scholarly journals Achieving of High Density/Utilization of Active Groups via Synergic Integration of C=N and C=O Bonds for Ultra-Stable and High-Rate Lithium-Ion Batteries

Research ◽  
2018 ◽  
Vol 2018 ◽  
pp. 1-10 ◽  
Author(s):  
Tao Sun ◽  
Zong-Jun Li ◽  
Xin-Bo Zhang

Organic electrode materials are receiving ever-increasing research interest due to their combined advantages, including resource renewability, low cost, and environmental friendliness. However, their practical applications are still terribly plagued by low conductivity, poor rate capability, solubility in electrolyte, and low density/utilization of active groups. In response, herein, as a proof-of-concept experiment, C=N and C=O bonds are synergically integrated into the backbone of pentacene to finely tune the electronic structures of pentacene. Unexpectedly, the firstly obtained unique 5,7,11,14-tetraaza-6,13-pentacenequinone/reduced graphene oxide (TAPQ/RGO) composite exhibits superior electrochemical performances, including an ultra-stable cycling stability (up to 2400 cycles) and good rate capability (174 mAh g−1 even at a high current density of 3.2 A g−1), which might be attributed to the abundant active groups, π-conjugated molecular structure, leaf-like morphology, and the interaction between TAPQ and graphene.

2019 ◽  
Vol 2019 ◽  
pp. 1-5 ◽  
Author(s):  
Zhen Bi ◽  
Lanyan Huang ◽  
Chaoqun Shang ◽  
Xin Wang ◽  
Guofu Zhou

Copper tin sulfides (CTSs) have widely been investigated as electrode materials for supercapacitors owing to their high theoretical pseudocapacitances. However, the poor intrinsic conductivity and volume change during redox reactions hindered their electrochemical performances and broad applications. In this study, carbon quantum dots (CQDs) were employed to modify CTSs. The structures and morphologies of obtained materials were characterized by X-ray diffraction (XRD) and transmission electron microscopy (TEM). XRD revealed CTSs were composed of Cu2SnS3 and Cu4SnS4, and TEM suggested the decoration of CQDs on the surface of CTSs. With the decoration of CQDs, CTSs@CQDs showed a remarkable specific capacitance of 856 F·g−1 at 2 mV·s−1 and a high rate capability of 474 F·g−1 at 50 mV·s−1, which were superior to those of CTSs (851 F·g−1 at 2 mV·s−1 and 192 F·g−1 at 50 mV·s−1, respectively). This was mainly ascribed to incorporation of carbon quantum dots, which improved the electrical conductivity and alleviated volume change of CTSs during charge/discharge processes.


2019 ◽  
Vol 19 (6) ◽  
pp. 3610-3615 ◽  
Author(s):  
Lifeng Wang ◽  
Kaiyuan Wei ◽  
Pengjun Zhang ◽  
Hong Wang ◽  
Xiujun Qi ◽  
...  

Potassium-ion batteries (PIBs), as one of the alternatives to lithium-ion batteries (LIBs), have attracted considerable attention on account of the affluence and low-cost of potassium. Moreover, CoC2O4 and graphene oxide (GO) have been used very well in lithium-ion batteries. Hence, the hybrid CoC2O4/GO was investigated as a new anode material for PIBs. The hybrid CoC2O4/GO was synthesized by a facile and cheap method combined with supersonic dispersion. Electrochemical measurements reveal that the hybrid CoC2O4/GO delivered an excellent cycling stability of 166 mAh g−1 at 50 mA g−1 and a superior rate capability even at 1 A g−1. These results demonstrate although the cycle ability was insufficient for practical applications, transition-metal oxalates composites can still bring new hope to the development of PIBs.


Author(s):  
Li Yang ◽  
Ye Tian ◽  
Jun Chen ◽  
Jinqiang Gao ◽  
Long Zhen ◽  
...  

As a high-safety and low-cost cathode material for lithium-ion batteries, LiFePO4 is predominately suffered from undesirable rate performance arising from its inferior conductivity in the practical application. Herein, LiFePO4 modified...


2015 ◽  
Vol 814 ◽  
pp. 358-364
Author(s):  
Peng Xiao Huang ◽  
Shui Hua Tang ◽  
Hui Peng ◽  
Xing Li

Graphitized-Carbon coated Li4Ti5O12/C (Li4Ti5O12/GC) composites were prepared from Li2CO3, TiO2 and aromatic resorcinol via a facile rheological phase method. The microstructure and morphology of the samples were determined by XRD and SEM. The electrochemical performances of the samples were characterized by galvanostatic charge-discharge test and electrochemical impedance spectroscopy (EIS). The results reveal that the coating of graphitized carbon could effectively enhance the charge/transfer kinetics of the Li4Ti5O12 electrode. The Li4Ti5O12/GC could deliver a discharge specific capacity of 166 mAh/g at 0.2 C, 148 mAh/g at 1.0 C, 142 mAh/g at 3.0 C, 138 mAh/g at 5.0 C and 127 mAh/g at 10.0 C, respectively, and it still could remain at 132 mAh/g after cycled at 5.0 C for 100 cycles. The excellent rate capability of the Li4Ti5O12/C makes it a promising anode material for high rate lithium ion batteries.


Energies ◽  
2021 ◽  
Vol 14 (5) ◽  
pp. 1299
Author(s):  
Jaeho Choi ◽  
Woo Jin Byun ◽  
DongHwan Kang ◽  
Jung Kyoo Lee

A mesoporous MnOx network (MMN) structure and MMN/C composites were prepared and evaluated as anodes for high-energy and high-rate lithium-ion batteries (LIB) in comparison to typical manganese oxide nanoparticle (MnNP) and graphite anodes, not only in a half-cell but also in a full-cell configuration (assembled with an NCM523, LiNi0.5Co0.2Mn0.3O2, cathode). With the mesoporous features of the MMN, the MMN/C exhibited a high capacity (approximately 720 mAh g−1 at 100 mA g−1) and an excellent cycling stability at low electrode resistance compared to the MnNP/C composite. The MMN/C composite also showed much greater rate responses than the graphite anode. Owing to the inherent high discharge (de-lithiation) voltage of the MMN/C than graphite as anodes, however, the MMN‖NCM523 full cell showed approximately 87.4% of the specific energy density of the Gr‖NCM523 at 0.2 C. At high current density above 0.2 C, the MMN‖NCM523 cell delivered much higher energy than the Gr‖NCM523 mainly due to the excellent rate capability of the MMN/C anode. Therefore, we have demonstrated that the stabilized and high-capacity MMN/C composite can be successfully employed as anodes in LIB cells for high-rate applications.


Author(s):  
Xianzhong Sun ◽  
Penglei Wang ◽  
Yabin An ◽  
Xiong Zhang ◽  
Shuanghao Zheng ◽  
...  

Abstract Lithium-ion capacitors (LICs) bridge the gap between lithium-ion batteries (LIBs) and electrical double-layer capacitors (EDLCs) owing to their unique energy storage mechanisms. From the viewpoints of electrode materials and cell design, the pre-lithiation process is indispensable for improving the working voltage and energy density of LICs. However, the conventional physical short-circuit (PSC) method is time-consuming, which limits the mass-production of practical large-capacity LIC cells. Three alternative pre-lithiation protocols have been proposed, combining the PSC protocol and electrochemical approaches to shorten the pre-lithiation time. The prototype LIC pre-lithiated by using the open-circuit potential cycling (OPC) protocol has the lowest internal resistance and superior high-rate capability (even at 200C-rate). The 900-F large-capacity laminated LIC cells have been assembled and pre-lithiated to validate the feasibility of this method. The pre-lithiation time has been reduced from 470 h (PSC protocol) to 19 h (OPC protocol). This combined protocol is presumed to counteract the voltage loss and enhance the Li+ ion diffusion between multiple anode electrodes during the pre-lithiation process.


Nanomaterials ◽  
2020 ◽  
Vol 10 (9) ◽  
pp. 1731
Author(s):  
Veronika Šedajová ◽  
Petr Jakubec ◽  
Aristides Bakandritsos ◽  
Václav Ranc ◽  
Michal Otyepka

Supercapacitors offer a promising alternative to batteries, especially due to their excellent power density and fast charging rate capability. However, the cycling stability and material synthesis reproducibility need to be significantly improved to enhance the reliability and durability of supercapacitors in practical applications. Graphene acid (GA) is a conductive graphene derivative dispersible in water that can be prepared on a large scale from fluorographene. Here, we report a synthesis protocol with high reproducibility for preparing GA. The charging/discharging rate stability and cycling stability of GA were tested in a two-electrode cell with a sulfuric acid electrolyte. The rate stability test revealed that GA could be repeatedly measured at current densities ranging from 1 to 20 A g−1 without any capacitance loss. The cycling stability experiment showed that even after 60,000 cycles, the material kept 95.3% of its specific capacitance at a high current density of 3 A g−1. The findings suggested that covalent graphene derivatives are lightweight electrode materials suitable for developing supercapacitors with extremely high durability.


2018 ◽  
Vol 6 (48) ◽  
pp. 24869-24876 ◽  
Author(s):  
Junru Wang ◽  
Feng Li ◽  
Yuanyuan Qu ◽  
Yang Liu ◽  
Yanmei Yang ◽  
...  

Organic electrode materials for rechargeable alkali-metal ion batteries have drawn increasing interest in recent years because of their distinctive advantages including low cost, environmental friendliness, and safety.


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