Self-Assembled Protein Nanofilm Regulating Uniform Zn Nucleation and Deposition Enabling Long-Life Zn Anodes.

Rechargeable zinc-ion batteries (RZIBs) have gained promising attention as a feasible alternative for large-scale energy storage by the virtue of their intrinsic security, environmental benignity, low cost, and high volumetric capacity (5849 mAh cm-3 ). Nevertheless, the deep-rooted issues of dendrite formation and side reactions in unstable Zn metal anode have impeded RZIBs from being dependably deployed in their proposed applications. Herein, silk fibroin (SF) and lysozyme (ly), as natural biomacromolecules with abundant polar groups arranged in polypeptide backbones, are in situ self-assembled on the Zn anode surface to construct a homogeneous and compact protein nanofilm. Such protein nanofilm protecting layer presents a negative charge surface and significantly regulates Zn2+ deposition behavior. Meanwhile, synergistic flexible and robust features of protein nanofilm function as artificial solid electrolyte interface (SEI), accommodates the dynamic volume deformation during deposition/dissolution, and blocks corrosion of side reactions. Consequently, the electrochemical stability of protein nanofilm-modified Zn anode is greatly improved, with an excellent extended lifespan of over 1100 h at a high current density of 10 mA cm-2 and a high cycling capacity of 10 mAh cm-2 , corresponding to a high depth of discharge (83% DODZn ). Furthermore, the highly reversible Zn electrode remarkably improved the overall performance of MnO2 ||Zn full-cells.

Sea Urchin-like NiCo2O4 Catalyst Activated Peroxymonosulfate for Degradation of Phenol: Performance and Mechanism.

How to efficiently activate peroxymonosulfate (PMS) in a complex water matrix to degrade organic pollutants still needs greater efforts, and cobalt-based bimetallic nanomaterials are desirable catalysts. In this paper, sea urchin-like NiCo2O4 nanomaterials were successfully prepared and comprehensively characterized for their structural, morphological and chemical properties via techniques, such as X-ray diffraction (XRD), transmission electron microscopy (TEM), scanning electron microscopy (SEM), X-ray photoelectron spectroscopy (XPS), among others. The sea urchin-like NiCo2O4 nanomaterials exhibited remarkable catalytic performance in activating PMS to degrade phenol. Within the NiCo2O4/PMS system, the removal rate of phenol (50 mg L-1, 250 mL) reached 100% after 45 min, with a reaction rate constant k of 0.091 min-1, which was 1.4-times higher than that of the monometallic compound Co3O4/PMS system. The outstanding catalytic activity of sea urchin-like NiCo2O4 primarily arises from the synergistic effect between Ni and Co ions. Additionally, a comprehensive analysis of key parameters influencing the catalytic activity of the sea urchin-like NiCo2O4/PMS system, including reaction temperature, initial pH of solution, initial concentration, catalyst and PMS dosages and coexisting anions (HCO3-, Cl-, NO3- and humic acid), was conducted. Cycling experiments show that the material has good chemical stability. Electron paramagnetic resonance (EPR) and quenching experiments verified that both radical activation (SO4•-, •OH, O2•-) and nonradical activation (1O2) are present in the NiCo2O4/PMS system. Finally, the possible degradation pathways in the NiCo2O4/PMS system were proposed based on gas chromatography-mass spectrometry (GC-MS). Favorably, sea urchin-like NiCo2O4-activated PMS is a promising technology for environmental treatment and the remediation of phenol-induced water pollution problems.

Effects of ethylene on berry ripening and anthocyanin accumulation of 'Fujiminori' grape in protected cultivation.

BACKGROUND: Although the grape berries are deliberated as a non-climacteric fruit, ethylene seems to be involved in grape berry ripening. However, the precise role of ethylene in regulating the ripening of non-climacteric fruits is poorly understood. RESULTS: Exogenous ethephon (ETH) can stimulate the concentration of internal ethylene and accelerate the accumulation of anthocyanins in berries of 'Fujiminori', including malvidin-, delphinidin-, and petunidin-derivatives (3',4',5'-trihydroxylated anthocyanins) and cyanidin-derivatives (3',4'-dihydroxylated anthocyanins). The content of 3',4',5'-trihydroxylated anthocyanins was extremely higher than 3',4'-dihydroxylated anthocyanins, and ethylene did not affect the composition of anthocyanins in grape. Furthermore, we observed the expression of anthocyanin structural and regulatory genes as well as ethylene biosynthesis and response genes in response to ETH treatment. The anthocyanins accumulation is significantly associated with increased expression of anthocyanin structural (VvPAL, Vv4CH, VvCHS, VvCHI, VvF3H, and VvUFGT) and regulatory genes (VvMYBA1, VvMYBA2, and VvMYBA3), which persisted over the 12 days. In addition, exogenous ETH affected the endogenous ethylene biosynthesis (VvACO2 and VvACO4) and the downstream ethylene regulatory network (VvERS1, VvETR2, VvCTR1, and VvERF005). CONCLUSIONS: These findings bring new insights into the physiological and molecular function of ethylene during berry development and ripening in grapes. © 2021 Society of Chemical Industry.

Nitrogen-Doped Carbon-Coating Disproportionated SiO Materials as Long Cycling Stable Anode for Lithium Ion Batteries.

Silicon monoxide (SiO) is a kind of promising anode material for lithium-ion batteries because of its smaller volume change during the charge and discharge process than pure silicon and its higher theoretical capacity than commercialized graphite. However, its fast-fading capacity still restricts the development of practical application of SiO. A simple and cheap strategy to dope nitrogen and coat carbon on the surface of disproportionated SiO is proposed to improve the cycling stability significantly even at a high specific current. The capacity retention is nearly 85% after 250 cycles and more than 69% after 500 cycles at a specific current of 1000 mA g-1. Even at a specific current of 2000 mA g-1, its cycling performance behaves similarly to that of 1000 mA g-1. Nitrogen doping in materials could improve the conductivity of materials because pyridinic nitrogen and pyrrolic nitrogen could improve the electron conductivity and provide defects to contribute to the diffusion of lithium ions. The use of pitch and melamine, which are easily available industrial raw materials, makes it possible to contribute to the practical application.

Growth of 3D hierarchical porous NiO@carbon nanoflakes on graphene sheets for high-performance lithium-ion batteries.

Nickel oxide (NiO) as one of the anode electrode materials for lithium ion batteries (LIBs) has attracted considerable research attention. However, the poor electron conductivity and bad capacity retention performance greatly hinder its wide application. Herein, we prepared a novel three-dimensional (3D) hierarchical porous graphene@NiO@carbon composite via a simple solvothermal process, in which the graphene sheets were uniformly wrapped by porous NiO@carbon nanoflakes. In this case, nickelocene was creatively used as the precursor for both NiO and amorphous carbon, while graphene oxide sheets were employed as a template for the two-dimensional nanostructure and the conductive graphene backbone. The resultant composites possess high surface area (196 m(2) g(-1)) and large pore volume (0.46 cm(3) g(-1)). When it is applied as an anode for LIBs, the carbon outer-layer can effectively suppress the large volume change and serious aggregation of NiO nanoparticles during the charge-discharge process. Therefore, the graphene@NiO@carbon composites show a high reversible capacity of 1042 mA h g(-1) at a current density of 200 mA g(-1), an excellent rate performance and long cycle life. We believe that our method provides a new route for the fabrication of novel transition metal oxide composites.

Rational Design of a Cross-Linked Composite Solid Electrolyte for Li-Metal Batteries.

The interfacial problem caused by solid-solid contact is an important issue faced by a solid-state electrolyte (SSE). Herein, a cross-linked composite solid electrolyte (CSE) poly(vinylene carbonate) (PVCA)─ethoxylated trimethylolpropane triacrylate (ETPTA)─Li1.5Al0.5Ge1.5(PO4)3 (LAGP) (PEL) is prepared by in situ thermal polymerization. The ionic conductivity and Li+ transference number (tLi+) of PEL increase significantly due to the addition of LAGP, which can reach 1.011 × 10-4 S cm-1 and 0.451 respectively. The electrochemical stable window is also widened to 4.68 V. Benefiting from the integrated interfacial structure, the assembled coin cell shows low interfacial resistance. The all-solid-state NCM622|PEL|Li coin cell exhibits an initial discharge capacity of 169.7 mA h g-1 and 70% capacity retention over 100 cycles at 0.2 C, demonstrating excellent cycling stability.

In Situ Thermal Polymerization of a Succinonitrile-Based Gel Polymer Electrolyte for Lithium-Oxygen Batteries.

For lithium-oxygen batteries (LOBs), the leakage and volatilization of a liquid electrolyte and its poor electrochemical performance are the main reasons for the slow industrial advancement. Searching for more stable electrolyte substrates and reducing the use of liquid solvents are crucial to the development of LOBs. In this work, a well-designed succinonitrile-based (SN) gel polymer electrolyte (GPE-SLFE) is prepared by in situ thermal cross-linking of an ethoxylate trimethylolpropane triacrylate (ETPTA) monomer. The continuous Li+ transfer channel, formed by the synergistic effect of an SN-based plastic crystal electrolyte and an ETPTA polymer network, endows the GPE-SLFE with a high room-temperature ionic conductivity (1.61 mS cm-1 at 25 °C), a high lithium-ion transference number (tLi+ = 0.489), and excellent long-term stability of the Li/GPE-SLFE/Li symmetric cell at a current density of 0.1 mA cm-2 for over 220 h. Furthermore, cells with the GPE-SLFE exhibit a high discharge specific capacity of 4629.7 mAh g-1 and achieve 40 cycles.

Capacity fade in Sn-C nanopowder anodes due to fracture.

Sn based anodes allow for high initial capacities, which however cannot be retained due to the severe mechanical damage that occurs during Li-insertion and de-insertion. To better understand the fracture process during electrochemical cycling three different nanopowders comprised of Sn particles attached on artificial graphite, natural graphite or micro-carbon microbeads were examined. Although an initial capacity of 700 mAh g(-1) was obtained for all Sn-C nanopowders, a significant capacity fade took place with continuous electrochemical cycling. The microstructural changes in the electrodes corresponding to the changes in electrochemical behavior were studied by transmission and scanning electron microscopy. The fragmentation of Sn observed by microscopy correlates with the capacity fade, but this fragmentation and capacity fade can be controlled by controlling the initial microstructure. It was found that there is a dependence of the capacity fade on the Sn particle volume and surface area fraction of Sn on carbon.

High-Energy-Density and Long-Lifetime Lithium-Ion Battery Enabled by a Stabilized Li2O2 Cathode Prelithiation Additive.

Lithium-ion batteries (LIBs) typically suffer from large irreversible capacities caused by active lithium loss during formation of a solid electrolyte interface (SEI) at the anode side. Cathode prelithiation with preloaded additives has emerged as an effective strategy to solve the above issue. With ultrahigh theoretical capacity, Li2O2 serves as an excellent cathode prelithiation additive, whereas poor ambient stability limits its further development. In this study, we report a surface protection strategy to enable ambient processing of the Li2O2 additive. Li2O2 is well confined in poly(methyl methacrylate) (PMMA) nanofibers (P-Li2O2) via electrospinning, which exhibits greatly enhanced ambient stability compared with the unprotected one. Notably, when P-Li2O2 is preloaded in LiNi0.5Co0.2Mn0.3O2 cathodes (NCM-P-Li2O2), PMMA nanofibers remain stable during cathode slurry processing but readily dissolve in electrolytes and expose Li2O2 for effective electrochemical oxidation. Fabrication of P-Li2O2 allows systematic investigation of prelithiation behavior in full cells (NCM-P-Li2O2 cathodes paired with Si/Graphite anodes) and its impact on the electrochemical performance. Rational tuning of the prelithiation degree provides guidance for optimizing the amount of the cathode additive, which brings appealing cell lifetime and energy density.

Effects of Co/Mn Content Variation on Structural and Electrochemical Properties of Single-Crystal Ni-Rich Layered Oxide Materials for Lithium Ion Batteries.

The development of single-crystal nickel-rich layered LiNixCoyMn1-x-yO2 materials (S-NCMs) represents the most significant progress for the electrification applications of nickel-rich ternary materials. There has been prior research on the important role of transition metal elements in agglomerated materials, supplemented by surface and internal lattice optimization to drive the performance improvements. However, studies on S-NCMs, especially on the role of transition metals (TM, i.e., Co and Mn), have not been reported. In this study, we synthesized four kinds of S-NCMs with different Co/Mn contents and studied their structural, electrochemical, kinetic, and thermodynamic properties with different Co/Mn contents. The results were as follows: (1) Electrochemically, Co was more effective than Mn at 25 °C at enhancing the intercalation/deintercalation kinetics, which resulted in an increased discharge capacity, an improved rate capability, and a reduced energy loss. (2) Thermodynamically, Mn was more effective at maintaining a higher thermal stability than Co, especially at a low cutoff voltage, but at a high cutoff voltage, the difference between the action of Co and Mn decreased. The main finding of this work was the enhanced structural stability provided by Co, which could be attributed to the following: (i) the absence of the H2/H3 phase transformation when Co exceeded 15%, which inhibited the irreversible phase transformation and reduced the volume strain, and (ii) the lower degrees of decrease in the cell parameters a and c with higher contents of Co, which contributed to a low cracking degree along the (003) crystal plane. The current work provides an important reference for the single-crystallization strategy of nickel-rich materials.

Rice husk-derived nano-SiO2 assembled on reduced graphene oxide distributed on conductive flexible polyaniline frameworks towards high-performance lithium-ion batteries.

By combining rice husk-derived nano-silica and reduced graphene oxide and then polymerizing PANI by in situ polymerization, we created polyaniline-coated rice husk-derived nano-silica@reduced graphene oxide (PANI-SiO2@rGO) composites with excellent electrochemical performance. ATR-FTIR and XRD analyses confirm the formation of PANI-SiO2@rGO, implying that SiO2@rGO served as a template in the formation of composites. The morphology of PANI-SiO2@rGO was characterized by SEM, HRTEM, and STEM, in which SiO2 nanoparticles were homogeneously loaded on graphene sheets and the PANI fibrous network uniformly covers the SiO2@rGO composites. The structure can withstand the large volume change as well as retain electronic conductivity during Li-ion insertion/extraction. Over 400 cycles, the assembled composite retains a high reversible specific capacity of 680 mA h g-1 at a current density of 0.4 A g-1, whereas the SiO2@rGO retains only 414 mA h g-1 at 0.4 A g-1 after 215 cycles. The enhanced electrochemical performance of PANI-SiO2@rGO was a result of the dual protection provided by the PANI flexible layer and graphene sheets. PANI-SiO2@rGO composites may pave the way for the development of advanced anode materials for high-performance lithium-ion batteries.

Double-Protected Layers with Solid-Liquid Hybrid Electrolytes for Long-Cycle-Life Lithium Batteries.

Lithium-ion batteries (LIBs) with liquid electrolytes (LEs) have problems such as electrolyte leakage, low safety profiles, and low energy density, which limit their further development. However, LIBs with solid electrolytes are safer with better energy and high-temperature performance. Thus, solid electrolyte system batteries have attracted widespread attention. However, due to the inherent rigidity of the LATP solid electrolyte, there is a high interface impedance at the LATP/electrode. In addition, the Ti element in LATP easily reacts with the Li metal. Here, we dripped an LE at the LATP/electrode interface (solid-liquid hybrid electrolytes) to reduce its interface impedance. A composite polymer electrolyte (CPE) protective film (containing PVDF, SN, and LiTFSI) was then cured in situ at the LATP/Li interface to avoid side reactions of LATP. The discharge specific capacity of the LiFePO4/LATP-12% LE-CPE/Li system is up to 150 mAh g-1, and the capacity retention rate is still 96% after 250 cycles. In addition, the NCM622/PVDF-LATP-12% LE/Li system has an initial reversible capacity of 170 mAh g-1. This study reports an approach that can protect solid electrolytes from lithium metal instability.

Dual Structure-Material Design of Separators toward Dendrite-Free Lithium Metal Anodes.

The practical applications of lithium metal anodes have been severely hindered by the Li dendrite issue. Herein, a dual structure-material design strategy was developed to fabricate a new type of separator using interconnected hollow porous polyacrylonitrile (PAN) nanofibers (HPPANF), which delivered controllable and dendrite-free Li depositions. The interconnected mesopores on HPPANF bridged the hollow interiors with the outside voids among the fibers, enabling outstanding electrolyte uptake capabilities for high ion conductivity, and nano-level wetted electrolyte/anode interface for uniform Li plating/stripping. In parallel, the HPPANF separator enriched with polar groups acted as an exceptional polymer-based solid-state electrolyte, providing 3D ion channels for the transport of Li ions. Benefiting from the dual structure-material design, the HPPANF separator induced uniform Li ion flux for dendrite-free Li depositions, which caused enhanced cycling stability (1300 h, 3 mA cm-2 ). This work demonstrates a new method to stabilize Li metal anodes through rational separator design.

Transcriptome and metabolite integrated analysis reveals that exogenous ethylene controls berry ripening processes in grapevine.

Although grapevine (Vitis vinifera L.) is generally classified as a non-climacteric fruit, the regulatory mechanisms of ethylene in the ripening of non-climacteric fruit are still poorly understood. In this study, exogenous ethephon (ETH) strongly stimulated fruit color and anthocyanin accumulation, which was consistent with the increased expression of anthocyanin structural, regulatory, and transport genes. ETH application increased ABA content and decreased IAA content by coordinating ABA and auxin biosynthesis regulatory network. ETH treatment also accelerated sugar (glucose and fructose) accumulation by enhancing the gene expression involved in sugar transport and sucrose cleavage. ETH treatment blocked the synthesis of cellulose and accelerated the degradation of pectin, which was strongly associated with berry softening. To further confirm the function of ethylene biosynthesis and signaling genes, transient overexpression of VvACO4 and VvEIL3 were performed in both in tomato and strawberry fruits. These findings of the ethylene cascade add to our understanding of ethylene in non-climacteric berry ripening regulation and revealed a complex involvement of ethylene and its interplay with phytohormones during grapevine berry ripening.

Fast-Charging Anode Materials and Novel Nanocomposite Design of Rice Husk-Derived SiO2 and Sn Nanoparticles Self-Assembled on TiO2(B) Nanorods for Lithium-Ion Storage Applications.

A novel microstructure of anode materials for lithium-ion batteries with ternary components, comprising tin (Sn), rice husk-derived silica (SiO2), and bronze-titanium dioxide (TiO2(B)), has been developed. The goal of this research is to utilize the nanocomposite design of rice husk-derived SiO2 and Sn nanoparticles self-assembled on TiO2(B) nanorods, Sn-SiO2@TiO2(B), through simple chemical route methods. Following that, the microstructure and electrochemical performance of as-prepared products were investigated. The major patterns of the X-ray diffraction technique can be precisely indexed as monoclinic TiO2(B). The patterns of SiO2 and Sn were found to be low in intensity since the particles were amorphous and in the nanoscale range, respectively. Small spherical particles, Sn and SiO2, attached to TiO2(B) nanorods were discovered. Therefore, the influence mechanism of Sn-SiO2@TiO2(B) fabrication was proposed. The Sn-SiO2@TiO2(B) anode material performed exceptionally well in terms of electrochemical and battery performance. The as-prepared electrode demonstrated outstanding stability over 500 cycles, with a high discharge capacity of ∼150 mA h g-1 at a fast-charging current of 5000 mA g-1 and a low internal resistance of around 250.0 Ω. The synthesized Sn-SiO2@TiO2(B) nanocomposites have a distinct structure, the potential for fast charging, safety in use, and good stability, indicating their use as promising and effective anode materials in better power batteries for the next-generation applications.

Tetramethylpyrazine: an electrolyte additive for high capacity and energy efficiency lithium-oxygen batteries.

Lithium-oxygen batteries have attracted great attention in recent years owing to their extremely high theoretical energy density, however, factors such as low actual capacity and poor rate performance hinder the practical application of lithium-oxygen batteries. In this work, a novel electrolyte additive, tetramethylpyrazine (TMP), is introduced into an electrolyte system to enhance the electrochemical performance of the lithium-oxygen batteries. TMP does not undergo its own redox reaction within the charge-discharge voltage range, which will not affect the electrochemical stability of the electrolyte. The results show that the addition of TMP can increase the reduction current of oxygen, which will promote the ORR process, and with an optimal TMP content (50 mM), the cell shows a high discharge capacity of 5712.3 mA h g-1 at 0.1 mA cm-2. And its rate capability is almost doubled compared with the system without TMP additive at a large current density of 1 mA cm-2. Further analysis by SEM and XRD reveals that the addition of TMP can reduce the formation of by-products and promote the solution growth of large-size Li2O2 particles to achieve a large discharge capacity. This approach could provide a new idea for improving the electrochemical performance of lithium-oxygen batteries.

Revealing the Role of W-Doping in Enhancing the Electrochemical Performance of the LiNi0.6Co0.2Mn0.2O2 Cathode at 4.5 V.

More and more attention has been focused on Ni-rich ternary materials due to their superior specific capacity, but they still suffer inherent structural irreversibility and rapid capacity degradation under a high voltage. Oxidation of unstable oxygen will lead to the irreversible transformation of the structure. Taking into account the strong W-O bond, an appropriate amount of W-doping is studied to reinforce the thermal stability and electrochemical performance of LiNi0.6Co0.2Mn0.2O2 (NCM622) at 4.5 V. Combining experiments and theoretical calculations, it can be found that W-doping is most preferred at Co sites, and the average charge around O in the NiO6 octahedron becomes more negative after W-doping, which can successfully restrain the release of oxygen, thereby improving the stability of the crystal structure during deep delithiation. In addition, W-doping decreases the energy barrier of the Li+ migration slightly and boosts the kinetic diffusion of lithium ions. As a result, NCM622 doped with 0.5% W boasts an outstanding capacity retention of 96.7% at 1 C after 100 cycles and a discharge specific capacity of up to 152.8 mA h g-1 at 5 C between 3.0 and 4.5 V. Furthermore, analysis of the cycled electrodes indicates that the lattice expansion and the formation of microcracks during long cycling are suppressed after W-doping, thereby elevating the structure and interface stability. Therefore, doping an appropriate amount of W via simple methods is helpful to obtain Ni-rich cathode materials with admirable performance.

In Situ Room-Temperature Cross-Linked Highly Branched Biopolymeric Binder Based on the Diels-Alder Reaction for High-Performance Silicon Anodes in Lithium-Ion Batteries.

Silicon (Si) is an auspicious anode material in next-generation lithium-ion batteries due to its exceptional theoretical gravimetric capacity, environmental friendliness, and high natural abundance. However, the practical application of Si anodes remains a "must-solve" challenge because of its drastic capacity fading that results from the inherent property of drastic volume expansion of Si during repeated lithiation and delithiation. Developing binders employed in robust electrodes has been considered an economical and practical method to affect the electrochemical performance of Si-based electrodes. Some natural polymers have demonstrated good adhesive properties with Si-active materials. However, they have limited capacity to keep the structural integrity of electrodes because the network structures solely based on weak hydrogen bonds are susceptible to deformation during cycling. Herein, we develop an in situ covalently cross-linked three-dimensional (3D) supramolecular network and apply it to the Si electrode to improve cycling performance. This network architecture is constructed using furan-modified branched arabinoxylan of corn fiber gum (CFG) and an ionically conductive cross-linker of maleimido-poly(ethylene glycol) (PEG) through the Diels-Alder reaction. The maleimide groups in PEG can react spontaneously with the furan groups in CFG at room temperature without any other stimulation, thus forming strong covalent bonds in the network. The cross-linked CFG-PEG binder has demonstrated robust adhesive properties with Si-active materials and the current collector. The branching of CFG and functional groups of PEG are conducive to improving the lithium-ion conductivity in the silicon anode, resulting in excellent rate performances. The Si anode with a cross-linked CFG-PEG binder exhibits superior cycling stability. As a result, an in situ cross-linking 3D network as a novel binder has a great potential for fabricating an advanced Si anode in next-generation Li-ion batteries.

Uniform Deposition and Effective Confinement of Lithium in Three-Dimensional Interconnected Microchannels for Stable Lithium Metal Anodes.

Lithium dendrite formation has hindered the practical implementation of lithium metal batteries with higher energy densities compared with those of conventional lithium-ion batteries. Herein, a nanoconfinement strategy to access dendrite-free lithium metal anodes comprising three-dimensional (3D) hollow porous multi-nanochannel carbon fiber embedded with TiO2 nanocrystals (HTCNF) is reported. The transport of the lithium ions is facilitated by the 3D architecture. Functioning as nanoseeds, the TiO2 nanocrystals guide the lithium ions toward forming uniform deposits, which are further confined inside the hollow carbon fibers and the 3D HTCNF layer. Site-selective deposition coupled with the nanoconfinement of lithium metal modifies the Li plating/stripping behavior and effectively suppresses the dendrite growth. The HTCNF-Li cell delivers a stable cycling performance of 1300 h with a voltage hysteresis as low as 6 mV. The assembled HTCNF-Li//LiFePO4 full cell displays a compelling rate performance and enhanced cycling stability with high capacity retention (90% after 400 cycles at 0.5 C). Our results demonstrate a new and potentially scalable route to resolve the lithium dendrite growth issue for enhanced electrochemical performances, which can be further extended to other metal battery systems.

Effect of Organic Electrolyte on the Performance of Solid Electrolyte for Solid-Liquid Hybrid Lithium Batteries.

The interface problem caused by the contact between the electrodes and the solid electrolyte was the main factor hindering the development of solid-state batteries. To enhance the electrode|solid electrolyte interface property, we designed a hybrid electrolyte, the combination of x vol % Li1.3Al0.3Ti1.7(PO4)3 (LATP) inorganic solid electrolyte and 1 - x vol % liquid organic electrolyte (LE). In this work, the 1 - x vol % LE was dropped between the electrode and the solid electrolyte, and it is found that the electrochemical performance of the LiFePO4|Li solid-liquid hybrid battery is significantly improved. At the current density of 0.1 and 0.5 C, the LATP with 15% liquid organic electrolyte could deliver a specific capacity of 160.5 and 124.3 mAh g-1, respectively; moreover, the specific discharge capacity remained as high as 111 mAh g-1 at 0.5 C after 100 cycles, indicating that the larger interface impedance was eliminated. The LE may have three functions: (1) forming a solid-liquid electrolyte interphase on the surface of the LATP particles to prevent further reduction of LATP, (2) wetting the electrode and solid electrolyte to reduce the interface resistance, and (3) improving interfacial Li-ion transport.