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1.
冷却速度对Ml(NiCoMnTi)_5贮氢合金电化学性能的影响   总被引:6,自引:0,他引:6  
对不同冷却速度下制成的具有同一成分的贮氢合金做了电化学充放电循环实验,比较了它们的容量、电化学循环稳定性及放电电压性能高的冷却速度导致放电容量特别是大电流放电容量较大幅度下降,活化困难,放电电压也有所降低,但改善了合金的循环稳定性及放电电压平台特性.  相似文献   

2.
冷却速度时Ml(NiCoMoTi)5贮氢合金电化学性能的影响   总被引:3,自引:0,他引:3  
对不同冷却速度下制成的具有同一成分的贮氢合金做了电化学充放电循环实验,比较了它们的容量、电化学循环稳定性及放电电压性能。高的冷却速度导致放电容量的特别是大电流放电容量较大幅度下降,活化困难,放电电压也有所降低,但改善了合金的循环稳定性及放电电压平台特性。  相似文献   

3.
为改善低钴贮氢合金的综合电化学性能,对其进行不同速度的快淬处理。结果表明,合适的快淬速度不仅可以大幅度的提高放电容量,而且明显的改善合金的循环稳定性和放电电压特性。18 m/s快淬低钴合金具有较好的综合电化学性能,但快淬使合金的活化性能有所降低。利用X射线、扫描电镜对铸态及快淬合金进行微观分析。分析了快淬对低钴贮氢合金电化学性能的影响机理。  相似文献   

4.
为改善低钴贮氢合金的综合电化学性能,对其进行不同速度的快淬处理.结果表明:合适的快淬速度不仅可以大幅度的提高放电容量,而且明显的改善合金的循环稳定性和放电电压特性.18 m/s快淬低钴合金具有较好的综合电化学性能.但快淬使得合金的活化性能有所降低.利用X射线衍射、扫描电镜对铸态及快淬合金进行微观分析,讨论了快淬对低钴贮氢合金电化学性能的影响机理.  相似文献   

5.
应用铸造及快淬工艺制备了La0 7Mg0.3Co0.45Ni2.55-xCux (x=0, 0.1, 0.2, 0.3, 0.4)贮氢电极合金,研究了快淬工艺对合金微观结构及电化学性能的影响.XRD,SEM及TEM的分析结果表明,铸态及快淬态合金具有多相结构,包括(La,Mg)Ni3相,LaNi5相以及LaNi2相.快淬对合金的相组成没有明显影响,但显著地改变了合金的相丰度.快淬还显著地改善合金的成分均匀性,并使合金的晶粒明显细化.电化学测试的结果表明,快淬大幅度提高合金的电化学循环稳定性,但使合金的放电容量和活化性能下降.快淬对合金的放电电压特性具有明显的影响,当淬速大于15m/s时,快淬降低合金的放电电压,并使放电平台的斜率明显增大.  相似文献   

6.
为改善低钴贮氢合金的综合电化学性能,对其进行不同速度的快淬处理。结果表明:合适的快淬速度不仅可以大幅度的提高放电容量,而且明显的改善合金的循环稳定性和放电电压特性。18m/s快淬低钴合金具有较好的综合电化学性能。但快淬使得合金的活化性能有所降低。利用X射线衍射、扫描电镜对铸态及快淬合金进行微观分析,讨论了快淬对低钴贮氢合金电化学性能的影响机理。  相似文献   

7.
铸态和快淬态Mm(NiCoMnAl)5合金的电化学性能及相结构   总被引:3,自引:0,他引:3  
本文研究了铸态和快淬态MmNi3.7Co0.6Mn0.4Al0.3贮氢合金的电化学性能和相结构。电化学测试结果表明:快淬态合金的活化性能比铸态合金差,淬速为10m/s和16m/s的快淬态合金的最大放电容量高于铸态合金,放电电压平台更为平坦。淬速为22m/s和28m/s的快淬态合金的最大放电容量低于铸态合金。随着淬速的增加,合金电极的循环稳定性提高。X射线衍射结果表明:铸态和快淬态合金均由CaCu5型主相和一个第二相组成,快淬使得第二相衍射峰减弱。合金成分更为均匀。快淬态合金的晶格参数大于铸态合金。晶格参数的增加是快淬合金具有良好循环稳定性的一个重要原因。  相似文献   

8.
研究了快淬、热处理、快淬+热处理制备工艺对铸态(LaCe)1.0(NiCoMnAl)5.0高容量贮氢合金电化学性能的影响。XRD分析表明所有合金均为单相CaCu5型结构,快淬+热处理合金相的成分和结构的均匀性最好。电化学测试结果表明,与铸态合金相比,热处理合金的放电容量和循环性能有所提高,但其倍率性能明显降低;快淬合金的活化性能、放电容量、倍率性能以及循环性能均降低;快淬+热处理合金综合电化学性能最好,具有较好的活化性能、最大的放电容量(344.7mA/g)、最大容量保持率(S100,85.67%)以及较好的倍率性能。  相似文献   

9.
为了改善A2B7型La0.8Mg0.2Ni3.5Co0.2合金的电化学性能,采用熔体快淬技术制备了合金。用XRD、SEM分析了合金的微观结构,用电化学方法测试了合金的电化学性能。结果表明,快淬后,合金具有多相结构,包括两个主相(La,Mg)Ni5及(La,Mg)2(Ni,Co)7和残留相LaNi2.28相,快淬使合金的微观应变增加,柱状晶区域面积较大,合金的晶粒明显细化。快淬使合金的放电容量、平台中值电压降低,电化学循环稳定性提高。  相似文献   

10.
为了提高合金的电化学性能,采用Ce部分替代La,并结合快淬方法制备了La_(1–x)CexMgNi_(3.5)Mn_(0.5)(x=0,0.1,0.2,0.3,0.4)贮氢合金。XRD和SEM测试结果表明,合金由LaMgNi_4主相以及LaNi_5第二相组成。随着快淬速度的增加,合金的晶格参数及晶胞体积逐渐增大,晶粒明显得到细化。电化学测试结果表明,铸态及快淬态合金具有优异的活化性能,其放电容量均在第一次循环时即可达到最大值。随着快淬速度的增加,合金的放电容量先增大后减小,但其循环稳定性逐渐提高。此外,合金电极的电化学动力学性能均随快淬速度的增加先提高后降低。  相似文献   

11.
1 Introduction Ni-MH batteries have been used widely by virtue of several of their advantages, such as high capacity, capable of performing a high rate charge/discharge, high resistance to overcharging and over-discharging, a long cycle life, environment…  相似文献   

12.
In order to improve the electrochemical performances of La-Mg-Ni based electrode alloys with PuNi3-type structure, a trace of boron was added in La0.7Mg0.3Ni2.55Co0.45 alloy. The La0.7Mg0.3Ni2.55Co0.45Bx(a=0, 0.05, 0.1, 0.15 and 0.2) alloys were prepared by casting and rapid quenching. The electrochemical performances and microstructures of the as-cast and quenched alloys were investigated. The effects of rapid quenching on the microstructures and electrochemical performances of the above alloys were investigated. The results show that the as-cast and quenched alloys are composed of (La, Mg)Ni3 phase, LaNi5 phase and LaNi2 phase. A trace of the Ni2B phase exists in the as-cast alloys containing boron, and the Ni2B phase in the B-contained alloys nearly disappears after rapid quenching. Rapid quenching increases the amount of the LaNi2 phase in the B-free alloy, but it decreases the amount of the LaNi2 phase in the boron-containing alloys. The effects of rapid quenching on the capacities of the boron-containing and boron-free alloys are different. The capacity of the B-free alloy monotonously decreases with increasing quenching rate, whereas the capacities of the B-contained alloys have a maximum value with the change of the quenching rate. The rapid quenching can improve the stability of La-Mg-Ni based electrode alloy but lowers the discharge plateau voltage and decreases the plateau length. The effect of rapid quenching on the activation capabilities of the alloys was complicated.  相似文献   

13.
用铸造及快淬工艺制备了低钴AB5型Mm(NiCoMnAl)5Bx(x=0~0.2)贮氢合金,测试了合金的微观结构及电化学性能,研究了B含量及快淬工艺的变化对合金晶格常数、热力学参数、微观结构及电化学性能的影响。结果表明:合金的晶格常数、晶胞体积及标准生成焓均随B含量的增加而增大;在一定的淬速范围内,快淬处理可以提高合金的放电容量,但淬速超过某一临界淬速时,快淬合金的容量低于铸态合金;合金的循环寿命随淬速的增加而单调增加。  相似文献   

14.
The La-Mg-Ni system PuNi3-type La0.5Ce0.2Mg0.3Co0.4Ni2.6-xMnx (x=0, 0.1, 0.2, 0.3, 0.4) hydrogen storage alloys were prepared by casting and rapid quenching. The effects of the rapid quenching on the structure and electrochemical characteristics of the alloys were studied. The results obtained by XRD, SEM and TEM indicate that the as-cast and quenched alloys mainly consist of two major phases, (La,Mg)Ni3 and LaNi5, as well as a residual phase LaNi. The rapid quenching does not exert an obvious influence on the phase composition of the alloys, but it leads to an increase of the LaNi5 phase and a decrease of the (La, Mg)Ni3 phase. The as-quenched alloys have a nano-crystalline structure, and the grain sizes of the alloys are in the range of 20-30 nm. The results by the electrochemical measurements indicate that both the discharge capacity and the high rate discharge(HRD) ability of the alloy first increase and then decrease with the variety of quenching rate and obtain the maximum values at the special quenching rate which is changeable with the variety of Mn content. The rapid quenching significantly improves the cycle stabilities of the alloys, but it slightly impairs the activation capabilities of the alloys.  相似文献   

15.
为了提高La-Mg-Ni系(PuNi3)型贮氢合金的电化学循环稳定性,在La2Mg(Ni0.85Co0.15)9合金中加入微量Cr,用铸造及快淬工艺制备了La2Mg(Ni0.85Co0.15)9Crx(x=0,0.1,0.2)贮氢合金.分析测试了铸态及快淬态合金的电化学性能及微观结构,研究了Cr对铸态及快淬态合金微观结构及电化学性能的影响.结果表明,铸态及快淬态合金具有多相结构,包括(La,Mg)Ni3相(PuNi3结构)),LaNi5相和一定量的LaNi2相.快淬对合金的相组成没有影响,但使合金的相丰度产生变化.Cr的加入提高了铸态及快淬态合金的循环稳定性,但使合金的容量下降.合金的循环寿命随淬速的增加而增加,铸态及快淬态合金均有优良的活化性能.  相似文献   

16.
In order to improve the electrochemical cycle stability of La-Mg-Ni system (PuNi3-type) hydrogen storage alloy, Ni in the alloys was partially substituted by M (M=Cu, Al, Mn). A new La-Mg-Ni system electrode alloys La0.7Mg0.3Ni2.55-xCo0.45Mx (M=Cu, Al, Mn;x =0,0.1) were prepared by casting and rapid quenching. The effects of element substitution and rapid quenching on the microstructures and electrochemical performances of the alloys were investigated. The results by XRD, SEM and TEM show that the alloys havea multiphase structure, including the (La, Mg)Ni3 phase, the LaNi5 phase and the LaNi2 phase. The rapid quenching and element substitution have an imperceptible influence on the phase compositions of the alloys, but both change the phase abundance of the alloys. The rapid quenching significantly improves the composition homogeneity of the alloys and markedly decreases the grain size of the alloys. The Cu substitution promotes the formation of an amorphous phase in the as-quenched alloy, and a reversal result by the Al substitution. The electrochemical measurement indicates that the element substitution decreases the discharge capacity of the alloys, whereas it obviously improves the cycle stability of the alloys. The positive influence of element substitution on the cycle life of the alloys is in sequence Al>Cu>Mn, and negative influence on the discharge capacity is in sequence Al>Mn>Cu. The rapid quenching significantly enhances the cycle stability of the alloys, but it leads to a different extent decrease of thedischarge capacity of the alloys.  相似文献   

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