Minxian Wu

Electrodeposition of germanium from the ionic liquid 1-butyl-1-methylpyrrolidinium dicyanamide

The electrodeposition of germanium from the ionic liquid 1-butyl-1-methylpyrrolidinium dicyanamide ([BMP][DCA]) and a mixture of [BMP][DCA] and 1-butyl-1-methylpyrrolidinium chloride ([BMP]Cl) was studied using cyclic voltammetry and using an electrochemical quartz crystal microbalance (EQCM). [GeCl4(BuIm)2] (BuIm = N-butylimidazole) was used as germanium source as it has a solubility of 0.47 M, up to 13 times the solubility of GeCl4 in [BMP][DCA]. Cyclic voltammograms show an irreversible electrochemical behavior and two reduction waves were observed. The wave at the more positive potential was assigned to the reduction of Ge(4+) to Ge(2+). The wave at the more negative potential was attributed to the formation of Ge(0). The diffusion coefficient of Ge(4+) in [BMP][DCA] containing 0.1 M [GeCl4(BuIm)2] is 1.1 × 10(-12) m(2) s(-1), and the exchange current density is 2 × 10(-4) A m(-2) at 50 °C. Polymerization of dicyanamide anions took place at the anode in the solution of [BMP][DCA]. The polymerization reaction could be avoided by using an equimolar [BMP]Cl-[BMP][DCA] mixture as electrolyte. Smooth, porous germanium films were electrodeposited on both copper and silicon substrates.

Electro-precipitation via oxygen reduction: a new technique for thin film manganese oxide deposition

Manganese oxide was deposited from a non-aqueous solution, dimethyl sulfoxide (DMSO), via the reduction of dissolved oxygen. The formed superoxide radical ion (O2−˙) reacts rapidly with the manganese ions forming a smooth and thin film (80 nm) of manganese oxide. From an in situ EQCM study, it could be concluded that MnO2 was the most probable oxide which was deposited at an average growth rate of 0.049 μg s−1 or 0.077 nm s−1. Since the direct deposition of a phase pure MnO2 layer was not confirmed by XRD, it is more likely that a variety of manganese oxides has been deposited during the electro-precipitation reaction and thus further optimization or post-treatments are required to obtain an active manganese oxide layer for thin film deposits. The key property of this new deposition technique is the self-limiting behavior, proven by rotating ring-disk electrode experiments. This is crucial to electrodeposit thin films conformally on high aspect ratio structures for 3D all-solid-state lithium-ion batteries or supercapacitors.

Bis(ethyl­eneglycolato-κ2O,O′)tellurium(IV)

The title compound, C4H8O4Te, crystallized from a solution of Te4+ in ethylene glycol. The TeIV atom is in a distorted seesaw coordination defined by four O atoms from two different ethyleneglycate ligands. The C atoms of the ethyleneglycate ligands are disorderd over two positions, with population parameters of 50.3 (6) and 49.7 (6)% indicating a statistical distribution. Due to the possibility to transform the primitive monoclinic unit cell into a metrically orthorhombic C unit cell, the data are twinned and were refined with the twin law -100/0-10/101 with the relative scale factor refining to 1.82 (4)% for the minor component.