2023年LIS期刊论文研究方法应用态势

研究方法的选择和运用影响研究的深度和可靠性,对科学研究发展十分重要。文章在总结LIS领域方法论研究的基础上,将LIS领域常用的研究方法整理、汇总、编码,以LIS领域11种TOP期刊2023年收录的论文为数据源,统计分析LIS期刊论文的研究方法应用态势,探讨LIS学科性质、研究对象、作者学科背景等因素对研究方法的影响。研究发现:LIS领域论文使用的研究方法内容不断演进,跨学科和新兴理论方法以及多元研究方法的应用促进了研究的深入和丰富。

热处理对Mg-3Sn-2Al-1Zn-5Li合金耐蚀性能的影响

对Mg-3Sn-2Al-1Zn-5Li合金进行了不同方式的热处理。利用电化学测试研究了不同热处理状态合金在3.5%NaCl溶液中的腐蚀电化学行为,并通过扫描电镜、能谱以及X射线衍射分析了合金腐蚀形貌及腐蚀产物的成分。结果表明:经固溶处理和时效处理后,合金的耐蚀性能有所提高,并且固溶态的Mg-3Sn-2Al-1Zn-5Li合金有着最佳的耐蚀性能;合金的腐蚀特征为丝状腐蚀,腐蚀产物主要为Mg(OH)_(2)。

察尔汗北部东陵湖Li、B资源分布特征与物质来源

柴达木盆地盐湖锂、硼资源是青海省建设世界级盐湖产业基地的重要资源组成部分,盆地内接续性锂、硼资源储量的增加意义重大。柴达木盆地东南部的察尔汗盐湖锂、硼资源差异分布明显,位于察尔汗盐湖北部的东陵湖,近两年勘查工作揭露其湖表卤水和湖区晶间卤水LiCl品位(315.16 mg/L)和B_(2)O_(3)品位(429.32 mg/L)均超过边界品位。本文以东陵湖湖表卤水、钻孔晶间卤水、承压卤水、浅层钻孔(0~8 m)盐类沉积物为研究对象,分析研究了东陵湖不同卤水和钻孔沉积物的锂、硼含量特征,并与察尔汗盐湖锂、硼含量分布特征对比,结合盆地补给河流和尾闾盐湖的Li^(+)含量和δ^(11)B值,分析了东陵湖锂、硼资源元素分布特征与物质来源,主要得出如下结论:①东陵湖湖表卤水(61.91 mg/L)和湖区钻孔晶间卤水(27.05 mg/L)的Li^(+)含量最高,而与察尔汗盐湖别勒滩区段(204.48 mg/L)相比,其Li含量低3.3~7.6倍;东陵湖湖表卤水的B^(3+)平均含量为177.25 mg/L,钻孔晶间卤水和承压卤水的B^(3+)平均含量为81.65 mg/L,较之察尔汗盐湖,东陵湖不同卤水硼含量普遍较高。②东陵湖11个钻孔沉积物样品Li^(+)含量介于1×10^(-6)~8.24×10^(-6)之间,B3+含量在0.005%~0.024%之间,湖区钻孔沉积物锂含量高于凹地钻孔;钻孔沉积剖面石盐层和碎屑层沉积物Li、B含量无明显变化。③东陵湖与察尔汗盐湖锂、硼含量空间分布差异明显,东陵湖较察尔汗盐湖别勒滩区段明显贫锂,较达布逊、察尔汗和霍布逊区段更富硼,总体表现为富硼贫锂的特征。④东陵湖δ^(11)B介于+20.33‰~+29.17‰之间,平均为+24.23‰,与柴北缘补给河流和Ca-Cl水补给形成的盐湖均位于高δ^(11)B端元区,结合东陵湖不同卤水样品的Ca^(2+)与Li^(+)、B^(3+)相关性研究,认为东陵湖锂、硼资源元素与含盐溶质具有相似的物源,高硼低锂的元素分布特征和高δ^(11)B值显示东陵湖地区水文补给来源与柴北缘水文体系有关,主要物质来源受察尔汗盐湖北部断裂带Ca-Cl水的补给。

猪胞内劳森菌抗体间接ELISA检测方法的建立及应用

猪增生性肠病(PPE),通常被称为猪回肠炎(PI),由胞内劳森氏菌(LI)感染引起。为建立检测LI抗体的间接ELISA方法,本研究构建LI外膜蛋白基因(LI0841)的重组表达质粒p ET28a-LI0841,经测序无误后转化BL21(DE3)宿主菌,经IPTG诱导表达,采用SDS-PAGE检测重组蛋白LI0841蛋白(rLI0841)的表达形式,经Ni柱纯化后采用western blot鉴定其反应原性。SDS-PAGE结果显示,在32 ku处出现目的条带,且其主要以可溶性形式表达;western blot结果显示,r LI0841能够与兔LI多克隆抗体特异性反应,表明纯化的r LI0841具有较强的反应原性,可作为包被抗原用于建立间接ELISA检测方法,经各反应条件优化初步建立LI抗体的间接ELISA检测方法。各反应条件的优化结果显示,4.38 ng/孔的r LI0841以4℃过夜包被最佳;血清最佳稀释度为1∶100,37℃反应0.5 h;羊抗猪Ig G-HRP最佳稀释度为1∶10000,37℃作用0.5 h;TMB底物37℃显色15 min。利用建立的间接ELISA方法检测猪繁殖与呼吸障碍综合征病毒、猪伪狂犬病病毒、副猪嗜血杆菌、猪链球菌、传染性胸膜肺炎放线杆菌及经美国Biostone PPE抗体检测试剂盒检测为阳性的猪血清,评估该方法的特异性;将LI阳性血清2倍倍比稀释(1∶100~1∶51200)后,采用本研究建立的间接ELISA方法检测,评估该方法的敏感性;以同一批次和不同批次包被的酶标板分别检测5份不同LI抗体水平的猪血清,评估该方法的重复性。结果显示,该方法除能检测到LI阳性血清外,其余相关病原的阳性血清均为阴性,特异性较强;LI阳性血清1∶800稀释时检测结果仍为阳性,敏感性较高;对5份不同抗体水平的LI阳性血清的批内、批间重复性试验的变异系数均小于10%,重复性较好。利用该ELISA方法与美国Biostone公司PPE抗体检测试剂盒同时检测104份临床猪血清样品,比较二者的检测结果,并计算二者的符合率;采用建立的间接ELISA方法检测黑龙江、吉林等地区413份临床猪血清样品,分析LI在上述地区的流行状况。结果显示,两种方法的阳性符合率为90.91%,阴性符合率为91.84%,总符合率为91.35%;413份临床猪血清样品中LI的阳性检出率为59.81%(247/413),表明LI在黑龙江、吉林等地区的猪群中普遍存在。本研究建立了检测LI抗体的间接ELISA方法,该方法特异性强、敏感性高、重复性与准确性均较好,为临床PI血清流行病学调查提供技术支持。

Al−Cu−Li−Mg合金纳米相之间溶质配分行为的第一性原理研究

采用一性原理计算考察25种合金化元素在大多数商业牌号Al−Cu−Li−Mg合金中主要纳米相(δʹ-Al3Li、θʹ-Al2Cu、T1-Al6Cu4Li3和S-Al2CuMg)之间的溶质配分能和配分行为。计算结果表明,主合金化元素Li不能直接影响θʹ和S相,Cu不能直接影响δʹ相,Mg不能直接影响θʹ和δʹ相,但可以较弱地固溶于T1相。对于微合金化元素,Si是唯一一种可以固溶于4种纳米相的元素。Au能固溶于δʹ、θʹ和S相,Cd能固溶于δʹ、T1和S相,Zr能固溶于δʹ和T1相,Ni仅有微弱的趋势固溶于θʹ和S相。Ti、V、Zn、Ag和Mo只能固溶于δʹ相,而Cr、Mn、Fe和Co对这4种纳米相均没有直接影响。几乎所有的稀土元素均能强烈固溶于T1、δʹ和S相,但无法固溶于θʹ相。仅Sc略显特殊,对S相没有明显的固溶趋势。计算预测的溶质配分能构成了一个原型数据库,有利于指导和加速Al−Li合金及其他相关Al合金的设计。

Lithium-Ion Charged Polymer Channels Flattening Lithium Metal Anode

The concentration difference in the near-surface region of lithium metal is the main cause of lithium dendrite growth.Resolving this issue will be key to achieving high-performance lithium metal batteries(LMBs).Herein,we construct a lithium nitrate(LiNO_(3))-implanted electroactiveβphase polyvinylidene fluoride-co-hexafluoropropylene(PVDF-HFP)crystalline polymorph layer(PHL).The electronegatively charged polymer chains attain lithium ions on the surface to form lithium-ion charged channels.These channels act as reservoirs to sustainably release Li ions to recompense the ionic flux of electrolytes,decreasing the growth of lithium dendrites.The stretched molecular channels can also accelerate the transport of Li ions.The combined effects enable a high Coulombic efficiency of 97.0%for 250 cycles in lithium(Li)||copper(Cu)cell and a stable symmetric plating/stripping behavior over 2000 h at 3 mA cm^(-2)with ultrahigh Li utilization of 50%.Furthermore,the full cell coupled with PHL-Cu@Li anode and Li Fe PO_(4) cathode exhibits long-term cycle stability with high-capacity retention of 95.9%after 900 cycles.Impressively,the full cell paired with LiNi_(0.87)Co_(0.1)Mn_(0.03)O_(2)maintains a discharge capacity of 170.0 mAh g^(-1)with a capacity retention of 84.3%after 100 cycles even under harsh condition of ultralow N/P ratio of 0.83.This facile strategy will widen the potential application of LiNO_(3)in ester-based electrolyte for practical high-voltage LMBs.

高强耐蚀1420Al-Li/Mg-9Li/1420Al-Li复合板制备及力学性能

采用高强耐蚀超轻1420 Al-Li合金作为覆板,通过一道次热轧制备了1420Al-Li/Mg-9Li/1420Al-Li复合板,研究了不同压下量、450℃热轧复合板界面的微观组织和力学性能。结果表明:当轧制压下量为35%时,复合板仅为部分结合—机械结合+冶金结合,界面无化合物生成,复合板的抗拉强度为236 MPa,伸长率为26%;当轧制压下量为50%时,复合板实现完全冶金结合,无界面化合物生成,复合板的抗拉强度高达272 MPa,伸长率为14%,在提高抗腐蚀性的同时,大幅提高了Mg-9Li合金的强度。

Trend of Developing Aqueous Liquid and Gel Electrolytes for Sustainable,Safe,and High‑Performance Li‑Ion Batteries

Current lithium-ion batteries(LIBs)rely on organic liquid electrolytes that pose significant risks due to their flammability and toxicity.The potential for environmental pollution and explosions resulting from battery damage or fracture is a critical concern.Water-based(aqueous)electrolytes have been receiving attention as an alternative to organic electrolytes.However,a narrow electrochemicalstability window,water decomposition,and the consequent low battery operating voltage and energy density hinder the practical use of aqueous electrolytes.Therefore,developing novel aqueous electrolytes for sustainable,safe,high-performance LIBs remains challenging.This Review first commences by summarizing the roles and requirements of electrolytes–separators and then delineates the progression of aqueous electrolytes for LIBs,encompassing aqueous liquid and gel electrolyte development trends along with detailed principles of the electrolytes.These aqueous electrolytes are progressed based on strategies using superconcentrated salts,concentrated diluents,polymer additives,polymer networks,and artificial passivation layers,which are used for suppressing water decomposition and widening the electrochemical stability window of water of the electrolytes.In addition,this Review discusses potential strategies for the implementation of aqueous Li-metal batteries with improved electrolyte–electrode interfaces.A comprehensive understanding of each strategy in the aqueous system will assist in the design of an aqueous electrolyte and the development of sustainable and safe high-performance batteries.

Li掺杂对铜锌锡硫硒太阳电池的影响研究

开展了基于二甲基亚砜溶剂体系的溶胶凝胶法制备铜锌锡硫硒薄膜中掺杂Li的相关研究。对不同Li掺杂量的CZTSSe薄膜分别进行了表截面形貌、晶体结构、成分比例测试,结果表明:在CZTSSe薄膜中掺杂Li可以提升薄膜的结晶质量,且随着Li掺杂量的增加,结晶质量变好。分析原因为,高温硒化过程中形成的Li_(2)Se相辅助生长改善了薄膜的结晶质量,抑制了ZnCu和SnCu等施主能级缺陷生成。但是,同样发现在Li/Cu摩尔比为1%~10%之间存在阈值,过量的Li并不能进入晶格而富集在晶界处。对不同Li掺杂的CZTSSe薄膜进行太阳电池的制备,结果表明Li/Cu为1%的太阳电池具有最高的转换效率,达到8.5%。

Construction of Dynamic Alloy Interfaces for Uniform Li Deposition in Li-Metal Batteries

It is well accepted that a lithiophilic interface can effectively regulate Li deposition behaviors,but the influence of the lithiophilic interface is gradually diminished upon continuous Li deposition that completely isolates Li from the lithiophilic metals.Herein,we perform in-depth studies on the creation of dynamic alloy interfaces upon Li deposition,arising from the exceptionally high diffusion coefficient of Hg in the amalgam solid solution.As a comparison,other metals such as Au,Ag,and Zn have typical diffusion coefficients of 10-20 orders of magnitude lower than that of Hg in the similar solid solution phases.This difference induces compact Li deposition pattern with an amalgam substrate even with a high areal capacity of 55 mAh cm^(-2).This finding provides new insight into the rational design of Li anode substrate for the stable cycling of Li metal batteries.

铸态Udimet720Li合金热变形行为及热加工图研究

在变形温度为1 040~1 160℃、真应变速率为0.01~10 s^(-1)和变形量为60%条件下,对铸态Udimet720Li合金开展了热压缩实验.基于真应力-真应变数据,运用Arrhenius方程、动态材料模型理论和流变失稳判据理论建立了本构方程模型和热加工图,分析了合金热变形行为并结合微观组织验证了所建热加工图的准确性.结果表明:流变真应力对温度和真应变速率具有较强的敏感性,随着变形温度的升高和变形速率的减小流变真应力不断降低,温度越高,流变真应力达到稳态时对应的真应力和真应变越小,所建本构方程模型对合金流变真应力预测具有较高的准确性.当变形量为60%时,变形温度1 040~1 070℃和真应变速率5~10 s^(-1)范围内为合金变形失稳区,变形温度1 140~1 160℃、真应变速率0.01~0.20 s^(-1)范围内合金具有最优热加工性,该区功率耗散系数为0.32~0.40,合金可以获得晶粒细小的等轴匀晶组织.

Li/SF_(6)反应动力学参数及燃烧现象研究

为探究不同温度及压力条件下锂/六氟化硫(Li/SF_(6))燃烧现象及反应动力学参数,利用激波诱导高压热载荷激励Li/SF_(6)燃烧实验台测量了温度范围为830~1400 K,压力范围为0.8~11 atm时的点火滞燃期;利用可视化实验段探究了Li/SF_(6)燃烧过程和基本发光现象等规律;利用点火滞燃期与温度和压力呈现出的典型Arrhenius依赖关系,通过多元线性回归法得出反应动力学参数。研究结果表明,Li/SF_(6)燃烧的点火滞燃期随温度和压力的升高而减少,发光现象随压力的升高由红色孤立火核逐渐转化为白色明亮火焰,并结合实验测定的点火滞燃期求出了指前因子A、指数因子n和活化能Ea,为明晰燃烧特性、构建数值仿真提供了重要依据。

有源层厚度对Li-ZTO TFT电学性能的影响

本研究旨在制备Li-ZTO单有源层薄膜晶体管,并研究有源层厚度对其性能的影响。该研究采用磁控溅射方法,使用Li-ZTO靶材制备出了有源层厚度分别为70 nm,90 nm,110 nm的器件。采用了X射线光电子能谱(XPS)、原子粒显微镜(AFM)、X射线衍射仪(XRD)等设备对制备出的Li-ZTO薄膜进行测试分析。通过对不同有源层厚度的薄膜物质组成、表面形貌、晶粒生长情况的测试分析,进一步研究了有源层厚度对Li-ZTO薄膜性能的影响。除此之外,我们还利用半导体参数仪对Li-ZTO的电学性能进行了测试。结果表明,过厚的有源层将影响电荷传输,增加散射中心,影响器件性能。因此,有源层厚度为70 nm的Li-ZTO具有最好的性能,包括12.33 cm^(2)/vs的饱和迁移率、0.66 V的阈值电压、2.12 V/dec的亚阈值摆幅以及>10~8的开关比。

Carbon-based interface engineering and architecture design for high-performance lithium metal anodes

Metallic lithium(Li)is considered the“Holy Grail”anode material for the nextgeneration of Li batteries with high energy density owing to the extraordinary theoretical specific capacity and the lowest negative electrochemical potential.However,owing to inhomogeneous Li-ion flux,Li anodes undergo uncontrollable Li deposition,leading to limited power output and practical applications.Carbon materials and their composites with controllable structures and properties have received extensive attention to guide the homogeneous growth of Li to achieve high-performance Li anodes.In this review,the correlation between the behavior of Li anode and the properties of carbon materials is proposed.Subsequently,we review emerging strategies for rationally designing high-performance Li anodes with carbon materials,including interface engineering(stabilizing solid electrolyte interphase layer and other functionalized interfacial layer)and architecture design of host carbon(constructing three-dimension structure,preparing hollow structure,introducing lithiophilic sites,optimizing geometric effects,and compositing with Li).Based on the insights,some prospects on critical challenges and possible future research directions in this field are concluded.It is anticipated that further innovative works on the fundamental chemistry and theoretical research of Li anodes are needed.

Electrolyte Design for Low‑Temperature Li‑Metal Batteries:Challenges and Prospects

Electrolyte design holds the greatest opportunity for the development of batteries that are capable of sub-zero temperature operation.To get the most energy storage out of the battery at low temperatures,improvements in electrolyte chemistry need to be coupled with optimized electrode materials and tailored electrolyte/electrode interphases.Herein,this review critically outlines electrolytes’limiting factors,including reduced ionic conductivity,large de-solvation energy,sluggish charge transfer,and slow Li-ion transportation across the electrolyte/electrode interphases,which affect the low-temperature performance of Li-metal batteries.Detailed theoretical derivations that explain the explicit influence of temperature on battery performance are presented to deepen understanding.Emerging improvement strategies from the aspects of electrolyte design and electrolyte/electrode interphase engineering are summarized and rigorously compared.Perspectives on future research are proposed to guide the ongoing exploration for better low-temperature Li-metal batteries.

Thin polymer electrolyte with MXene functional layer for uniform Li^(+) deposition in all-solid-state lithium battery

Solid polymer electrolyte(SPE) shows great potential for all-solid-state batteries because of the inherent safety and flexibility;however, the unfavourable Li+deposition and large thickness hamper its development and application. Herein, a laminar MXene functional layer-thin SPE layer-cathode integration(MXene-PEO-LFP) is designed and fabricated. The MXene functional layer formed by stacking rigid MXene nanosheets imparts higher compressive strength relative to PEO electrolyte layer. And the abundant negatively-charged groups on MXene functional layer effectively repel anions and attract cations to adjust the charge distribution behavior at electrolyte–anode interface. Furthermore,the functional layer with rich lithiophilic groups and outstanding electronic conductivity results in low Li nucleation overpotential and nucleation energy barrier. In consequence, the cell assembled with MXene-PEO-LFP, where the PEO electrolyte layer is only 12 μm, much thinner than most solid electrolytes, exhibits uniform, dendrite-free Li+deposition and excellent cycling stability. High capacity(142.8 mAh g-1), stable operation of 140 cycles(capacity decay per cycle, 0.065%), and low polarization potential(0.5 C) are obtained in this Li|MXene-PEO-LFP cell,which is superior to most PEO-based electrolytes under identical condition. This integrated design may provide a strategy for the large-scale application of thin polymer electrolytes in all-solid-state battery.

Dual Additives for Stabilizing Li Deposition and SEI Formation in Anode-Free Li-Metal Batteries

Anode-free Li-metal batteries are of significant interest to energy storage industries due to their intrinsically high energy.However,the accumulative Li dendrites and dead Li continuously consume active Li during cycling.That results in a short lifetime and low Coulombic efficiency of anode-free Li-metal batteries.Introducing effective electrolyte additives can improve the Li deposition homogeneity and solid electrolyte interphase(SEI)stability for anode-free Li-metal batteries.Herein,we reveal that introducing dual additives,composed of LiAsF6 and fluoroethylene carbonate,into a low-cost commercial carbonate electrolyte will boost the cycle life and average Coulombic efficiency of NMC‖Cu anode-free Li-metal batteries.The NMC‖Cu anode-free Li-metal batteries with the dual additives exhibit a capacity retention of about 75%after 50 cycles,much higher than those with bare electrolytes(35%).The average Coulombic efficiency of the NMC‖Cu anode-free Li-metal batteries with additives can maintain 98.3%over 100 cycles.In contrast,the average Coulombic efficiency without additives rapidly decline to 97%after only 50 cycles.In situ Raman measurements reveal that the prepared dual additives facilitate denser and smoother Li morphology during Li deposition.The dual additives significantly suppress the Li dendrite growth,enabling stable SEI formation on anode and cathode surfaces.Our results provide a broad view of developing low-cost and high-effective functional electrolytes for high-energy and long-life anode-free Li-metal batteries.

Li-promoted C_(3)N_(4) catalyst for efficient isomerization of glucose into fructose at 50℃ in water

Efficient and selective glucose-to-fructose isomerization is a crucial step for production of oxygenated chemicals derived from sugars,which is usually catalyzed by base or Lewis acid heterogeneous catalyst.However,high yield and selectivity of fructose cannot be simultaneously obtained under mild conditions which hamper the scale of application compared with enzymatic catalysis.Herein,a Li-promoted C_(3)N_(4) catalyst was exploited which afforded an excellent fructose yield(40.3 wt%)and selectivity(99.5%)from glucose in water at 50℃,attributed to the formation of stable Li–N bond to strengthen the basic sites of catalysts.Furthermore,the so-formed N_(6)–Li–H_(2)O active site on Li–C_(3)N_(4) catalyst in aqueous phase changes the local electronic structure and strengthens the deprotonation process during glucose isomerization into fructose.The superior catalytic performance which is comparable to biological pathway suggests promising applications of lithium containing heterogeneous catalyst in biomass refinery.

Tuning Li/Ni mixing by reactive coating to boost the stability of cobalt-free Ni-rich cathode

Cobalt-free cathode materials are attractive for their high capacity and low cost,yet they still encounter issues with structural and surface instability.AlPO_(4),in particular,has garnered attention as an effective stabilizer for bulk and surface.However,the impact of interfacial reactions and elemental interdiffusion between AlPO_(4) and LiNi_(0.95)Mn_(0.05)O_(2) upon sintering on the bulk and surface remains elusive.In this study,we demonstrate that during the heat treatment process,AlPO_(4) decomposes,resulting in Al doping into the bulk of the cathode through elemental interdiffusion.Simultaneously,PO_(4)^(3-)reacts with the surface Li of material to form a Li_3PO_(4) coating,inducing lithium deficiency,thereby increasing Li/Ni mixing.The suitable Li/Ni mixing,previously overlooked in AlPO_(4) modification,plays a pivotal role in stabilizing the bulk and surface,exceeding the synergy of Al doping and Li_3PO_(4) coating.The presence of Ni^(2+)ions in the lithium layers contributes to the stabilization of the delithiated structure via a structural pillar effect.Moreover,suitable Li/Ni mixing can stabilize the lattice oxygen and electrode-electrolyte interface by increasing oxygen removal energy and reducing the overlap between the Ni^(3+/4+)e_g and O^(2-)2p orbitals.These findings offer new perspectives for the design of stable cobalt-free cathode materials.

Sc元素添加对双辊铸轧Al−Cu−Li−Mg−Zr基合金热处理的影响

提出制备含Sc的Al−Cu−Li−Mg−Zr基合金带材的工艺方案。即先采用双辊铸轧技术制备近净形状的3 mm厚带材,再对其进行均匀化/固溶处理。研究两种Al−Cu−Li−Mg−Zr基双辊铸轧合金,其中一种添加质量分数为0.17%的Sc,另一种未添加Sc。两种合金均先在300℃下退火30 min,然后在450℃下退火30 min以及530℃下退火30 min,随后进行室温水淬。前两段退火后组织中生成了细小、弥散的Al_(3)Zr/Al_(3)(Sc,Zr)颗粒。最后的退火步骤起到了均匀化/固溶处理的作用。双辊铸轧材料的细小晶粒结构使含有主要合金元素的原始颗粒在较短的退火时间内溶解。缩短保温时间可以限制表面层中Li的耗尽和Al_(3)Zr/Al_(3)(Sc,Zr)弥散相的明显粗化。铸态含Sc材料已经具有明显细小的晶粒结构,而经均匀化/固溶处理后生成的Al_(3)(Sc,Zr)弥散相抑制了晶粒在高温下发生粗化。在后续180℃下时效处理后,形成了θʹ(Al_(2)Cu)、T1(Al_(2)CuLi)和S'(Al_(2)CuMg)强化相。在峰值时效状态下,屈服强度提高了200 MPa,这一数值与类似直接冷却铸造材料的相当,从而证实了所提方案的合理性。