scholarly journals Salt-Mediated Au-Cu Nanofoam and Au-Cu-Pd Porous Macrobeam Synthesis

Molecules ◽  
2018 ◽  
Vol 23 (7) ◽  
pp. 1701 ◽  
Author(s):  
Fred Burpo ◽  
Enoch Nagelli ◽  
Lauren Morris ◽  
Kamil Woronowicz ◽  
Alexander Mitropoulos
Keyword(s):  
Surface Area ◽  
Electrochemical Impedance ◽  
High Surface ◽  
Electronic Conductivity ◽  
High Surface Area ◽  
Three Dimensional ◽  
Synthesis Methods ◽  
X Ray ◽  
Sensing Applications ◽  
Metal Composition

Multi-metallic and alloy nanomaterials enable a broad range of catalytic applications with high surface area and tuning reaction specificity through the variation of metal composition. The ability to synthesize these materials as three-dimensional nanostructures enables control of surface area, pore size and mass transfer properties, electronic conductivity, and ultimately device integration. Au-Cu nanomaterials offer tunable optical and catalytic properties at reduced material cost. The synthesis methods for Au-Cu nanostructures, especially three-dimensional materials, has been limited. Here, we present Au-Cu nanofoams and Au-Cu-Pd macrobeams synthesized from salt precursors. Salt precursors formed from the precipitation of square planar ions resulted in short- and long-range ordered crystals that, when reduced in solution, form nanofoams or macrobeams that can be dried or pressed into freestanding monoliths or films. Metal composition was determined with X-ray diffraction and energy dispersive X-ray spectroscopy. Nitrogen gas adsorption indicated an Au-Cu nanofoam specific surface area of 19.4 m2/g. Specific capacitance determined with electrochemical impedance spectroscopy was 46.0 F/g and 52.5 F/g for Au-Cu nanofoams and Au-Cu-Pd macrobeams, respectively. The use of salt precursors is envisioned as a synthesis route to numerous metal and multi-metallic nanostructures for catalytic, energy storage, and sensing applications.

scholarly journals Syntheses of Nanostructured Magnesium Carbonate Powders with Mesoporous Structures from Carbon Dioxide

2021 ◽  
Vol 11 (3) ◽  
pp. 1141
Author(s):  
Fernando J. Rodríguez-Macías ◽  
José E. Ortiz-Castillo ◽  
Erika López-Lara ◽  
Alejandro J. García-Cuéllar ◽  
José L. López-Salinas ◽  
...  
Keyword(s):  
Carbon Dioxide ◽  
Surface Area ◽  
High Surface ◽  
High Surface Area ◽  
Magnesium Carbonate ◽  
Synthesis Methods ◽  
X Ray Diffraction ◽  
Aqueous Synthesis ◽  
Synthesis Time ◽  
X Ray

In this work, we present the results of two synthesis approaches for mesoporous magnesium carbonates, that result in mineralization of carbon dioxide, producing carbonate materials without the use of cosolvents, which makes them more environmentally friendly. In one of our synthesis methods, we found that we could obtain nonequilibrium crystal structures, with acicular crystals branching bidirectionally from a denser core. Both Raman spectroscopy and X-ray diffraction showed these crystals to be a mixture of sulfate and hydrated carbonates. We attribute the nonequilibrium morphology to coprecipitation of two salts and short synthesis time (25 min). Other aqueous synthesis conditions produced mixtures of carbonates with different morphologies, which changed depending on drying temperature (40 or 100 °C). In addition to aqueous solution, we used supercritical carbon dioxide for synthesis, producing a hydrated magnesium carbonate, with a nesquehonite structure, according to X-ray diffraction. This second material has smaller pores (1.01 nm) and high surface area. Due to their high surface area, these materials could be used for adsorbents and capillary transport, in addition to their potential use for carbon capture and sequestration.

Toward the control of graphenic foams

2017 ◽  
Vol 89 (4) ◽  
pp. 565-577 ◽  
Author(s):  
Lucie Speyer ◽  
Océane Louppe ◽  
Sébastien Fontana ◽  
Sébastien Cahen ◽  
Claire Hérold
Keyword(s):  
Surface Area ◽  
High Surface ◽  
High Surface Area ◽  
Three Dimensional ◽  
Solvothermal Reaction ◽  
Synthesis Methods ◽  
Structure And Properties ◽  
Optimal Conditions ◽  
Experimental Conditions ◽  
Wide Range

AbstractGraphene-based materials are extensively studied, due to their excellent properties and their wide range of possible applications. Attention has recently been paid to three-dimensional-like graphenic structures, such as crumpled graphene sheets and graphenic foams: these kinds of materials can combine the properties of graphene associating high surface area and porosity, what is particularly interesting for energy or catalysis applications. Most of the synthesis methods leading to such structures are based on graphite oxide exfoliation and re-assembly, but in this work we focus on the preparation of graphenic foams by a solvothermal-based process. We performed a solvothermal reaction between ethanol and sodium at 220°C, during 72 h, under 200 bar, followed by a pyrolysis under nitrogen flow. An extended study of the influence of the temperature (800°C–900°C) of pyrolysis evidences an unexpected strong effect of this parameter on the characteristics of the materials. The optimal conditions provide multi-layer graphene (10 layers) foam with a surface area of 2000 m2·g−1. This work is an important step for the understanding of the mechanisms of the thermal treatment. Post-treatments in different experimental conditions are performed in order to modulate the structure and properties of the graphenic foams.

Three-dimensional characterization of electrodeposited lithium microstructures using synchrotron X-ray phase contrast imaging

2015 ◽  
Vol 51 (2) ◽  
pp. 266-268 ◽  
Author(s):  
David S. Eastwood ◽  
Paul M. Bayley ◽  
Hee Jung Chang ◽  
Oluwadamilola O. Taiwo ◽  
Joan Vila-Comamala ◽  
...  
Keyword(s):  
Surface Area ◽  
Phase Contrast ◽  
High Surface ◽  
High Surface Area ◽  
Three Dimensional ◽  
Phase Contrast Imaging ◽  
Contrast Imaging ◽  
X Ray ◽  
Phase Contrast Tomography

The morphology of electrodeposited high surface area lithium microstructures was imaged in 3D using synchrotron X-ray phase contrast tomography.

Hierarchical Nano/Micro-structured Surfaces with High Surface Area/Volume Ratios

2021 ◽  
pp. 1-36
Author(s):  
Ketki Lichade ◽  
Yizhou Jiang ◽  
Yayue Pan
Keyword(s):  
Surface Structure ◽  
Surface Area ◽  
Light Trapping ◽  
High Surface ◽  
High Surface Area ◽  
Three Dimensional ◽  
Structure Design ◽  
Surface Structures ◽  
Structured Surfaces ◽  
Design And Manufacture

Abstract Recently, many studies have investigated additive manufacturing of hierarchical surfaces with high surface area/volume (SA/V) ratios, and their performance has been characterized for applications in next-generation functional devices. Despite recent advances, it remains challenging to design and manufacture high SA/V ratio structures with desired functionalities. In this study, we established the complex correlations among the SA/V ratio, surface structure geometry, functionality, and manufacturability in the Two-Photon Polymerization (TPP) process. Inspired by numerous natural structures, we proposed a 3-level hierarchical structure design along with the mathematical modeling of the SA/V ratio. Geometric and manufacturing constraints were modeled to create well-defined three-dimensional hierarchically structured surfaces with a high accuracy. A process flowchart was developed to design the proposed surface structures to achieve the target functionality, SA/V ratio, and geometric accuracy. Surfaces with varied SA/V ratios and hierarchy levels were designed and printed. The wettability and antireflection properties of the fabricated surfaces were characterized. It was observed that the wetting and antireflection properties of the 3-level design could be easily tailored by adjusting the design parameter settings and hierarchy levels. Furthermore, the proposed surface structure could change a naturally-hydrophilic surface to near-superhydrophobic. Geometrical light trapping effects were enabled and the antireflection property could be significantly enhanced (>80% less reflection) by the proposed hierarchical surface structures. Experimental results implied the great potential of the proposed surface structures for various applications such as microfluidics, optics, energy, and interfaces.

scholarly journals Organomineral nanocomposite carbon burial during Oceanic Anoxic Event 2

2014 ◽  
Vol 11 (5) ◽  
pp. 6815-6844
Author(s):  
S. C. Löhr ◽  
M. J. Kennedy
Keyword(s):  
Surface Area ◽  
High Surface ◽  
High Surface Area ◽  
Mineral Surfaces ◽  
Mineral Surface ◽  
X Ray ◽  
Oceanic Anoxic Event ◽  
Carbon Burial ◽  
Anoxic Events ◽  
Mineral Surface Area

Abstract. Organic carbon (OC) enrichment in sediments deposited during Oceanic Anoxic Events (OAEs) is commonly attributed to elevated productivity and marine anoxia. We find that OC enrichment in the late Cenomanian aged OAE2 at Demerara Rise was controlled by co-occurrence of anoxic bottom-water, sufficient productivity to saturate available mineral surfaces and variable deposition of high surface area detrital smectite clay. Redox indicators show consistently oxygen-depleted conditions, while a strong correlation between OC concentration and sediment mineral surface area (R2=0.92) occurs across a range of TOC values from 9–33%. X-ray diffraction data indicates intercalation of OC in smectite interlayers while electron, synchrotron infrared and X-ray microscopy show an intimate association between clay minerals and OC, consistent with preservation of OC as organomineral nanocomposites and aggregates rather than discrete, μm-scale pelagic detritus. Since the consistent ratio between TOC and mineral surface area suggests that excess OC relative to surface area is lost, we propose that it is the varying supply of smectite that best explains variable organic enrichment against a backdrop of continuous anoxia, which is conducive to generally high TOC during OAE2 at Demerara Rise. Smectitic clays are unique in their ability to form stable organomineral nanocomposites and aggregates that preserve organic matter, and are common weathering products of continental volcanic deposits. An increased flux of smectite coinciding with high carbon burial is consistent with evidence for widespread volcanism during OAE2, so that organomineral carbon burial may represent a potential feedback to volcanic degassing of CO2.

Three-Dimensional Cage Type Mesoporous CN-Based Hybrid Material with Very High Surface Area and Pore Volume

2007 ◽  
Vol 19 (17) ◽  
pp. 4367-4372 ◽  
Author(s):  
Ajayan Vinu ◽  
Pavuluri Srinivasu ◽  
Dhanashri P. Sawant ◽  
Toshiyuki Mori ◽  
Katsuhiko Ariga ◽  
...  
Keyword(s):  
Surface Area ◽  
Hybrid Material ◽  
Pore Volume ◽  
High Surface ◽  
High Surface Area ◽  
Three Dimensional ◽  
Very High

Synthesis and Analysis of High Surface Area Vanadium Carbide Nanoparticles

2012 ◽  
Vol 585 ◽  
pp. 95-99 ◽  
Author(s):  
M. Mahajan ◽  
K. Singh ◽  
O.P. Pandey
Keyword(s):  
Surface Area ◽  
Vanadium Carbide ◽  
High Surface ◽  
High Surface Area ◽  
X Ray Diffraction ◽  
High Melting Point ◽  
X Ray ◽  
Transmission Electron ◽  
Product Powder ◽  
Scanning Electron

Vanadium carbide is known for its applications due to extreme hardness and high melting point. In this present work, vanadium carbide nanoparticles have been synthesized in a specially designed stainless steel autoclave by solvothermal route using vanadium pentoxide (V2O5) as precursor along with a hydrocarbon acetone (C3H6O) in the presence of reducing agent magnesium (Mg). The optimization of reaction time was studied at constant temperature of 800oC. The product powder was characterized by X-ray diffraction (XRD), Scanning electron microscopy (SEM), Transmission electron microscope (TEM) and Brunauer – Emmett – Teller (BET) techniques. The results indicate that the product was vanadium carbide having particle size of about 30 nm with high surface area.

Fabrication of Ultra-Low Density, High Surface Area Carbon Aerogels and their Application in Supercapacitors

2016 ◽  
Vol 852 ◽  
pp. 1349-1355
Author(s):  
Jia Yi Zhu ◽  
Xi Yang ◽  
Zhi Bing Fu ◽  
Chao Yang Wang ◽  
Wei Dong Wu ◽  
...  
Keyword(s):  
Aqueous Solution ◽  
Surface Area ◽  
High Surface ◽  
High Surface Area ◽  
Three Dimensional ◽  
Carbon Aerogel ◽  
Carbon Aerogels ◽  
Low Density ◽  
Organic Aerogel ◽  
Cyclic Voltammetry Test

The ultra-low density carbon aerogel, as low as 20 mg/cm3, was fabricated by pyrolysis of the organic aerogel formed by aqueous condensation of resorcinol and formaldehyde. Its surface area was as high as 1783 m2/g and it was used for investigation of electrochemical capacitive behaviours. The ultra-low density carbon aerogel displayed capacitive performance (110 F/g at 0.2 A/g) in 6 M KOH aqueous solution. Additionally, over 98% of the initial capacitance was retained after repeating the cyclic voltammetry test for 1000 cycles. The electrochemical performance might be attributed to the combination of three dimensional “opened” structure and high surface area of the carbon aerogel.

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