本文研究了草酸铁(Ⅲ)负载在 HZSM-5和 HY 沸石上的性质和热分解.草酸铁(Ⅲ)在沸石表面发生离解吸附,CO与表面的 Al 配位,热分解时产生β峰.草酸铁(Ⅲ)与 HZSM-5沸石作用较弱,在氢气中500℃时的还原产物为α-Fe,而Fe(CO)—HY 体系在氢气...本文研究了草酸铁(Ⅲ)负载在 HZSM-5和 HY 沸石上的性质和热分解.草酸铁(Ⅲ)在沸石表面发生离解吸附,CO与表面的 Al 配位,热分解时产生β峰.草酸铁(Ⅲ)与 HZSM-5沸石作用较弱,在氢气中500℃时的还原产物为α-Fe,而Fe(CO)—HY 体系在氢气中500℃时除得到α-Fe 外,还有少量高分散的零价铁和部分难以还原的铁离子.展开更多
The development of high-energy-density Li-ion batteries is hindered by the irreversible capacity loss during the initial charge-discharge process.Therefore,pre-lithiation technology has emerged in the past few decades...The development of high-energy-density Li-ion batteries is hindered by the irreversible capacity loss during the initial charge-discharge process.Therefore,pre-lithiation technology has emerged in the past few decades as a powerful method to supplement the undesired lithium loss,thereby maximizing the energy utilization of LIBs and extending their cycle life.Lithium oxalate(Li_(2)C_(2)O_(4)),with a high lithium content and excellent air stability,has been considered one of the most promising materials for lithium compensation.However,the sluggish electrochemical decomposition kinetics of the material severely hinders its further commercial application.Here,we introduce a recrystallization strategy combined with atomic Ni catalysts to modulate the mass transport and decomposition reaction kinetics.The decomposition potential of Li_(2)C_(2)O_(4)is significantly decreased from~4.90V to~4.30V with a high compatibility with the current battery systems.In compared to the bare NCM//Li cell,the Ni/N-rGO and Li_(2)C_(2)O_(4)composite(Ni-LCO)modified cell releases an extra capacity of~11.7%.Moreover,this ratio can be magnified in the NCM//SiOx full cell,resulting in a 30.4%higher reversible capacity.Overall,this work brings the catalytic paradigm into the pre-lithiation technology,which opens another window for the development of high-energy-density battery systems.展开更多
Micro-arc oxidation （MAO） coatings with different concentrations of K2TiO（C2O4）2 in the sodium silicate base electrolyte were prepared on 6061 aluminum alloy with the aim of promoting a better understanding of the...Micro-arc oxidation （MAO） coatings with different concentrations of K2TiO（C2O4）2 in the sodium silicate base electrolyte were prepared on 6061 aluminum alloy with the aim of promoting a better understanding of the formation mechanisms and tribological behaviors of the coatings. Scanning electron microscopy （SEM） assisted with energy-dis- persive X-ray spectroscopy （EDS）, X-ray photoelectron spectroscopy （XPS） and friction test were employed to charac- terize the MAO processes and microstructure of the resultant coatings. Results showed that the composition and microstructure of the coatings were significantly affected by the addition of KETiO（CaO4）2. A sealing microstructure of MAO coating was obtained with the addition of K2TiO（C2O4）2. Ti element from K2TiO（C2O4）2 was only absorbed into the defects of micropores under surface energy in the early stage, while in the later stage, Ti element was predominant in the micropores and distributed on the coatings under plasma discharge to form TiO2. It was demonstrated that Ti and Si elements from the electrolyte could interact with each other during the MAO process and the interaction mechanism was systematically analyzed. Wear resistance of the MAO coatings with K2TiO（C2O4）2 addition was significantly improved compared with that of the MAO coatings without K2TiO（C2O4）2 addition.展开更多
用热重-差热(TG-DTA)技术,在不同升温速率条件下,研究了十水草酸镧在空气气氛下的热分解过程.分别采用Ozawa-Flynm-Wall法、Kissinger法、Crane法和同步热分析法确定其热分解动力学参数.TG-DTA曲线表明:十水草酸镧分解为四个阶段,前两...用热重-差热(TG-DTA)技术,在不同升温速率条件下,研究了十水草酸镧在空气气氛下的热分解过程.分别采用Ozawa-Flynm-Wall法、Kissinger法、Crane法和同步热分析法确定其热分解动力学参数.TG-DTA曲线表明:十水草酸镧分解为四个阶段,前两个阶段为脱水过程,后两个阶段为La_2(C_2O_4)_3的分解过程.实验计算得出四步反应表观活化能E分别为83.92、76.04、136.26、162.61 k J·mol-1左右;指前因子A分别为4.92×10^(10)、6.1×10~7、2.1×10~9、8.46×10~6s-1左右;反应级数n均为1左右,并用Coats-Redfem积分法得出第三步分解机理受F1控制.展开更多
文摘本文研究了草酸铁(Ⅲ)负载在 HZSM-5和 HY 沸石上的性质和热分解.草酸铁(Ⅲ)在沸石表面发生离解吸附,CO与表面的 Al 配位,热分解时产生β峰.草酸铁(Ⅲ)与 HZSM-5沸石作用较弱,在氢气中500℃时的还原产物为α-Fe,而Fe(CO)—HY 体系在氢气中500℃时除得到α-Fe 外,还有少量高分散的零价铁和部分难以还原的铁离子.
基金supported by National Natural Science Foundation of China(Grant No.52002094)Guangdong Basic and Applied Basic Research Foundation(Grant No.2019A1515110756)+2 种基金Shenzhen Science and Technology Program(Grant No.JCYJ20210324121411031,JSGG202108021253804014,RCBS20210706092218040)the Shenzhen Steady Support Plan(GXWD20221030205923001,GXWD20201230155427003-20200824103000001)School Research Startup Expenses of Harbin Institute of Technology(Shenzhen)(Grant No.DD29100027,DD45001022).
文摘The development of high-energy-density Li-ion batteries is hindered by the irreversible capacity loss during the initial charge-discharge process.Therefore,pre-lithiation technology has emerged in the past few decades as a powerful method to supplement the undesired lithium loss,thereby maximizing the energy utilization of LIBs and extending their cycle life.Lithium oxalate(Li_(2)C_(2)O_(4)),with a high lithium content and excellent air stability,has been considered one of the most promising materials for lithium compensation.However,the sluggish electrochemical decomposition kinetics of the material severely hinders its further commercial application.Here,we introduce a recrystallization strategy combined with atomic Ni catalysts to modulate the mass transport and decomposition reaction kinetics.The decomposition potential of Li_(2)C_(2)O_(4)is significantly decreased from~4.90V to~4.30V with a high compatibility with the current battery systems.In compared to the bare NCM//Li cell,the Ni/N-rGO and Li_(2)C_(2)O_(4)composite(Ni-LCO)modified cell releases an extra capacity of~11.7%.Moreover,this ratio can be magnified in the NCM//SiOx full cell,resulting in a 30.4%higher reversible capacity.Overall,this work brings the catalytic paradigm into the pre-lithiation technology,which opens another window for the development of high-energy-density battery systems.
基金supported by the National Science Foundation of China(Grant Nos.51571114 and 51201120)the Science and Technology Coordination and Innovation Project of Shaanxi Province(No.2016KTZDGY-04-01)the Shaanxi Provincial Education Department(Grant No.16JK1377)
文摘Micro-arc oxidation （MAO） coatings with different concentrations of K2TiO（C2O4）2 in the sodium silicate base electrolyte were prepared on 6061 aluminum alloy with the aim of promoting a better understanding of the formation mechanisms and tribological behaviors of the coatings. Scanning electron microscopy （SEM） assisted with energy-dis- persive X-ray spectroscopy （EDS）, X-ray photoelectron spectroscopy （XPS） and friction test were employed to charac- terize the MAO processes and microstructure of the resultant coatings. Results showed that the composition and microstructure of the coatings were significantly affected by the addition of KETiO（CaO4）2. A sealing microstructure of MAO coating was obtained with the addition of K2TiO（C2O4）2. Ti element from K2TiO（C2O4）2 was only absorbed into the defects of micropores under surface energy in the early stage, while in the later stage, Ti element was predominant in the micropores and distributed on the coatings under plasma discharge to form TiO2. It was demonstrated that Ti and Si elements from the electrolyte could interact with each other during the MAO process and the interaction mechanism was systematically analyzed. Wear resistance of the MAO coatings with K2TiO（C2O4）2 addition was significantly improved compared with that of the MAO coatings without K2TiO（C2O4）2 addition.
文摘用热重-差热(TG-DTA)技术,在不同升温速率条件下,研究了十水草酸镧在空气气氛下的热分解过程.分别采用Ozawa-Flynm-Wall法、Kissinger法、Crane法和同步热分析法确定其热分解动力学参数.TG-DTA曲线表明:十水草酸镧分解为四个阶段,前两个阶段为脱水过程,后两个阶段为La_2(C_2O_4)_3的分解过程.实验计算得出四步反应表观活化能E分别为83.92、76.04、136.26、162.61 k J·mol-1左右;指前因子A分别为4.92×10^(10)、6.1×10~7、2.1×10~9、8.46×10~6s-1左右;反应级数n均为1左右,并用Coats-Redfem积分法得出第三步分解机理受F1控制.
