Cobalt Single Atom Incorporated in Ruthenium Oxide Sphere: A Robust Bifunctional Electrocatalyst for HER and OER

2021 ◽  
Author(s):  
Khadim Shah ◽  
Ruoyun Dai ◽  
Muhammad Mateen ◽  
Zubair Hassan ◽  
Zewen Zhuang ◽  
...  
Author(s):  
Khadim Shah ◽  
Ruoyun Dai ◽  
Muhammad Mateen ◽  
Zubair Hassan ◽  
Zewen Zhuang ◽  
...  

2020 ◽  
Author(s):  
Srikanth Pedireddy ◽  
Mahesh Kumar Ravva ◽  
Chandrani Nayak ◽  
Dalaver Anjum ◽  
Shambhu Nath Jha ◽  
...  

Single-atom metal (SA-M) catalysts with high dispersion of active metal sites allow maximum atomic utilization. However, conventional synthesis of SA-M catalysts involves high-temperature treatments, leading to a low yield with random distribution of atoms. Herein, a facile method to synthesize SA-M catalysts (M = Fe, Ir, Pt, Ru, Cu, or Pd) in a single step at ambient temperature, using the extracellular electron transfer capability of Geobacter sulfurreducens (GS), is presented. Interestingly, the SA-M is coordinated to three nitrogen (N) atoms adopting an MN3 on the surface of GS. Dry samples of SA-Ir@GS without further heat treatments show exceptionally high activity for OER when compared to benchmark IrO2 catalyst and comparable HER activity to commercial 10 wt.% Pt/C. The SA-Ir@GS electrocatalyst exhibits the best water‐splitting performance compared to other SA-M@GS, showing a low applied potential of 1.65 V to achieve 10 mA cm−2 in 1.0 M KOH solution with cycling over 5 h. The density functional calculations reveal that the large adsorption energy of H2O and moderate adsorption energies of reactants and reaction intermediates for SA-Ir@GS favorably improve its activity. This nature-based facile synthesis method of SA-M at room temperature provides a versatile platform for the preparation of other transition metal SA-M catalysts for various energy-related applications by merely altering the metal precursors. <br>


Author(s):  
Yuli Ma ◽  
Fangming Jin ◽  
Yun Hang Hu

Catalysts play a critical role in oxygen evolution reaction (OER) and oxygen reduction reaction (ORR) for energy storage, conversion, and utilization. Herein, first-principle density functional theory (DFT) calculations demonstrated that...


2021 ◽  
Vol 12 (1) ◽  
Author(s):  
Zhiqi Zhang ◽  
Jiapeng Liu ◽  
Jian Wang ◽  
Qi Wang ◽  
Yuhao Wang ◽  
...  

AbstractSingle-atom catalysts have been widely investigated for several electrocatalytic reactions except electrochemical alcohol oxidation. Herein, we synthesize atomically dispersed platinum on ruthenium oxide (Pt1/RuO2) using a simple impregnation-adsorption method. We find that Pt1/RuO2 has good electrocatalytic activity towards methanol oxidation in an alkaline media with a mass activity that is 15.3-times higher than that of commercial Pt/C (6766 vs. 441 mA mg‒1Pt). In contrast, single atom Pt on carbon black is inert. Further, the mass activity of Pt1/RuO2 is superior to that of most Pt-based catalysts previously developed. Moreover, Pt1/RuO2 has a high tolerance towards CO poisoning, resulting in excellent catalytic stability. Ab initio simulations and experiments reveal that the presence of Pt‒O3f (3-fold coordinatively bonded O)‒Rucus (coordinatively unsaturated Ru) bonds with the undercoordinated bridging O in Pt1/RuO2 favors the electrochemical dehydrogenation of methanol with lower energy barriers and onset potential than those encountered for Pt‒C and Pt‒Ru.


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