The Role of Nitrogen and Sulfur Dual Coordination of Cobalt in Co-N4−xSx/C Single-Atom Catalysts in Oxygen Reduction Reaction

Author(s):  
Asnake Sahele Haile ◽  
Heine Anton Hansen ◽  
Weldegebriel Yohannes ◽  
Yedilfana Setarge Mekonnen

Single-atom catalysts (SACs) have been considered as a potential candidate for fuel cell application due to the fact that they exhibited good oxygen reduction reaction (ORR) activity. In this study,...

2019 ◽  
Vol 7 (45) ◽  
pp. 26062-26070 ◽  
Author(s):  
Qiong Peng ◽  
Jian Zhou ◽  
Jiatian Chen ◽  
Tian Zhang ◽  
Zhimei Sun

MXene supported single-atom catalysts catalyze the oxygen reduction reaction in a proton exchange membrane fuel cell.


2018 ◽  
Vol 115 (26) ◽  
pp. 6626-6631 ◽  
Author(s):  
Liu Yang ◽  
Daojian Cheng ◽  
Haoxiang Xu ◽  
Xiaofei Zeng ◽  
Xin Wan ◽  
...  

It is still a grand challenge to develop a highly efficient nonprecious-metal electrocatalyst to replace the Pt-based catalysts for oxygen reduction reaction (ORR). Here, we propose a surfactant-assisted method to synthesize single-atom iron catalysts (SA-Fe/NG). The half-wave potential of SA-Fe/NG is only 30 mV less than 20% Pt/C in acidic medium, while it is 30 mV superior to 20% Pt/C in alkaline medium. Moreover, SA-Fe/NG shows extremely high stability with only 12 mV and 15 mV negative shifts after 5,000 cycles in acidic and alkaline media, respectively. Impressively, the SA-Fe/NG-based acidic proton exchange membrane fuel cell (PEMFC) exhibits a high power density of 823 mW cm−2. Combining experimental results and density-functional theory (DFT) calculations, we further reveal that the origin of high-ORR activity of SA-Fe/NG is from the Fe-pyrrolic-N species, because such molecular incorporation is the key, leading to the active site increase in an order of magnitude which successfully clarifies the bottleneck puzzle of why a small amount of iron in the SA-Fe catalysts can exhibit extremely superior ORR activity.


Author(s):  
Hee Soo Kim ◽  
CHI HO LEE ◽  
Jue-Hyukk Jang ◽  
Min Seok Kang ◽  
Haneul Jin ◽  
...  

Development of non Pt-based catalysts (non-PBCs) that show excellent oxygen reduction reaction (ORR) activity for high-performance Zn-air battery (ZAB) and anion exchange membrane fuel cell (AEMFC) is highly necessitated. Here,...


Polymers ◽  
2018 ◽  
Vol 10 (9) ◽  
pp. 1002 ◽  
Author(s):  
Sait Elmas ◽  
Wesley Beelders ◽  
Xun Pan ◽  
Thomas Nann

The oxygen reduction reaction (ORR) is still the most research-intensive aspect of a fuel cell. The sluggish kinetics of the electrocatalysts toward the ORR requires large amounts of platinum to be used as cathode material, which calls for alternatives to replace or minimize the amount of the noble metals used. This study describes the synthesis and complete characterization of a copper metallopolymer (Cu MP) based on a conducting polymer (CP) and single-site catalytic centers for the electrocatalytic ORR. The copper (II) catalyst, embedded in a redox-active and conducting polymeric environment, was pursued as a potential candidate to replace noble metals in fuel cell applications. Performance studies at a rotating disk electrode (RDE) showed that the metallopolymer exhibited a direct four-electron reduction at potentials between −150 and −350 mV vs. the reversible hydrogen electrode (RHE) and high kinetic current densities of over 22.62 mA/cm2. The kinetic current densities obtained at the Cu MP electrode outperformed most of the reported state-of-the art electrocatalysts toward the ORR. Further analysis of the Cu/CP hybrid revealed the copper being largely reduced to the oxidation state +I.


Author(s):  
Xiaoyang Cheng ◽  
Jian Yang ◽  
Wei Yan ◽  
Yu Han ◽  
Ximing Qu ◽  
...  

Co single-atom (CoSA) catalysts of the CoN4 moiety usually show an unsatisfactory oxygen reduction reaction (ORR) activity due to poor O2 activation.


2020 ◽  
Vol 11 (23) ◽  
pp. 5994-5999 ◽  
Author(s):  
Huishan Shang ◽  
Zhuoli Jiang ◽  
Danni Zhou ◽  
Jiajing Pei ◽  
Yu Wang ◽  
...  

A sulfur modified Mn–N–C single atom catalyst was constructed through an atomic interface strategy, with outstanding ORR activity in alkaline media.


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