Confined heat treatment of a Prussian blue analogue for enhanced electrocatalytic oxygen evolution

2018 ◽  
Vol 6 (33) ◽  
pp. 15942-15946 ◽  
Author(s):  
Yanhua Zeng ◽  
Gao-Feng Chen ◽  
Zhouyang Jiang ◽  
Liang-Xin Ding ◽  
Suqing Wang ◽  
...  

A simple and feasible in situ synthesis and surface optimization strategy to enable the Ni-based Prussian blue analogue (NiFeII-PBA) with excellent electrocatalytic oxygen evolution performance by boosting its electron transport and the exposure of active sites.

Nano Letters ◽  
2021 ◽  
Vol 21 (7) ◽  
pp. 3016-3025
Author(s):  
Guangxun Zhang ◽  
Yanle Li ◽  
Xiao Xiao ◽  
Yang Shan ◽  
Yang Bai ◽  
...  

Nanoscale ◽  
2020 ◽  
Vol 12 (27) ◽  
pp. 14514-14523 ◽  
Author(s):  
Jiamin Huo ◽  
Ying Wang ◽  
Liting Yan ◽  
Yingying Xue ◽  
Shuni Li ◽  
...  

Design an in-situ semi-transformation strategy for the development of Fe-Ni LDH/MOF hierarchical architecture exhibiting large accessible surface, open electron transport channel and multiple active sites to promote the electrocatalytic capacity.


2018 ◽  
Vol 6 (22) ◽  
pp. 10304-10312 ◽  
Author(s):  
Ziliang Chen ◽  
Renbing Wu ◽  
Miao Liu ◽  
Yang Liu ◽  
Shuangyu Xu ◽  
...  

Construction of nanocomposites with tunable coupling effects to obtain the synergetic effects and optimal performance has been realized through annealing a Prussian blue analogue at controlled temperatures.


2019 ◽  
Author(s):  
Lichen Bai ◽  
Chia-Shuo Hsu ◽  
Duncan Alexander ◽  
Hao Ming Chen ◽  
Xile Hu

Single atom catalysts exhibit well-defined active sites and potentially maximum atomic efficiency. However, they are unsuitable for reactions that benefit from bimetallic promotion such as the oxygen evolution reaction (OER) in alkaline medium. Here we show that a single atom Co precatalyst can be in-situ transformed into a Co-Fe double atom catalyst for OER. This catalyst exhibits one of the highest turnover frequencies among metal oxides. Electrochemical, microscopic, and spectroscopic data including those from operando X-ray absorption spectroscopy, reveal a dimeric Co-Fe moiety as the active site of the catalyst. This work demonstrates double-atom catalysis as a promising approach for the developed of defined and highly active OER catalysts.


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