Please use this identifier to cite or link to this item: https://hdl.handle.net/20.500.14279/10511
Title: Nanoporous activated carbon cloth as a versatile material for hydrogen adsorption, selective gas separation and electrochemical energy storage
Authors: Kostoglou, Nikolaos 
Koczwara, Christian 
Prehal, Christian 
Terziyska, Velislava 
Babic, Biljana 
Matovic, Branko 
Constantinides, Georgios 
Tampaxis, Christos 
Charalambopoulou, Georgia 
Steriotis, Theodore 
Hinder, Steve 
Baker, Mark A. 
Polychronopoulou, Kyriaki 
Doumanidis, Charalabos 
Paris, Oskar 
Mitterer, Christian 
Rebholz, Claus 
Major Field of Science: Natural Sciences
Field Category: Chemical Sciences
Keywords: Activated carbon cloth;Nanoporous material;Adsorption;H-2 storage;CO2/CH4 selectivity;Supercapacitor electrode
Issue Date: Oct-2017
Source: Nano Energy, 2017, vol. 40, pp. 49-64
Volume: 40
Start page: 49
End page: 64
Journal: Nano Energy 
Abstract: The efficient storage of energy combined with a minimum carbon footprint is still considered one of the major challenges towards the transition to a progressive, sustainable and environmental friendly society on a global scale. The energy storage in pure chemical form using gas carriers with high heating values, including H-2 and CH4, as well as via electrochemical means using state-of-the-art devices, such as batteries or supercapacitors, are two of the most attractive alternatives for the combustion of finite, carbon-rich and environmentally harmful fossil fuels, such as diesel and gasoline. A few-step, reproducible and scalable method is presented in this study for the preparation of an ultra-microporous (average pore size around 0.6 nm) activated carbon cloth (ACC) with large specific area (> 1200 m(2)/g) and pore volume (similar to 0.5 cm(3)/g) upon combining chemical impregnation, carbonization and CO2 activation of a low-cost cellulose-based polymeric fabric. The ACC material shows a versatile character towards three different applications, including H2 storage via cryo-adsorption, separation of energy-dense CO2/CH4 mixtures via selective adsorption and electrochemical energy storage using super-capacitor technology. Fully reversible H-2 uptake capacities in excess of 3.1 wt% at 77 K and similar to 72 bar along with a significant heat of adsorption value of up to 8.4 kJ/mol for low surface coverage have been found. Upon incorporation of low-pressure sorption data in the ideal adsorbed solution theory model, the ACC is predicted to selectively adsorb about 4.5 times more CO2 than CH4 in ambient conditions and thus represents an appealing adsorbent for the purification of such gaseous mixtures. Finally, an electric double-layer capacitor device was assembled and tested for its electrochemical performance, constructed of binder-free and flexible ACC electrodes and aqueous CsCl electrolyte. The full-cell exhibits a gravimetric capacitance of similar to 121 F/g for a specific current of 0.02 A/g, which relative to the ACC's specific area, is superior to commercially available activated carbons. A capacitance retention of more than 97% was observed after 10,000 charging/discharging cycles, thus indicating the ACC's suitability for demanding and high-performance energy storage on a commercial scale. The enhanced performance in all tested applications seems to be attributed to the mean ultra-micropore size of the ACC material instead of the available specific area and/or pore volume.
URI: https://hdl.handle.net/20.500.14279/10511
ISSN: 22112855
DOI: 10.1016/j.nanoen.2017.07.056
Rights: © Elsevier
Type: Article
Affiliation : Cyprus University of Technology 
University of Leoben 
University of Cyprus 
University of Surrey 
Khalifa University 
University of Belgrade 
Publication Type: Peer Reviewed
Appears in Collections:Άρθρα/Articles

CORE Recommender
Show full item record

SCOPUSTM   
Citations

84
checked on Nov 9, 2023

WEB OF SCIENCETM
Citations 50

85
Last Week
2
Last month
0
checked on Oct 29, 2023

Page view(s) 20

476
Last Week
0
Last month
6
checked on Dec 3, 2024

Google ScholarTM

Check

Altmetric


Items in KTISIS are protected by copyright, with all rights reserved, unless otherwise indicated.