Spontaneous power source in ambient air of a well-directionally reduced graphene oxide bulk

2018 ◽  
Vol 11 (10) ◽  
pp. 2839-2845 ◽  
Author(s):  
Huhu Cheng ◽  
Yaxin Huang ◽  
Fei Zhao ◽  
Ce Yang ◽  
Panpan Zhang ◽  
...  

Spontaneous electric generation (voltage up to 450 mV) in ambient atmosphere has been achieved on a functional groups-reconfigured graphene oxide membrane.

Nanomaterials ◽  
2021 ◽  
Vol 11 (3) ◽  
pp. 623
Author(s):  
Monika Gupta ◽  
Huzein Fahmi Hawari ◽  
Pradeep Kumar ◽  
Zainal Arif Burhanudin ◽  
Nelson Tansu

The demand for carbon dioxide (CO2) gas detection is increasing nowadays. However, its fast detection at room temperature (RT) is a major challenge. Graphene is found to be the most promising sensing material for RT detection, owing to its high surface area and electrical conductivity. In this work, we report a highly edge functionalized chemically synthesized reduced graphene oxide (rGO) thin films to achieve fast sensing response for CO2 gas at room temperature. The high amount of edge functional groups is prominent for the sorption of CO2 molecules. Initially, rGO is synthesized by reduction of GO using ascorbic acid (AA) as a reducing agent. Three different concentrations of rGO are prepared using three AA concentrations (25, 50, and 100 mg) to optimize the material properties such as functional groups and conductivity. Thin films of three different AA reduced rGO suspensions (AArGO25, AArGO50, AArGO100) are developed and later analyzed using standard FTIR, XRD, Raman, XPS, TEM, SEM, and four-point probe measurement techniques. We find that the highest edge functionality is achieved by the AArGO25 sample with a conductivity of ~1389 S/cm. The functionalized AArGO25 gas sensor shows recordable high sensing properties (response and recovery time) with good repeatability for CO2 at room temperature at 500 ppm and 50 ppm. Short response and recovery time of ~26 s and ~10 s, respectively, are achieved for 500 ppm CO2 gas with the sensitivity of ~50 Hz/µg. We believe that a highly functionalized AArGO CO2 gas sensor could be applicable for enhanced oil recovery, industrial and domestic safety applications.


2020 ◽  
Vol 44 (44) ◽  
pp. 19022-19027
Author(s):  
Zegao Wang ◽  
Yuqing Wang ◽  
Xin Hao ◽  
Jingbo Liu ◽  
Yuanfu Chen ◽  
...  

Through tuning the oxygen function groups, it was demonstrated that the specific capacitance of reduced graphene oxide can increase from 136 F g−1 to 182 F g−1.


Solar Energy ◽  
2019 ◽  
Vol 194 ◽  
pp. 415-430 ◽  
Author(s):  
Gong Cheng ◽  
Xinzhi Wang ◽  
Xing Liu ◽  
Yurong He ◽  
Boris V. Balakin

RSC Advances ◽  
2016 ◽  
Vol 6 (57) ◽  
pp. 52339-52346 ◽  
Author(s):  
X. Wang ◽  
X. Li ◽  
Y. Zhao ◽  
Y. Chen ◽  
J. Yu ◽  
...  

Three methods were used to prepare reduced graphene oxide (rGO) with various ratios of oxygen functional groups, such as –OOH, –OH and CO, to study their effects on the NO2 sensing properties at room temperature.


2016 ◽  
Vol 34 (3) ◽  
pp. 481-486 ◽  
Author(s):  
Łukasz Majchrzycki ◽  
Mariusz Walkowiak ◽  
Agnieszka Martyła ◽  
Mikhail Y. Yablokov ◽  
Marek Nowicki ◽  
...  

AbstractNowadays reduced graphene oxide (rGO) is regarded as a highly interesting material which is appropriate for possible applications in electrochemistry, especially in lithium-ion batteries (LIBs). Several methods were proposed for the preparation of rGO-based electrodes, resulting in high-capacity LIBs anodes. However, the mechanism of lithium storage in rGO and related materials is still not well understood. In this work we focused on the proposed mechanism of favorable bonding sites induced by additional functionalities attached to the graphene planes. This mechanism might increase the capacity of electrodes. In order to verify this hypothesis the composite of non-reduced graphene oxide (GO) with multiwalled carbon nanotubes electrodes was fabricated. Electrochemical properties of GO composite anodes were studied in comparison with similarly prepared electrodes based on rGO. This allowed us to estimate the impact of functional groups on the reversible capacity changes. As a result, it was shown that oxygen containing functional groups of GO do not create, in noticeable way, additional active sites for the electrochemical reactions of lithium storage, contrary to what has been postulated previously.


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