Functionalization of 0-D and 2-D Carbon Nitride Nanostructures on Bio-Derived Carbon spheres for Sustainable Electrochemical Supercapacitors

2021 ◽  
pp. 115808
Author(s):  
N. Ramesh Reddy ◽  
Arghya Narayan Banerjee ◽  
P. Mohan Reddy ◽  
Sang Woo Joo
Keyword(s):  
Carbon Nitride ◽  
Electrochemical Supercapacitors ◽  
Carbon Spheres

Nitrogen-enriched carbon spheres coupled with graphitic carbon nitride nanosheets for high performance supercapacitors

2018 ◽  
Vol 47 (29) ◽  
pp. 9724-9732 ◽  
Author(s):  
Jun Zhu ◽  
Lirong Kong ◽  
Xiaoping Shen ◽  
Hu Zhou ◽  
Guoxing Zhu ◽  
...  
Keyword(s):  
Electrochemical Performance ◽  
High Performance ◽  
Carbon Nitride ◽  
Clean Energy ◽  
Carbon Spheres ◽  
Energy Storage Devices ◽  
Step Method ◽  
Storage Devices ◽  
Excellent Electrochemical Performance ◽  
Carbon Nitride Nanosheets

A facile two-step method is proposed to synthesize g-CN/NCS composites, which exhibit an excellent electrochemical performance in clean energy storage devices.

Size dependence of uniformed carbon spheres in promoting graphitic carbon nitride toward enhanced photocatalysis

2017 ◽  
Vol 204 ◽  
pp. 358-364 ◽  
Author(s):  
Shizhen Liu ◽  
Jun Ke ◽  
Hongqi Sun ◽  
Jian Liu ◽  
Moses O. Tade ◽  
...  
Keyword(s):  
Carbon Nitride ◽  
Size Dependence ◽  
Graphitic Carbon ◽  
Graphitic Carbon Nitride ◽  
Carbon Spheres

Preparation and characterization of thin films of carbon nitride

1995 ◽  
Vol 53 ◽  
pp. 104-105
Author(s):  
L. Wan ◽  
R. F. Egerton
Keyword(s):  
Carbon Nitride ◽  
Arc Discharge ◽  
Ion Beam ◽  
Chemical Vapor ◽  
Reactive Sputtering ◽  
Vacuum Arc ◽  
Specimen Preparation ◽  
Bonding Structure ◽  
Electron Energy Loss

INTRODUCTION Recently, a new compound carbon nitride (CNx) has captured the attention of materials scientists, resulting from the prediction of a metastable crystal structure β-C3N4. Calculations showed that the mechanical properties of β-C3N4 are close to those of diamond. Various methods, including high pressure synthesis, ion beam deposition, chemical vapor deposition, plasma enhanced evaporation, and reactive sputtering, have been used in an attempt to make this compound. In this paper, we present the results of electron energy loss spectroscopy (EELS) analysis of composition and bonding structure of CNX films deposited by two different methods.SPECIMEN PREPARATION Specimens were prepared by arc-discharge evaporation and reactive sputtering. The apparatus for evaporation is similar to the traditional setup of vacuum arc-discharge evaporation, but working in a 0.05 torr ambient of nitrogen or ammonia. A bias was applied between the carbon source and the substrate in order to generate more ions and electrons and change their energy. During deposition, this bias causes a secondary discharge between the source and the substrate.

Enhanced catalytic activity of low-Pt content nanocatalysts supported on hollow carbon spheres for the ORR in alkaline media

MRS Advances ◽  
2020 ◽  
Vol 5 (57-58) ◽  
pp. 2961-2972
Author(s):  
P.C. Meléndez-González ◽  
E. Garza-Duran ◽  
J.C. Martínez-Loyola ◽  
P. Quintana-Owen ◽  
I.L. Alonso-Lemus ◽  
...  
Keyword(s):  
Catalytic Activity ◽  
Anion Exchange ◽  
Average Particle Size ◽  
Synthesis Method ◽  
Alkaline Media ◽  
High Catalytic Activity ◽  
Average Particle ◽  
Carbon Spheres ◽  
Hollow Carbon ◽  
Hollow Carbon Spheres

In this work, low-Pt content nanocatalysts (≈ 5 wt. %) supported on Hollow Carbon Spheres (HCS) were synthesized by two routes: i) colloidal conventional polyol, and ii) surfactant-free Bromide Anion Exchange (BAE). The nanocatalysts were labelled as Pt/HCS-P and Pt/HCS-B for polyol and BAE, respectively. The physicochemical characterization of the nanocatalysts showed that by following both methods, a good control of chemical composition was achieved, obtaining in addition well dispersed nanoparticles of less than 3 nm TEM average particle size (d) on the HCS. Pt/HCS-B contained more Pt0 species than Pt/HCS-P, an effect of the synthesis method. In addition, the structure of the HCS remains more ordered after BAE synthesis, compared to polyol. Regarding the catalytic activity for the Oxygen Reduction Reaction (ORR) in 0.5 M KOH, Pt/HCS-P and Pt/HCS-B showed a similar performance in terms of current density (j) at 0.9 V vs. RHE than the benchmark commercial 20 wt. % Pt/C. However, Pt/HCS-P and Pt/HCS-B demonstrated a 6 and 5-fold increase in mass catalytic activity compared to Pt/C, respectively. A positive effect of the high specific surface area of the HCS and its interactions with metal nanoparticles and electrolyte, which promoted the mass transfer, increased the performance of Pt/HCS-P and Pt/HCS-B. The high catalytic activity showed by Pt/HCS-B and Pt/HCS-P for the ORR, even with a low-Pt content, make them promising cathode nanocatalysts for Anion Exchange Membrane Fuel Cells (AEMFC).

Dissolution and Performing Homogeneous Photocatalysis of Polymeric Carbon Nitride

2018 ◽  
Author(s):  
Chaofeng Huang ◽  
Jing Wen ◽  
Yanfei Shen ◽  
Fei He ◽  
Li Mi ◽  
...  
Keyword(s):  
Conjugated Polymer ◽  
Carbon Nitride ◽  
Heterogeneous Catalysts ◽  
Methane Sulfonic Acid ◽  
Environment Friendly ◽  
The Poor ◽  
Catalytic Sites ◽  
Homogeneous Photocatalysis ◽  
Polymeric Carbon ◽  
First Time

<a></a><a>As a metal-free conjugated polymer, carbon nitride (CN) has attracted tremendous attention as heterogeneous (photo)catalysts. </a><a></a><a>By following prototype of enzymes, making all catalytic sites of accessible via homogeneous reactions is a promising approach toward maximizing CN activity, but hindered due to </a><a></a><a>the poor insolubility of CN</a>. Herein, we report the dissolution of CN in environment-friendly methane sulfonic acid and the homogeneous photocatalysis driven by CN for the first time with the activity boosted up to 10-times, comparing to the heterogeneous counterparts. Moreover, facile recycling and reusability, the <a>hallmark</a> of heterogeneous catalysts, were kept for the homogeneous CN photocatalyst via reversible precipitation using poor solvents. It opens new vista of CN in homogeneous catalysis and offers a successful example of polymeric catalysts in bridging gaps of homo/heterogeneous catalysis.

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