Revealing the structural transformation of rutile RuO2via in situ X-ray absorption spectroscopy during the oxygen evolution reaction

2019 ◽  
Vol 48 (21) ◽  
pp. 7122-7129 ◽  
Author(s):  
Chia-Jui Chang ◽  
You-Chiuan Chu ◽  
Hao-Yu Yan ◽  
Yen-Fa Liao ◽  
Hao Ming Chen
Keyword(s):  
Oxygen Evolution ◽  
Structural Transformation ◽  
Absorption Spectroscopy ◽  
Oxygen Evolution Reaction ◽  
The State ◽  
X Ray ◽  
Alkaline Conditions ◽  
X Ray Absorption ◽  
State Of Art

The state-of-art RuO2 catalyst for the oxygen evolution reaction (OER) is measured by using in situ X-ray absorption spectroscopy (XAS) to elucidate the structural transformation during catalyzing the reaction in acidic and alkaline conditions.

scholarly journals Redox Processes of Manganese Oxide in Catalyzing Oxygen Evolution and Reduction: An in Situ Soft X-ray Absorption Spectroscopy Study

2017 ◽  
Vol 121 (33) ◽  
pp. 17682-17692 ◽  
Author(s):  
Marcel Risch ◽  
Kelsey A. Stoerzinger ◽  
Binghong Han ◽  
Tom Z. Regier ◽  
Derek Peak ◽  
...  
Keyword(s):  
Manganese Oxide ◽  
Oxygen Evolution ◽  
Absorption Spectroscopy ◽  
Redox Processes ◽  
Spectroscopy Study ◽  
X Ray ◽  
X Ray Absorption

scholarly journals A Cobalt-Iron Double-Atom Catalyst for the Oxygen Evolution Reaction

2019 ◽  
Author(s):  
Lichen Bai ◽  
Chia-Shuo Hsu ◽  
Duncan Alexander ◽  
Hao Ming Chen ◽  
Xile Hu
Keyword(s):  
Oxygen Evolution ◽  
Active Site ◽  
Oxygen Evolution Reaction ◽  
Active Sites ◽  
Single Atom ◽  
X Ray ◽  
Highly Active ◽  
Cobalt Iron ◽  
X Ray Absorption

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.

Photoexcited Hole Transfer to a MnOxCocatalyst on a SrTiO3Photoelectrode during Oxygen Evolution Studied by In Situ X-ray Absorption Spectroscopy

2014 ◽  
Vol 118 (42) ◽  
pp. 24302-24309 ◽  
Author(s):  
Masaaki Yoshida ◽  
Takumi Yomogida ◽  
Takehiro Mineo ◽  
Kiyofumi Nitta ◽  
Kazuo Kato ◽  
...  
Keyword(s):  
Oxygen Evolution ◽  
Absorption Spectroscopy ◽  
Hole Transfer ◽  
X Ray ◽  
X Ray Absorption

scholarly journals In Situ Observations of Oxygen Evolution Cocatalysts on Photoelectrodes by X-ray Absorption Spectroscopy: Comparison between Cobalt-Phosphate and Cobalt-Borate

2016 ◽  
Vol 84 (10) ◽  
pp. 779-783 ◽  
Author(s):  
Hirokatsu KUROSU ◽  
Masaaki YOSHIDA ◽  
Yosuke MITSUTOMI ◽  
Sho ONISHI ◽  
Hitoshi ABE ◽  
...  
Keyword(s):  
Oxygen Evolution ◽  
Absorption Spectroscopy ◽  
X Ray ◽  
In Situ Observations ◽  
Cobalt Phosphate ◽  
X Ray Absorption

scholarly journals A Cobalt-Iron Double-Atom Catalyst for the Oxygen Evolution Reaction

2019 ◽  
Author(s):  
Lichen Bai ◽  
Chia-Shuo Hsu ◽  
Duncan Alexander ◽  
Hao Ming Chen ◽  
Xile Hu
Keyword(s):  
Oxygen Evolution ◽  
Active Site ◽  
Oxygen Evolution Reaction ◽  
Active Sites ◽  
Single Atom ◽  
X Ray ◽  
Highly Active ◽  
Cobalt Iron ◽  
X Ray Absorption

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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