CNFs/S1-xSex Composites as Promising Cathode Materials for High-Energy Lithium-Sulfur Batteries

MRS Advances ◽  
2019 ◽  
Vol 4 (14) ◽  
pp. 821-828 ◽  
Author(s):  
Gaind P. Pandey ◽  
Kobi Jones ◽  
Lamartine Meda
Keyword(s):  
Cathode Material ◽  
High Performance ◽  
Coulombic Efficiency ◽  
Specific Capacity ◽  
Rate Capability ◽  
Composite Cathode ◽  
High Energy ◽  
High Mass ◽  
High Performance Composite ◽  
Lithium Sulfur

ABSTRACTHigh-energy lithium-sulfur (Li-S) batteries still suffer from poor rate capability and short cycle life caused by the polysulfides shuttle and insulating nature of S (and the discharge product, Li2S). Selenium disulfide (SeS2), with a theoretical specific capacity of 1342 mAh g−1, is a promising cathode material as it has better conductivity compared to sulfur. The electrochemical reaction kinetics of CNFs-S/SeS2 composites (denoted as CNFs/S1-xSex, where x ≤ 0.1) are expected to be remarkably improved because of the better conductivity of SeS2 compared to sulfur. Here, a high-performance composite cathode material of CNFs/S1-xSex for novel Li-S batteries is reported. The CNFs/S1-xSex composites combine the higher conductivity and higher density of SeS2 with high specific capacity of sulfur. The CNFs/S1-xSex electrode shows good initial discharge capacity of ∼1050 mAh g−1 at 0.05 C rate with high mass loading of materials (∼6-7 mg cm−2 of composites) and > 97% initial coulombic efficiency. The CNFs/S1-xSex electrode shows more than 600 mAh g-1 specific capacity after 50 charge-discharge cycles at 0.5C rate, much higher compared to the CNFs/S cathodes.

scholarly journals High-Energy and High-Power Pseudocapacitor–Battery Hybrid Sodium-Ion Capacitor with Na+ Intercalation Pseudocapacitance Anode

2021 ◽  
Vol 13 (1) ◽  
Author(s):  
Qiulong Wei ◽  
Qidong Li ◽  
Yalong Jiang ◽  
Yunlong Zhao ◽  
Shuangshuang Tan ◽  
...  
Keyword(s):  
Energy Density ◽  
High Power ◽  
Anode Materials ◽  
High Performance ◽  
Coulombic Efficiency ◽  
Specific Capacity ◽  
Rate Capability ◽  
High Energy ◽  
Sodium Ion ◽  
High Energy Density

AbstractHigh-performance and low-cost sodium-ion capacitors (SICs) show tremendous potential applications in public transport and grid energy storage. However, conventional SICs are limited by the low specific capacity, poor rate capability, and low initial coulombic efficiency (ICE) of anode materials. Herein, we report layered iron vanadate (Fe5V15O39 (OH)9·9H2O) ultrathin nanosheets with a thickness of ~ 2.2 nm (FeVO UNSs) as a novel anode for rapid and reversible sodium-ion storage. According to in situ synchrotron X-ray diffractions and electrochemical analysis, the storage mechanism of FeVO UNSs anode is Na+ intercalation pseudocapacitance under a safe potential window. The FeVO UNSs anode delivers high ICE (93.86%), high reversible capacity (292 mAh g−1), excellent cycling stability, and remarkable rate capability. Furthermore, a pseudocapacitor–battery hybrid SIC (PBH-SIC) consisting of pseudocapacitor-type FeVO UNSs anode and battery-type Na3(VO)2(PO4)2F cathode is assembled with the elimination of presodiation treatments. The PBH-SIC involves faradaic reaction on both cathode and anode materials, delivering a high energy density of 126 Wh kg−1 at 91 W kg−1, a high power density of 7.6 kW kg−1 with an energy density of 43 Wh kg−1, and 9000 stable cycles. The tunable vanadate materials with high-performance Na+ intercalation pseudocapacitance provide a direction for developing next-generation high-energy capacitors.

scholarly journals Metal-Based Electrocatalysts for High-Performance Lithium-Sulfur Batteries: A Review

Catalysts ◽  
2020 ◽  
Vol 10 (10) ◽  
pp. 1137
Author(s):  
Kiran Mahankali ◽  
Sudhan Nagarajan ◽  
Naresh Kumar Thangavel ◽  
Sathish Rajendran ◽  
Munaiah Yeddala ◽  
...  
Keyword(s):  
Energy Storage ◽  
Coulombic Efficiency ◽  
Specific Capacity ◽  
Rate Capability ◽  
High Energy ◽  
High Energy Density ◽  
Storage Device ◽  
Next Generation ◽  
End Products ◽  
Lithium Sulfur

The lithium-sulfur (Li-S) redox battery system is considered to be the most promising next-generation energy storage technology due to its high theoretical specific capacity (1673 mAh g−1), high energy density (2600 Wh kg−1), low cost, and the environmentally friendly nature of sulfur. Though this system is deemed to be the next-generation energy storage device for portable electronics and electric vehicles, its poor cycle life, low coulombic efficiency and low rate capability limit it from practical applications. These performance barriers were linked to several issues like polysulfide (LiPS) shuttle, inherent low conductivity of charge/discharge end products, and poor redox kinetics. Here, we review the recent developments made to alleviate these problems through an electrocatalysis approach, which is considered to be an effective strategy not only to trap the LiPS but also to accelerate their conversion reactions kinetics. Herein, the influence of different chemical interactions between the LiPS and the catalyst surfaces and their effect on the conversion of liquid LiPS to solid end products are reviewed. Finally, we also discussed the challenges and perspectives for designing cathode architectures to enable high sulfur loading along with the capability to rapidly convert the LiPS.

scholarly journals Confine sulfur in double-hollow carbon sphere integrated with carbon nanotubes for advanced lithium–sulfur batteries

2021 ◽  
Vol 10 (1) ◽  
Author(s):  
Maru Dessie Walle ◽  
You-Nian Liu
Keyword(s):  
Carbon Nanotubes ◽  
Coulombic Efficiency ◽  
Specific Capacity ◽  
High Energy ◽  
High Energy Density ◽  
Carbon Sphere ◽  
Hollow Carbon Sphere ◽  
Lithium Sulfur Batteries ◽  
Hollow Carbon ◽  
Lithium Sulfur

AbstractThe lithium–sulfur (Li–S) batteries are promising because of the high energy density, low cost, and natural abundance of sulfur material. Li–S batteries have suffered from severe capacity fading and poor cyclability, resulting in low sulfur utilization. Herein, S-DHCS/CNTs are synthesized by integration of a double-hollow carbon sphere (DHCS) with carbon nanotubes (CNTs), and the addition of sulfur in DHCS by melt impregnations. The proposed S-DHCS/CNTs can effectively confine sulfur and physically suppress the diffusion of polysulfides within the double-hollow structures. CNTs act as a conductive agent. S-DHCS/CNTs maintain the volume variations and accommodate high sulfur content 73 wt%. The designed S-DHCS/CNTs electrode with high sulfur loading (3.3 mg cm−2) and high areal capacity (5.6 mAh mg cm−2) shows a high initial specific capacity of 1709 mAh g−1 and maintains a reversible capacity of 730 mAh g−1 after 48 cycles at 0.2 C with high coulombic efficiency (100%). This work offers a fascinating strategy to design carbon-based material for high-performance lithium–sulfur batteries.

Calcium Cobalt Hexacyanoferrate Cathodes for Rechargeable Divalent Ion Batteries

2016 ◽  
Vol 19 (2) ◽  
pp. 057-064 ◽  
Author(s):  
Prasanna Padigi ◽  
Neal Kuperman ◽  
Joseph James Thiebes ◽  
Gary Goncher ◽  
David Evans ◽  
...  
Keyword(s):  
Cathode Material ◽  
Divalent Cations ◽  
Coulombic Efficiency ◽  
Empirical Relationship ◽  
Specific Capacity ◽  
Rate Capability ◽  
Capacity Utilization ◽  
Rechargeable Batteries ◽  
Host Lattice ◽  
Cobalt Hexacyanoferrate

Calcium cobalt hexacyanoferrate (CaCoHCF) was synthesized and tested as a cathode material for rechargeable batteries, using divalent cations (Mg2+, Ca2+, Ba2+). CaCoHCF demonstrated reversible specific capacity and coulombic efficiency (in parentheses) of 45.49 mAh/g (99.18%) for Mg2+, 55.04 mAh/g (99.2%) for Ca2+, and 44.09 mAh/g (99.42%) for Ba2+, at a current density of 25 mA/g. Of the three ions, Ca2+ resulted in the highest absolute specific capacity as well as high specific capacity utilization. The cathodes were also subjected to rate capability measurements using current densities of 50 mA/g (30 cycles) and 0.1 A/g (100 cycles). Upon addition of 2 mL water to the non-aqueous electrolyte, the fraction of theoretical specific capacity increased to 0.55 for Mg2+, 94.8% for Ca2+, and 95.53% forBa2+. This increase has been interpreted as the ability of the cathode material to intercalate and de-intercalate more ions due to the electrostatic shielding provided by water molecules between the host lattice and the guest cations. An empirical relationship between the cation size and specific capacity utilization is presented.Calcium cobalt hexacyanoferrate (CaCoHCF) was synthesized and tested as a cathode material for rechargeable batteries, using divalent cations (Mg2+, Ca2+, Ba2+). CaCoHCF demonstrated reversible specific capacity and coulombic efficiency (in parentheses) of 45.49 mAh/g (99.18%) for Mg2+, 55.04 mAh/g (99.2%) for Ca2+, and 44.09 mAh/g (99.42%) for Ba2+, at a current density of 25 mA/g. Of the three ions, Ca2+ resulted in highest absolute specific capacity as well as high specific capacity utilization. The cathodes were also subjected to rate capability measurements using current densities of 50 mA/g (30 cycles) and 0.1 A/g (100 cycles). Upon addition of 2 mL water to the non-aqueous electrolyte, the fraction of theoretical specific capacity increased to 0.55 for Mg2+, 94.8% for Ca2+, and 95.53% forBa2+. This increase has been interpreted as the ability of the cathode material to intercalate and de-intercalate more ions due to the electrostatic shielding provided by water molecules between the host lattice and the guest cations. An empirical relationship between the cation size and specific capacity utilization is presented.

Fabrication of layered Ti3C2 with an accordion-like structure as a potential cathode material for high performance lithium–sulfur batteries

2015 ◽  
Vol 3 (15) ◽  
pp. 7870-7876 ◽  
Author(s):  
Xiaoqin Zhao ◽  
Min Liu ◽  
Yong Chen ◽  
Bo Hou ◽  
Na Zhang ◽  
...  
Keyword(s):  
Cathode Material ◽  
Discharge Capacity ◽  
High Performance ◽  
Coulombic Efficiency ◽  
Initial Discharge Capacity ◽  
Capacity Retention ◽  
Initial Discharge ◽  
Lithium Sulfur Batteries ◽  
Lithium Sulfur

L-Ti3C2 was prepared by exfoliating Ti3AlC2 in 40% HF. With sulfur-loaded L-Ti3C2 as cathodes, Li–S batteries deliver a high initial discharge capacity of 1291 mA h g−1, an excellent capacity retention of 970 mA h g−1 and coulombic efficiency of 99% after 100 cycles.

Graphene oxide-polypyrrole composite as sulfur hosts for high-performance lithium-sulfur batteries

2018 ◽  
Vol 11 (06) ◽  
pp. 1840007 ◽  
Author(s):  
Qian Wang ◽  
Chengkai Yang ◽  
Hui Tang ◽  
Kai Wu ◽  
Henghui Zhou
Keyword(s):  
Graphene Oxide ◽  
High Performance ◽  
Density Functional ◽  
Specific Capacity ◽  
High Energy ◽  
High Energy Density ◽  
Composite Cathodes ◽  
Lithium Sulfur Batteries ◽  
Lithium Sulfur ◽  
Capacity Decay

Lithium-sulfur batteries are considered as a promising candidate for the next-generation high energy density storage devices. However, they are still hindered by serious capacity decay on cycling caused by the dissolution of redox intermediates. Here, we designed a unique structure with polypyrrole (ppy) inserting into the graphene oxide (GO) sheet for accommodating sulfur. Such a sulfur host not only exhibits a good electronic and ionic conductivity, but also can suppress polysulfide dissolution effectively. With this advanced design, the composite cathode showed a high specific capacity of 548.4[Formula: see text]mA[Formula: see text]h[Formula: see text]g[Formula: see text] at 5.0 C. A stable Coulombic efficiency of [Formula: see text]99.5% and a capacity decay rate as low as 0.089% per cycle along with 300 cycles at 1.0 C were achieved for composite cathodes with 78[Formula: see text]wt.% of S. Besides, the interaction mechanism between PPy and lithium polysulfides (LPS) was investigated by density-functional theory (DFT), suggesting that only the polymerization of N atoms can bind strongly to Li ions of LPS rather than single N atoms. The 3D structure GO-PPy host with high conductivity and excellent trapping ability to LPS offered a viable strategy to design high-performance cathodes for Li–S batteries.

An in-situ catalytic-insoluble strategy enabled by sulfurized polyacrylonitrile-based composite cathode for potassium–sulfur batteries

2021 ◽  
pp. 2143003
Author(s):  
Xiaomin Yuan ◽  
Bo Zhu ◽  
Jinkui Feng ◽  
Chengguo Wang ◽  
Xun Cai ◽  
...  
Keyword(s):  
High Performance ◽  
Metal Oxide Nanoparticles ◽  
Specific Capacity ◽  
Reversible Capacity ◽  
Composite Cathode ◽  
High Energy ◽  
Host Materials ◽  
Catalytic Kinetics ◽  
One Step

Owing to the insoluble organosulfur mechanism and stable cycling life, sulfurized polyacrylonitrile (SPAN) developed as a promising cathode material for high-energy potassium–sulfur batteries (KSBs). However, it is yet a major challenge to achieve fast catalytic kinetics and high reversible capacity in SPAN-based cathodes. Here, one-step electrospun SPAN nanofibers embedded with Fe[Formula: see text]Nb[Formula: see text]O metal oxide nanoparticles (FeNb@SPAN) have been successfully developed to construct sulfur electrodes with high electrochemical activity, high sulfur utilization, and high cycling stability. The as-prepared freestanding FeNb@SPAN composite cathode, which featuring interwoven nanofibers with Fe[Formula: see text]Nb[Formula: see text]O nanoparticles homogeneously implanted, possesses high storage space for volume expansion and suppresses polysulfide dissolution during potassiation/depotassiation. Benefiting from its unique structure and composition in electrode design, the FeNb@SPAN cathode is endowed with outstanding energy storage performances with a high initial specific capacity of 776 mAh [Formula: see text] g[Formula: see text] under 50 mA [Formula: see text] g[Formula: see text] and an excellent cycling capability of 201 mAh [Formula: see text] g[Formula: see text] after 80 charge/discharge processes. This work heralds a feasible strategy toward SPAN-based sulfur host materials in the structural design of next-generation high-performance cathode materials for KSBs and other metal–sulfur batteries.

Cellulose-Derived Carbon Microfiber Mesh for Binder-Free Lithium—Sulfur Batteries

2020 ◽  
Vol 20 (9) ◽  
pp. 5629-5635
Author(s):  
Shiqi Li ◽  
Zhiqun Cheng ◽  
Tian Xie ◽  
Zhihua Dong ◽  
Guohua Liu
Keyword(s):  
High Performance ◽  
Carbon Materials ◽  
Electronic Conductivity ◽  
Specific Capacity ◽  
Rate Capability ◽  
Lithium Sulfide ◽  
Lithium Sulfur Batteries ◽  
Binder Free ◽  
Carbon Microfiber ◽  
Lithium Sulfur

The practical application of lithium–sulfur batteries (LSBs) has been impeded by several chronic problems related to the insulating nature of sulfur and lithium sulfide, in addition to the dissolution and diffusion of lithium polysulfides. In view of these problems, a large variety of carbonaceous materials have been employed to enhance the electronic conductivity of the cathode and/or sequester lithium polysulfides within conductive matrixes. Although they may exhibit impressive electrochemical performance, the fabrication of most carbon materials involves costly precursors and complicated procedures. Waste paper—the main constituent of municipal waste—is composed of carbohydrates, and can be an ideal precursor for carbon materials. Herein, carbon microfiber meshes (CMFMs) obtained by the pyrolysis of common filter paper in argon (A-CMFM) or ammonia (N-CMFM) were used to form sulfur cathodes. Compared with LSBs based on A-CMFM, those based on N-CMFM demonstrated higher specific capacity and better rate capability, with a capacity of 650 mA h g−1 at 0.2 C and 550 mA h g−1 at 0.5 C. This was owing to the strong immobilization of lithium polysulfides resulting from the heteroatom doping and hydrophilicity of N-CMFM. The results indicate that cellulose paper-derived carbon is a promising candidate for application in high-performance LSBs.

scholarly journals High-Performance Lithium Sulfur Batteries Based on Multidimensional Graphene-CNT-Nanosulfur Hybrid Cathodes

Batteries ◽  
2021 ◽  
Vol 7 (2) ◽  
pp. 26
Author(s):  
Álvaro Doñoro ◽  
Álvaro Muñoz-Mauricio ◽  
Vinodkumar Etacheri
Keyword(s):  
High Performance ◽  
Coulombic Efficiency ◽  
Electronic Conductivity ◽  
Specific Capacity ◽  
Synthesis Method ◽  
Graphene Nanoplatelets ◽  
Practical Implementation ◽  
Electrochemical Performances ◽  
High Electronic Conductivity ◽  
Lithium Sulfur

Although lithium-sulfur (Li-S) batteries are one of the promising candidates for next-generation energy storage, their practical implementation is limited by rapid capacity fading due to lithium polysulfide (LiPSs) formation and the low electronic conductivity of sulfur. Herein, we report a high-performance lithium-sulfur battery based on multidimensional cathode architecture consisting of nanosulfur, graphene nanoplatelets (2D) and multiwalled carbon nanotubes (1D). The ultrasonic synthesis method results in the generation of sulfur nanoparticles and their intercalation into the multilayered graphene nanoplatelets. The optimized multidimensional graphene-sulfur-CNT hybrid cathode (GNS58-CNT10) demonstrated a high specific capacity (1067 mAh g−1 @ 50 mA g−1), rate performance (539 @ 1 A g−1), coulombic efficiency (~95%) and cycling stability (726 mAh g−1 after 100 cycles @ 200 mA g−1) compared to the reference cathode. Superior electrochemical performances are credited to the encapsulation of nanosulfur between the individual layers of graphene nanoplatelets with high electronic conductivity, and effective polysulfide trapping by MWCNT bundles.

scholarly journals Supercritical CO2 Synthesis of Freestanding Se1-xSx Foamy Cathodes for High-Performance Li-Se1-xSx Battery

2021 ◽  
Vol 9 ◽  
Author(s):  
Chengwei Lu ◽  
Ruyi Fang ◽  
Kun Wang ◽  
Zhen Xiao ◽  
G. Gnana kumar ◽  
...  
Keyword(s):  
High Performance ◽  
Specific Capacity ◽  
Three Dimensional ◽  
Rate Capability ◽  
Carbon Matrix ◽  
High Energy ◽  
Rechargeable Batteries ◽  
High Energy Density ◽  
Rechargeable Lithium Batteries ◽  
Practical Applications

Selenium-sulfur solid solutions (Se1-xSx) are considered to be a new class of promising cathodic materials for high-performance rechargeable lithium batteries owing to their superior electric conductivity than S and higher theoretical specific capacity than Se. In this work, high-performance Li-Se1-xSx batteries employed freestanding cathodes by encapsulating Se1-xSx in a N-doped carbon framework with three-dimensional (3D) interconnected porous structure (NC@SWCNTs) are proposed. Se1-xSx is uniformly dispersed in 3D porous carbon matrix with the assistance of supercritical CO2 (SC-CO2) technique. Impressively, NC@SWCNTs host not only provides spatial confinement for Se1-xSx and efficient physical/chemical adsorption of intermediates, but also offers a highly conductive framework to facilitate ion/electron transport. More importantly, the Se/S ratio of Se1-xSx plays an important role on the electrochemical performance of Li- Se1-xSx batteries. Benefiting from the rationally designed structure and chemical composition, NC@[email protected] cathode exhibits excellent cyclic stability (632 mA h g−1 at 200 cycle at 0.2 A g−1) and superior rate capability (415 mA h g−1 at 2.0 A g−1) in carbonate-based electrolyte. This novel NC@[email protected] cathode not only introduces a new strategy to design high-performance cathodes, but also provides a new approach to fabricate freestanding cathodes towards practical applications of high-energy-density rechargeable batteries.

Sign in / Sign up

Export Citation Format

Share Document