The effect of the low-oxidation-state metal ion reagent tris-picolinatovanadium(II) formate on the surface morphology and composition of crystalline iron oxides

Author(s):  
Geoffrey C. Allen ◽  
Colin Kirby ◽  
Robin M. Sellers
1999 ◽  
Vol 585 ◽  
Author(s):  
Douglas H. Lowndes ◽  
Vladimir I. Merkulov ◽  
L. R. Baylor ◽  
G. E. Jellison ◽  
D. B. Poker ◽  
...  

AbstractThe principal interests in this work are energetic-beam control of carbon-film properties and the roles of doping and surface morphology in field emission. Carbon films with variable sp3-bonding fraction were deposited on n-type Si substrates by ArF (193 nm) pulsed-laser ablation (PLA) of a pyrolytic graphite target, and by direct metal ion beam deposition (DMIBD) using a primary Cs+ beam to generate the secondary C- deposition beam. The PLA films are undoped while the DMIBD films are doped with Cs. The kinetic energy (KE) of the incident C atoms/ions was controlled and varied over the range from ∼25 eV to ∼175 eV. Earlier studies have shown that C films' sp3-bonding fraction and diamond-like properties can be maximized by using KE values near 90 eV. The films' surface morphology, sp3–bonding fraction, and Cs-content were determined as a function of KE using atomic force microscopy, TEM/EELS, Rutherford backscattering and nuclear reaction measurements, respectively. Field emission (FE) from these very smooth undoped and Cs-containing films is compared with the FE from two types of deliberately nanostructured carbon films, namely hot-filament chemical vapor deposition (HF-CVD) carbon and carbon nanotubes grown by plasma-enhanced CVD. Electron field emission (FE) characteristics were measured using ∼25-μm, ∼5-μm and ∼1-μm diameter probes that were scanned with ∼75 nm resolution in the x-, y-, and z-directions in a vacuum chamber (∼5 × 10-7 torr base pressure) equipped with a video camera for viewing. The hydrogen-free and very smooth a-D or a-C films (with high or low sp3 content, and with or without ∼1% Cs doping) produced by PLD and DMIBD are not good field emitters. Conditioning accompanied by arcing was required to obtain emission, so that their subsequent FE is characteristic of the arc-produced damage site. However, deliberate surface texturing can eliminate the need for conditioning, apparently by geometrical enhancement of the local electric field. But the most promising approach for producing macroscopically flat FE cathodes is to use materials that are highly nanostructured, either by the deposition process (e.g. HF-CVD carbon) or intrinsically (e.g. carbon nanotubes). HF-CVD films were found to combine a number of desirable properties for FE displays and vacuum microelectronics, including the absence of conditioning, low turn-on fields, high emission site density, and apparent stability and durability during limited long-term testing. Preliminary FE measurements revealed that vertically aligned carbon nanotubes are equally promising.


2013 ◽  
Vol 11 (6) ◽  
pp. 1497-1502 ◽  
Author(s):  
V. A. Castillo ◽  
M. A. Barakat ◽  
M. H. Ramadan ◽  
H. L. Woodcock ◽  
J. N. Kuhn

2017 ◽  
Vol 10 (4) ◽  
pp. 1059
Author(s):  
Fabiana Cristina Meira Zaparoli ◽  
Nelson Vicente Lovatto Gasparetto

This research aimed to compare the surface morphology of quartz grains of the E and Bt horizons of an Ultisol of the Aratu stream basin, in the city of Floraí, Paraná. The Ultisol is derived from sandstones of the Caiuá Formation and it is subjected to mesothermal humid subtropical climate. The materials from the E horizon showed abundant porosity compared to the Bt horizon ones, due to the filling of pores by coating of clay and iron oxides. On the surface of the quartz grains of the E horizon, several features were identified such as ";craters";, pyramidal microfeatures, gulfs of dissolution, elongated cavities, and silica reprecipitation, resulting from the chemical change, and fragmented grains resulting from a phenomenon called ";plasma infusion."; In the Bt horizon, nearly all the detrital grains were surrounded by clay and iron oxide. The detrital grains of the Bt horizon were better preserved, showing little corrosion features and rare fragmented grains, compared to the E horizon. These analyzes showed that the water flow accounts for the superficial alteration of detrital quartz grains when they are under the influence of humid subtropical climate.  R E S U M OA pesquisa teve como objetivo comparar a morfologia superficial de grãos de quartzo dos horizontes E e Bt de um Argissolo da bacia do córrego Aratu, no município de Floraí, PR. O Argissolo é derivado de arenitos da Formação Caiuá e submetido a clima subtropical úmido mesotérmico. Os materiais do horizonte E apresentam porosidade abundante quando comparados com os do horizonte Bt, em razão do preenchimento dos poros por revestimentos de argila e óxidos de ferro. Foram identificadas na superfície dos grãos de quartzo do horizonte E várias feições tipo “crateras”, microfeições piramidais, golfos de dissolução, cavidades alongadas, reprecipitação de sílica, oriundas da alteração química, e grãos fragmentados devido ao fenômeno denominado “plasma infusion”. No horizonte Bt, praticamente todos os grãos detritais estão envolvidos por argila e óxidos de ferro. Os grãos detritais do horizonte Bt estão mais preservados, exibindo poucas feições de corrosão e raros grãos fragmentados, se comparados com os do horizonte E. Essas análises demonstraram que o fluxo hídrico é o responsável pela alteração superficial dos grãos detritais de quartzo quando sob a influência de clima subtropical úmido. Palavras-chave: Argissolo, morfologia de grãos de quartzo, alteração geoquímica, fluxo hídrico 


Inorganics ◽  
2021 ◽  
Vol 9 (9) ◽  
pp. 72
Author(s):  
Dafydd D. L. Jones ◽  
Samuel Watts ◽  
Cameron Jones

Sterically bulky β-diketiminate (or Nacnac) ligand systems have recently shown the ability to kinetically stabilize highly reactive low-oxidation state main group complexes. Metal halide precursors to such systems can be formed via salt metathesis reactions involving alkali metal complexes of these large ligand frameworks. Herein, we report the synthesis and characterization of lithium and potassium complexes of the super bulky anionic β-diketiminate ligands, known [TCHPNacnac]− and new [TCHP/DipNacnac]− (ArNacnac = [(ArNCMe)2CH]−) (Ar = 2,4,6-tricyclohexylphenyl (TCHP) or 2,6-diisopropylphenyl (Dip)). The reaction of the proteo-ligands, ArNacnacH, with nBuLi give the lithium etherate compounds, [(TCHPNacnac)Li(OEt2)] and [(TCHP/DipNacnac)Li(OEt2)], which were isolated and characterized by multinuclear NMR spectroscopy and X-ray crystallography. The unsolvated potassium salts, [{K(TCHPNacnac)}2] and [{K(TCHP/DipNacnac)}∞], were also synthesized and characterized in solution by NMR spectroscopy. In the solid state, these highly reactive potassium complexes exhibit differing alkali metal coordination modes, depending on the ligand involved. These group 1 complexes have potential as reagents for the transfer of the bulky ligand fragments to metal halides, and for the subsequent stabilization of low-oxidation state metal complexes.


2019 ◽  
Vol 2019 (44) ◽  
pp. 4719-4726 ◽  
Author(s):  
Kevin Schwedtmann ◽  
Alexander Hepp ◽  
Kai Schwedtmann ◽  
Jan J. Weigand ◽  
Felicitas Lips

2006 ◽  
Vol 70 (11) ◽  
pp. 2679-2698 ◽  
Author(s):  
M. Ponthieu ◽  
F. Juillot ◽  
T. Hiemstra ◽  
W.H. van Riemsdijk ◽  
M.F. Benedetti

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