scholarly journals Synthesis of Clustered Mn3O4 Nanoparticles through a Polymer Surfactant Mediated Route on Few-Layer Graphene Nanoplatelet Surface and its Application for Electrochemical Energy Storage: Lithium-ion Battery Anode

Author(s):  
Debkumar Saha ◽  
Lawrence T. Drzal

<p>Composites synthesized through the deposition of Mn<sub>3</sub>O<sub>4</sub> on graphene, carbon nanotube and other carbon based materials have attracted much attention recently as potential electrode materials for different electrochemical applications such as pseudocapacitor; Lithium-ion battery; and catalysis. The primary reason Mn<sub>3</sub>O<sub>4</sub> is grown on these substrates in spite of having high charge storage capacity as pseudocapacitor or Lithium-ion battery electrodes on its own is to enhance its electrical conductivity and/or to impart flexibility to the electrode, which is difficult for a fully metallic electrode. Higher electrical conductivity prolongs the cycle life of an electrode. In addition, the substrate contributes capacity and thus, enhances the overall energy density of an electrode. Mn<sub>3</sub>O<sub>4 </sub>acts as a spacer and keeps graphene nanosheets separated when used as the substrate for capacitor electrode fabrication. This helps retain the high surface area of graphene nanosheets in the electrode which contributes additional capacitance. Mn<sub>3</sub>O<sub>4 </sub>supported on graphene and other carbon substrates have recently been investigated as catalyst for methanol electro-oxidation in alkaline media; CO oxidation; and Oxygen reduction reaction (ORR). High surface area substrate uniformly distributes metal particles and prevents their agglomeration and dissolution during catalytic process. In addition, high electrical conductivity of graphene and carbon substrates enhances the electronic conductivity of Mn<sub>3</sub>O<sub>4</sub> which is of importance for superior catalytic activity. Composite of Mn<sub>3</sub>O<sub>4</sub> combined with carbon based substrate has also found non-electrochemical application such as the removal of Pb and Cu ions from aqueous solution because of their adsorptive behaviour.<b></b></p> <p>A myriad of procedures have been adopted for the synthesis of Mn<sub>3</sub>O<sub>4</sub> on graphene or other carbonaceous substrates. All of these methods involve one or more of the following factors that complicate the process, such as: long synthesis time; high synthesis temperature; use of hazardous/toxic chemicals; multistep process and the requirement for sophisticated device or highly controlled environment. In fact, the complicacies associated with the synthesis of Mn<sub>3</sub>O<sub>4</sub> have already been acknowledged and investigations have been directed at finding relatively simpler route such as the use of microwave technique. <b></b></p> <p>In this research, we report the synthesis of clusters of nearly octahedral shapedn Mn<sub>3</sub>O<sub>4</sub> nanoparticles on few-layer graphene nanoplatalet (GnP) surface through a simple, wet-chemical, polyethyleneimine (PEI) mediated route. Few-layer graphene nanoplatelets are ultrathin particles of graphite prepared through proprietary intercalation and exfoliation method (XG Sciences, Inc., Lansing, MI, USA). The components involved in this synthesis method are manganese salts (KMnO<sub>4</sub> and MnSO<sub>4</sub>.H<sub>2</sub>O); water; PEI; and GnP as the substrate. The synthesis is carried out at a temperature of 80°C only and in open air. Highly crystallized Mn<sub>3</sub>O<sub>4</sub> particles, as observed by X-Ray Diffraction (XRD), can be synthesized on GnP surface. It has also been observed that PEI acts as a reducing agent and as a capping agent on a continuous network of ribbon-like Birnessite-MnO<sub>2</sub> (IV) to produce a nearly octahedral shaped nanoparticles of Mn<sub>3</sub>O<sub>4</sub> (II, III). It has already been mentioned that composites of Mn<sub>3</sub>O<sub>4</sub> on graphene or other carbonaceous substrates find a myriad of applications. Thus, our research findings to synthesize GnP-Mn<sub>3</sub>O<sub>4</sub> composite through a simple method should be of interest to a broad group of researchers. In this research, we have investigated the performance of this composite system as a Lithium-ion battery anode only. Our preliminary investigations reveal that the Mn<sub>3</sub>O<sub>4</sub> composite synthesized through this method has just as much potential as the ones prepared through other alternative methods.</p>

2020 ◽  
Author(s):  
Debkumar Saha ◽  
Lawrence T. Drzal

<p>Composites synthesized through the deposition of Mn<sub>3</sub>O<sub>4</sub> on graphene, carbon nanotube and other carbon based materials have attracted much attention recently as potential electrode materials for different electrochemical applications such as pseudocapacitor; Lithium-ion battery; and catalysis. The primary reason Mn<sub>3</sub>O<sub>4</sub> is grown on these substrates in spite of having high charge storage capacity as pseudocapacitor or Lithium-ion battery electrodes on its own is to enhance its electrical conductivity and/or to impart flexibility to the electrode, which is difficult for a fully metallic electrode. Higher electrical conductivity prolongs the cycle life of an electrode. In addition, the substrate contributes capacity and thus, enhances the overall energy density of an electrode. Mn<sub>3</sub>O<sub>4 </sub>acts as a spacer and keeps graphene nanosheets separated when used as the substrate for capacitor electrode fabrication. This helps retain the high surface area of graphene nanosheets in the electrode which contributes additional capacitance. Mn<sub>3</sub>O<sub>4 </sub>supported on graphene and other carbon substrates have recently been investigated as catalyst for methanol electro-oxidation in alkaline media; CO oxidation; and Oxygen reduction reaction (ORR). High surface area substrate uniformly distributes metal particles and prevents their agglomeration and dissolution during catalytic process. In addition, high electrical conductivity of graphene and carbon substrates enhances the electronic conductivity of Mn<sub>3</sub>O<sub>4</sub> which is of importance for superior catalytic activity. Composite of Mn<sub>3</sub>O<sub>4</sub> combined with carbon based substrate has also found non-electrochemical application such as the removal of Pb and Cu ions from aqueous solution because of their adsorptive behaviour.<b></b></p> <p>A myriad of procedures have been adopted for the synthesis of Mn<sub>3</sub>O<sub>4</sub> on graphene or other carbonaceous substrates. All of these methods involve one or more of the following factors that complicate the process, such as: long synthesis time; high synthesis temperature; use of hazardous/toxic chemicals; multistep process and the requirement for sophisticated device or highly controlled environment. In fact, the complicacies associated with the synthesis of Mn<sub>3</sub>O<sub>4</sub> have already been acknowledged and investigations have been directed at finding relatively simpler route such as the use of microwave technique. <b></b></p> <p>In this research, we report the synthesis of clusters of nearly octahedral shapedn Mn<sub>3</sub>O<sub>4</sub> nanoparticles on few-layer graphene nanoplatalet (GnP) surface through a simple, wet-chemical, polyethyleneimine (PEI) mediated route. Few-layer graphene nanoplatelets are ultrathin particles of graphite prepared through proprietary intercalation and exfoliation method (XG Sciences, Inc., Lansing, MI, USA). The components involved in this synthesis method are manganese salts (KMnO<sub>4</sub> and MnSO<sub>4</sub>.H<sub>2</sub>O); water; PEI; and GnP as the substrate. The synthesis is carried out at a temperature of 80°C only and in open air. Highly crystallized Mn<sub>3</sub>O<sub>4</sub> particles, as observed by X-Ray Diffraction (XRD), can be synthesized on GnP surface. It has also been observed that PEI acts as a reducing agent and as a capping agent on a continuous network of ribbon-like Birnessite-MnO<sub>2</sub> (IV) to produce a nearly octahedral shaped nanoparticles of Mn<sub>3</sub>O<sub>4</sub> (II, III). It has already been mentioned that composites of Mn<sub>3</sub>O<sub>4</sub> on graphene or other carbonaceous substrates find a myriad of applications. Thus, our research findings to synthesize GnP-Mn<sub>3</sub>O<sub>4</sub> composite through a simple method should be of interest to a broad group of researchers. In this research, we have investigated the performance of this composite system as a Lithium-ion battery anode only. Our preliminary investigations reveal that the Mn<sub>3</sub>O<sub>4</sub> composite synthesized through this method has just as much potential as the ones prepared through other alternative methods.</p>


2019 ◽  
Vol 55 (2) ◽  
pp. 186-189 ◽  
Author(s):  
Xingang Kong ◽  
Xing Wang ◽  
Dingying Ma ◽  
Jianfeng Huang ◽  
Jiayin Li ◽  
...  

Fe2+ doped Fe0.8Ti1.2O40.8− nanosheets were prepared via delaminating H0.8Fe0.8Ti1.2O4 precursor and further photo reduction. It shows improved electrochemical performance due to the enhanced electrical conductivity by the introduction of Fe2+.


Molekul ◽  
2021 ◽  
Vol 16 (3) ◽  
pp. 235
Author(s):  
Annisa Syifaurrahma ◽  
Arnelli Arnelli ◽  
Yayuk Astuti

A lithium ion battery anode active material comprised of LiOH (Li) and coconut shell activated carbon (AC) has been synthesized with Li/AC ratios of (w/w) 1/1, 2/1, 3/1, and 4/1 through the sol gel method. The present study aims to ascertain the best Li/AC ratio that produces an anode active material with the best electrical conductivity value and determine the characteristics of the anode active material in terms of functional groups, surface area, crystallinity, and capacity. Based on the electrical conductivity test using LCR, the active material Li/AC 2/1 had the highest electrical conductivity with a value of 2.064x10-3 Sm-1. The conductivity achieved was slightly smaller than that of the active material with no addition of LiOH on the activated carbon at an electrical conductivity of 5.434x10-3 Sm-1. The FTIR spectra of the activated carbon and Li/AC 2/1 showed differences with in the Li-O-C group absorption at 1075 cm-1 wavenumber and the wide absorption in the area of 547.5 cm-1 that represents Li-O vibration. Based on the results of SAA, the activated carbon had a larger surface area than Li/AC 2/1 at 17.057 m2g-1 and 5.615 m2g-1, respectively. The crystallinity of both active materials was low shown by the widening of the diffraction peaks. Tests with cyclic voltammetry (CV) proved that there was a reduction-oxidation reaction for the two samples in the first cycle with a large charge and discharge capacities of the activated carbon of 150.989 mAh and 92.040 mAh, while for Li/AC 2/1 they were 91.103 mAh and 47.580 mAh.


2015 ◽  
Vol 23 (3) ◽  
pp. 569-575 ◽  
Author(s):  
Ruijin Meng ◽  
Hongying Hou ◽  
Xianxi Liu ◽  
Jixiang Duan ◽  
Song Liu

2016 ◽  
Vol 206 ◽  
pp. 10-16 ◽  
Author(s):  
Hong Chen ◽  
Hui Gao ◽  
Houwen Xiao ◽  
Xiuhua Zhou ◽  
Wengong Zhang ◽  
...  

2015 ◽  
Vol 379 (37) ◽  
pp. 2245-2251 ◽  
Author(s):  
Xiao-Yong Fang ◽  
Xiao-Xia Yu ◽  
Hong-Mei Zheng ◽  
Hai-Bo Jin ◽  
Li Wang ◽  
...  

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