Bifunctional electrocatalysts of MOF-derived Co–N/C on bamboo-like MnO nanowires for high-performance liquid- and solid-state Zn–air batteries

2018 ◽  
Vol 6 (20) ◽  
pp. 9716-9722 ◽  
Author(s):  
Ya-Nan Chen ◽  
Yibo Guo ◽  
Huijuan Cui ◽  
Zhaojun Xie ◽  
Xin Zhang ◽  
...  

MnO@Co–N/C composites were fabricated with excellent bifunctional catalytic activity and outstanding performance for both liquid- and solid-state Zn–air batteries. The excellent electrocatalytic activities are attributed to the unique 1D nanowire structure with abundant Co–Nx active sites and a high specific surface area.

Nanomaterials ◽  
2021 ◽  
Vol 11 (12) ◽  
pp. 3429
Author(s):  
Lei Zhao ◽  
Ziwei Lan ◽  
Wenhao Mo ◽  
Junyu Su ◽  
Huazhu Liang ◽  
...  

Non-platinum carbon-based catalysts have attracted much more attention in recent years because of their low cost and outstanding performance, and are regarded as one of the most promising alternatives to precious metal catalysts. Activated carbon (AC), which has a large specific surface area (SSA), can be used as a carrier or carbon source at the same time. In this work, stable pine peel bio-based materials were used to prepare large-surface-area activated carbon and then compound with cobalt phthalocyanine (CoPc) to obtain a high-performance cobalt/nitrogen/carbon (Co-N-C) catalyst. High catalytic activity is related to increasing the number of Co particles on the large-specific-area activated carbon, which are related with the immersing effect of CoPc into the AC and the rational decomposed temperature of the CoPc ring. The synergy with N promoting the exposure of CoNx active sites is also important. The Eonset of the catalyst treated with a composite proportion of AC and CoPc of 1 to 2 at 800 °C (AC@CoPc-800-1-2) is 1.006 V, higher than the Pt/C (20 wt%) catalyst. Apart from this, compared with other AC/CoPc series catalysts and Pt/C (20 wt%) catalyst, the stability of AC/CoPc-800-1-2 is 87.8% in 0.1 M KOH after 20,000 s testing. Considering the performance and price of the catalyst in a practical application, these composite catalysts combining biomass carbon materials with phthalocyanine series could be widely used in the area of catalysts and energy storage.


2021 ◽  
Vol 45 (12) ◽  
pp. 5712-5719
Author(s):  
Yongxiang Zhang ◽  
Peifeng Yu ◽  
Mingtao Zheng ◽  
Yong Xiao ◽  
Hang Hu ◽  
...  

Porous carbons with a high specific surface area (2314–3470 m2 g−1) are prepared via a novel KCl-assisted activation strategy for high-performance supercapacitor.


2016 ◽  
Vol 6 (9) ◽  
pp. 3238-3252 ◽  
Author(s):  
Sumit Chabri ◽  
Arnab Dhara ◽  
Bibhutibhushan Show ◽  
Deepanjana Adak ◽  
Arijit Sinha ◽  
...  

Mesoporous and core–shell like (p)CuO–(n)ZnO nanocomposites were prepared using microstructural refinement and solid state reactions, which showed enhanced photochemical and electrochemical performances.


2021 ◽  
Vol 1036 ◽  
pp. 130-136
Author(s):  
Ting Qun Tan ◽  
Lei Geng ◽  
Yan Lin ◽  
Yan He

In order to prepare carbon nanotubes with high specific surface area, small diameter, low resistivity, high purity and high catalytic activity, the Fe-Mo/Al2O3 catalyst was prepared based on the microreactor. The influence of different Fe/Al molar ratios on the catalyst and the carbon nanotubes prepared was studied through BET, SEM, TEM and other detection methods. Studies have shown that the pore structure of the catalyst is dominated by slit pores at a lower Fe/Al molar ratio. The catalytic activity is the highest when the Fe/Al molar ratio is 1:1, reaching 74.1%. When the Fe/Al molar ratio is 1:2, the catalyst has a higher specific surface area, the maximum pore size is 8.63 nm, and the four-probe resistivity and ash content of the corresponding carbon nanotubes are the lowest. The higher the proportion of aluminum, the higher the specific surface area of the catalyst and the carbon nanotubes, and the finer the diameter of the carbon nanotubes, which gradually tends to relax. The results show that when the Fe/Al molar ratio is 1:2, although the catalytic activity of the catalyst is not the highest, the carbon nanotubes prepared have the best performance.


RSC Advances ◽  
2019 ◽  
Vol 9 (66) ◽  
pp. 38531-38537 ◽  
Author(s):  
Hao Kan ◽  
Min Li ◽  
Hui Li ◽  
Chong Li ◽  
Jian Zhou ◽  
...  

A high-performance QCM humidity sensor was prepared based on In2O3 QDs with a high specific surface area.


Clay Minerals ◽  
2015 ◽  
Vol 50 (2) ◽  
pp. 211-219 ◽  
Author(s):  
Bo Xue ◽  
Hongmei Guo ◽  
Lujie Liu ◽  
Min Chen

AbstractA new yttrium-zirconium-pillared montmorillonite (Y-Zr-MMT), was synthesized, characterized and used as a Ce catalyst support. The Y-Zr-MMT is a good support for dispersing cerium active sites and it is responsible for the high activity in the total oxidation of acetone, toluene and ethyl acetate. The Y-Zr-MMT shows greater advantages than the conventional alumina/cordierite honeycomb supports such as large specific surface area, lower cost and easier preparation. Catalytic tests demonstrated that Ce/Y-Zr-MMT (Ce loading 8.0%) was the most active, with the total oxidation of acetone, toluene and ethyl acetate being achieved at 220, 300 and 220°C, respectively. The catalyst displayed better activity for the oxidation of acetone and ethyl acetate than a conventional, supported Pd-catalyst under similar conditions. The special structure of the yttrium-doped zirconium-pillared montmorillonite can strengthen the interaction between the CeO2 and Zr-MMT support and improve the dispersion of the Ce particles, which enhances the catalytic activity for the oxidation of VOCs. The new catalyst, 8.0%Ce/Y-Zr-MMT, could be promising for industrial applications due to its high catalytic activity and low cost. The support and the catalysts were characterized by X-ray diffraction (XRD), transmission electron microscopy (TEM) and BET specific surface area measurements.


Author(s):  
Chenyu Liu ◽  
Haitong Wei ◽  
Yanhui Gao ◽  
Ning Wang ◽  
Xiaoying Yuan ◽  
...  

Abstract Metal-Organic Frameworks (MOFs) have unique properties and stable structure, which have been widely used as templates/precursors to prepare well-developed pore structure and high specific surface area materials. In this article, an innovative and facile method of crystal reorganization was designed by using MOFs as sacrificial templates to prepare LDH nano-layer sheet structure through a pseudomorphic conversion process under alkaline conditions. The obtained CoMn-LDH and CoFe-LDH catalysts broke the ligand of MOFs and reorganized the structure on the basis of retaining a high specific surface area and a large number of pores, which have higher specific surface area and well-developed pore structure than LDH catalysts prepared by traditional methods, and thus provide more active sites to activate PMS. Due to the unique framework structure of MOFs, the MOF derived CoMn-LDH and CoFe-LDH catalysts could provide more active sites to activate PMS, and achieve a 2, 4-dichlorophenol (2, 4-DCP) degradation of 99.3% and 99.2% within 20 min, respectively. Besides, the two LDH catalysts displayed excellent degradation performance for bisphenol A (BPA), ciprofloxacin (CIP) and 2, 4-dichlorophenoxyacetic acid (2, 4-D). XPS indicated that the valence state transformation of metal elements participated in PMS activation. EPR manifested sulfate radical () and singlet oxygen (1O2) were the main species for degrading pollutants. In addition, after the three-cycle experiment, the CoMn-LDH and CoFe-LDH catalysts also showed long-term stability with a slight activity decrease in the third cycle. The phytotoxicity assessment determined by the germination of mung beans proved that PMS activation by MOFs-derived LDH catalyst can basically eliminate the phytotoxicity of 2, 4-D solution. This research not only developed high-activity LDH catalysts for PMS activation, but also expanded the environmental applications of MOFs derivants.


Sign in / Sign up

Export Citation Format

Share Document