Solvothermally synthesized nanoporous hypercrosslinked polyaniline: studies of the gas sorption and charge storage behavior

RSC Advances ◽  
2016 ◽  
Vol 6 (61) ◽  
pp. 56421-56428 ◽  
Author(s):  
Vivek Sharma ◽  
Santimoy Khilari ◽  
Debabrata Pradhan ◽  
Paritosh Mohanty

High surface area hypercrosslinked polyaniline samples synthesized by solvothermal method have shown efficient performance for gas sorption and charge storage.

2017 ◽  
Vol 46 (7) ◽  
pp. 2122-2128 ◽  
Author(s):  
Suresh Kannan Balasingam ◽  
Minoh Lee ◽  
Byung Hoon Kim ◽  
Jae Sung Lee ◽  
Yongseok Jun

High surface area MoS2 sponge electrodes were synthesized via a facile hydrothermal method followed by a freeze drying process and showed high specific capacitance and better charge storage behavior.


RSC Advances ◽  
2016 ◽  
Vol 6 (72) ◽  
pp. 68092-68099 ◽  
Author(s):  
J. Archana ◽  
S. Harish ◽  
M. Sabarinathan ◽  
M. Navaneethan ◽  
S. Ponnusamy ◽  
...  

High surface area mesoporous anatase TiO2 spheres are synthesized using ethylene glycol as a template by a solvothermal method.


RSC Advances ◽  
2016 ◽  
Vol 6 (100) ◽  
pp. 97560-97565 ◽  
Author(s):  
Bader Ghanem ◽  
Youssef Belmabkhout ◽  
Yingge Wang ◽  
Yunfeng Zhao ◽  
Yu Han ◽  
...  

A novel 3D ultramicroporous triptycene-based polyimide framework with high surface area (1050 m2 g−1) and high CO2 sorption capacity (3.4 mmol g−1 at 273 K and 1 bar), good CO2/N2 (45) and CO2/CH4 (9.6) selectivity was synthesized and characterized.


2016 ◽  
Vol 4 (15) ◽  
pp. 5578-5591 ◽  
Author(s):  
Dattakumar Mhamane ◽  
Vanchiappan Aravindan ◽  
Myeong-Seong Kim ◽  
Hyun-Kyung Kim ◽  
Kwang Chul Roh ◽  
...  

A silica-assisted method was developed to prepare graphene-like carbon displaying excellent capacitive charge storage.


RSC Advances ◽  
2015 ◽  
Vol 5 (57) ◽  
pp. 45749-45754 ◽  
Author(s):  
Vivek Sharma ◽  
Asit Sahoo ◽  
Yogesh Sharma ◽  
Paritosh Mohanty

Microwave-assisted synthesis of high surface area (SABET = 1059 m2 g−1) nanoporous hypercrosslinked polyaniline for gas storage and supercapacitor applications.


2018 ◽  
Vol 2 (10) ◽  
pp. 2314-2324 ◽  
Author(s):  
Hao Zhang ◽  
Mingjie Lu ◽  
Huanlei Wang ◽  
Yan Lyu ◽  
Dong Li ◽  
...  

The porosity and heteroatom doping level can be tuned for jellyfish-derived carbons to adjust capacitive and pseudocapacitive contributions.


2014 ◽  
Vol 07 (06) ◽  
pp. 1440012 ◽  
Author(s):  
Mui Yen Ho ◽  
Poi Sim Khiew ◽  
Dino Isa ◽  
Wee Siong Chiu

In present study, the electrochemical performance of eco-friendly and cost-effective titanium oxide ( TiO 2)-based and zinc oxide-based nanocomposite electrodes were studied in neutral aqueous Na 2 SO 3 electrolyte, respectively. The electrochemical properties of these composite electrodes were studied using cyclic voltammetry (CV), galvanostatic charge–discharge (CD) and electrochemical impedance spectroscopy (EIS). The experimental results reveal that these two nanocomposite electrodes achieve the highest specific capacitance at fairly low oxide loading onto activated carbon (AC) electrodes, respectively. Considerable enhancement of the electrochemical properties of TiO 2/AC and ZnO /AC nanocomposite electrodes is achieved via synergistic effects contributed from the nanostructured metal oxides and the high surface area mesoporous AC. Cations and anions from metal oxides and aqueous electrolyte such as Ti 4+, Zn 2+, Na + and [Formula: see text] can occupy some pores within the high-surface-area AC electrodes, forming the electric double layer at the electrode–electrolyte interface. Additionally, both TiO 2 and ZnO nanoparticles can provide favourable surface adsorption sites for [Formula: see text] anions which subsequently facilitate the faradaic processes for pseudocapacitive effect. These two systems provide the low cost material electrodes and the low environmental impact electrolyte which offer the increased charge storage without compromising charge storage kinetics.


CrystEngComm ◽  
2015 ◽  
Vol 17 (3) ◽  
pp. 532-539 ◽  
Author(s):  
I. Spanopoulos ◽  
I. Bratsos ◽  
Ch. Tampaxis ◽  
A. Kourtellaris ◽  
A. Tasiopoulos ◽  
...  

The gas-sorption properties of a high surface area α-magnesium formate with an expanded unit cell are reported. The material is stable in NH3 and shows very high CH4/N2 (5.2) selectivity.


2015 ◽  
Vol 275 ◽  
pp. 159-166 ◽  
Author(s):  
Abdoulaye Djire ◽  
Olabode T. Ajenifujah ◽  
Alice E.S. Sleightholme ◽  
Paul Rasmussen ◽  
Levi T. Thompson

Author(s):  
Kailun Yang ◽  
Recep Kas ◽  
Wilson A. Smith

<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>


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