Three-dimensional structures of Mn doped CoP on flexible carbon cloth for effective oxygen evolution reaction

2017 ◽  
Vol 33 (9) ◽  
pp. 1258-1267 ◽  
Author(s):  
Jiajin Lin ◽  
Shilei Xie ◽  
Peng Liu ◽  
Min Zhang ◽  
Shoushan Wang ◽  
...  

Abstract

2016 ◽  
Vol 9 (11) ◽  
pp. 3411-3416 ◽  
Author(s):  
Muhammad-Sadeeq Balogun ◽  
Weitao Qiu ◽  
Hao Yang ◽  
Wenjie Fan ◽  
Yongchao Huang ◽  
...  

Herein, a three-dimensional monolithic and metal-free N-doped porous carbon cloth electrocatalyst was fabricated.


2021 ◽  
pp. 160388
Author(s):  
Xin Yu ◽  
Siran Xu ◽  
Xian Liu ◽  
Xiaohong Cheng ◽  
Yeshuang Du ◽  
...  

CrystEngComm ◽  
2020 ◽  
Vol 22 (23) ◽  
pp. 3984-3990 ◽  
Author(s):  
Guijin Yang ◽  
Botao Zhu ◽  
Daqiang Gao ◽  
Yujun Fu ◽  
Jing Zhao ◽  
...  

A Co3O4/MnCO3 heterojunction on NF with a unique architecture exhibits prominent OER activity and stability that is superior to most Co3O4-based catalysts.


2019 ◽  
Vol 7 (16) ◽  
pp. 9690-9697 ◽  
Author(s):  
Jie-Song Sun ◽  
Yi-Tong Zhou ◽  
Rui-Qi Yao ◽  
Hang Shi ◽  
Zi Wen ◽  
...  

Chromium-doped NiFe oxyhydroxide nanosheets that are quasi-vertically oriented on three-dimensional nanoporous gold exhibit superior catalytic activity towards the oxygen evolution reaction.


2021 ◽  
Vol 9 ◽  
Author(s):  
Yubing Yan

Developing efficient and low-cost replacements for noble metals as electrocatalysts for the oxygen evolution reaction (OER) remain a great challenge. Herein, we report a needle-like cobalt carbonate hydroxide hydrate (Co(CO3)0.5OH·0.11H2O) nanoarrays, which in situ grown on the surface of carbon cloth through a facile one-step hydrothermal method. Scanning electron microscopy (SEM) and transmission electron microscopy (TEM) characterizations demonstrate that the Co(CO3)0.5OH nanoarrays with high porosity is composed of numerous one-dimensional (1D) nanoneedles. Owing to unique needle-like array structure and abundant exposed active sites, the Co(CO3)0.5OH@CC only requires 317 mV of overpotential to reach a current density of 10 mA cm−2, which is much lower than those of Co(OH)2@CC (378 mV), CoCO3@CC (465 mV) and RuO2@CC (380 mV). For the stability, there is no significant attenuation of current density after continuous operation 27 h. This work paves a facile way to the design and construction of electrocatalysts for the OER.


2012 ◽  
Vol 22 (13) ◽  
pp. 6010 ◽  
Author(s):  
Wei Hu ◽  
Yaqin Wang ◽  
Xiaohong Hu ◽  
Yuanquan Zhou ◽  
Shengli Chen

2020 ◽  
Vol 34 (2) ◽  
pp. 353-363
Author(s):  
F. Kanwal ◽  
A. Batool ◽  
R. Akbar ◽  
S. Asim ◽  
M. Saleem

Electrochemical water splitting is the most promising pathway to produce high-purity hydrogen to alleviate global energy crisis. This reaction demands inexpensive, efficient and robust electrocatalyst for its commercial use. Herein, we demonstrate an effective, facile and scalable method for the synthesis of cerium doped Ni3Fe nanostructures as an electrocatalyst for oxygen evolution reaction (OER) by following simple chemical bath deposition route. The different molar ratios (3, 6 and 12 mM) of cerium in the chemical bath were used to study its effect on the structural and the electrochemical properties of the Ni3Fe nanostructured films. Doping of cerium contents induced variations in the morphology of deposited Ni3Fe nanostructures. The optimized electrocatalyst Ni3Fe/Ce-6 yielded high surface area catalyst nanosheets uniformly deposited on three-dimensional conductive scaffold to ensure increase in the exposure of doped Ni3Fe catalytic sites with high electrical conductivity. As a result, this earth-abundant electrocatalyst affords high OER performance with a small overpotential of 310 mV versus reversible hydrogen electrode (RHE) at 10 mA cm-2 and retains good stability up to ~ 10 h in alkaline electrolyte. This scalable strategy has great potential in future advancement of efficient and low-cost electrocatalysts for their large-scale application in energy conversion systems.                     KEY WORDS: Oxygen evolution, Electrocatalyst, Ni3Fe nanostructures, Cerium, Alkaline electrolyte   Bull. Chem. Soc. Ethiop. 2020, 34(2), 353-363 DOI: https://dx.doi.org/10.4314/bcse.v34i2.12


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