Nickel Multi-walled Carbon Nanotube Composite Electrode for Hydrogen Generation

2012 ◽  
Vol 1387 ◽  
Author(s):  
Nitin Kalra ◽  
Kalathur Santhanam ◽  
David Olney
Keyword(s):  
Carbon Nanotube ◽  
Hydrogen Production ◽  
Large Scale ◽  
Coulombic Efficiency ◽  
Superior Performance ◽  
Efficient Production ◽  
Scale Production ◽  
Production Of Hydrogen ◽  
Carbon Nanotube Composite ◽  
Decomposition Of Water

ABSTRACTThe electrochemical decomposition of water is an attractive method, however, the performance of the electrodes and efficiencies are of great concern in its large scale production. In this context, we wish to report here the superior performance of Ni-multiwalled carbon nanotube composite as cathode in the decomposition of water. The current voltage curves recorded with this electrode in different media showed a significant electrocatalysis in the reduction of hydrogen ion; the background electrolysis is shifted in the anodic direction. The nanocomposite composition has been found to be crucial in the efficient production of hydrogen. A coulombic efficiency of about 68% has been obtained at this electrode with a hydrogen production rate of 130L/m2 d. This electrode is more efficient than the 316L stainless steel (composition in percentage: C 0.019, Cr 17.3, Mo 2.04, Ni 11.3, Mn 1.04, N 0.041, Fe bulk) cathode that produces 10 ml/h at an area of 20 cm2 (5L/m2.h) (2). The results obtained with different electrolytes, performance variation with electrode composition, and current densities will be presented. The trials carried out using solar panel instead of DC power source showed similar hydrogen production rates and efficiencies.

Preliminary Cost Estimates for Massive Hydrogen Production Using SI Process

2008 ◽  
Author(s):  
K. J. Yang ◽  
K. Y. Lee ◽  
T. H. Lee
Keyword(s):  
Hydrogen Production ◽  
Large Scale ◽  
Fossil Fuels ◽  
Production Costs ◽  
Scale Production ◽  
Cost Estimates ◽  
Production Of Hydrogen ◽  
Major Factors ◽  
The Cost ◽  
Hydrogen Systems

As a preliminary study of cost estimates for nuclear hydrogen systems, the hydrogen production costs of the nuclear energy sources benchmarking GT-MHR and PBMR are estimated in the necessary input data on a Korean specific basis. G4-ECONS was appropriately modified to calculate the cost for hydrogen production of SI process with VHTR as a thermal energy source rather than the LUEC. The estimated costs presented in this paper show that hydrogen production by the VHTR could be competitive with current techniques of hydrogen production from fossil fuels if CO2 capture and sequestration is required. Nuclear production of hydrogen would allow large-scale production of hydrogen at economic prices while avoiding the release of CO2. Nuclear production of hydrogen could thus become the enabling technology for the hydrogen economy. The major factors that would affect the cost of hydrogen were also discussed.

scholarly journals Hydrogen production from water electrolysis: role of catalysts

2021 ◽  
Vol 8 (1) ◽  
Author(s):  
Shan Wang ◽  
Aolin Lu ◽  
Chuan-Jian Zhong
Keyword(s):  
Hydrogen Production ◽  
Water Splitting ◽  
Noble Metal ◽  
Active Sites ◽  
Current Knowledge ◽  
Low Cost ◽  
Critical Role ◽  
Water Electrolysis ◽  
Efficient Production ◽  
Production Of Hydrogen

AbstractAs a promising substitute for fossil fuels, hydrogen has emerged as a clean and renewable energy. A key challenge is the efficient production of hydrogen to meet the commercial-scale demand of hydrogen. Water splitting electrolysis is a promising pathway to achieve the efficient hydrogen production in terms of energy conversion and storage in which catalysis or electrocatalysis plays a critical role. The development of active, stable, and low-cost catalysts or electrocatalysts is an essential prerequisite for achieving the desired electrocatalytic hydrogen production from water splitting for practical use, which constitutes the central focus of this review. It will start with an introduction of the water splitting performance evaluation of various electrocatalysts in terms of activity, stability, and efficiency. This will be followed by outlining current knowledge on the two half-cell reactions, hydrogen evolution reaction (HER) and oxygen evolution reaction (OER), in terms of reaction mechanisms in alkaline and acidic media. Recent advances in the design and preparation of nanostructured noble-metal and non-noble metal-based electrocatalysts will be discussed. New strategies and insights in exploring the synergistic structure, morphology, composition, and active sites of the nanostructured electrocatalysts for increasing the electrocatalytic activity and stability in HER and OER will be highlighted. Finally, future challenges and perspectives in the design of active and robust electrocatalysts for HER and OER towards efficient production of hydrogen from water splitting electrolysis will also be outlined.

Iron and Nitrogen Co-doped CoSe2 Nanosheet Arrays for Robust Electrocatalytic Water Oxidation

2021 ◽  
Author(s):  
Di Li ◽  
Yingying Xing ◽  
Changjian Zhou ◽  
Yikai Lu ◽  
Shengjie Xu ◽  
...  
Keyword(s):  
Water Splitting ◽  
Water Oxidation ◽  
Energy Barrier ◽  
Large Scale ◽  
Scale Production ◽  
Reaction Energy ◽  
Large Scale Production ◽  
Nanosheet Arrays ◽  
Production Of Hydrogen ◽  
Co Doped

The high reaction energy barrier of the oxygen evolution reaction (OER) extremely reduces the efficiency of water splitting, which is not conducive to large-scale production of hydrogen. Due to the...

(Invited) Improve Electrodes' Electrochemical Performance for HER and OER By Hydrogenation Treatment

2018 ◽  
Vol MA2018-01 (31) ◽  
pp. 1840-1840
Author(s):  
Xiaobo Chen
Keyword(s):  
Hydrogen Production ◽  
Large Scale ◽  
Electrode Materials ◽  
Scale Production ◽  
Structure Property ◽  
Large Scale Production ◽  
Property Performance ◽  
Splitting Process ◽  
New Discovery ◽  
Hydrogenation Treatment

Hydrogen production through electrolysis has been regarded as one of the most promising solutions for large-scale production of clean fuels. However, most electrodes have large overpotentials in the HER and OER reactions during the water splitting process. Many approaches and methods have been developed to enhance the electrodes' performance. Here, we would like to present our studies on the hydrogenation of various electrode materials for HER and OER applications. We aim to reveal the structure-property-performance relationship for those electrodes after hydrogenation treatment. We wish our work could provide useful information and will be honored if our work can inspire new discovery and finding in the related fields to advance our understanding and technologies for efficient hydrogen production through electrolysis.

scholarly journals Electrochemically derived functionalized graphene for bulk production of hydrogen peroxide

2020 ◽  
Vol 11 ◽  
pp. 432-442 ◽  
Author(s):  
Munaiah Yeddala ◽  
Pallavi Thakur ◽  
Anugraha A ◽  
Tharangattu N Narayanan
Keyword(s):  
Large Scale ◽  
Reduction Reaction ◽  
Single Step ◽  
Scale Production ◽  
Functionalized Graphene ◽  
Large Scale Production ◽  
Production Of Hydrogen ◽  
Electron Reduction ◽  
Bulk Production ◽  
Carbon Based

On-site peroxide generation via electrochemical reduction is gaining tremendous attention due to its importance in many fields, including water treatment technologies. Oxidized graphitic carbon-based materials have been recently proposed as an alternative to metal-based catalysts in the electrochemical oxygen reduction reaction (ORR), and in this work we unravel the role of C=O groups in graphene towards sustainable peroxide formation. We demonstrate a versatile single-step electrochemical exfoliation of graphite to graphene with a controllable degree of oxygen functionalities and thickness, leading to the formation of large quantities of functionalized graphene with tunable rate parameters, such as the rate constant and exchange current density. Higher oxygen-containing exfoliated graphene is known to undergo a two-electron reduction path in ORR having an efficiency of about 80 ± 2% even at high overpotential. Bulk production of H2O2 via electrolysis was also demonstrated at low potential (0.358 mV vs RHE), yielding ≈34 mg/L peroxide with highly functionalized (≈23 atom %) graphene and ≈16 g/L with low functionalized (≈13 atom %) graphene, which is on par with the peroxide production using state-of-the-art precious-metal-based catalysts. Hence this method opens a new scheme for the single-step large-scale production of functionalized carbon-based catalysts (yield ≈45% by weight) that have varying functionalities and can deliver peroxide via the electrochemical ORR process.

scholarly journals Efficient Production of l-Ribose with a Recombinant Escherichia coli Biocatalyst

2008 ◽  
Vol 74 (10) ◽  
pp. 2967-2975 ◽  
Author(s):  
Ryan D. Woodyer ◽  
Nathan J. Wymer ◽  
F. Michael Racine ◽  
Shama N. Khan ◽  
Badal C. Saha
Keyword(s):  
Escherichia Coli ◽  
Large Scale ◽  
Active Form ◽  
Apium Graveolens ◽  
Efficient Production ◽  
Scale Production ◽  
Gene Encoding ◽  
Large Scale Production ◽  
One Step ◽  
Rare Sugars

ABSTRACT A new synthetic platform with potential for the production of several rare sugars, with l-ribose as the model target, is described. The gene encoding the unique NAD-dependent mannitol-1-dehydrogenase (MDH) from Apium graveolens (garden celery) was synthetically constructed for optimal expression in Escherichia coli. This MDH enzyme catalyzes the interconversion of several polyols and their l-sugar counterparts, including the conversion of ribitol to l-ribose. Expression of recombinant MDH in the active form was successfully achieved, and one-step purification was demonstrated. Using the created recombinant E. coli strain as a whole-cell catalyst, the synthetic utility was demonstrated for production of l-ribose, and the system was improved using shaken flask experiments. It was determined that addition of 50 to 500 μM ZnCl2 and addition of 5 g/liter glycerol both improved production. The final levels of conversion achieved were >70% at a concentration of 40 g/liter and >50% at a concentration of 100 g/liter. The best conditions determined were then scaled up to a 1-liter fermentation that resulted in 55% conversion of 100 g/liter ribitol in 72 h, for a volumetric productivity of 17.4 g liter−1 day−1. This system represents a significantly improved method for the large-scale production of l-ribose.

scholarly journals Performance of rGO/TiO2 Photocatalytic Membranes for Hydrogen Production

Membranes ◽  
2020 ◽  
Vol 10 (9) ◽  
pp. 218 ◽  
Author(s):  
Juan Corredor ◽  
Eduardo Perez-Peña ◽  
Maria J. Rivero ◽  
Inmaculada Ortiz
Keyword(s):  
Hydrogen Production ◽  
High Performance ◽  
Large Scale ◽  
Membrane Surface ◽  
Life Time ◽  
Dip Coating ◽  
Production Of Hydrogen ◽  
Nafion Membranes ◽  
The Matrix ◽  
Low Efficiency

Although there are promising environmental and energy characteristics for the photocatalytic production of hydrogen, two main drawbacks must be overcome before the large- scale deployment of the technology becomes a reality, (i) the low efficiency reported by state of the art photocatalysts and, (ii) the short life time and difficult recovery of the photocatalyst, issues that need research and development for new high performance catalysts. In this work 2% rGO/TiO2 composite photocatalysts were supported over Nafion membranes and the performance of the photocatalytic membrane was tested for hydrogen production from a 20% vol. methanol solution. Immobilization of the composite on Nafion membranes followed three different simple methods which preserve the photocatalyst structure: solvent-casting (SC), spraying (SP), and dip-coating (DP). The photocatalyst was included in the matrix membrane using the SC method, while it was located on the membrane surface in the SP and DP membranes showing less mass transfer limitations. The performance of the synthesized photocatalytic membranes for hydrogen production under UVA light irradiation was compared. Leaching of the catalytic membranes was tested by measuring the turbidity of the solution. With respect to catalyst leaching, both the SC and SP membranes provided very good results, the leaching being lower with the SC membrane. The best results in terms of initial hydrogen production rate (HPR) were obtained with the SP and DP membrane. The SP was selected as the most suitable method for photocatalytic hydrogen production due to the high HPR and the negligible photocatalyst leaching. Moreover, the stability of this membrane was studied for longer operation times. This work helps to improve the knowledge on the application of photocatalytic membranes for hydrogen production and contributes in facilitating the large-scale application of this process.

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