离子液体
电化学
循环伏安法
基质(水族馆)
扩散
X射线光电子能谱
材料科学
阴极
离子键合
分析化学(期刊)
化学
核化学
离子
电极
化学工程
物理化学
色谱法
有机化学
催化作用
工程类
海洋学
物理
热力学
地质学
作者
Xiao-qing LU,Aimin Liu,Fengguo Liu,Xianwei Hu,Zhongning Shi
标识
DOI:10.1016/s1003-6326(24)66524-6
摘要
The feasibility and reaction mechanism of NdFeB film electrodeposition in 1,3-dimethyl-2-imidazolidinone (DMI)−LiNO3 ionic liquid analogs at room temperature were investigated. Cyclic voltammetry indicated that the reduction peak at −1.83 V (vs Ag) was related to the reduction of Fe(II) to Fe, while the reduction peak at −2.01 V (vs Ag) was related to the reduction of B(III) to B. The electrochemical reduction reaction of Fe(II) and B(III) were irreversible processes controlled by diffusion, and the diffusion coefficients of Fe(II) and B(III) at 313 K were 3.03×10−6 and 6.74×10−7 cm2/s, respectively. In addition, XRD analysis suggested that the product obtained by the electrodeposition in DMI−LiNO3−Nd(CF3SO3)3−FeCl2−H3BO3 ionic liquid analogs for 2 h on the Al substrate contained NdFe3B3. SEM and EDS analysis showed that Nd, Fe, and B in the cathode product were uniformly distributed. XPS analysis revealed that the mass fractions of Nd, Fe, and B on the W substrate were 27.44%, 27.90%, and 7.51%, respectively.
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