Rational Design of Perovskite Oxide Nanofibers As Electrocatalysts for Oxygen Evolution Reaction

Author(s):  
Hanwen Xu ◽  
Jiawei Zhu ◽  
Pengyan Wang ◽  
Ding Chen ◽  
Chengtian Zhang ◽  
...  

Rational design and construction of high-efficiency bifunctional catalysts for hydrogen evolution reaction (HER) and oxygen evolution reaction (OER) is crucial for large-scale hydrogen production by water splitting. Herein, by a...


2021 ◽  
Vol 393 ◽  
pp. 202-206
Author(s):  
Michael John Craig ◽  
Romain Barda-Chatain ◽  
Max García-Melchor

Catalysts ◽  
2019 ◽  
Vol 9 (5) ◽  
pp. 459 ◽  
Author(s):  
Heng Luo ◽  
Hang Lei ◽  
Yufei Yuan ◽  
Yongyin Liang ◽  
Yi Qiu ◽  
...  

The rational design and development of the low-cost and effective electrocatalysts toward oxygen evolution reaction (OER) are essential in the storage and conversion of clean and renewable energy sources. Herein, a ternary copper-cobalt sulfide nanosheets electrocatalysts (denoted as CuCoS/CC) for electrochemical water oxidation has been synthesized on carbon cloth (CC) via the sulfuration of CuCo-based precursors. The obtained CuCoS/CC reveals excellent electrocatalytic performance toward OER in 1.0 M KOH. It exhibits a particularly low overpotential of 276 mV at current density of 10 mA cm−2, and a small Tafel slope (58 mV decade−1), which is superior to the current commercialized noble-metal electrocatalysts, such as IrO2. Benefiting from the synergistic effect of Cu and Co atoms and sulfidation, electrons transport and ions diffusion are significantly enhanced with the increase of active sites, thus the kinetic process of OER reaction is boosted. Our studies will serve as guidelines in the innovative design of non-noble metal electrocatalysts and their application in electrochemical water splitting


2019 ◽  
Vol 55 (17) ◽  
pp. 2445-2448 ◽  
Author(s):  
Haoran Yu ◽  
Fuqiang Chu ◽  
Xiao Zhou ◽  
Junling Ji ◽  
Yang Liu ◽  
...  

A porous perovskite oxide is fabricated by an inorganic salt-template strategy, which exhibits remarkable performance for the oxygen evolution reaction.


ACS Catalysis ◽  
2015 ◽  
Vol 5 (9) ◽  
pp. 5380-5387 ◽  
Author(s):  
Oscar Diaz-Morales ◽  
Isis Ledezma-Yanez ◽  
Marc T. M. Koper ◽  
Federico Calle-Vallejo

2021 ◽  
pp. 2101632
Author(s):  
Thi Xuyen Nguyen ◽  
Yi‐Cheng Liao ◽  
Chia‐Chun Lin ◽  
Yen‐Hsun Su ◽  
Jyh‐Ming Ting

2019 ◽  
Author(s):  
Denis Kuznetsov ◽  
Jiayu Peng ◽  
Livia Giordano ◽  
Yuriy Román-Leshkov ◽  
Yang Shao-Horn

In this study, we employ the strategy of substitution with more electronegative/acidic A-site ions in the cobalt perovskites to alter O 2p-band center, surface hydroxide affinity, and oxygen evolution reaction (OER) activity and stability in the basic electrolyte. Galvanostatically charged Bi<sub>0.2</sub>Sr<sub>0.8</sub>CoO<sub>3-δ</sub> (δ close to zero) was shown to exhibit record OER specific activity exceeding not only La<sub>x</sub>Sr<sub>1-x</sub>CoO<sub>3-δ</sub> but also charged SrCoO<sub>3-δ</sub> (δ close to zero), one of the most active oxide OER catalysts reported so far. The enhanced OER activity of charged Bi<sub>0.2</sub>Sr<sub>0.8</sub>CoO<sub>3-δ</sub> can be attributed to greater hydroxide affinity facilitating the deprotonation of surface bound intermediates due to the presence of strong Lewis acidic A-site Bi<sup>3+</sup> ions, while the high stability can result from lowered O 2p-band center relative to the Fermi level. This work provides a novel example in the rational design of highly active oxide catalysts for OER by leveraging the inductive effect.


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