Towards high-efficiency nanoelectrocatalysts for oxygen reduction through engineering advanced carbon nanomaterials

2016 ◽  
Vol 45 (5) ◽  
pp. 1273-1307 ◽  
Author(s):  
Ming Zhou ◽  
Hsing-Lin Wang ◽  
Shaojun Guo

We summarize and discuss recent developments of different-dimensional advanced carbon nanomaterial-based noble-metal-free high-efficiency oxygen reduction electrocatalysts, including heteroatom-doped, transition metal-based nanoparticle-based, and especially iron carbide (Fe3C)-based carbon nanomaterial composites.

2016 ◽  
Vol 7 (7) ◽  
pp. 4167-4173 ◽  
Author(s):  
Wenling Gu ◽  
Liuyong Hu ◽  
Wei Hong ◽  
Xiaofang Jia ◽  
Jing Li ◽  
...  

A high-efficiency noble-metal-free oxygen reduction reaction (ORR) catalyst was obtained based on the pyrolysis of the inexpensive precursor cobalt dithiolene (an S4-chelate complex) on simultaneously reduced graphene oxide (GO) as a support matrix.


RSC Advances ◽  
2016 ◽  
Vol 6 (112) ◽  
pp. 110820-110830 ◽  
Author(s):  
Juanhong Xue ◽  
Ling Zhao ◽  
Zhiyu Dou ◽  
Yan Yang ◽  
Yue Guan ◽  
...  

Functionalized 3D porous carbons comprising encased iron carbide species, derived from a MOF, display outstanding ORR performance in both acidic and alkaline solutions.


2014 ◽  
Vol 271 ◽  
pp. 522-529 ◽  
Author(s):  
Jian Zhang ◽  
Siyu Wu ◽  
Xu Chen ◽  
Mu Pan ◽  
Shichun Mu

2019 ◽  
Vol 44 (45) ◽  
pp. 24922-24933 ◽  
Author(s):  
Sagar B. Ingavale ◽  
Indrajit Patil ◽  
Haridas Parse ◽  
Divya Catherin Sesu ◽  
Phiralang Marbaniang ◽  
...  

2020 ◽  
Vol 26 (67) ◽  
pp. 15397-15415 ◽  
Author(s):  
Ioanna K. Sideri ◽  
Nikos Tagmatarchis

Synlett ◽  
2018 ◽  
Vol 29 (05) ◽  
pp. 548-555 ◽  
Author(s):  
Liang-Nian He ◽  
Xiao-Fang Liu ◽  
Xiao-Ya Li ◽  
Chang Qiao

Reductive functionalization of CO2 with amines and a reductant, which combines both reduction of CO2 and C–N bond formation in one pot to produce versatile chemicals and energy-storage materials such as formamides, aminals, and methylamines that are usually derived from petroleum feedstock, would be appealing and promising. Herein, we give a brief review on recent developments in the titled CO2 chemistry by employing transition-metal-free catalysis, which can be catalogued as below according to the diversified energy content of the products, that is formamides, aminals, and methylamines being consistent with 2-, 4-, and 6-electron reduction of CO2, respectively. Notably, hierarchical reduction of CO2 with amines to afford at least two products, for example, formamides and methylamines, could be realized with the same catalyst through tuning the hydrosilane type, reaction temperature, or CO2 pressure. Finally, the opportunities and challenges of the reductive functionalization of CO2 with amines are also highlighted.1 Introduction2 2-Electron Reduction of CO2 to Formamide3 6-Electron Reduction of CO2 to Methylamine4 4-Electron Reduction of CO2 to Aminal5 Hierarchical Reduction of CO2 with Amines6 Conclusion


2017 ◽  
Vol 5 (5) ◽  
pp. 1930-1934 ◽  
Author(s):  
Daping He ◽  
Yuli Xiong ◽  
Jinlong Yang ◽  
Xu Chen ◽  
Zhaoxiang Deng ◽  
...  

A highly active bifunctional electrocatalyst for oxygen reduction and evolution reactions was developed based on nanocarbon-intercalated and Fe–N-codoped graphene materials.


2015 ◽  
Vol 1 (1) ◽  
pp. e1400129 ◽  
Author(s):  
Jianglan Shui ◽  
Min Wang ◽  
Feng Du ◽  
Liming Dai

The availability of low-cost, efficient, and durable catalysts for oxygen reduction reaction (ORR) is a prerequisite for commercialization of the fuel cell technology. Along with intensive research efforts of more than half a century in developing nonprecious metal catalysts (NPMCs) to replace the expensive and scarce platinum-based catalysts, a new class of carbon-based, low-cost, metal-free ORR catalysts was demonstrated to show superior ORR performance to commercial platinum catalysts, particularly in alkaline electrolytes. However, their large-scale practical application in more popular acidic polymer electrolyte membrane (PEM) fuel cells remained elusive because they are often found to be less effective in acidic electrolytes, and no attempt has been made for a single PEM cell test. We demonstrated that rationally designed, metal-free, nitrogen-doped carbon nanotubes and their graphene composites exhibited significantly better long-term operational stabilities and comparable gravimetric power densities with respect to the best NPMC in acidic PEM cells. This work represents a major breakthrough in removing the bottlenecks to translate low-cost, metal-free, carbon-based ORR catalysts to commercial reality, and opens avenues for clean energy generation from affordable and durable fuel cells.


ACS Omega ◽  
2019 ◽  
Vol 4 (1) ◽  
pp. 130-139 ◽  
Author(s):  
Tamás Varga ◽  
Lívia Vásárhelyi ◽  
Gergő Ballai ◽  
Henrik Haspel ◽  
Albert Oszkó ◽  
...  

Synlett ◽  
2020 ◽  
Author(s):  
Lei Jiao ◽  
Fei-Yu Zhou

AbstractPyridine is an important structural motif that is prevalent in natural products, drugs, and materials. Methods that functionalize and derivatize pyridines have gained significant attention. Recently, a large number of transition-metal-free reactions have been developed. In this review, we provide a brief summary of recent advances in transition-metal-free functionalization and derivatization reactions of pyridines, categorized according to their reaction modes.1 Introduction2 Metalated Pyridines as Nucleophiles2.1 Deprotonation2.2 Halogen–Metal exchange3 Activated Pyridines as Electrophiles3.1 Asymmetric 2-Allylation by Chiral Phosphite Catalysis3.2 Activation of Pyridines by a Bifunctional Activating Group3.3 Alkylation of Pyridines by 1,2-Migration3.4 Alkylation of Pyridines by [3+2] Addition3.5 Pyridine Derivatization by Catalytic In Situ Activation Strategies3.6 Reactions via Heterocyclic Phosphonium Salts4 Radical Reactions for Pyridine Functionalization4.1 Pyridine Functionalization through Radical Addition Reactions4.2 Pyridine Functionalization through Radical–Radical Coupling Reactions5 Derivatization of Pyridines through the Formation of Meisenheimer-Type Pyridyl Anions6 Conclusion


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