Revealing the potential of apparent critical current density of Li/garnet interface with capacity perturbation strategy

Apparent critical current density(j_(Ac)^(a))of garnet all-solid-state lithium metal symmetric cells(ASSLSCs)is a fundamental parameter for designing all-solid-state lithium metal batteries.Nevertheless,how much the possible maximum apparent current density that a given ASSLSC system can endure and how to reveal this potential still require study.Herein,a capacity perturbation strategy aiming to better measure the possible maximum j_(Ac)^(a)is proposed for the first time.With garnet-based plane-surface structure ASSLSCs as an exemplification,the j_(Ac)^(a)is quite small when the capacity is dramatically large.Under a perturbed capacity of 0.001 mA h cm^(-2),the j_(Ac)^(a)is determined to be as high as 2.35 mA cm^(-2)at room temperature.This investigation demonstrates that the capacity perturbation strategy is a feasible strategy for measuring the possible maximum j_(Ac)^(a)of Li/solid electrolyte interface,and hopefully provides good references to explore the critical current density of other types of electrochemical systems.

Boosting the performance of LiNi_(0.90)Co_(0.06)Mn_(0.04)O_(2) electrode by uniform Li_(3)PO_(4) coating via atomic layer deposition

Ultra-high nickel material is considered to be a promising cathode material.However,with the increase of nickel content,the interfacial side reactions between the cathode and electrolyte become increasingly serious.Herein,an atomically controllable ionic conductor Li_(3)PO_(4)(LPO)coating is deposited on the LiNi_(0.90)Co_(0.06)Mn_(0.04)O_(2)(NCM9064)based electrode by the atomic layer deposition method.The results shows that the LPO coating is uniformly and densely covered on the surface of secondary particles of NCM9064,helping to prevent the direct contact between the electrolyte and cathode during the chargingdischarging process.In addition,the coating layer is electrochemically stable.As a result,the interfacial side reactions during the long cycle are effectively suppressed,and the solid electrolyte interphase layer at the interface is stabilized.The electrode with 20 layers of LPO deposition(ALD-LPO-20)exhibits an excellent capacity retention of 81%after 200 cycles in 2.8-4.3 V at 25℃,which is 18%higher than the unmodified material(ALD-LPO-0).Besides,the moderate LPO coating improves the rate capability and high temperature cycling performance of NCM9064.This study provides a method for the modification of ultra-high nickel cathode materials and corresponding electrodes.

Rapid conversion of alkaline bauxite residue through co-pyrolysis with waste biomass and its revegetation potential

The extreme alkalinity of bauxite residue(BR)leads to difficulty with its reuse.Alkaline leachate and dust generation during the stacking process can pollute surrounding soil,air and water.In this work,co-pyrolysis of bauxite residue and sawdust was applied to rapidly produce a soil-like matrix that met the conditions for plant growth as demonstrated by ryegrass pot experiments.The present study aimed to characterize the detailed changes in physicochemical,mineral weathering,and microbial communities of the pyrolyzed BR with different ratios of saw dust after plant colonization for 2 months.With increasing sawdust addition during co-pyrolysis,the pH of BR decreased from 11.21 to 8.16,the fraction of macro-aggregates 0.25-2 mm in the water-stable agglomerates increased by 29.3%,and the organic carbon concentration increased from 12.5 to 320 mg/kg,whilst facilitating the degree of humification,which were all beneficial to its revegetation performance.The backscattered electron-scanning electron microscope-energy-dispersive X-ray spectrometry(BSE-SEM-EDS)results confirmed the occurrence of sodalite and calcite weathering on aggregate surfaces,and X-ray photoelectron spectroscopy(XPS)results of surface Al and Si compounds identified that some weathering products were clay minerals such as kaolinite.Furthermore,bacterial community composition and structure shifted towards typical soil taxonomic groups.These results demonstrate soil development of treated BR at an early stage.The technique is a combination of alkalinity regulation and agglomerate construction,which accelerates soil formation of BR,thus proving highly promising for potential application as an artificial soil substitute.

The effect of extracellular polymeric substances (EPS) of iron-oxidizing bacteria (Ochrobactrum EEELCW01) on mineral transformation and arsenic (As) fate

Extracellular polymeric substances(EPS)are an importantmedium for communication and material exchange between iron-oxidizing bacteria and the external environment and could induce the iron(oxyhydr)oxides production which reduced arsenic(As)availability.The main component of EPS secreted by iron-oxidizing bacteria(Ochrobactrum EEELCW01)was composed of polysaccharides(150.76-165.33 mg/g DW)followed by considerably smaller amounts of proteins(12.98–16.12 mg/g DW).Low concentrations of As(100 or 500μmol/L)promoted the amount of EPS secretion.FTIR results showed that EPS was composed of polysaccharides,proteins,and a miniscule amount of nucleic acids.The functional groups including-COOH,-OH,-NH,-C=O,and-C-O played an important role in the adsorption of As.XPS results showed that As was bound to EPS in the form of As3+.With increasing As concentration,the proportion of As3+adsorbed on EPS increased.Ferrihydrite with a weak crystalline state was only produced in the system at 6 hr during the mineralization process of Ochrobactrum sp.At day 8,the minerals were composed of goethite,galena,and siderite.With the increasing mineralization time,the main mineral phases were transformed from weakly crystalline hydrous iron ore into higher crystallinity siderite(FeCO_(3))or goethite(α-FeOOH),and the specific surface area and active sites of minerals were reduced.It can be seen from the distribution of As elements that As is preferentially adsorbed on the edges of iron minerals.This study is potential to understand the biomineralizationmechanism of iron-oxidizing bacteria and As remediation in the environment.