scholarly journals Towards Control of the Size, Composition and Surface Area of NiO Nanostructures by Sn Doping

Nanomaterials ◽  
2021 ◽  
Vol 11 (2) ◽  
pp. 444
Author(s):  
María Taeño ◽  
David Maestre ◽  
Julio Ramírez-Castellanos ◽  
Shaohui Li ◽  
Pooi See Lee ◽  
...  
Keyword(s):  
Surface Area ◽  
High Surface ◽  
High Surface Area ◽  
Size Composition ◽  
Charge Compensation ◽  
Potential Candidate ◽  
Sno2 Nanostructures ◽  
Experimental Conditions ◽  
Sn Doping ◽  
Compensation Mechanisms

Achieving nanostructures with high surface area is one of the most challenging tasks as this metric usually plays a key role in technological applications, such as energy storage, gas sensing or photocatalysis, fields in which NiO is gaining increasing attention recently. Furthermore, the advent of modern NiO-based devices can take advantage of a deeper knowledge of the doping process in NiO, and the fabrication of p-n heterojunctions. By controlling experimental conditions such as dopant concentration, reaction time, temperature or pH, NiO morphology and doping mechanisms can be modulated. In this work, undoped and Sn doped nanoparticles and NiO/SnO2 nanostructures with high surface areas were obtained as a result of Sn incorporation. We demonstrate that Sn incorporation leads to the formation of nanosticks morphology, not previously observed for undoped NiO, promoting p-n heterostructures. Consequently, a surface area value around 340 m2/g was obtained for NiO nanoparticles with 4.7 at.% of Sn, which is nearly nine times higher than that of undoped NiO. The presence of Sn with different oxidation states and variable Ni3+/Ni2+ ratio as a function of the Sn content were also verified by XPS, suggesting a combination of two charge compensation mechanisms (electronic and ionic) for the substitution of Ni2+ by Sn4+. These results make Sn doped NiO nanostructures a potential candidate for a high number of technological applications, in which implementations can be achieved in the form of NiO–SnO2 p-n heterostructures.

Production and Characterization of Activated Carbon from Waste Tire by H3PO4 Treatment for Ethylene Adsorbent Used in Active Packaging

2012 ◽  
Vol 506 ◽  
pp. 214-217 ◽  
Author(s):  
Athiwat Sirimuangjinda ◽  
Khanthima Hemra ◽  
Duangduen Atong ◽  
Chiravoot Pechyen
Keyword(s):  
Activated Carbon ◽  
Surface Area ◽  
Activated Carbons ◽  
Adsorption Property ◽  
High Surface ◽  
High Surface Area ◽  
Fixed Bed ◽  
Activation Process ◽  
Experimental Conditions ◽  
Waste Tire

Pyrolysis is one form of energy recovery process which has the potential to generate oil, gas and char products. The char becomes an attractive by-product, with applications including production of activated carbons, which is useful as a ethylene sorbent for climacteric fruit packaging. In this work, activated carbon prepared from waste tire, produced as a by product of the bio-diesel extraction industry was prepared via chemical treatment with phosphoric acid (H3PO4) at three different char:H3PO4 ratios (1:1, 1:2 and 1:3) under fixed bed pyrolysis at 400, 500 and 600°C for 30 minutes in nitrogen (N2) flow rate of 1000 mL/min and heating rate of 20°C/min. Result shows that char pyrolyzed at 800°C contained high fixed carbon and low volatile content favorable for subsequent activation process compared to other cases.(data not show here) Under the experimental conditions investigated, impregnation ratio of 1:2 were found to be suitable for producing high-surface area activated carbon. It was shown that H3PO4 did work effectively as dehydration reagent at approximately 600°C. The obtained carbons were characterized by nitrogen adsorptiondesorption isotherms at-196 °C. The surface area of activated carbons, which were determined by application of the BrunauerEmmettTeller (BET) and t-plot methods, were achieved as high as 833.50 m2/g. The chemically activated carbons were found to be mainly type II carbons and high adsorption property (Methylene blue adsorption = 622 mg/g and Iodine number = 899 mg/g).

Preparation of N-Doped Nanoporous Carbon from Crude Biomass and its Electrochemical Activity

NANO ◽  
2016 ◽  
Vol 11 (03) ◽  
pp. 1650028 ◽  
Author(s):  
Zezhong Xu ◽  
Jingyu Si
Keyword(s):  
Surface Area ◽  
Low Cost ◽  
High Surface ◽  
High Surface Area ◽  
Lithium Ion ◽  
Nanoporous Carbon ◽  
High Specific Surface Area ◽  
Electrochemical Sensing ◽  
Potential Candidate ◽  
Surface Areas

H2O2 detection plays an important role in electrochemical sensing since H2O2 often acts as an intermediate product or regulator in various reactions. Nanoporous carbon (NPC) can be a potential candidate in electrochemical sensing because of its high specific surface area, various pore sizes and structures. In this work, we reported the preparation of N-doped NPC derived from the highly available, accessible and recyclable plant Typha orientalis. The products have high surface area (highest surface areas of 1439.0 m2 g[Formula: see text] and a number of nanopores. Highest content of nitrogen atom in the product is 3.66 at.%). Typical product exhibits high electrocatalytic activity for reduction of hydrogen peroxide. The product may have further use for glucose biosensing. We developed a low-cost, simple and readily scalable approach to prepare the excellent carbon electrocatalyst directly from crude biomass. In addition, because of high surface area and doping of nitrogen element, the product may find broad applications in the fields of supercapacitors, lithium-ion batteries, gas uptake and so on.

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.

Tenacious Mass Transfer Limitations Drive Catalytic Selectivity during Electrochemical Carbon Dioxide Reduction

2019 ◽  
Author(s):  
Kailun Yang ◽  
Recep Kas ◽  
Wilson A. Smith
Keyword(s):  
Surface Area ◽  
High Surface ◽  
High Surface Area ◽  
Catalyst Layer ◽  
Active Surface ◽  
Active Surface Area ◽  
High Concentration ◽  
Copper Electrodes ◽  
Surface Enhanced ◽  
Local Current

<p>This study evaluated the performance of the commonly used strong buffer electrolytes, i.e. phosphate buffers, during CO<sub>2</sub> electroreduction in neutral pH conditions by using in-situ surface enhanced infrared absorption spectroscopy (SEIRAS). Unfortunately, the buffers break down a lot faster than anticipated which has serious implications on many studies in the literature such as selectivity and kinetic analysis of the electrocatalysts. Increasing electrolyte concentration, surprisingly, did not extend the potential window of the phosphate buffers due to dramatic increase in hydrogen evolution reaction. Even high concentration phosphate buffers (1 M) break down within the potentials (-1 V vs RHE) where hydrocarbons are formed on copper electrodes. We have extended the discussion to high surface area electrodes by evaluating electrodes composed of copper nanowires. We would like highlight that it is not possible to cope with high local current densities on these high surface area electrodes by using high buffer capacity solutions and the CO<sub>2</sub> electrocatalysts are needed to be evaluated by casting thin nanoparticle films onto inert substrates as commonly employed in fuel cell reactions and up to now scarcely employed in CO<sub>2</sub> electroreduction. In addition, we underscore that normalization of the electrocatalytic activity to the electrochemical active surface area is not the ultimate solution due to concentration gradient along the catalyst layer.This will “underestimate” the activity of high surface electrocatalyst and the degree of underestimation will depend on the thickness, porosity and morphology of the catalyst layer. </p> <p> </p>

scholarly journals Rugae-like FeP nanocrystal assembly on a carbon cloth: an exceptionally efficient and stable cathode for hydrogen evolution

Nanoscale ◽  
2015 ◽  
Vol 7 (25) ◽  
pp. 10974-10981 ◽  
Author(s):  
Xiulin Yang ◽  
Ang-Yu Lu ◽  
Yihan Zhu ◽  
Shixiong Min ◽  
Mohamed Nejib Hedhili ◽  
...  
Keyword(s):  
Gas Phase ◽  
Surface Area ◽  
Hydrogen Evolution ◽  
Hydrogen Generation ◽  
High Surface ◽  
High Surface Area ◽  
Catalytic Efficiency ◽  
Carbon Cloth ◽  
Nanocrystal Assembly

High surface area FeP nanosheets on a carbon cloth were prepared by gas phase phosphidation of electroplated FeOOH, which exhibit exceptionally high catalytic efficiency and stability for hydrogen generation.

High Surface Area NiCoP Nanostructure as Efficient Water Splitting Electrocatalyst for the Oxygen Evolution Reaction

2021 ◽  
pp. 111312
Author(s):  
Sisir Maity ◽  
Dheeraj Kumar Singh ◽  
Divya Bhutani ◽  
Suchitra Prasad ◽  
Umesh V. Waghmare ◽  
...  
Keyword(s):  
Surface Area ◽  
Water Splitting ◽  
Oxygen Evolution ◽  
Oxygen Evolution Reaction ◽  
High Surface ◽  
High Surface Area

scholarly journals Fast synthesis of high surface area bio-based porous carbons for p-nitrophenol removal

MethodsX ◽  
2021 ◽  
pp. 101464
Author(s):  
Yichen Wu ◽  
Nan Zhang ◽  
Charles-François de Lannoy
Keyword(s):  
Surface Area ◽  
High Surface ◽  
High Surface Area ◽  
Porous Carbons ◽  
Fast Synthesis

Synthesis of high surface area and functionalized nanoporous biocarbons and their efficiency for CO2 capture and supercapacitors

2021 ◽  
Author(s):  
Gurwinder Singh ◽  
Rohan Bahadur ◽  
Ajanya Maria Ruban ◽  
Jefrin Marykala Davidraj ◽  
Dawei Su ◽  
...  
Keyword(s):  
Energy Storage ◽  
Surface Area ◽  
Co2 Capture ◽  
Water Purification ◽  
High Surface ◽  
High Surface Area ◽  
Energy Storage And Conversion ◽  
Waste Biomass ◽  
Fabrication Technology ◽  
Significant Attention

Nanoporous biocarbons derived from waste biomass have created significant attention owing to their great potential for energy storage and conversion and water purification. However, the fabrication technology for these materials...

scholarly journals Developing Eco-Friendly and Cost-Effective Porous Adsorbent for Carbon Dioxide Capture

Molecules ◽  
2021 ◽  
Vol 26 (7) ◽  
pp. 1962
Author(s):  
Mahboubeh Nabavinia ◽  
Baishali Kanjilal ◽  
Noahiro Fujinuma ◽  
Amos Mugweru ◽  
Iman Noshadi
Keyword(s):  
Carbon Dioxide ◽  
Surface Area ◽  
Co2 Capture ◽  
High Surface ◽  
Scale Up ◽  
Polymer Networks ◽  
High Surface Area ◽  
Excellent Thermal Stability ◽  
Doped Polymers ◽  
Metal Doped

To address the issue of global warming and climate change issues, recent research efforts have highlighted opportunities for capturing and electrochemically converting carbon dioxide (CO2). Despite metal doped polymers receiving widespread attention in this respect, the structures hitherto reported lack in ease of synthesis with scale up feasibility. In this study, a series of mesoporous metal-doped polymers (MRFs) with tunable metal functionality and hierarchical porosity were successfully synthesized using a one-step copolymerization of resorcinol and formaldehyde with Polyethyleneimine (PEI) under solvothermal conditions. The effect of PEI and metal doping concentrations were observed on physical properties and adsorption results. The results confirmed the role of PEI on the mesoporosity of the polymer networks and high surface area in addition to enhanced CO2 capture capacity. The resulting Cobalt doped material shows excellent thermal stability and promising CO2 capture performance, with equilibrium adsorption of 2.3 mmol CO2/g at 0 °C and 1 bar for at a surface area 675.62 m2/g. This mesoporous polymer, with its ease of synthesis is a promising candidate for promising for CO2 capture and possible subsequent electrochemical conversion.

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