Fast microwave-induced synthesis of solid cobalt hydroxide nanorods and their thermal conversion into porous cobalt oxide nanorods for efficient oxygen evolution reaction

2019 ◽  
Vol 3 (7) ◽  
pp. 1713-1719 ◽  
Author(s):  
Dattatray S. Dhawale ◽  
Pradnya Bodhankar ◽  
Neharani Sonawane ◽  
Pradip B. Sarawade

Oxygen evolution reaction (OER) in water splitting is one of the most critical and more demanding half-reactions in electrochemical devices; therefore, the design of highly efficient and nonprecious metal-based electrocatalysts is required.

Nanomaterials ◽  
2021 ◽  
Vol 11 (3) ◽  
pp. 657
Author(s):  
Geul Han Kim ◽  
Yoo Sei Park ◽  
Juchan Yang ◽  
Myeong Je Jang ◽  
Jaehoon Jeong ◽  
...  

Developing high performance, highly stable, and low-cost electrodes for the oxygen evolution reaction (OER) is challenging in water electrolysis technology. However, Ir- and Ru-based OER catalysts with high OER efficiency are difficult to commercialize as precious metal-based catalysts. Therefore, the study of OER catalysts, which are replaced by non-precious metals and have high activity and stability, are necessary. In this study, a copper–cobalt oxide nanosheet (CCO) electrode was synthesized by the electrodeposition of copper–cobalt hydroxide (CCOH) on Ni foam followed by annealing. The CCOH was annealed at various temperatures, and the structure changed to that of CCO at temperatures above 250 °C. In addition, it was observed that the nanosheets agglomerated when annealed at 300 °C. The CCO electrode annealed at 250 °C had a high surface area and efficient electron conduction pathways as a result of the direct growth on the Ni foam. Thus, the prepared CCO electrode exhibited enhanced OER activity (1.6 V at 261 mA/cm2) compared to those of CCOH (1.6 V at 144 mA/cm2), Co3O4 (1.6 V at 39 mA/cm2), and commercial IrO2 (1.6 V at 14 mA/cm2) electrodes. The optimized catalyst also showed high activity and stability under high pH conditions, demonstrating its potential as a low cost, highly efficient OER electrode material.


2018 ◽  
Vol 6 (7) ◽  
pp. 3224-3230 ◽  
Author(s):  
Li-Ming Cao ◽  
Jia-Wei Wang ◽  
Di-Chang Zhong ◽  
Tong-Bu Lu

The development of readily available, highly efficient and stable electrocatalysts for the oxygen evolution reaction (OER) is extremely significant to facilitate water splitting for the generation of clean hydrogen energy.


2017 ◽  
Vol 10 (1) ◽  
pp. 121-128 ◽  
Author(s):  
Baicheng Weng ◽  
Fenghua Xu ◽  
Changlei Wang ◽  
Weiwei Meng ◽  
Corey R. Grice ◽  
...  

Novel layered Na1−xNiyFe1−yO2OER catalysts outperform IrO2, RuO2, and NiFe-LDH, reaching an 11.22% solar/H2efficiency for a perovskite solar cell.


2019 ◽  
Vol 7 (13) ◽  
pp. 7636-7643 ◽  
Author(s):  
Qin Wang ◽  
Hongyang Zhao ◽  
Fumin Li ◽  
Wenyan She ◽  
Xiaoming Wang ◽  
...  

It was found that Mo-doped Ni2P hollow nanostructures display excellent hydrogen evolution reaction and oxygen evolution reaction performance.


Polymers ◽  
2019 ◽  
Vol 11 (8) ◽  
pp. 1268 ◽  
Author(s):  
Fangfang Zhang ◽  
Minchen Yang ◽  
Siyi Zhang ◽  
Pengfei Fang

Improving the electrocatalytic performance of oxygen evolution reaction (OER) is essential for oxygen-involved electrochemical devices, including water splitting and rechargeable metal–air batteries. In this work, we report that the OER performance of commercial catalysts of IrO2, Co3O4, and Pt-C can be improved by replacing the traditional Nafion® ionomer with newly synthesized copolymers consisting of protonated imidazolium moieties such as ion conductors and binders in electrodes. Specifically, such an improvement in OER performance for all the tested catalysts is more significant in basic and neutral environments than that under acidic conditions. We anticipate that the results will provide new ideas for the conceptual design of electrodes for oxygen-involved electrochemical devices.


2015 ◽  
Vol 3 (18) ◽  
pp. 9707-9713 ◽  
Author(s):  
Xiaomin Liu ◽  
Jing Jiang ◽  
Lunhong Ai

CoC2O4·2H2O microstructures as nonprecious metal-based electrocatalysts exhibited remarkable activity for catalyzing OER in alkaline medium.


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