds from T3, T4, and T5 had a higher (P < 0.05) Occludin protein expression levels in duodenum on day 42 than those from T2. These results indicate that dietary pattern of Cu, Fe, Mn, Zn, and Se influenced gut flora and intestinal health of broilers, and the appropriate pattern of Cu, Fe, Mn, Zn, and Se in the diet for intestinal health of broilers would be Cu 12 mg, Fe 229 mg, Mn 81 mg, Zn 78 mg, and Se 0.24 mg/kg (1 to 21 d of age), and Cu 11 mg, Fe 193 mg, Mn 80 mg, Zn 73 mg, and Se 0.22 mg/kg (22 to 42 d of age), when the trace minerals as inorganic sources were added to diets according to the recommendations of the current NRC.

Information is still scarce regarding the effect of dietary trace mineral patterns on the intestinal health of broilers. The results indicated that dietary trace mineral pattern influenced intestinal health of broilers, and the appropriate pattern of trace minerals in the diet for intestinal health of broilers would be Cu 12 mg, Fe 229 mg, Mn 81 mg, Zn 78 mg, and Se 0.24 mg/kg (1 to 21 d of age), and Cu 11 mg, Fe 193 mg, Mn 80 mg, Zn 73 mg, and Se 0.22 mg/kg (22 to 42 d of age), when the trace minerals as inorganic sources were added to diets according to the recommendations of the current National Research Council. Our results provided scientific experimental bases for improving intestinal health of broilers by nutritional strategy.

The organic zinc with moderate chelation strength enhances the expression of related transporters in the jejunum and ileum of broilers.

Our previous study demonstrated that the zinc (Zn) proteinate with moderate chelation strength (Zn-Prot M) enhanced the Zn absorption in the small intestine partially via increasing the expression of some Zn and amino acid transporters in the duodenum of broilers. However, it remains unknown whether the Zn-Prot M could also regulate the expression of related transporters in the jejunum and ileum of broilers in the above enhancement of Zn absorption. The present study was conducted to investigate the effect of the Zn-Prot M on the expression of related transporters in the jejunum and ileum of broilers compared to the Zn sulfate (ZnS). Zinc-deficient broilers (13-d-old) were fed with the Zn-unsupplemented basal diets (control) or the basal diets supplemented with 60 mg Zn/kg as ZnS or Zn-Prot M for 26 d. The results showed that in the jejunum, compared to the control, supplementation of the organic or inorganic Zn increased (P < 0.05) mRNA and protein expression of b0,+-type amino acid transporter (rBAT), Zn transporter 10 (ZnT10), and peptide-transporter 1 (PepT1) mRNA expression and Zn transporter 7 (ZnT7) protein expression on d 28, while y+L-type amino transporter 2 (y+LAT2) mRNA and protein expression, and protein expression of ZnT7 and ZnT10 on 28 d and zrt-irt-like protein 3 (ZIP3) and zrt-irt-like protein 5 (ZIP5) on d 39 were higher (P < 0.05) for Zn-Prot M than for ZnS. In the ileum, Zn addition regardless of Zn source up-regulated (P < 0.05) mRNA expression of Zn transporter 9 (ZnT9) and ZIP3, ZIP5, and y+LAT2 protein expression on d 28, and PepT1 mRNA and protein expression, ZIP3 and y+LAT2 mRNA expression and ZnT10 protein expression on d 39. Furthermore, Zn transporter 4 (ZnT4) and ZnT9 mRNA expression and Zn transporter 1 (ZnT1) protein expression on d 28, and y+LAT2 mRNA expression and ZnT10 and PepT1 protein expression on d 39 were higher (P < 0.05) for Zn-Prot M than for ZnS. It was concluded that the Zn-Prot M enhanced the expression of the ZnT1, ZnT4, ZnT9, ZnT10, ZIP3, ZIP5, y+LAT2, and PepT1 in the jejunum or ileum of broilers compared to the ZnS.

Organic zinc with moderate chelation strength enhances zinc absorption in the small intestine and expression of related transporters in the duodenum of broilers.

Our previous study demonstrated that the absorption of zinc (Zn) from the organic Zn proteinate with moderate chelation strength was significantly higher than that of Zn from the inorganic Zn sulfate in the in situ ligated duodenal segment of broilers, but the underlying mechanisms are unknown. The present study aimed to determine the effect of organic Zn with moderate chelation strength and inorganic Zn on the Zn absorption in the small intestine and the expression of related transporters in the duodenum of broilers. The Zn-deficient broilers (13 days old) were fed with the Zn-unsupplemented basal diets (control) containing 25.72 and 25.64 mg Zn/kg by analysis or the basal diets supplemented with 60 mg Zn/kg as the Zn sulfate or the Zn proteinate with moderate chelation strength (Zn-Prot M) for 26 days. The results showed that the plasma Zn contents from the hepatic portal vein of broilers at 28 days and 39 days of age were increased (p < 0.05) by Zn addition and greater (p < 0.05) in the Zn-Prot M than in the Zn sulfate. On d 28, Zn addition upregulated (p < 0.05) mRNA expression of zinc transporter 1 (ZnT1), Zrt-irt-like protein 5 (ZIP5), y + L-type amino transporter 2 (y + LAT2) and b0,+-type amino acid transporter (rBAT), zinc transporter 4 (ZnT4) protein expression, and zinc transporter 9 (ZnT9) mRNA and protein expression in the duodenum. Moreover, ZnT9 mRNA expression, ZnT4, ZIP5, and rBAT protein expression, zinc transporter 7 (ZnT7), and y + LAT2 mRNA and protein expression in the duodenum of broilers on 28 days were higher (p < 0.05) in the Zn-Prot M than in the Zn sulfate. On d 39, supplemental Zn increased (p < 0.05) peptide-transporter 1 (PepT1) mRNA expression and y + LAT2 protein expression, while the mRNA expression of ZnT7 and Zrt-irt-like protein 3 (ZIP3) were higher (p < 0.05) for the Zn-Prot M than for the Zn sulfate in the duodenum. It was concluded that the Zn-Prot M enhanced the Zn absorption in the small intestine partially via upregulating the expression of ZnT4, ZnT7, ZnT9, ZIP3, ZIP5, y + LAT2, and rBAT in the duodenum of broilers.

Extending the low-temperature operation of sodium metal batteries combining linear and cyclic ether-based electrolyte solutions.

Nonaqueous sodium-based batteries are ideal candidates for the next generation of electrochemical energy storage devices. However, despite the promising performance at ambient temperature, their low-temperature (e.g., < 0 °C) operation is detrimentally affected by the increase in the electrolyte resistance and solid electrolyte interphase (SEI) instability. Here, to circumvent these issues, we propose specific electrolyte formulations comprising linear and cyclic ether-based solvents and sodium trifluoromethanesulfonate salt that are thermally stable down to -150 °C and enable the formation of a stable SEI at low temperatures. When tested in the Na||Na coin cell configuration, the low-temperature electrolytes enable long-term cycling down to -80 °C. Via ex situ physicochemical (e.g., X-ray photoelectron spectroscopy, cryogenic transmission electron microscopy and atomic force microscopy) electrode measurements and density functional theory calculations, we investigate the mechanisms responsible for efficient low-temperature electrochemical performance. We also report the assembly and testing between -20 °C and -60 °C of full Na||Na3V2(PO4)3 coin cells. The cell tested at -40 °C shows an initial discharge capacity of 68 mAh g-1 with a capacity retention of approximately 94% after 100 cycles at 22 mA g-1.

Evaluation of optimal dietary calcium level by bone characteristics and calcium metabolism-related gene expression of broilers from 22 to 42 d of age.

The current dietary Ca recommendation of broilers is primarily based on the previous studies carried out more than 30 yr ago. However, the modern commercial broilers are quite different from those more than 30 yr ago. The present experiment was conducted to evaluate an optimal dietary Ca level by bone characteristics and Ca metabolism-related gene expression of broilers fed a corn-soybean meal diet from 22 to 42 d of age. A total of 252 22-d-old Arbor Acres male broilers were randomly assigned to 1 of 7 treatments with 6 replicate cages of 6 birds per cage for each treatment. Broilers were fed the corn-soybean meal diets containing 0.50%, 0.60%, 0.70%, 0.80%, 0.90%, 1.00%, or 1.10% Ca for 21 d, and each diet contained 0.31% non-phytate P. The results showed that the mineral contents in tibia and middle toe bone, mineral density in tibia and middle toe bone, middle toe ash percentage, middle toe ash Ca percentage, and tibia alkaline phosphatase mRNA expression level of broilers were influenced (P < 0.04) by dietary Ca level and increased quadratically (P < 0.05) as dietary Ca level increased. The estimates of optimal dietary Ca levels were 0.55%, 0.60%, 0.70%, 0.72%, 0.63%, 0.66%, and 0.70%, respectively, based on the best fitted broken-line, quadratic, or asymptotic models (P < 0.02) of the above sensitive indices. These results indicate that the optimal dietary Ca level would be 0.72% to support all of the Ca metabolism and bone development of broilers fed the corn-soybean meal diet from 22 to 42 d of age.

The present experiment was conducted to evaluate an optimal dietary Ca level by bone characteristics and Ca metabolism-related gene expression of broilers fed a corn-soybean meal diet from 22 to 42 d of age. A total of 252 22-d-old Arbor Acres male broilers were randomly assigned to 1 of 7 treatments with 6 replicate cages of 6 birds per cage for each treatment. Broilers were fed the corn-soybean meal diets containing 0.50%, 0.60%, 0.70%, 0.80%, 0.90%, 1.00%, or 1.10% Ca for 21 d, and each diet contained 0.31% non-phytate P. The results showed that the tibia and middle toe bone mineral contents, tibia and middle toe bone mineral density, middle toe ash percentage, middle toe ash Ca percentage, and tibia alkaline phosphatase mRNA expression level were sensitive criteria to estimate the optimal dietary Ca levels of broilers. The estimates of optimal dietary Ca levels were 0.55% to 0.72% based on the above sensitive criteria. These results indicate that the optimal dietary Ca level would be 0.72% to support all of the Ca metabolism and bone development of broilers fed the corn-soybean meal diet from 22 to 42 d of age.

Stabilizing Sodium Metal Anodes with Surfactant-Based Electrolytes and Unraveling the Atomic Structure of Interfaces by Cryo-TEM.

Sodium (Na) metal batteries are promising as next-generation energy storage systems due to the high specific capacity of the Na metal anode as well as rich natural abundance and low cost of Na resources. Nevertheless, uncontrolled growth of dendritic/mossy Na arising from the unstable solid-electrolyte interphase (SEI) leads to rapid electrode degradation and severe safety issues. In this work, we introduce cetyltrimethylammonium bromide (CTAB) as an electrolyte additive that enables a synergistic effect from both the CTA+ cation and Br- anion in stabilizing the Na metal anode. Notably, cryogenic transmission electron microscopy is utilized to investigate the effect of the additive, revealing the critical morphology and structure of the SEIs and Na electrodes at the nano/atomic scale. Benefiting fromthe additive, a stable Na anode can be realized at an ultrahigh capacity of 30 mAh cm-2 at 10 mA cm-2 over 400 h.

Determination of optimal dietary selenium levels by full expression of selenoproteins in various tissues of broilers from 22 to 42 d of age.

The current NRC dietary selenium (Se) requirement (0.15 mg/kg) of broilers from 22 to 42 d of age is primarily based on a previous study reported in 1986, which might not be applicable to modern classes of rapidly growing broilers. The present experiment was conducted to determine the optimal dietary Se level for meeting metabolic and functional Se requirements of broilers fed a corn-soybean meal diet from 22 to 42 d of age. A total of 336 Arbor Acres male broilers at 22 d old were randomly assigned to 1 of 6 treatments with 7 replicates and fed a basal corn-soybean meal diet (control, containing 0.014 mg Se/kg) and the basal diet supplemented with 0.10, 0.20, 0.30, 0.40, or 0.50 mg Se/kg from Na2SeO3 for 21 d. The results showed that the Se concentrations in plasma, liver, kidney, pancreas, breast and thigh muscles, the activity of glutathione peroxidase (GPX) in plasma, liver and kidney, the mRNA expression levels of Gpx4, selenoprotein (Seleno) h and Selenou in liver, S elenop and Selenoh in kidney, and the protein expression levels of GPX4 in the liver and kidney of broilers were affected (P < 0.05) by supplemental Se level, and increased quadratically (P < 0.05) with the increase of supplemental Se level. The estimates of optimal dietary Se levels were 0.10 to 0.49 mg/kg based on the fitted broken-line or asymptotic models (P < 0.0001) of the above Se concentration indices, and 0.08 to 0.37 mg/kg based on the fitted broken-line, quadratic or asymptotic models (P < 0.007) of the above selenoprotein expression indices. These results indicate that the optimal dietary Se levels would be 0.49 mg/kg to support the maximum Se concentrations and 0.37 mg/kg to support the full expression of selenoproteins in plasma and various tissues of broilers fed a corn-soybean meal diet from 22 to 42 d of age.

Stable sodium-sulfur electrochemistry enabled by phosphorus-based complexation.

A series of sodium phosphorothioate complexes are shown to have electrochemical properties attractive for sodium-sulfur battery applications across a wide operating temperature range. As cathode materials, they resolve a long-standing issue of cyclic liquid-solid phase transition that causes sluggish reaction kinetics and poor cycling stability in conventional, room-temperature sodium-sulfur batteries. The cathode chemistry yields 80% cyclic retention after 400 cycles at room temperature and a superior low-temperature performance down to -60 °C. Coupled experimental characterization and density functional theory calculations revealed the complex structures and electrochemical reaction mechanisms. The desirable electrochemical properties are attributed to the ability of the complexes to prevent the formation of solid precipitates over a fairly wide range of voltage.

Vibration Band Gap Characteristics of Two-Dimensional Periodic Double-Wall Grillages.

In this article, the wave finite element method (WFEM) is used to calculate the band gap characteristics of two-dimensional (2D) periodic double-wall grillages (DwGs), which are verified by the grillage model vibration measurement experiment and finite element calculation. To obtain the band gap characteristics of periodic DwGs, the finite element calculation model is established according to the lattice and energy band theory and the characteristic equation of the periodic unit cell under the given wave vector condition is solved based on Bloch theorem. Then, the frequency transfer functions of finite-length manufactured and finite element models are obtained to verify the band gap characteristics of periodic DwGs. Finally, the effects of material parameters and structural forms on band gap characteristics and transfer functions are analyzed, which can provide a reference for engineering structure vibration and noise reduction design.

Deeply Cycled Sodium Metal Anodes at Low Temperature and in Lean Electrolyte Conditions.

Enabling high-performing alkali metal anodes at low temperature and in lean electrolyte conditions is critical for the advancement of next-generation batteries with high energy density and improved safety. We present an ether-ionic liquid composite electrolyte to tackle the problem of dendrite growth of metallic sodium anode at low temperatures ranging from 0 to -40 °C. This composite electrolyte enables a stable sodium metal anode to be deeply cycled at 2 mA cm-2 with an ultrahigh reversible capacity of 50 mAh cm-2 for 500 hours at -20 °C in lean electrolyte (1.0 µL mAh-1 ) conditions. Using the composite electrolyte, full cells with Na3 V2 (PO4 )3 as cathode and sodium metal as anode present a high capacity retention of 90.7 % after 1,000 cycles at 2C at -20 °C. The sodium-carbon dioxide batteries also exhibit a reversible capacity of 1,000 mAh g-1 over 50 cycles across a range of temperatures from -20 to 25 °C.

Tunable MXene-Derived 1D/2D Hybrid Nanoarchitectures as a Stable Matrix for Dendrite-Free and Ultrahigh Capacity Sodium Metal Anode.

Although sodium (Na) is one of the most promising alternatives to lithium as an anode material for next-generation batteries, uncontrollable Na dendrite growth still remains the main challenge for Na metal batteries. Herein, a novel 1D/2D Na3Ti5O12-MXene hybrid nanoarchitecture consisting of Na3Ti5O12 nanowires grown between the MXene nanosheets is synthesized by a facile approach using cetyltrimethylammonium bromide (CTAB)-pretreated Ti3C2 MXene. Used as a matrix for the Na metal anode, the Na3Ti5O12 nanowires, formed benefiting from the CTAB stabilization, have chemical interaction with Na and thus provide abundant Na nucleation sites. These 1D nanostructures, together with the unique confinement effect from the 2D nanosheets, effectively guide and control the Na deposition within the interconnected nanochannels, preventing the "hot spot" formation for dendrite growth. A stable cycling performance can be achieved at a high current density up to 10 mA cm-2 along with an ultrahigh capacity up to 20 mAh cm-2.

Designing an All-Solid-State Sodium-Carbon Dioxide Battery Enabled by Nitrogen-Doped Nanocarbon.

All-solid-state sodium-carbon dioxide (Na-CO2) battery is an emerging technology that effectively utilizes the greenhouse gas, CO2, for energy storage with the virtues of minimized electrolyte leakage and suppressed Na dendrite growth for the Na metal anode. However, the sluggish reduction/evolution reactions of CO2 on the solid electrolyte/CO2 cathode interface have caused premature battery failure. Herein, nitrogen (N)-doped nanocarbon derived from metal-organic frameworks is designed as a cathode catalyst to solve this challenge. The porous and highly conductive N-doped nanocarbon possesses superior uptake and binding capability with CO2, which significantly accelerates the CO2 electroreduction and promotes the formation of thin sheetlike discharged products (200 nm in thickness) that can be easily decomposed upon charging. Accordingly, reduced discharge/charge overpotential, high discharge capacity (>10 000 mAh g-1), long cycle life, and high energy density (180 Wh kg-1 in pouch cells) are achieved at 50 °C.

Rapid and Scalable Synthesis of Cuprous Halide-Derived Copper Nano-Architectures for Selective Electrochemical Reduction of Carbon Dioxide.

Electrochemical reduction of carbon dioxide (CO2) into value-added chemicals and fuels provides a promising pathway for environmental and energy sustainability. Copper (Cu) demonstrates a unique ability to catalyze the electrochemical conversion of CO2 into valuable multicarbon products. However, developing a rapid, scalable and cost-effective method to synthesize efficient and stable Cu catalysts with high selectivity toward multicarbon products at a low overpotential is still hard to achieve and highly desirable. In this work, we present a facile wet chemistry approach to yield well-defined cuprous halide (CuX, X = Cl, Br or I) microcrystals with different degrees of truncations at edges/vertices, which can be ascribed to the oxidative etching mechanism of halide ions. More importantly, the as-obtained cuprous halides can be electrochemically transformed into varied Cu nanoarchitectures, thus exhibiting distinct CO2 reduction behaviors. The CuI-derived Cu nanofibers composed of self-assembled nanoparticles are reported for the first time, which favor the formation of C2+3 products at a low overpotential with a particular selectivity toward ethane. In comparison, the Cu nanocubes evolved from CuCl are highly selective toward C1 products. For CuBr-derived Cu nanodendrites, C1 products are subject to form at a low overpotential, while C2+3 products gradually become dominant with a favorable formation of ethylene when the potential turns more negative. This work explicitly reveals the critical morphology effect of halide-derived Cu nanostructures on the CO2 product selectivity, and also provides an ideal platform to investigate the structure-property relationship for CO2 electroreduction.

Graphene Regulated Ceramic Electrolyte for Solid-State Sodium Metal Battery with Superior Electrochemical Stability.

Employing solid ceramic electrolyte in sodium (Na) metal batteries enables safe and cost-effective energy storage solution toward the advent of sustainable energy. Nevertheless, the development of solid-state Na batteries is hindered by the large interfacial charge transfer resistance between electrodes and solid electrolyte. Here, a novel and scalable design approach is utilized to significantly reduce the interfacial resistance through the direct growth of graphene-like interlayer on Na+ superionic conductor (NASICON) ceramic electrolyte, resulting in a 10-fold decrease of interfacial resistance. Benefiting from the graphene regulated NASICON, extremely stable Na plating/stripping cycling performance using solid electrolyte at a current density up to 1 mA/cm2 with a cycling capacity of 1 mAh/cm2 for 500 cycles (1000 h) is demonstrated for the first time. The surface of Na electrode after 1000 h of cycling remained smooth because of uniform Na+ flux across graphene-coated-NASICON/Na interface enabled by the abundant graphene defects network for efficient Na+ transport. Solid-state room temperature battery consists of graphene-regulated NASICON electrolyte, Na3V2(PO4)3 cathode and Na anode delivered a reversible initial capacity of 108 mAh/g at 1C current density for 300 cycles with 85% capacity retention, far superior than the battery with pristine NASICON. This work can be a valuable contribution toward a safe and stable solid-state Na metal battery system, and provide insights for solid-state lithium metal batteries as well.

Facile Stabilization of the Sodium Metal Anode with Additives: Unexpected Key Role of Sodium Polysulfide and Adverse Effect of Sodium Nitrate.

Sodium metal is an attractive anode for next-generation energy storage systems owing to its high specific capacity, low cost, and high abundance. Nevertheless, uncontrolled Na dendrite growth caused by the formation of unstable solid electrolyte interphase (SEI) leads to poor cycling performance and severe safety concerns. Sodium polysulfide (Na2 S6 ) alone is revealed to serve as a positive additive or pre-passivation agent in ether electrolyte to improve the long-term stability and reversibility of the Na anode, while Na2 S6 -NaNO3 as co-additive has an adverse effect, contrary to the prior findings in the lithium anode system. A superior cycling behavior of Na anode is first demonstrated at a current density up to 10 mA cm-2 and a capacity up to 5 mAh cm-2 over 100 cycles. As a proof of concept, a high-capacity Na-S battery was prepared by pre-passivating the Na anode with Na2 S6 . This study gives insights into understanding the differences between Li and Na systems.

Critical Role of Ultrathin Graphene Films with Tunable Thickness in Enabling Highly Stable Sodium Metal Anodes.

Sodium (Na) metal has shown great promise as an anode material for the next-generation energy storage systems because of its high theoretical capacity, low cost, and high earth abundance. However, the extremely high reactivity of Na metal with organic electrolyte leads to the formation of unstable solid electrolyte interphase (SEI) and growth of Na dendrites upon repeated electrochemical stripping/plating, causing poor cycling performance, and serious safety issues. Herein, we present highly stable and dendrite-free Na metal anodes over a wide current range and long-term cycling via directly applying free-standing graphene films with tunable thickness on Na metal surface. We systematically investigate the dependence of Na anode stability on the thickness of the graphene film at different current densities and capacities. Our findings reveal that only a few nanometer (∼2-3 nm) differences in the graphene thickness can have decisive influence on the stability and rate capability of Na anodes. To achieve the optimal performance, the thickness of the graphene film covered on Na surface needs to be meticulously selected based on the applied current density. We demonstrate that with a multilayer graphene film (∼5 nm in thickness) as a protective layer, stable Na cycling behavior was first achieved in carbonate electrolyte without any additives over 100 cycles at a current density as high as 2 mA/cm2 with a high capacity of 3 mAh/cm2. We believe our work could be a viable route toward high-energy Na battery systems, and can provide valuable insights into the lithium batteries as well.