Electrodeposition of Zn, Cu, and Zn-Cu Alloys from Deep Eutectic Solvents

Deep eutectic solvents (DESs) comprising choline chloride (ChCl) with either urea or ethylene glycol (EG) have been successfully used as powerful and potential electrolytes for extracting metals from their corresponding metal oxide precursors. In this work, for electrodeposition of Zn and Zn-Cu alloys, ChCl/urea-based DES was employed. Cyclic voltammetry study demonstrates that the reduction of Zn(II) to Zn is a diffusion-controlled quasi-reversible, one-step, two electrons transfer process. Micro-/nanostructured Zn and Zn-Cu alloys films have been electrodeposited directly from their metal oxide precursors in DES, and the Zn and Zn-Cu alloy films exhibit homogeneous morphologies with controlled particle sizes. Besides, the electrodeposition of Cu from CuO in the eutectics based on ChCl with urea and EG has been investigated, respectively. The higher coordinated Cu species in the ChCl/urea-based DES are obviously more difficult to reduce, and higher overpotential is needed to drive the nucleation process compared with the lower coordinated Cu species in the ChCl/EG-based DES. The surface morphology of the Cu electrodeposits is significantly affected by the type of DES and the electrodeposition potentials. Furthermore, the Cu electrodeposits obtained in the ChCl/urea-based DES possess more dense microstructures than those produced in the ChCl/EG-based DES

Electrolysis of Converter Matte in Molten CaCl2-NaCl

The electrolytic production of nickel-copper alloy by electrochemical reduction of converter matte in molten salt has been investigated. The sintered solid porous pellets of Ni3S2, Cu2S and converter matte were electrolyzed at a voltage of 3.0 V in molten CaCl2-NaCl under the protection of argon gas at 700?, respectively. The electro-reduction processes were investigated and the products were characterized. The results show that the molten salt electro-reduction process can be used to produce nickel, copper and nickel-copper alloy directly from Ni3S2, Cu2S and converter matte precursors in molten CaCl2-NaCl, respectively. CaS would be formed as the intermediate compound during the electro-reduction process, and then the formed CaS can be gradually decomposed and removed with the increase of the electrolysis time. The experimental results show that the molten salt electro-reduction process has the potential to be used for the reduction of sulfide minerals in molten CaCl2-NaClpublishersversionPeer reviewe

3D dendritic-Fe2O3@C nanoparticles as an anode material for lithium ion batteries

3D dendritic Fe2O3 nanoparticles wrapped with carbon (denoted as 3DD-Fe2O3@C hereafter) were synthesized.</p

Pt nanoparticles decorated rose-like Bi2O2CO3 configurations for efficient photocatalytic removal of water organic pollutants

Pt nanoparticles decorated with rose-like Bi2O2CO3 configurations were synthesized via a simple photoreduction method at room temperature. The structure, morphology, optical and electronic properties, and photocatalytic performance of the as-prepared materials were characterized. Compared to pure Bi2O2CO3, the Pt/Bi2O2CO3 photocatalysts show better performance in decomposing RhB, BPA and OTC under visible light (? > 420 nm). The enhanced photocatalytic activity of Pt/Bi2O2CO3 could be attributed to the modification in light absorption (? > 420 nm) charge migration and the separation of photo-generated electrons (e?) and holes (h+). Free radical trapping experiments demonstrated that the main active species of the catalytic reaction are different in decomposing RhB and BPA.publishersversionPeer reviewe

Electrochemical Reducation of TiO2/Al2O3/C to Ti3AlC2 and Its Derived Two-Dimensional (2D) Carbides

Ti3AlC2 has been directly synthesized from TiO2/Al2O3/C mixture precursors (3TiO2/0.5Al2O3/1.5C and 2TiO2/0.5Al2O3/C) by a molten salt electrolysis process at 900?C and 3.2 V in molten CaCl2. The influence of initial carbon content on the electrosynthesized products has been investigated. The result shows that the main phase of the electrosynthesized products changes from Ti3AlC to Ti2AlC and then to Ti3AlC2 with the increasing carbon content, and the electrosynthesized Ti3AlC2 is carbon deficient. The morphology observation shows that the electrosynthesized Ti3AlC2 particles possess smooth surfaces and dense flake-like microstructure. The reaction mechanism of the electroreduction of TiO2/Al2O3/C mixture precursor has been discussed based on the time- and position-dependent phase constitution analysis. In addition, two-dimensional (2D) Ti3AlC2-derived carbides, i.e., Ti3C2Tx and TiCx have been successfully prepared from the electrosynthesized Ti3AlC2 by a chemical etching process and an electrochemical etching process, respectively. Both derived carbides exhibit the similar layered structure, in which single layer carbides are composed of plentiful nanometer carbides. It is suggested that the molten salt electrolysis process has a great potential to be used for the facile synthesis of Mn+1AXn phases (such as Ti3AlC2) from their oxides precursors, and the synthesized Mn+1AXn phases can be further converted into 2D carbidesauthorsversionPeer reviewe

Wafer-Scale Synthesis of WS2 Films with In Situ Controllable p-Type Doping by Atomic Layer Deposition

Wafer-scale synthesis of p-type TMD films is critical for its commercialization in next-generation electro/optoelectronics. In this work, wafer-scale intrinsic n-type WS2 films and in situ Nb-doped p-type WS2 films were synthesized through atomic layer deposition (ALD) on 8-inch α-Al2O3/Si wafers, 2-inch sapphire, and 1 cm2 GaN substrate pieces. The Nb doping concentration was precisely controlled by altering cycle number of Nb precursor and activated by postannealing. WS2 n-FETs and Nb-doped p-FETs with different Nb concentrations have been fabricated using CMOS-compatible processes. X-ray photoelectron spectroscopy, Raman spectroscopy, and Hall measurements confirmed the effective substitutional doping with Nb. The on/off ratio and electron mobility of WS2 n-FET are as high as 105 and 6.85 cm2 V-1 s-1, respectively. In WS2 p-FET with 15-cycle Nb doping, the on/off ratio and hole mobility are 10 and 0.016 cm2 V-1 s-1, respectively. The p-n structure based on n- and p- type WS2 films was proved with a 104 rectifying ratio. The realization of controllable in situ Nb-doped WS2 films paved a way for fabricating wafer-scale complementary WS2 FETs.This work is partially supported by the NSFC (62004044 and 61904033) and by State Key Laboratory of ASIC & System (2021MS004). This research was partially supported by the National Science Foundation through the Center for Dynamics and Control of Materials: an NSF MRSEC under Cooperative Agreement No. DMR-1720595. Li Ji acknowl- edges the support of starting research fund from Fudan Uni- versity and the Young Scientist Project of MOE Innovation platform. Deji Akinwande acknowledges the support of ARO via a PECASE award.Center for Dynamics and Control of Material