离子液体[BMIM]PF_6中铬的电沉积行为  被引量:2

Electrodeposition Behavior of Chromium in Ionic Liquid [BMIM]PF_6 

在线阅读下载全文

作  者:玉山江.哈斯木 刘瑞泉[1] 米红宇[1] 

机构地区:[1]新疆大学化学化工学院,乌鲁木齐830046

出  处:《高等学校化学学报》2014年第1期140-145,共6页Chemical Journal of Chinese Universities

基  金:新疆维吾尔自治区高校科研计划项目(批准号:XJEDU2012I05);国家自然科学基金(批准号:21063013)资助~~

摘  要:以一氯丁烷、N-甲基咪唑和KPF6为原料,合成了1-丁基-3-甲基咪唑六氟磷酸盐离子液体([BMIM]PF6),用红外光谱(IR)对产物进行了结构分析.用循环伏安法测试该离子液体在85℃下的电化学窗口为4.7 V.考察了[BMIM]PF6-Cr(Ⅲ)电解液的电化学行为,结果表明,在85℃下Cr(Ⅲ)的还原过程是受扩散控制的一步还原不可逆过程,Cr(Ⅲ)的传递系数α=0.023,阴极扩散系数D0=1.142×10-6cm2/s.在85℃和-1.5 V条件下,用恒电势法在铜片上电沉积Cr(Ⅲ),并通过扫描电子显微镜(SEM)观察了铜片上镀层的表面结构,发现该镀层呈颗粒状,且颗粒的体积随沉积时间的延长而增大.X射线能量色散谱(EDS)和X射线粉末衍射(XRD)测试结果表明,该镀层为无定形的金属铬.1-Butyl-3-methylimidazolium hexafluorophosphate ([ BMIM] PF6 ) ionic liquid was synthesized by 1-chlorobutane, N-methylimidazole and KPF6. The structure of ionic liquid was investigated by IR spectrum. The electrochemical window of [ BMIM ] PF6 was determined to be 4.7 V at 85 ℃ by cyclic vohammetry. The electrochemical behavior of the[ BMIM ] PF6-Cr( Ill ) electrolyte was studied. The reduction of chromium from Cr( HI ) to Cr(0) in the solution is a one-step irreversible growth process which is controlled by diffusion. The cathodal transfer coefficient (α) is 0. 023 and the cathode diffusion coefficient ( Do ) is 1. 142 x 10-6 cm2/s. The electrodeposition of chromium on copper substrate from [ BMIM ] PF6-Cr( m ) were experimented by potentio- static method at -1.5 V. The surface morphology of chromium coating was characterized by means of scanning electron microscopy (SEM) and its morphology was granular structure. The size of granulae increase with the increase of deposition time. The chemical composition and structure of chromium coating were tested by energy dispersive spectrometry(EDS) and X-ray diffraction (XRD). The results indicate that the coating consist of amorphous metallic chromium.

关 键 词: 离子液体 循环伏安 电化学窗口 电沉积 

分 类 号:O646[理学—物理化学]

 

参考文献:

正在载入数据...

 

二级参考文献:

正在载入数据...

 

耦合文献:

正在载入数据...

 

引证文献:

正在载入数据...

 

二级引证文献:

正在载入数据...

 

同被引文献:

正在载入数据...

 

相关期刊文献:

正在载入数据...

相关的主题
相关的作者对象
相关的机构对象