Synergistically enhanced oxygen reduction reaction composites of specific surface area and manganese valence controlled α-MnO2 nanotube decorated by silver nanoparticles in Al-air batteries

2019 ◽  
Vol 305 ◽  
pp. 360-369 ◽  
Author(s):  
Binbin Xu ◽  
Huimin Lu ◽  
Wei Cai ◽  
Yuan Cao ◽  
Yan Deng ◽  
...  
2020 ◽  
Vol 44 (18) ◽  
pp. 7417-7423
Author(s):  
Jiannan Cai ◽  
Xiaofeng Zhang ◽  
Yi Zhang ◽  
Mingxing Yang ◽  
Baohua Huang ◽  
...  

The enhanced electrocatalytic properties of rGO/TiO2NTs for the ORR are a result of increased specific surface area, number of active sites and accelerated electron conductivity.


Catalysts ◽  
2021 ◽  
Vol 11 (11) ◽  
pp. 1354
Author(s):  
Vera Bogdanovskaya ◽  
Inna Vernigor ◽  
Marina Radina ◽  
Vladimir Sobolev ◽  
Vladimir Andreev ◽  
...  

In order to develop highly efficient and stable catalysts for oxygen reduction reaction (ORR) that do not contain precious metals, it is necessary to modify carbon nanotubes (CNT) and define the effect of the modification on their activity in the ORR. In this work, the modification of CNTs included functionalization by treatment in NaOH or HNO3 (soft and hard conditions, respectively) and subsequent doping with nitrogen (melamine was used as a precursor). The main parameters that determine the efficiency of modified CNT in ORR are composition and surface area (XPS, BET), hydrophilic–hydrophobic surface properties (method of standard contact porosimetry (MSP)) and zeta potential (dynamic light scattering method). The activity of CNT in ORR was assessed following half-wave potential, current density within kinetic potential range and the electrochemically active surface area (SEAS). The obtained results show that the modification of CNT with oxygen-containing groups leads to an increase in hydrophilicity and, consequently, SEAS, as well as the total (overall) current. Subsequent doping with nitrogen ensures further increase in SEAS, higher zeta potential and specific activity in ORR, reflected in the shift of the half-wave potential by 150 mV for CNTNaOH-N and 110 mV for CNTHNO3-N relative to CNTNaOH and CNTHNO3, respectively. Moreover, the introduction of N into the structure of CNTHNO3 increases their corrosion stability.


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