Regulating zinc ion transport behavior and solvated structure towards stable aqueous Zn metal batteries

Aqueous Zn metal batteries(AZMBs)with intrinsic safety,high energy density and low cost have been regarded as promising electrochemical energy storage devices.However,the parasitic reaction on metallic Zn anode and the incompatibility between electrode and electrolytes lead to the deterioration of electrochemical performance of AZMBs during the cycling.The critical point to achieve the stable cycling of AZMBs is to properly regulate the zinc ion solvated structure and transfer behavior between metallic Zn anode and electrolyte.In recent years,numerous achievements have been made to resolve the formation of Zn dendrite and interface incompatible issues faced by AZMBs via optimizing the sheath structure and transport capability of zinc ions at electrode-electrolyte interface.In this review,the challenges for metallic Zn anode and electrode-electrolyte interface in AZMBs including dendrite formation and interface characteristics are presented.Following the influences of different strategies involving designing advanced electrode structu re,artificial solid electrolyte interphase(SEI)on Zn anode and electrolyte engineering to regulate zinc ion solvated sheath structure and transport behavior are summarized and discussed.Finally,the perspectives for the future development of design strategies for dendrite-free Zn metal anode and long lifespan AZMBs are also given.

An aqueous BiI_(3)-Zn battery with dual mechanisms of Zn^(2+)(de)intercalation and I^(-)/I_(2)redox

The development of aqueous battery with dual mechanisms is now arousing more and more interest.The dual mechanisms of Zn^(2+)(de)intercalation and I^(-)/I_(2)redox bring unexpected effects.Herein,differing from previous studies using Zn I_(2)additive,this work designs an aqueous Bi I_(3)-Zn battery with selfsupplied I^(-).Ex situ tests reveal the conversion of Bi I_(3)into Bi(discharge)and Bi OI(charge)at the 1st cycle and the dissolved I^(-)in electrolyte.The active I^(-)species enhances the specific capacity and discharge medium voltage of electrode as well as improves the generation of Zn dendrite and by-product.Furthermore,the porous hard carbon is introduced to enhance the electronic/ionic conductivity and adsorb iodine species,proven by experimental and theoretical studies.Accordingly,the well-designed Bi I_(3)-Zn battery delivers a high reversible capacity of 182 m A h g^(-1)at 0.2 A g^(-1),an excellent rate capability with 88 m A h g^(-1)at 10 A g^(-1),and an impressive cyclability with 63%capacity retention over 20 K cycles at 10 A g^(-1).An excellent electrochemical performance is obtained even at a high mass loading of 6 mg cm^(-2).Moreover,a flexible quasi-solid-state Bi I_(3)-Zn battery exhibits satisfactory battery performances.This work provides a new idea for designing high-performance aqueous battery with dual mechanisms.

Enhanced energy density and fast-charging ability via directional particle configuration

The limited energy density of lithium-ion capacitors poses a significant obstacle to their widespread application,primarily stemming from the inability of the electrodes to simultaneously fulfill both high energy density and rapid charging requirements.Experimental data demonstrate that a directional particle configuration can enhance charging speed while maintaining high-capacity density,but it is rarely discussed.Here,we have developed a particle-level electrochemical model capable of reconstructing an electrode with a directional particle configuration.By employing this method,an investigation was conducted to explore how the spatial morphology characteristics of particle configuration impact the energy storage characteristics of electrodes.Results demonstrate that rational particle configuration can effectively enhance the transport of lithium ions and create additional space for lithium-ion storage.With the same particle size distribution,the best electrode can increase the discharge capacity by up to132.4% and increase the charging SOC by 11.3% compared to the ordinary electrode under the condition of 6 C.These findings provide a further understanding of the energy storage mechanism inside the anisotropic particle distribution electrode,which is important for developing high-performance lithium-ion capacitors.

Sn-doped BiOCl nanosheet with synergistic H^(+)/Zn^(2+)co-insertion for“rocking chair”zinc-ion battery

The development of insertion-type anodes is the key to designing“rocking chair”zinc-ion batteries.However,there is rare report on high mass loading anode with high performances.Here,{001}-oriented Bi OCl nanosheets with Sn doping are proposed as a promising insertion-type anode.The designs of cross-linked CNTs conductive network,{001}-oriented nanosheet,and Sn doping significantly enhance ion/electron transport,proved via experimental tests and theoretical calculations(density of states and diffusion barrier).The H^(+)/Zn^(2+)synergistic co-insertion mechanism is proved via ex situ XRD,Raman,XPS,and SEM tests.Accordingly,this optimized electrode delivers a high reversible capacity of 194 m A h g^(-1)at 0.1 A g^(-1)with a voltage of≈0.37 V and an impressive cyclability with 128 m A h g^(-1)over 2500 cycles at 1 A g^(-1).It also shows satisfactory performances at an ultrahigh mass loading of 10 mg cm^(-2).Moreover,the Sn-Bi OCl//MnO_(2)full cell displays a reversible capacity of 85 m A h g^(-1)at 0.2 A g^(-1)during cyclic test.

Impact of State-Owned Capital Participation on ESG Performance of Private Enterprises

As global investors and stakeholders increasingly prioritize environmental,social,and governance(ESG)performance,corporate social responsibility and sustainability have become crucial factors in determining corporate success.In the context of China’s robust economy,the involvement of state-owned capital exerts a profound impact on the ESG performance of private enterprises.This paper,starting from the perspective of ESG,analyzes how state-owned capital participation influences the ESG performance of private enterprises.Additionally,it proposes recommendations for the involvement of state-owned enterprises in private enterprises,aiming to foster the sustainable development of private enterprises and enhance their social responsibility.

Constructing a lithiophilic polyaniline coating via in situ polymerization for dendrite-free lithium metal anode

Metallic lithium is regarded as one of the most promising electrode materials to break through the energy density bottleneck of current commercial lithium-ion batteries.However,the practical implementation of lithium metal anode is limited by the unstable electrode interface significantly,which directly induces a low Coulombic efficiency,short cycling lifespan,and dendritic lithium growth behavior.In this study,via in situ electropolymerization,lithiophilic and conformal polyaniline layer is developed to improve the initial lithium nucleation and plating process,reducing the interface charge transfer resistance and promoting uniform lithium plating/stripping behavior.Meanwhile,the polyaniline layer exhibits good adhesion to the substrate.As a result,the Li/Cu half cell delivers a high Coulombic efficiency of 99.1%for 400 cycles at 1.0 mA·cm^(−2)with polyaniline layer.In addition,long-term stable cycling at a current density of 1.0 mA·cm^(−2)for 1300 h has been achieved for lithium metal anode.This strategy provides a new perspective for the practical lithium metal batteries.

Progress on Li3VO4 as a Promising Anode Material for Li-ion Batteries

Vanadium oxide Li3VO4 has attracted much attention as anode material for Li-ion batteries in recent years since it has a low and safe redox potential （vs. Li metal）, high specific capacity and its cost is low. However, the poor electronic conductivity and initial low coulombic efficiency limit its practical application. In this mini-review, the state-of-the-art results associated with Li3VO4 are summarized including structure, lithium insertion mechanism, preparation, modification, and electrochemical properties. Finally, the challenges and prospects are also discussed.

An Aqueous Asymmetric Supercapacitor Based on Activated Carbon and Tungsten Trioxide Nanowire Electrodes

An asymmetric supercapacitor （ASC） was assembled by using an activated carbon as positive electrode and WO3 nanowire as negative electrode, and its electrical performances were tested in voltage windows ranging from 0 to 1.5 V. A high specific capacitance of 51 Fog-1 could be achieved at the current density of 0.25 A·g-1 . Moreover, the ASC displays a good cycling stability with 86% of capacitance retention after 800 cycles, its energy density can be up to 11.9 Wh·kg-1 at the power density of 210 W·kg -1, and remains 7.7 Wh·kg-1 at a power density of 1250 W· kg-1. The excellent electrical performance is perhaps due to the crystal orientation of （001） planes for the WO3 nanowire, which favors the rapid reaction between W（VI） and H＋ cations. This aqueous asymmetric WO3//AC supercapacitor is promising for practical applications due to its easy preparation of WO3.

Directly conversion the biomass-waste to Si/C composite anode materials for advanced lithium ion batteries

The necessity to explore high-efficiency and high-value utilization strategy for biomass-waste is desirable.Herein,the strategy for direct conversion biomass-waste(rice husks) to Si/C composite structure anode was built.The Si/C composite materials were successfully obtained via the typical thermal reduction with magnesium,and the Si nanopa rticle was uniformly embedded in carbon frame,as revealed by Raman,X-ray diffraction(XRD) and transmission electron microscope(TEM) measurement.The carbon structure among rice husks was effectively used as a protective layer to accommodate the volume variation of Si anode during the repeated lithiation/delithiation process.Benefitting from the structure design,the batteries show a superior electrochemical stability with the capacity retention rate above 90% after 150 cycles at the charge/discha rge rate of 0.5 C(1 C=600 mAh/g),and hold a high charge capacity of 420.7 mAh/g at the rate of 3 C.Therefore,our finding not only provides a promising design strategy for directly conversion biomass-waste to electrochemical storage materials but broadens the high-efficiency utilization method for other biomass by-products.