Facile synthesis and characterization of the Mn-MOF electrode material for flexible supercapacitors

Author(s):  
Yanhong Liu ◽  
Jiahong Liu ◽  
Yijun Cao ◽  
Wei Shang ◽  
Ning Peng ◽  
...  

Abstract Metal-organic frameworks (MOFs) due to their porosity and well-defined structures are considered to be very promising electrode materials for the construction of high-performance supercapacitor. In this paper, manganese-based metal organic frameworks (Mn-MOF) were prepared on the surface of carbon cloth (CC) by hydrothermal method. The morphology and structure of the electrode material were characterized by SEM, XRD, FT-IR, and XPS. Its electrochemical studies show that the Mn-MOF electrode materials exhibit low charge transfer resistance, the excellent specific capacitance of 433.5 mF·cm−2 in 1.0 M Na2SO4 aqueous solution at the current density of 0.8 mA·cm−2. It is noteworthy that the flexible electrode has excellent cycle stability and 105% capacitance retention even after 5000 cycles at a current density of 5 mA·cm−2. The high electrochemical performance of Mn-MOF/CC flexible electrode materials can be attributed to its three-dimensional porous structure.

2017 ◽  
Vol 5 (3) ◽  
pp. 1094-1102 ◽  
Author(s):  
Yang Jiao ◽  
Jian Pei ◽  
Dahong Chen ◽  
Chunshuang Yan ◽  
Yongyuan Hu ◽  
...  

Metal–organic frameworks (MOFs) have obtained increasing attention as a kind of novel electrode material for energy storage devices.


Author(s):  
Wen-Wei Song ◽  
Bing Wang ◽  
Xiao-Man Cao ◽  
Qiang Chen ◽  
Zhengbo Han

Metal-organic frameworks (MOFs)-derived transition-metal oxides and transition-metal phosphides have great application potential as electrode materials for supercapacitors, owing to the excellent redox activity and high conductivity. However, their electrochemical performances...


2019 ◽  
Vol 30 (3) ◽  
pp. 605-609 ◽  
Author(s):  
Shaofei Zhao ◽  
Lizhen Zeng ◽  
Gao Cheng ◽  
Lin Yu ◽  
Huaqiang Zeng

2019 ◽  
Vol 12 (01) ◽  
pp. 1850104 ◽  
Author(s):  
Jinggao Wu ◽  
Qi Lai ◽  
Canyu Zhong

MoO3@CoMoO4 hybrid is fabricated by a facile one-step hydrothermal method and is used as anode for lithium-ion battery (LIB). Compared to pristine MoO3, galvanostatic charge–discharge tests show that the hybrid electrode delivered a remarkable rate capability of 586.69[Formula: see text]mAh[Formula: see text]g[Formula: see text] at the high current density of 1000[Formula: see text]mA[Formula: see text]g[Formula: see text] and a greatly enhanced cyclic capacity of 887.36[Formula: see text]mA[Formula: see text]h[Formula: see text]g[Formula: see text] after 140 cycles at the current density of 200[Formula: see text]mA[Formula: see text]g[Formula: see text] (with capacity retention, 85.3%). The superior electrochemical properties could be ascribed to the synergistic effect of MoO3 and CoO nanostructure that results in the lower charge transfer resistance and the higher Li[Formula: see text] diffusion coefficient, thus leading to high performance Li[Formula: see text] reversibility storage.


2020 ◽  
Vol 7 (6) ◽  
pp. 1428-1436 ◽  
Author(s):  
Dandan Han ◽  
Jinhe Wei ◽  
Yuan Zhao ◽  
Ye Shen ◽  
Yifan Pan ◽  
...  

Starting from 2D Co-based metal-organic frameworks, novel petal-like core-shell Co3O4@CoNi2S4 nanowall arrays are synthesized on carbon cloth using a facile two-step method and investigated as promising electrode materials for supercapacitors.


NANO ◽  
2020 ◽  
pp. 2150005
Author(s):  
Meng Sun ◽  
Zhipeng Cui ◽  
Huanqing Liu ◽  
Sijie Li ◽  
Qingye Zhang ◽  
...  

FeOOH nanorods (NRs) wrapped by reduced graphene oxide (rGO) were fabricated using a facile solvothermal method. When used as anode materials for lithium-ion batteries (LIBs), the FeOOH NRs/rGO composites show a higher capacity (490[Formula: see text]mAh g[Formula: see text] after 100 cycles at a current density of 100[Formula: see text]mA g[Formula: see text] and better rate capability than pure FeOOH NRs. The enhanced electrochemical performance can be ascribed to the hybrid structure of FeOOH and rGO. On one hand, the introduction of rGO can improve electronic conductivity and reduce charge-transfer resistance for electrode materials. On the other hand, the distinctive structure (FeOOH NRs surrounded by flexible rGO) can effectively buffer large volume change during the Li[Formula: see text] insertion/extraction process. Our work provides a feasible strategy to obtain high-performance LIBs.


2021 ◽  
Author(s):  
Zhichao Liu ◽  
Dong Wang ◽  
Hongliang Mu ◽  
Chunjie Zhang ◽  
Liqing Wu ◽  
...  

Abstract Two-phase heterostructure with rich phase boundaries holds great potential in engineering advanced electrode materials. However, current heterostructures are largely generated by introducing exotic cations or anions, complicating synthetic procedures and disturbing real insights into the intrinsic effect of heterostructure. Herein, nanosized monometallic selenides heterostructures are developed by precisely controlled selenylation of metal organic frameworks, which are implanted into in-situ formed carbon (NiSe/NiSe2@C, CoSe/CoSe2@C). The disordered atoms arrangement at two-phase boundary leads to the redistribution of interfacial charge and generation of lattice distortions, promoting easy adsorption and swift transfer of Li+, and providing extra active sites. As a proof of concept, the NiSe/NiSe2@C exhibits far surpassing lithium storage properties to single-phase counterparts (NiSe@C and NiSe2@C), including higher reversible capacity of 1015.5 mAh g− 1, better rate capability (500.8 mAh g− 1 at 4 A g− 1), and superior cyclic performance. As expected, the NiSe/NiSe2@C manifests lower charge transfer resistance, higher Li+ diffusion coefficient, and accelerated capacitive kinetics. Ex-situ X-ray diffraction, high-resolution transmission electron microscopy, and selected area electron diffraction combined with differential capacity versus voltage plots reveal multi-step redox mechanism of NiSe/NiSe2@C and the reason of conspicuous capacity enhancement. This work demonstrates the enormous potential of monometallic monoanionic heterostructure in energy-related field.


2020 ◽  
Author(s):  
Sai Rashmi M. ◽  
Ashish Singh ◽  
Chandra sekhar Rout ◽  
Akshaya Samal ◽  
Manav Saxena

<p>The conversion of biomass into valuable carbon composites as an efficient non-precious energy storage electrode material have elicited extensive research interest. As synthesized partially graphitized iron oxide-carbon composite material (Fe<sub>3</sub>O<sub>4</sub>/Fe<sub>3</sub>C@C) shows an excellent property as an electrode material for supercapacitor. X-ray diffraction, High resolution transmission electron microscopy, X-ray photo-electron spectroscopy and Brunauer-Emmett-Teller analysis is used to study the structural, compositional and surface areal properties. The electrode material shows a specific surface area of 827.4 m<sup>2</sup>/g. Due to the synergistic effect of graphitic layers with iron oxide/carbide, Fe<sub>3</sub>O<sub>4</sub>/Fe<sub>3</sub>C@C hybrid electrode materials display high-performance for supercapacitor with excellent capacity of 878 F/g at a current density of 5A/g (3-electrode) and 211.6 F/g at a current density of 0.4A/g (2-electrode) in 6M KOH electrolyte with good cyclic stability.</p>


Polymers ◽  
2021 ◽  
Vol 13 (11) ◽  
pp. 1673
Author(s):  
Nagaraj Patil ◽  
Jesus Palma ◽  
Rebeca Marcilla

Aqueous zinc-polymer batteries (AZPBs) comprising abundant Zn metal anode and redox-active polymer (RAP) cathodes can be a promising solution for accomplishing viable, safe and sustainable energy storage systems. Though a limited number of RAPs have been successfully applied as organic cathodes in AZPBs, their macromolecular engineering towards improving electrochemical performance is rarely considered. In this study, we systematically compare performance of AZPB comprising Zn metal anode and either poly(catechol) homopolymer (named P(4VC)) or poly(catechol) copolymer (named P(4VC86-stat-SS14)) as polymer cathodes. Sulfonate anionic pendants in copolymer not only rendered lower activation energy and higher rate constant, but also conferred lower charge-transfer resistance, as well as facilitated Zn2+ mobility and less diffusion-controlled current responses compared to its homopolymer analogue. Consequently, the Zn||P(4VC86-stat-SS14) full-cell exhibits enhanced gravimetric (180 versus 120 mAh g−1 at 30 mg cm−2) and areal capacity (5.4 versus 3.6 mAh cm−2 at 30 mg cm−2) values, as well as superior rate capability both at room temperature (149 versus 105 mAh g−1 at 150 C) and at −35 °C (101 versus 35 mAh g−1 at 30 C) compared to Zn||P(4VC)100. This overall improved performance for Zn||P(4VC86-stat-SS14) is highly encouraging from the perspective applying macromolecular engineering strategies and paves the way for the design of advanced high-performance metal-organic batteries.


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