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Tuning Li/Ni mixing by reactive coating to boost the stability of cobalt-free Ni-rich cathode 被引量:1
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作者 Fanghui Du Xitong Zhang +7 位作者 Yingchao Wang Lei Ding Pengfang Zhang Lingyang Liu Dong Wang Jianzong Man Yuling Chen Yunwu Li 《Journal of Energy Chemistry》 SCIE EI CAS CSCD 2024年第10期20-29,I0002,共11页
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 s... 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. 展开更多
关键词 Cobalt-free Ni-rich cathode Li/Ni mixing al doping Li_(3)PO_(4) coating Lithium-ion batteries
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Penetration behavior of electrolyte into graphite cathode in NaF-KF-LiF-AlF_(3) system with low cryolite ratios
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作者 Bing-xu CHEN Jian-ping PENG +1 位作者 Yao-wu WANG Yue-zhong DI 《Transactions of Nonferrous Metals Society of China》 SCIE EI CAS CSCD 2022年第8期2727-2735,共9页
The current study focuses on the electrolyte penetration of the graphite cathode in a NaF−KF−LiF−AlF_(3) aluminum-electrolysis system with a cryolite ratio of 1.3.It involves a comprehensive investigation of the elect... The current study focuses on the electrolyte penetration of the graphite cathode in a NaF−KF−LiF−AlF_(3) aluminum-electrolysis system with a cryolite ratio of 1.3.It involves a comprehensive investigation of the electrolyte in the cathode before and after electrolysis by X-ray diffraction and analysis of the results by semi-quantitative calculation in MAUD.The results show that KF can promote electrolyte penetration,with higher KF contents resulting in greater penetration.During electrolyte penetration,K_(2)NaAlF_(6) and solid solutions containing KF play important roles in KF-containing systems.LiF effectively prevents the electrolyte penetration,while the Na_(3)Li_(3)Al_(2)F_(12) phase plays an essential role in systems with high LiF contents. 展开更多
关键词 aluminum electrolysis KF lif cathode penetration electrolyte composition low cryolite ratio
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The mechanism of side reaction induced capacity fading of Ni-rich cathode materials for lithium ion batteries 被引量:10
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作者 Daozhong Hu Yuefeng Su +7 位作者 Lai Chen Ning Li Liying Bao Yun Lu Qiyu Zhang Jing Wang Shi Chen Feng Wu 《Journal of Energy Chemistry》 SCIE EI CAS CSCD 2021年第7期1-8,共8页
Ni-rich cathode materials show great potential of applying in high-energy lithium ion batteries,but their inferior cycling stability hinders this process.Study on the electrode/electrolyte interfacial reaction is indi... Ni-rich cathode materials show great potential of applying in high-energy lithium ion batteries,but their inferior cycling stability hinders this process.Study on the electrode/electrolyte interfacial reaction is indispensable to understand the capacity failure mechanism of Ni-rich cathode materials and further address this issue.This work demonstrates the domain size effects on interfacial side reactions firstly,and further analyzes the inherent mechanism of side reaction induced capacity decay through comparing the interfacial behaviors before and after MgO coating.It has been determined that LiF deposition caused thicker SEI films may not increase the surface film resistance,while HF erosion induced surface phase transition will increase the charge transfer resistance,and the later plays the dominant factor to declined capacity of Ni-rich cathode materials.This work suggests strategies to suppress the capacity decay of layered cathode materials and provides a guidance for the domain size control to match the various applications under different current rates. 展开更多
关键词 Lithium-ion batteries Ni-rich cathode materials lif deposition HF erosion Failure mechanism
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Regeneration of Al-doped LiNi_(0.5)Co_(0.2)Mn_(0.3)O_(2) cathode material by simulated hydrometallurgy leachate of spent lithium-ion batteries 被引量:7
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作者 Fang-cheng LI Gang ZHANG +4 位作者 Zong-liang ZHANG Jian YANG Fang-yang LIU Ming JIA Liang-xing JIANG 《Transactions of Nonferrous Metals Society of China》 SCIE EI CAS CSCD 2022年第2期593-603,共11页
A uniform Al-doped LiNi_(0.5)Co_(0.2)Mn_(0.3)O_(2) cathode material was prepared using a coprecipitation method to take advantage of the positive effect of Al on regenerated NCM(Ni,Co,Mn)cathode materials and ameliora... A uniform Al-doped LiNi_(0.5)Co_(0.2)Mn_(0.3)O_(2) cathode material was prepared using a coprecipitation method to take advantage of the positive effect of Al on regenerated NCM(Ni,Co,Mn)cathode materials and ameliorate cumbersome and high-cost impurity removal processes during lithium-ion battery recycling.When the Al^(3+) content in the leachate was 1 at.%with respect to the total amount of transition metals(Ni,Co,and Mn),the produced Al-doped NCM cathode material increased concentrations of lattice oxygen and Ni^(2+).The initial specific capacity at 0.1C was 167.4 mA·h/g,with a capacity retention of 79.1%after 400 cycles at 1C.Further,this Al-doped sample showed improved rate performance and a smaller electrochemical impedance.These findings provide a reference for developing industrial processes to resynthesize cathode materials with improved electrochemical performance by incorporating Al^(3+) impurities produced during lithium-ion battery recycling. 展开更多
关键词 spent lithium-ion battery REGENERATION al doping ternary cathode material coprecipitation
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Synthesis and electrochemical properties of Al-doped LiVPO_4F cathode materials for lithium-ion batteries 被引量:6
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作者 ZHONG Shengkui YIN Zhoulan +1 位作者 WANG Zhixing CHEN Qiyuan 《Rare Metals》 SCIE EI CAS CSCD 2007年第5期445-449,共5页
Al-doped LiVPO4F cathode materials LiAlxV1-xPO4F were prepared by two-step reactions based on a car-bothermal reduction (CTR) process. The properties of the Al-doped LiVPO4F were investigated by X-ray diffraction (... Al-doped LiVPO4F cathode materials LiAlxV1-xPO4F were prepared by two-step reactions based on a car-bothermal reduction (CTR) process. The properties of the Al-doped LiVPO4F were investigated by X-ray diffraction (XRD),scanning electron microscopy (SEM),and electrochemical measurements. XRD studies show that the Al-doped LiVPO4F has the same triclinic structure (space group p-↑1 ) as the undoped LiVPO4F. The SEM images exhibit that the particle size of Al-doped LiVPO4F is smaller than that of the undoped LiVPO4F and that the smallest particle size is only about 1 μm. The Al-doped LiVPO4F was evaluated as a cathode material for secondary lithium batteries,and exhibited an improved reversibility and cycleability,which may be attributed to the addition of Al^3+ ion by stabilizing the triclinic structure. 展开更多
关键词 lithium-ion batteries cathode material LIVPO4F al-doping carbothermal reduction method cyclic voltammetry (CV)
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STUDY ON THE TANTALIZING ON THE SURFACE OF TITANIUM ALLOY BY NET-SHAPE CATHODE GLOW DISCHARGING 被引量:1
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作者 F.Chen H.Zhou +1 位作者 Y.F.Zhang J.D.Pan 《Acta Metallurgica Sinica(English Letters)》 SCIE EI CAS CSCD 2005年第3期375-379,共5页
A new net-shape cathode sputtering target which has a simple structure and a hig h sputtering was put forward. The multiple-structure made of alloying and coatin g layers of tantalum was achieved on the surface of TC4... A new net-shape cathode sputtering target which has a simple structure and a hig h sputtering was put forward. The multiple-structure made of alloying and coatin g layers of tantalum was achieved on the surface of TC4 (Ti6Al4V) using this met hod in double glow surface alloying process. The tantalized samples were investi gated by SEM, XRD and electrochemical corrosion method .Results show the complic ated tissue of pure tantalizing layer and diffusion layer was successfully forme d on the surface of TC4 with the method of net-shape cathode glow discharge, whi ch further improved the corrosion-resistance of TC4 and formed good corrosion-re sistant alloys. 展开更多
关键词 TC4 (Ti6al4V) cathode sputtering tantalizing
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Synthesis and electrochemical characterization of LiNi_(0.78)Co_(0.2)Al_(0.02)O_2 cathode material in a novel co-precipitation method 被引量:1
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作者 顾大明 田启友 《Journal of Harbin Institute of Technology(New Series)》 EI CAS 2008年第3期436-438,共3页
LiNi0.78 Co0.2 Al0.02O2 cathode materials were prepared with a novel co-precipitation method followed by heat-treating. The properties of the materials were characterized. XRD patterns showed that no secondary phase a... LiNi0.78 Co0.2 Al0.02O2 cathode materials were prepared with a novel co-precipitation method followed by heat-treating. The properties of the materials were characterized. XRD patterns showed that no secondary phase appeared and the hexagonal lattice parameter c of LiNi0.rsCoo.2AI^0202 was larger than that of LiNi0.8Co0.2O2. The SEM images indicated that the powders of the material were submicron size. The results of the ICP-AES analysis proved that elemental compositions of the material were similar to those of the targeted one. Cyclic voltammetry (3.0- 4. 2 V) illustrated that the new material had good lithium-ion intercalation/de-intercalation performance. The results of galvanostatic cycling showed that the initial specific discharge capacity of the prepared material was 181.4 mAh/g, and the specific discharge capacity was 177.3 mAh/g after 100 cycles (0. 2C, 3.0 - 4. 2 V, vs. Li^+/Li) with the capacity retention ratio of 97.7%. 展开更多
关键词 lithium ion battery CO-PRECIPITATION LINI0.8CO0.2O2 cathode material al doped
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Direct Synthesis of Al_2O_3-modified Li(Ni_(0.5)Co_(0.2)Mn_(0.3))O_2 Cathode Materials for Lithium Ion Batteries 被引量:1
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作者 王启岁 ZHANG Changchun +2 位作者 XING Junlong YANG Maoping XIE Jia 《Journal of Wuhan University of Technology(Materials Science)》 SCIE EI CAS 2018年第1期97-101,共5页
To improve the cyclic stability at high temperature and thermal stability, the spherical Al2O3-modified Li(Ni0.5Co0.2Mn0.3)O2 was synthesized by a modified co-precipitation method, and the physical and electrochemic... To improve the cyclic stability at high temperature and thermal stability, the spherical Al2O3-modified Li(Ni0.5Co0.2Mn0.3)O2 was synthesized by a modified co-precipitation method, and the physical and electrochemical properties were studied. The TEM images showed that Li(Ni0.5Co0.2Mn0.3)O2 was modified successfully with nano-Al2O3. The discharge capacity retention of Al2O3-modified Li(Ni0.5Co0.2Mn0.3)O2 maintained about 99% after 200 cycles at high temperature(55 ℃), while that of the bare one was only 86%. Also, unlike bare Li(Ni0.5Co0.2Mn0.3)O2, the Al2O3-modified material cathode exhibited good thermal stability. 展开更多
关键词 modified precipitation method layered cathode materials al2O3- modified cyclic stability DSC
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Preparation and properties of Os–Ir–Al alloy for impregnated tungsten cathodes
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作者 Yang Xia Yuan-Feng Xie +2 位作者 Heng Jiang Hong Lv Yu-Min Wang 《Rare Metals》 SCIE EI CAS CSCD 2013年第6期564-568,共5页
Os–Ir–Al alloy was fabricated by powder metallurgy technique.IrAl and OsIr interalloys were synthesized to reduce the Al evaporation and ensure the composition of the ternary alloy.Analysis on microstructures shows ... Os–Ir–Al alloy was fabricated by powder metallurgy technique.IrAl and OsIr interalloys were synthesized to reduce the Al evaporation and ensure the composition of the ternary alloy.Analysis on microstructures shows that each component is distributed homogeneously,and the green density reaches 94.9%.Ba–W cathodes with Os–Ir–Al alloy magnetic sputtered on the tips are prepared and directly current density tests are carried out on these cathodes.It is found that at 1,050℃,the average zero field emission density of the cathode reaches up to 20 Aácm-2.The improvements of cathodic current density and stability may indicate the prosperous application of Os–Ir–Al alloy on cathode. 展开更多
关键词 cathode Os–Ir–al alloy Interalloys HOMOGENEOUS Current density
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Studies on Synthesis and Electrochemical Performance of Li_(1+δ) Ni_(1-x)Co_xO_(2-y)F_y Cathode Materials for Lithium-ion Batteries?
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作者 LIN Xiao-jing LIU Xing-quan +1 位作者 HE Ze-zhen LI Shu-hua 《合成化学》 CAS CSCD 2004年第z1期128-128,共1页
关键词 Lithium-ion rechargeable batteries cathode materials Li1+Ni CoxO2-yFy SYNTHESIS co-doping lif.
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利用LiF/Al作为电极的有机电致发光器件 被引量:9
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作者 李传南 肖步文 +1 位作者 侯晶莹 刘式墉 《光子学报》 EI CAS CSCD 北大核心 2001年第1期86-89,共4页
本文报道了利用 L i F/ Al作为负电极的有机电致发光器件 ,器件结构为 ITO/ TPD/Alq3/ Li F/ Al,Li F层的加入增强了电子注入 ,当其厚度为 0 .4nm时 ,器件的性能最好 ,与单层 Al和 Mg/ Al电极的同类器件相比 ,此时器件的开启电压由 Al... 本文报道了利用 L i F/ Al作为负电极的有机电致发光器件 ,器件结构为 ITO/ TPD/Alq3/ Li F/ Al,Li F层的加入增强了电子注入 ,当其厚度为 0 .4nm时 ,器件的性能最好 ,与单层 Al和 Mg/ Al电极的同类器件相比 ,此时器件的开启电压由 Al电极时的 4.3V和 Mg/ Al电极时的 3.0 V降低到了 2 .0 V,器件的最大亮度分别由 40 0 0 cd/ m2、1 40 0 0 cd/ m2提高到1 960 0 cd/ m2 ,器件的发光效率也分别增加了 5倍和 2倍 ,达到 2 .66lm/ W. 展开更多
关键词 有机电致发光器件 氟化锂/铝 电极
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LiF对Na_3AlF_6-Al_2O_3熔盐电解阴极过程的影响 被引量:5
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作者 陶绍虎 狄跃忠 +3 位作者 彭建平 王耀武 赵坤 冯乃祥 《化工学报》 EI CAS CSCD 北大核心 2014年第2期633-640,共8页
电解铝工业中铝在阴极上析出,铝析出反应的机理对电解铝生产具有理论指导意义。在运用循环伏安法研究的基础上,通过理论计算,对Na3AlF6-Al2O3和Na3AlF6-Al2O3-LiF体系中金属铝在钨电极上的电化学沉积行为以及铝钨金属间化合物的形成机... 电解铝工业中铝在阴极上析出,铝析出反应的机理对电解铝生产具有理论指导意义。在运用循环伏安法研究的基础上,通过理论计算,对Na3AlF6-Al2O3和Na3AlF6-Al2O3-LiF体系中金属铝在钨电极上的电化学沉积行为以及铝钨金属间化合物的形成机理进行了研究。结果表明:两体系中铝钨金属间化合物在50 mV·s-1≤ν≤150mV·s-1扫描速率下的形成过程是受扩散控制的准可逆过程。在化合物形成的过程中,两体系中Al3+的扩散系数从4.54×10-9 cm2·s-1增长到5.71×10-9 cm2·s-1,Al3+反应的活化能分别为11.14 kJ·mol-1和10.47 kJ·mol-1。在Na3AlF6-Al2O3-LiF体系的还原过程中,Li并没有还原析出,而在氧化过程中Al在金属间化合物中的氧化电流增大;在恒电流电解时,Al-W金属间化合物并不溶于熔盐中,会附着在工作电极表面,LiF的加入会使电极表面的WAl4量变小,取而代之的是Al2O3的增加,说明LiF的加入使电解更加稳定,抑制了电极表面WAl4的生长。 展开更多
关键词 铝电解 阴极电化学 循环伏安 铝钨金属间化合物
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LiF对Na_3AlF_6-K_3AlF_6-AlF_3熔体初晶温度和Al_2O_3溶解度的影响 被引量:11
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作者 黄有国 田忠良 +2 位作者 赖延清 李劼 刘业翔 《中国有色金属学报》 EI CAS CSCD 北大核心 2010年第5期903-907,共5页
采用步冷曲线法测定Na3AlF6-K3AlF6-AlF3-LiF熔体的初晶温度,采用旋转刚玉片质量损失法测定Al2O3在Na3AlF6-K3AlF6-AlF3-LiF熔体中的溶解度。结果表明:当LiF添加量在0~4%范围内时,每添加1%LiF使Na3AlF6-K3AlF6-AlF3熔体的初晶温度降低3... 采用步冷曲线法测定Na3AlF6-K3AlF6-AlF3-LiF熔体的初晶温度,采用旋转刚玉片质量损失法测定Al2O3在Na3AlF6-K3AlF6-AlF3-LiF熔体中的溶解度。结果表明:当LiF添加量在0~4%范围内时,每添加1%LiF使Na3AlF6-K3AlF6-AlF3熔体的初晶温度降低3~4.7℃,小于Na3AlF6-AlF3熔体中添加LiF后初晶温度的影响;在0~3%的范围内,每添加1%LiF将使Al2O3在Na3AlF6-K3AlF6-AlF3熔体中的溶解度降低0.23%~0.55%。 展开更多
关键词 al2O3 lif Na3alF6-K3alF6-alF3熔体 初晶温度 溶解度
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Al_2O_3:C、LiF:Mg,Ti、LiF:Mg,Cu,P对本底辐射的热释光响应比较 被引量:2
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作者 陈劲民 李永强 +5 位作者 熊正烨 王文华 封余军 黄存友 汤照 师文庆 《核技术》 CAS CSCD 北大核心 2012年第2期109-112,共4页
用Al2O3:C、LiF:Mg,Ti、LiF:Mg,Cu,P热释光剂量计(TLD)测量湛江市区本底辐射的热释光响应,以选取适合低辐射场辐射剂量测量的TLD。它们的最低响应剂量依次为Al2O3:C(1–2μGy)、LiF:Mg,Cu,P(约2μGy)和LiF:Mg,Ti(>10μGy)。Al2O3:C... 用Al2O3:C、LiF:Mg,Ti、LiF:Mg,Cu,P热释光剂量计(TLD)测量湛江市区本底辐射的热释光响应,以选取适合低辐射场辐射剂量测量的TLD。它们的最低响应剂量依次为Al2O3:C(1–2μGy)、LiF:Mg,Cu,P(约2μGy)和LiF:Mg,Ti(>10μGy)。Al2O3:C的热释光峰温较低,对较长时间段(>30 d)的累积剂量,存在较明显的热释光衰退,剂量响应曲线偏离线性;LiF:Mg,Cu,P和LiF:Mg,Ti的发光峰温较高,数年内都很稳定。综合考虑灵敏度和稳定性,LiF:Mg,Cu,P更宜于低辐射场的累积剂量测量。 展开更多
关键词 热释光 本底辐射 al2O3 lif
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前驱体掺杂-常温球磨还原法制备锂离子电池正极材料LiFe_(1-3y/2)Al_yPO_4 被引量:4
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作者 吕凡 伍凌 +2 位作者 管淼 钟胜奎 刘洁群 《中国有色金属学报》 EI CAS CSCD 北大核心 2014年第2期468-475,共8页
采用共沉淀法制备掺Al3+前驱体FePO4·2H2O,并以乙二酸为还原剂,与Li2CO3反应在常温下球磨合成LiFePO4前驱混合物,后经热处理得到橄榄石型LiFe1-3y/2AlyPO4。用XRD、SEM、HRTEM和恒流充放电等对样品进行表征。结果表明:适量Al3+掺... 采用共沉淀法制备掺Al3+前驱体FePO4·2H2O,并以乙二酸为还原剂,与Li2CO3反应在常温下球磨合成LiFePO4前驱混合物,后经热处理得到橄榄石型LiFe1-3y/2AlyPO4。用XRD、SEM、HRTEM和恒流充放电等对样品进行表征。结果表明:适量Al3+掺杂不会破坏LiFePO4的晶体结构,当掺杂量较低时(y=0.01),Al3+优先占据Fe位;当掺杂量较高时(y≥0.02),Al3+同时占据Li位和Fe位。电化学测试表明:LiFe0.985Al0.01PO4拥有最优的电化学性能,该样品在0.1C、1C和2C倍率下的首次放电比容量分别为162.4、152.2和142.0 mA·h/g,在1C倍率下循环100次后的放电比容量高达149.7 mA·h/g。 展开更多
关键词 正极材料 磷酸铁锂 al^3+掺杂 球磨 常温还原
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有或没有Alq_3参与情况下LiF和Al的化学反应
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作者 张寒洁 鲍世宁 +4 位作者 何丕模 王穗东 冯明凯 李振声 李述汤 《物理化学学报》 SCIE CAS CSCD 北大核心 2003年第8期770-773,共4页
利用X光电子能谱(XPS)和高分辨电子能量损失谱(HREELS)研究了几种条件下LiF和Al的化学反应.在有Alq3参与的情况下,LiF和Al在室温下发生反应.在Al/LiF/Alq3系统中,Li1s的峰发生了0.25eV的位移,同时F1s也发生了相应的位移.在没有Alq3参与... 利用X光电子能谱(XPS)和高分辨电子能量损失谱(HREELS)研究了几种条件下LiF和Al的化学反应.在有Alq3参与的情况下,LiF和Al在室温下发生反应.在Al/LiF/Alq3系统中,Li1s的峰发生了0.25eV的位移,同时F1s也发生了相应的位移.在没有Alq3参与的情况下,加热样品至350K后,在Li1s峰的低能端0.85eV处出现了一个伴峰.XPS研究表明,这个伴峰对应的是金属态的Li1s.HREELS的结果也验证了这一结论. 展开更多
关键词 alQ3 lif al 化学反应 氟化锂 X光电子能谱 高分辨电子能量损失谱 8-羟基喹啉铝络合物 有机发光器件
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Leaching kinetics of fluorine during the aluminum removal from spent Li-ion battery cathode materials 被引量:1
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作者 Shengjie Li Jianxin Zhu 《Journal of Environmental Sciences》 SCIE EI CAS CSCD 2024年第4期312-325,共14页
The high content of aluminum(Al)impurity in the recycled cathode powder seriously affects the extraction efficiency of Nickel,Cobalt,Manganese,and Lithium resources and the actual commercial value of recycled material... The high content of aluminum(Al)impurity in the recycled cathode powder seriously affects the extraction efficiency of Nickel,Cobalt,Manganese,and Lithium resources and the actual commercial value of recycled materials,so Al removal is crucially important to conform to the industrial standard of spent Li-ion battery cathode materials.In this work,we systematically investigated the leaching process and optimum conditions associated with Al removal from the cathode powder materials collected in a wet cathode-powder peeling and recycling production line of spent Li-ion batteries(LIBs).Moreover,we specifically studied the leaching of fluorine(F)synergistically happened along with the removal process of Al,which was not concerned about in other studies,but one of the key factors affecting pollution prevention in the recovery process.The mechanism of the whole process including the leaching of Al and F from the cathode powder was indicated by using NMR,FTIR,and XPS,and a defluoridation process was preliminarily investigated in this study.The leaching kinetics of Al could be successfully described by the shrinking core model,controlled by the diffusion process and the activation energy was 11.14 kJ/mol.While,the leaching of F was attributed to the dissolution of LiPF6and decomposition of PVDF,and the kinetics associated was described by Avrami model.The interaction of Al and F is advantageous to realize the defluoridation to some degree.It is expected that our investigation will provide theoretical support for the large-scale recycling of spent LIBs. 展开更多
关键词 al removal F leaching cathode powder Heating alkali leaching Leaching kinetics
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LiCl-KCl熔盐中Pu^(3+)在Al阴极上的电化学行为
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作者 孟照凯 林如山 +4 位作者 王有群 陈辉 宋鹏 何辉 叶国安 《核化学与放射化学》 CAS CSCD 北大核心 2023年第2期133-138,I0003,共7页
基于固体Al阴极分离锕系元素(An)与裂变产物(FP)的电解精炼技术是极具前景的干法后处理流程之一。本研究采用暂态电化学法系统研究了Pu^(3+)在固体Al阴极上的电化学行为。循环伏安法(CV)和方波伏安法(SWV)研究结果表明,Pu^(3+)在Al阴极... 基于固体Al阴极分离锕系元素(An)与裂变产物(FP)的电解精炼技术是极具前景的干法后处理流程之一。本研究采用暂态电化学法系统研究了Pu^(3+)在固体Al阴极上的电化学行为。循环伏安法(CV)和方波伏安法(SWV)研究结果表明,Pu^(3+)在Al阴极上可一步还原为合金,且该反应为不可逆,Pu^(3+)与Al形成合金的电位与温度的关系式为E^(θ,*)(Pu^(3+)/PuAl n)(vs.Cl-/Cl_(2))=-2.944+9.84×10^(-4)T。开路计时电位法(OCP)结合相图表明,Pu^(3+)在固体Al阴极上可生成Pu_(3)Al、PuAl、PuAl_(2)、PuAl_(3)和PuAl_(4)五种合金化合物,且计算得到了不同温度时PuAl_(4)的Gibbs生成自由能。 展开更多
关键词 LiCl-KCl熔盐 电化学行为 al阴极
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NaC l、LiF对K_3AlF_6-Na_3AlF_6-AlF_3体系初晶温度和Al_2O_3溶解度的影响 被引量:3
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作者 张亮 陈建设 +2 位作者 李斌川 韩庆 刘奎仁 《轻金属》 CSCD 北大核心 2018年第11期36-39,共4页
采用步冷微分曲线法测定了K_3AlF_6-Na_3AlF_6-AlF_3-NaCl-LiF体系的初晶温度,采用EDTA法测定该体系的Al_2O_3溶解度。结果表明:LiF和NaCl都可以降低电解质的初晶温度,当LiF和NaCl复合添加时,降温效果更加明显,当NaCl、LiF的添加量均为4... 采用步冷微分曲线法测定了K_3AlF_6-Na_3AlF_6-AlF_3-NaCl-LiF体系的初晶温度,采用EDTA法测定该体系的Al_2O_3溶解度。结果表明:LiF和NaCl都可以降低电解质的初晶温度,当LiF和NaCl复合添加时,降温效果更加明显,当NaCl、LiF的添加量均为4wt%时,初晶温度由841℃降至770℃。在K_3AlF_6-Na_3AlF_6-AlF_3体系中,随着NaCl和LiF的添加,Al_2O_3的溶解度降低,当NaCl、LiF的添加量均为4wt%时,氧化铝溶解度由5.85wt%降至4.04wt%。 展开更多
关键词 NACL lif K3alF6-Na3alF6-alF3 初晶温度 al2O3溶解度
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Al和Mg共掺杂LiFePO_4/C正极材料的电化学性能研究 被引量:5
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作者 肖资龙 张经济 +3 位作者 张志杰 王红强 李庆余 刘国壮 《矿冶工程》 CAS CSCD 北大核心 2018年第5期148-151,156,共5页
采用高温固相法合成了LiFePO_4/C和Al、Mg共掺杂的LiFe_(0.95)Al_(0.03)Mg_(0.02)PO_4/C复合材料。通过X射线衍射(XRD)、扫描电子显微镜(SEM)、能量仪(EDS)、恒流充放电测试、循环伏安法(CV)等手段对材料的结构、形貌及电化学性能进行... 采用高温固相法合成了LiFePO_4/C和Al、Mg共掺杂的LiFe_(0.95)Al_(0.03)Mg_(0.02)PO_4/C复合材料。通过X射线衍射(XRD)、扫描电子显微镜(SEM)、能量仪(EDS)、恒流充放电测试、循环伏安法(CV)等手段对材料的结构、形貌及电化学性能进行了表征。XRD结果表明,Al、Mg共掺杂后的样品并没有破坏LiFePO_4的橄榄石结构,同时还增强了LiFePO_4结构的稳定性、提高了电子导电性和Li+扩散速度;通过SEM和EDS观测到LiFePO_4呈球形颗粒,并在复合样品中检测到有Al和Mg元素存在。分别以0.5C、1C、3C和5C倍率充放电,LiFe_(0.95)Al_(0.03)Mg_(0.02)PO_4/C的放电比容量分别为145.1、142.6、133.2和124.9 m Ah/g; 1C倍率下循环30次后仍保持99.2%的初始容量,显示出良好的循环寿命。 展开更多
关键词 锂离子电池 正极材料 磷酸铁锂 lifEPO4/C 共掺杂 高温固相法 电化学性能
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