Dual Redox Reaction Sites for Pseudocapacitance Based on Ti and -P Functional Groups of Ti3C2PBrx MXene.

MXenes have extensive applications due to their different properties determined by intrinsic structures and various functional groups. Exploring different functional groups of MXenes leads to improved performance or potential applications. In this work, we prepared new Ti3C2PBrx (x=0.4-0.6) MXene with phosphorus functional groups (-P) through a two-step gas-phase reaction. The acquisition of -P is achieved by replacing bromine functional groups (-Br) of Ti3C2Br2 in the phosphorus vapor. After -Br is replaced with -P, Ti3C2PBrx MXene shows an improved areal capacitance (360 mF cm-2) at 20 mV s-1 compared with Ti3C2Br2 MXene (102 mF cm-2). At a current density of 5 mA cm-2 after 10000 cycles, the capacitance retention of Ti3C2PBrx MXene has not decreased. The pseudocapacitive enhancement mechanism has been discovered based on the dual redox sites of the functional groups -P and Ti.

Tuning Electrocatalytic Activities of Dealloyed Nanoporous Catalysts by Macroscopic Strain Engineering.

It is technically challenging to quantitatively apply strains to tune catalysis because most heterogeneous catalysts are nanoparticles, and lattice strains can only be applied indirectly via core-shell structures or crystal defects. Herein, we report quantitative relations between macroscopic strains and hydrogen evolution reaction (HER) activities of dealloyed nanoporous gold (NPG) by directly applying macroscopic strains upon bulk NPG. It was found that macroscopic compressive strains lead to a decrease, while macroscopic tensile strains improve the HER activity of NPG, which is in line with the d-band center model. The overpotential and onset potential of HER display approximately a linear relation with applied macroscopic strains, revealing an ∼2.9 meV decrease of the binding energy per 0.1% lattice strains from compressive to tensile. The methodology with the high strain sensitivity of electrocatalysis, developed in this study, paves a new way to investigate the insights of strain-dependent electrocatalysis with high precision.

Effect of Li6.4La3Zr1.4Ta0.6O12 Fillers on the Interfacial Properties between Composite PEO-LiTFSI Electrolytes with Li Metal during Cycling.

PEO-LiX solid polymer electrolyte (SPE) with the addition of Li6.4La3Zr1.4Ta0.6O12 (LLZTO) fillers is considered as a promising solid-state electrolyte for solid-state Li-ion batteries. However, the developments of the SPE have caused additional challenges, such as poor contact interface and SPE/Li interface stability during cycling, which always lead to potentially catastrophic battery failure. The main problem is that the real impact of LLZTO fillers on the interfacial properties between SPE and Li metal is still unclear. Herein, we combined the electrochemical measurement and in situ synchrotron-based X-ray absorption near-edge structure (XANES) imaging technology to study the role of LLZTO fillers in directing SPE/Li interface electrochemical performance. In situ XRF-XANES mapping during cycling showed that addition of an appropriate amount of LLZTO fillers (50 wt %) can improve the interfacial contact and stability between SPE and Li metal without reacting with the PEO and Li salts. Additionally, it also demonstrated the beneficial effect of LLZTO particles for suppressing the interface reactions between the Li metal and PEO-LiTFSI SPE and further inhibiting Li-metal dendrite growth. The Li|LiFePO4 batteries deliver long cycling for over 700 cycles with a low-capacity fade rate of 0.08% per cycle at a rate of 0.3C, revealing tremendous potential in promoting the large-scale application of future solid-state Li-ion batteries.

The involvement of spontaneous brain activity in natural recovery from internet gaming disorder: A resting-state fMRI study.

Objective: Internet gaming disorder (IGD) can seriously impair an individual's physical and mental health. However, unlike the majority of those suffering from substance addiction, individuals with IGD may recover without any professional intervention. Understanding the brain mechanisms of natural recovery from IGD may provide new insight into how to prevent addiction and implement more targeted interventions. Methods: Sixty individuals with IGD were scanned by using a resting-state fMRI to assess brain region changes associated with IGD. After 1 year, 19 individuals with IGD no longer met the IGD criteria and were considered recovered (RE-IGD), 23 individuals still met the IGD criteria (PER-IGD), and 18 individuals left the study. The brain activity in resting state between 19 RE-IGD individuals and 23 PER-IGD individuals was compared by using regional homogeneity (ReHo). Additionally, brain structure and cue-craving functional MRIs were collected to further support the results in the resting-state. Results: The resting-state fMRI results revealed that activity in brain regions responsible for reward and inhibitory control [including the orbitofrontal cortex (OFC), the precuneus and the dorsolateral prefrontal cortex (DLPFC)] was decreased in the PER-IGD individuals compared to RE-IGD individuals. In addition, significant positive correlations were found between mean ReHo values in the precuneus and self-reported craving scores for gaming, whether among the PER-IGD individuals or the RE-IGD individuals. Furthermore, we found similar results in that brain structure and cue-craving differences exist between the PER-IGD individuals and RE-IGD individuals, specifically in the brain regions associated with reward processing and inhibitory control (including the DLPFC, anterior cingulate gyrus, insula, OFC, precuneus, and superior frontal gyrus). Conclusion: These findings indicate that the brain regions responsible for reward processing and inhibitory control are different in PER-IGD individuals, which may have consequences on natural recovery. Our present study provides neuroimaging evidence that spontaneous brain activity may influence natural recovery from IGD.

Lanthanum nitrate as aqueous electrolyte additive for favourable zinc metal electrodeposition.

Aqueous zinc batteries are appealing devices for cost-effective and environmentally sustainable energy storage. However, the zinc metal deposition at the anode strongly influences the battery cycle life and performance. To circumvent this issue, here we propose the use of lanthanum nitrate (La(NO3)3) as supporting salt for aqueous zinc sulfate (ZnSO4) electrolyte solutions. Via physicochemical and electrochemical characterizations, we demonstrate that this peculiar electrolyte formulation weakens the electric double layer repulsive force, thus, favouring dense metallic zinc deposits and regulating the charge distribution at the zinc metal|electrolyte interface. When tested in Zn||VS2 full coin cell configuration (with cathode mass loading of 16 mg cm-2), the electrolyte solution containing the lanthanum ions enables almost 1000 cycles at 1 A g-1 (after 5 activation cycles at 0.05 A g-1) with a stable discharge capacity of about 90 mAh g-1 and an average cell discharge voltage of ∼0.54 V.

Improving Na/Na3 Zr2 Si2 PO12 Interface via SnOx /Sn Film for High-Performance Solid-State Sodium Metal Batteries.

Sodium (Na) metal batteries have attracted much attention due to their rich resources, low cost, and high energy density. As a promising solid electrolyte, Na3 Zr2 Si2 PO12 (NZSP) is expected to be used in solid-state Na metal batteries addressing the safety concerns. However, due to the poor contact between NZSP and the Na metal, the interfacial resistance is too large to gain proper performance for practical solid-state batteries (SSBs) application. Here, a SnOx /Sn film is successfully introduced to improve the interface between Na and NZSP for enhancing the electrochemical performance of SSBs. As a result, the Na/NZSP interfacial resistance is dramatically reduced from 581 to 3 Ω cm2 . The modified Na||Na symmetric cell keeps cycling over 1500 h with an overpotential of 40 mV at 0.1 mA cm-2 at room temperature. Even at current densities of 0.3 and 0.5 mA cm-2 , the cell still maintains an excellent cyclability. When coupled with NaTi2 (PO4 )3 and a Na3 V2 (PO4 )3 cathode, the full-cell demonstrates a good performance at 0.2 C and 1 C, respectively. The present work provides an effective way to solve the interface issue of SSBs.

Involvement of Phosphatidylserine and Triacylglycerol in the Response of Sweet Potato Leaves to Salt Stress.

Lipid remodeling plays an important role in the adaptation of plants to environmental factors, but the mechanism by which lipid remodeling mediates salt stress response remains unclear. In this study, we compared the root and leaf lipidome profiles of salt-tolerant and salt-sensitive sweet potato cultivars (Xu 22 and Xu 32, respectively) under salinity stress. After salt treatment, the leaf lipidome showed more significant remodeling than the root lipidome in both cultivars. Compared with Xu 32 leaves, Xu 22 leaves generally maintained higher abundance of phospholipids, glycolipids, sphingolipids, sterol derivatives, and diacylglycerol under salinity conditions. Interestingly, salinity stress significantly increased phosphatidylserine (PS) abundance in Xu 22 leaves by predominantly triggering the increase of PS (20:5/22:6). Furthermore, Xu 32 leaves accumulated higher triacylglycerol (TG) level than Xu 22 leaves under salinity conditions. The exogenous application of PS delayed salt-induced leaf senescence in Xu 32 by reducing salt-induced K+ efflux and upregulating plasma membrane H+-ATPase activity. However, the inhibition of TG mobilization in salinized-Xu 22 leaves disturbed energy and K+/Na+ homeostasis, as well as plasma membrane H+-ATPase activity. These results demonstrate alterations in the leaf lipidome of sweet potato under salinity condition, underscoring the importance of PS and TG in mediating salt-defensive responses in sweet potato leaves.

Facile Synthesis of Sn/Nitrogen-Doped Reduced Graphene Oxide Nanocomposites with Superb Lithium Storage Properties.

Sn/Nitrogen-doped reduced graphene oxide (Sn@N-G) composites have been successfully synthesized via a facile method for lithium-ion batteries. Compared with the Sn or Sn/graphene anodes, the Sn@N-G anode exhibits a superb rate capability of 535 mAh g-1 at 2C and cycling stability up to 300 cycles at 0.5C. The improved lithium-storage performance of Sn@N-G anode could be ascribed to the effective graphene wrapping, which accommodates the large volume change of Sn during the charge-discharge process, while the nitrogen doping increases the electronic conductivity of graphene, as well as provides a large number of active sites as reservoirs for Li+ storage.

Ultranarrow Graphene Nanoribbons toward Oxygen Reduction and Evolution Reactions.

Identification of catalytic sites for oxygen reduction and evolution reactions (ORR/OER) is critical to rationally develop highly efficient bifunctional carbon-based metal-free electrocatalyst. Here, a unique defect-rich N-doped ultranarrow graphene nanoribbon with a high aspect ratio that exhibits excellent ORR/OER bifunctional activities and impressive long-term cycling stability in Zn-air batteries is successfully fabricated. Density functional theory calculations indicates that the topological defects (e.g., pentagons and heptagons) cooperated with pyridinic-N dopants on the edges are more favorable to electrocatalytic activity toward ORR and OER. This work provides a new design principle for carbon-based electrocatalytic nanomaterials.

New P2-Type Honeycomb-Layered Sodium-Ion Conductor: Na2Mg2TeO6.

A novel solid sodium-ion conductor, Na2Mg2TeO6 (NMTO) with a P2-type honeycomb-layered structure, has been synthesized for the first time by a simple solid-state synthetic route. The conductor of NMTO exhibits high conductivity of 2.3 × 10-4 S cm-1 at room temperature (RT) and a large electrochemical window of ∼4.2 V (versus Na+/Na). The conductor is remarkably stable, both in the ambient environment and within its metallic Na anode. This facile sodium-ion conductor displays potential for use in all-solid-state sodium-ion batteries (SS-SIBs).

Promises, Challenges, and Recent Progress of Inorganic Solid-State Electrolytes for All-Solid-State Lithium Batteries.

All-solid-state lithium batteries (ASSLBs) have the potential to revolutionize battery systems for electric vehicles due to their benefits in safety, energy density, packaging, and operable temperature range. As the key component in ASSLBs, inorganic lithium-ion-based solid-state electrolytes (SSEs) have attracted great interest, and advances in SSEs are vital to deliver the promise of ASSLBs. Herein, a survey of emerging SSEs is presented, and ion-transport mechanisms are briefly discussed. Techniques for increasing the ionic conductivity of SSEs, including substitution and mechanical strain treatment, are highlighted. Recent advances in various classes of SSEs enabled by different preparation methods are described. Then, the issues of chemical stabilities, electrochemical compatibility, and the interfaces between electrodes and SSEs are focused on. A variety of research addressing these issues is outlined accordingly. Given their importance for next-generation battery systems and transportation style, a perspective on the current challenges and opportunities is provided, and suggestions for future research directions for SSEs and ASSLBs are suggested.

Synthesis of Cu2O Octadecahedron/TiO2 Quantum Dot Heterojunctions with High Visible Light Photocatalytic Activity and High Stability.

Since p-n heterojunction photocatalysts with higher energy facets exposed usually possess greatly enhanced photocatalytic activities than single-phase catalysts, a novel Cu2O octadecahedron/TiO2 quantum dot (Cu2O-O/TiO2-QD) p-n heterojunctions composite was designed and synthesized in this study. Cu2O octadecahedra (Cu2O-O) with {110} facets and {100} facets exposed were synthesized first, then highly dispersed TiO2 quantum dots (TiO2-QDs) were loaded on Cu2O-O by the precipitation of TiO2-QDs sol in the presence of absolute ethanol. The morphology, crystal structure, chemical composition, optical properties, photocatalytic activity, and stability of Cu2O-O/TiO2-QD heterojunctions were characterized and investigated. It was found that TiO2-QDs were firmly anchored on Cu2O-O single crystals with good dispersibility. The Cu2O-O/TiO2-QD heterojunctions with partial coverage of TiO2-QDs showed a strong absorbance of visible light and exhibited an effective transfer of photoexcited electrons. The degradation of methyl orange (MO) under visible light irradiation indicated that the photocatalytic activity of Cu2O-O/TiO2-QD heterojunctions was significantly enhanced compared with that of Cu2O-O. This Cu2O-O/TiO2-QD heterojunctions composite exhibited high stability in MO degradation process and after storage in air. The high visible light photocatalytic activity and good stability were attributed to high utilization of light, effective separation of photoexcited electron-hole pairs, and instant scavenging of holes in the unique heterojunction structure.