The Comparison of Characteristics in Tin Doped Indium Oxide (ITO) Synthesized via Nonaqueous Sol-Gel and Solvothermal Process

Tin doped indium oxide nanoparticles were synthesized by nonaqueous sol-gel method and solvothermal process from indium acetylacetonate (In(acac)3) and tin bis(acetylacetonate)dichloride (Sn(acac)2Cl2) in oleyamine as the starting materials. The structure and morphology of ITO samples were analyzed by XRD and TEM. The electrical conductivy and specific surface area of both ITO samples were also determined and compared to each other. The ITO prepared via solvothermal method showed better results that prepared by nonaqueous sol-gel method

High-Throughput Synthesis, Screening, and Scale-Up of Optimized Conducting Indium Tin Oxides

A high-throughput optimization and subsequent scale-up methodology has been used for the synthesis of conductive tin-doped indium oxide (known as ITO) nanoparticles. ITO nanoparticles with up to 12 at % Sn were synthesized using a laboratory scale (15 g/hour by dry mass) continuous hydrothermal synthesis process, and the as-synthesized powders were characterized by powder X-ray diffraction, transmission electron microscopy, energy-dispersive X-ray analysis, and X-ray photoelectron spectroscopy. Under standard synthetic conditions, either the cubic In2O3 phase, or a mixture of InO(OH) and In2O3 phases were observed in the as-synthesized materials. These materials were pressed into compacts and heat-treated in an inert atmosphere, and their electrical resistivities were then measured using the Van der Pauw method. Sn doping yielded resistivities of ∼10(-2) Ω cm for most samples with the lowest resistivity of 6.0 × 10(-3) Ω cm (exceptionally conductive for such pressed nanopowders) at a Sn concentration of 10 at %. Thereafter, the optimized lab-scale composition was scaled-up using a pilot-scale continuous hydrothermal synthesis process (at a rate of 100 g/hour by dry mass), and a comparable resistivity of 9.4 × 10(-3) Ω cm was obtained. The use of the synthesized TCO nanomaterials for thin film fabrication was finally demonstrated by deposition of a transparent, conductive film using a simple spin-coating process

Ge Nanowires Anode sheathed with Amorphous Carbon for Rechargeable Lithium batteries

Interdisciplinary School of Green EnergyThe composite electrode composed of single crystalline Ge NWs sheathed with amorphous carbon showed excellent electrochemical properties of large reversible capacity, high coulombic efficiency, excellent rate capability and stable cycle performance. c-Ge NWs synthesized by using thermal decomposition of C2H2 gas at 700 °C under Ar atmosphere after SLS (solution-liquid-solid) growth were found to have good performance during cycling with Li. The rate capability for charging was shown reversible capacity of 963 mAh/g with a coulombic efficiency of 90% and 700 mAh/g at the rate of 6C (= 4800mA/g). Capacity retention after 100 cycles was 72% at the rate of 0.5C. The improved electrochemical performance of c-Ge-NWs fabricated in our experiment was attributed to the formation of amorphous Ge NWs during cycling and a homogenous carbon coating on Ge NWs. Thus, these results suggest that the use of nanowires structure can be promising for alloy anode materials in lithium ion batteries

Microwave-Assisted Synthesis and Processing of Al-Doped, Ga-Doped, and Al, Ga Codoped ZnO for the Pursuit of Optimal Conductivity for Transparent Conducting Film Fabrication

This work reports the microwave-assisted fabrication of highly conducting Al-doped ZnO (AZO), Ga-doped ZnO (GZO), and Al, Ga codoped ZnO (AGZO) materials as cheaper earth abundant alternatives to indium tin oxide (ITO) for transparent conducting applications. All three doped ZnO powder samples were compressed into pellets, and their electrical properties were evaluated after the postsynthesis heat treatment. The heat treatment was performed by sintering the pellets at 600 °C in a reducing atmosphere using either conventional radiant annealing for 3 h or microwave annealing for 90 s. The Al and Ga dopant levels were systematically varied from 0.5 to 2.5 at. %, and it was found that the lowest resistivity values for the pelleted singly doped ZnO powders exist when the doping level is adjusted to 1.5 at. % for both AZO and GZO, giving resistivity values of 4.4 × 10–3 and 4.3 × 10–3 Ω·cm, respectively. The lowest resistivity of 5.6 × 10–4 Ω·cm was achieved for the pelleted codoped AGZO powder using the optimized Al and Ga dopant levels. Notably, this value is one magnitude lower than the best literature reported value for conventionally synthesized codoped AGZO powder. The resistivity values obtained for the pellets after radiant and microwave postsynthesis heat treatment are comparable, although the microwave heat treatment was performed only for 90 s, compared to 3 h for conventional radiant heat treatment. Hence, significant gains were made in the postannealing step by reducing time, cost, and energy required, benefiting our thrust for finding sustainable routes toward alternative low-cost transparent conducting oxides. As a proof of concept, transparent conducting thin films were fabricated via a simple aerosol-assisted deposition technique using our best conducting AGZO nanoparticles. The films exhibited a visible transmittance as good as 90% and a resistivity of 5.7 × 10–3 Ω·cm, which can compete with the existing high cost ITO films

Unravelling the surface chemistry of metal oxide nanocrystals, the role of acids and bases

We synthesized HfO2 nanocrystals from HfCl4 using a surfactant-free solvothermal process in benzyl alcohol and found that the resulting nanocrystals could be transferred to nonpolar media using a mixture of carboxylic acids and amines. Using solution 1H NMR, FTIR, and elemental analysis, we studied the details of the transfer reaction and the surface chemistry of the resulting sterically stabilized nanocrystals. As-synthesized nanocrystals are charge-stabilized by protons, with chloride acting as the counterion. Treatment with only carboxylic acids does not lead to any binding of ligands to the HfO2 surface. On the other hand, we find that the addition of amines provides the basic environment in which carboxylic acids can dissociate and replace chloride. This results in stable, aggregate-free dispersions of HfO2 nanocrystals, sterically stabilized by carboxylate ligands. Moreover, titrations with deuterated carboxylic acid show that the charge on the carboxylate ligands is balanced by coadsorbed protons. Hence, opposite from the X-type/nonstoichiometric nanocrystals picture prevailing in literature, one should look at HfO2/carboxylate nanocrystals as systems where carboxylic acids are dissociatively adsorbed to bind to the nanocrystals. Similar results were obtained with ZrO2 NCs. Since proton accommodation on the surface is most likely due to the high Brønsted basicity of oxygen, our model could be a more general picture for the surface chemistry of metal oxide nanocrystals with important consequences on the chemistry of ligand exchange reactions

Three-dimensional ZnO hierarchical nanostructures: Solution phase synthesis and applications

Zinc oxide (ZnO) nanostructures have been studied extensively in the past 20 years due to their novel electronic, photonic, mechanical and electrochemical properties. Recently, more attention has been paid to assemble nanoscale building blocks into three-dimensional (3D) complex hierarchical structures, which not only inherit the excellent properties of the single building blocks but also provide potential applications in the bottom-up fabrication of functional devices. This review article focuses on 3D ZnO hierarchical nanostructures, and summarizes major advances in the solution phase synthesis, applications in environment, and electrical/electrochemical devices. We present the principles and growth mechanisms of ZnO nanostructures via different solution methods, with an emphasis on rational control of the morphology and assembly. We then discuss the applications of 3D ZnO hierarchical nanostructures in photocatalysis, field emission, electrochemical sensor, and lithium ion batteries. Throughout the discussion, the relationship between the device performance and the microstructures of 3D ZnO hierarchical nanostructures will be highlighted. This review concludes with a personal perspective on the current challenges and future research

Nanostructured semiconductor materials for dye-sensitized solar cells

Since O'Regan and Grätzel's first report in 1991, dye-sensitized solar cells (DSSCs) appeared immediately as a promising low-cost photovoltaic technology. In fact, though being far less efficient than conventional silicon-based photovoltaics (being the maximum, lab scale prototype reported efficiency around 13%), the simple design of the device and the absence of the strict and expensive manufacturing processes needed for conventional photovoltaics make them attractive in small-power applications especially in low-light conditions, where they outperform their silicon counterparts. Nanomaterials are at the very heart of DSSC, as the success of its design is due to the use of nanostructures at both the anode and the cathode. In this review, we present the state of the art for both n-type and p-type semiconductors used in the photoelectrodes of DSSCs, showing the evolution of the materials during the 25 years of history of this kind of devices. In the case of p-type semiconductors, also some other energy conversion applications are touched upon. © 2017 Carmen Cavallo et al

Structural and Electrochemical Analysis of CIGS: Cr Crystalline Nanopowders and Thin Films Deposited onto ITO Substrates

A new approach for the synthesis of nanopowders and thin films of CuInGaSe2 (CIGS) chalcopyrite material doped with different amounts of Cr is presented. The chalcopyrite material CuInxGa1 − xSe2 was doped using Cr to form a new doped chalcopyrite with the structure CuInxCryGa1 − x − ySe2, where x = 0.4 and y = 0.0, 0.1, 0.2, or 0.3. The electrical properties of CuInx CryGa1 − x − ySe2 are highly dependent on the Cr content and results show these materials as promising dopants for the fabrication thin film solar cells. The CIGS nano-precursor powder was initially synthesized via an autoclave method, and then converted into thin films over transparent substrates. Both crystalline precursor powders and thin films deposited onto ITO substrates following a spin-coating process were subsequently characterized using XRD, SEM, HR-TEM, UV-visible and electrochemical impedance spectroscopy (EIS). EIS measurement was performed to evaluate the dc-conductivity of these novel materials as conductive films to be applied in solar cells