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1.
Vertically Aligned MoS2 Nanosheets Patterned on Electrochemically Exfoliated Graphene for High‐Performance Lithium and Sodium Storage
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Gang Wang Jian Zhang Sheng Yang Faxing Wang Xiaodong Zhuang Klaus Müllen Xinliang Feng 《Liver Transplantation》2018,8(8)
Molybdenum disulfide (MoS2) has been recognized as a promising anode material for high‐energy Li‐ion (LIBs) and Na‐ion batteries (SIBs) due to its apparently high capacity and intriguing 2D‐layered structure. The low conductivity, unsatisfied mechanical stability, and limited active material utilization are three key challenges associated with MoS2 electrodes especially at high current rates and mass active material loading. Here, vertical MoS2 nanosheets are controllably patterned onto electrochemically exfoliated graphene (EG). Within the achieved hierarchical architecture, the intimate contact between EG and MoS2 nanosheets, interconnected network, and effective exposure of active materials by vertical channels simultaneously overcomes the above three problems, enabling high mechanical integrity and fast charge transport kinetics. Serving as anode material for LIBs, EG‐MoS2 with 95 wt% MoS2 content delivered an ultrahigh‐specific capacity of 1250 mA h g?1 after 150 stable cycles at 1 A g?1, which is among the highest values in all reported MoS2 electrodes, and excellent rate performance (970 mA h g?1 at 5 A g?1). Moreover, impressive cycling stability (509 mA h g?1 at 1 A g?1 after 250 cycles) and rate capability (423 mA h g?1 at 2 A g?1) were also achieved for SIBs. The area capacities reached 1.27 and 0.49 mA h cm?2 at ≈1 mA cm?2 for LIBs and SIBs, respectively. This work may inspire the development of new 2D hierarchical structures for high efficiency energy storage and conversion. 相似文献
2.
Amorphous MoS3 Infiltrated with Carbon Nanotubes as an Advanced Anode Material of Sodium‐Ion Batteries with Large Gravimetric,Areal, and Volumetric Capacities
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Hualin Ye Lu Wang Shuo Deng Xiaoqiao Zeng Kaiqi Nie Paul N. Duchesne Bo Wang Simon Liu Junhua Zhou Feipeng Zhao Na Han Peng Zhang Jun Zhong Xuhui Sun Youyong Li Yanguang Li Jun Lu 《Liver Transplantation》2017,7(5)
The search for earth‐abundant and high‐performance electrode materials for sodium‐ion batteries represents an important challenge to current battery research. 2D transition metal dichalcogenides, particularly MoS2, have attracted increasing attention recently, but few of them so far have been able to meet expectations. In this study, it is demonstrated that another phase of molybdenum sulfide—amorphous chain‐like MoS3—can be a better choice as the anode material of sodium‐ion batteries. Highly compact MoS3 particles infiltrated with carbon nanotubes are prepared via the facile acid precipitation method in ethylene glycol. Compared to crystalline MoS2, the resultant amorphous MoS3 not only exhibits impressive gravimetric performance—featuring excellent specific capacity (≈615 mA h g?1), rate capability (235 mA h g?1 at 20 A g?1), and cycling stability but also shows exceptional volumetric capacity of ≈1000 mA h cm?3 and an areal capacity of >6.0 mA h cm?2 at very high areal loadings of active materials (up to 12 mg cm?2). The experimental results are supported by density functional theory simulations showing that the 1D chains of MoS3 can facilitate the adsorption and diffusion of Na+ ions. At last, it is demonstrated that the MoS3 anode can be paired with an Na3V2(PO4)3 cathode to afford full cells with great capacity and cycling performance. 相似文献
3.
Ion Transport Nanotube Assembled with Vertically Aligned Metallic MoS2 for High Rate Lithium‐Ion Batteries
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Yucong Jiao Alolika Mukhopadhyay Yi Ma Lei Yang Ahmed M. Hafez Hongli Zhu 《Liver Transplantation》2018,8(15)
Metallic phase molybdenum disulfide (MoS2) is well known for orders of magnitude higher conductivity than 2H semiconducting phase MoS2. Herein, for the first time, the authors design and fabricate a novel porous nanotube assembled with vertically aligned metallic MoS2 nanosheets by using the scalable solvothermal method. This metallic nanotube has the following advantages: (i) intrinsic high electrical conductivity that promotes the rate performance of battery and eliminates the using of conductive additive; (ii) hierarchical, hollow, porous, and aligned structure that assists the electrolyte transportation and diffusion; (iii) tubular structure that avoids restacking of 2D nanosheets, and therefore maintains the electrochemistry cycling stability; and (iv) a shortened ion diffusion path, that improves the rate performance. This 1D metallic MoS2 nanotube is demonstrated to be a promising anode material for lithium‐ion batteries. The unique structure delivers an excellent reversible capacity of 1100 mA h g?1 under a current density of 5 A g?1 after 350 cycles, and an outstanding rate performance of 589 mA h g?1 at a current density of 20 A g?1. Furthermore, attributed to the material's metallic properties, the electrode comprising 100% pure material without any additive provides an ideal system for the fundamental electrochemical study of metallic MoS2. This study first reveals the characteristic anodic peak at 1.5 V in cyclic voltammetry of metallic MoS2. This research sheds light on the fabrication of metallic 1D, 2D, or even 3D structures with 2D nanosheets as building blocks for various applications. 相似文献
4.
Inspired by the great success of graphite in lithium‐ion batteries, anode materials that undergo an intercalation mechanism are considered to provide stable and reversible electrochemical sodium‐ion storage for sodium‐ion battery (SIB) applications. Though MoS2 is a promising 2D material for SIBs, it suffers from deformation of its layered structure during repeated intercalation of Na+, resulting in undesirable electrochemical behaviors. In this study, vertically oriented MoS2 on nitrogenous reduced graphene oxide sheets (VO‐MoS2/N‐RGO) is presented with designed spatial geometries, including sheet density and height, which can deliver a remarkably high reversible capacity of 255 mA h g?1 at a current density of 0.2 A g?1 and 245 mA h g?1 at a current density of 1 A g?1, with a total fluctuation of 5.35% over 1300 cycles. These results are superior to those obtained with well‐developed hard carbon structures. Furthermore, a SIB full cell composed of the optimized VO‐MoS2/N‐RGO anode and a Na2V3(PO4)3 cathode reaches a specific capacity of 262 mA h g?1 (based on the anode mass) during 50 cycles, with an operated voltage range of 2.4 V, demonstrating the potentially rewarding SIB performance, which is useful for further battery development. 相似文献
5.
Carbon‐Sheathed MoS2 Nanothorns Epitaxially Grown on CNTs: Electrochemical Application for Highly Stable and Ultrafast Lithium Storage
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Zijia Zhang Hailei Zhao Yongqiang Teng Xiwang Chang Qing Xia Zhaolin Li Jiejun Fang Zhihong Du Konrad Świerczek 《Liver Transplantation》2018,8(7)
Molybdenum disulfide (MoS2), which possesses a layered structure and exhibits a high theoretical capacity, is currently under intensive research as an anode candidate for next generation of Li‐ion batteries. However, unmodified MoS2 suffers from a poor cycling stability and an inferior rate capability upon charge/discharge processes. Herein, a unique nanocomposite comprising MoS2 nanothorns epitaxially grown on the backbone of carbon nanotubes (CNTs) and coated by a layer of amorphous carbon is synthesized via a simple method. The epitaxial growth of MoS2 on CNTs results in a strong chemical coupling between active nanothorns and carbon substrate via C? S bond, providing a high stability as well as a high‐efficiency electron‐conduction/ion‐transportation system on cycling. The outer carbon layer can well‐accommodate the structural strain in the electrode upon lithium‐ion insertion/extraction. When employed as an anode for lithium storage, the prepared material exhibits remarkable electrochemical properties with a high specific capacity of 982 mA h g?1 at 0.1 A g?1, as well as excellent long‐cycling stability (905 mA h g?1 at 1 A g?1 after 500 cycles) and superior rate capability, confirming its potential application in high‐performance Li‐ion batteries. 相似文献
6.
Ice Templated Free‐Standing Hierarchically WS2/CNT‐rGO Aerogel for High‐Performance Rechargeable Lithium and Sodium Ion Batteries
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Ye Wang Dezhi Kong Wenhui Shi Bo Liu Glenn Joey Sim Qi Ge Hui Ying Yang 《Liver Transplantation》2016,6(21)
A hybrid nanoarchitecture aerogel composed of WS2 nanosheets and carbon nanotube‐reduced graphene oxide (CNT‐rGO) with ordered microchannel three‐dimensional (3D) scaffold structure was synthesized by a simple solvothermal method followed by freeze‐drying and post annealing process. The 3D ordered microchannel structures not only provide good electronic transportation routes, but also provide excellent ionic conductive channels, leading to an enhanced electrochemical performance as anode materials both for lithium‐ion batteries (LIBs) and sodium‐ion batteries (SIBs). Significantly, WS2/CNT‐rGO aerogel nanostructure can deliver a specific capacity of 749 mA h g?1 at 100 mA g?1 and a high first‐cycle coulombic efficiency of 53.4% as the anode material of LIBs. In addition, it also can deliver a capacity of 311.4 mA h g?1 at 100 mA g?1, and retain a capacity of 252.9 mA h g?1 at 200 mA g?1 after 100 cycles as the anode electrode of SIBs. The excellent electrochemical performance is attributed to the synergistic effect between the WS2 nanosheets and CNT‐rGO scaffold network and rational design of 3D ordered structure. These results demonstrate the potential applications of ordered CNT‐rGO aerogel platform to support transition‐metal‐dichalcogenides (i.e., WS2) for energy storage devices and open up a route for material design for future generation energy storage devices. 相似文献
7.
Novel 2D van der Waals heterostructures with innovative bimetallic oxychloride (Bi‐ and Sb‐based oxychloride) nanosheets that are well dispersed on reduced graphene oxide nanosheets, are established through element engineering for superior potassium ion battery (PIBs) anodes. This material displays an exceptional electrochemical performance, obtaining a discharge capacity as high as 360 mAh g?1 at 100 mA g?1 after running 1000 cycles for over 9 months with a capacity preservation percentage of 88.5% and achieving a discharge capacity as high as 319 mAh g?1 at 1000 mA g?1, in addition to the low charge/discharge plateaus for anodes and promising full cell performance. More significantly, the nature of such 2D van der Waals heterostructures, including the element engineering for morphology control, the function of each component of heterostructures, the mechanism of potassium ion storage, and the process of K+ intercalation accompanied with the lattice distortion and chemical bond breakages, is explored in depth. This study is critical for not only paving the way for the practical application of PIBs but also shedding light on fundamentals of potassium ion storage in 2D van der Waals heterostructures. 相似文献
8.
Hyeonyeol Jeon Jae‐Min Jeong Heon Gyu Kang Hyung‐Jin Kim Jeyoung Park Do Hyun Kim Young Mee Jung Sung Yeon Hwang Young‐Kyu Han Bong Gill Choi 《Liver Transplantation》2018,8(18)
Highly conductive and ultrathin 2D nanosheets are of importance for the development of portable electronics and electric vehicles. However, scalable production and rational design for highly electronic and ionic conductive 2D nanosheets still remain a challenge. Herein, an industrially adoptable fluid dynamic exfoliation process is reported to produce large quantities of ionic liquid (IL)‐functionalized metallic phase MoS2 (m‐MoS2) and defect‐free graphene (Gr) sheets. Hybrid 2D–2D layered films are also fabricated by incorporating Gr sheets into compact m‐MoS2 films. The incorporated IL functionalities and Gr sheets prevent aggregation and restacking of the m‐MoS2 sheets, thereby creating efficient and rapid ion and electron pathways in the hybrid films. The hybrid film with a high packing density of 2.02 g cm?3 has an outstanding volumetric capacitance of 1430.5 F cm?3 at 1 A g?1 and an extremely high rate capability of 80% retention at 1000 A g?1. The flexible supercapacitor assembled using a polymer‐gel electrolyte exhibits excellent resilience to harsh electrochemical and mechanical conditions while maintaining an impressive rate performance and long cycle life. Successful achievement of an ultrahigh volumetric energy density (1.14 W h cm?3) using an organic electrolyte with a wide cell voltage of ≈3.5 V is demonstrated. 相似文献
9.
Xin Fan Rohit Ranganathan Gaddam Nanjundan Ashok Kumar Xiu Song Zhao 《Liver Transplantation》2017,7(19)
The hybrid Mg2+/Li+ battery (MLIB) is a very promising energy storage technology that combines the advantage of the Li and Mg electrochemistry. However, previous research has shown that the battery performance is limited due to the strong dependence on the Li content in the dual Mg2+/Li+ electrolyte. This limitation can be circumvented by significantly improving the diffusion kinetics of Mg2+ in the electrode, so that both Li+ and Mg2+ ions can be utilized as charge carriers. Herein, a free‐standing interlayer expanded MoS2/graphene composite (E‐MG) is demonstrated as a cathode for MLIB. The key advantage of this cathode is to enable the efficient intercalation of both Mg2+ and Li+. The E‐MG electrode displays a reversible capacity of ≈300 mA h g?1 at 20 mA g?1 in an MLIB cell, corresponding to a specific energy density up to ≈316.9 W h kg?1, which is comparable to that of the state‐of‐the‐art Li‐ion batteries (LIBs) and has no dendrite formation. The composite electrode is stable against cycling with a coulombic efficiency close to 100% at 500 mA g?1. This new electrode design represents a significant step forward for building a safe and high‐density electrochemical energy storage system. 相似文献
10.
Shuai Wang Zhijing Yu Jiguo Tu Junxiang Wang Donghua Tian Yingjun Liu Shuqiang Jiao 《Liver Transplantation》2016,6(13)
Due to an ever‐increasing demand for electronic devices, rechargeable batteries are attractive for energy storage systems. A novel rechargeable aluminum‐ion battery based on Al3+ intercalation and deintercalation is fabricated with Ni3S2/graphene microflakes composite as cathode material and high‐purity Al foil as anode. This kind of aluminum‐ion battery comprises of an electrolyte containing AlCl3 in an ionic liquid of 1‐ethyl‐3‐methylimidazolium chloride ([EMIm]Cl). Galvanostatic charge/discharge measurements have been performed in a voltage range of 0.1–2.0 V versus Al/AlCl4 ?. An initial discharge specific capacity of 350 mA h g?1 at a current density of 100 mA g?1 is achieved, and the discharge capacity remains over 60 mA h g?1 and coulombic efficiency of 99% after 100 cycles. Typically, for the current density at 200 mA g?1, the initial charge and discharge capacities are 300 and 235 mA h g?1, respectively. More importantly, it should be emphasized that the battery has a high discharge voltage plateau (≈1.0 V vs Al/AlCl4 ?). These meaningful results represent a significant step forward in the development of aluminum‐ion batteries. 相似文献
11.
Dinh Chuong Nguyen Duy Thanh Tran Thi Luu Luyen Doan Do Hwan Kim Nam Hoon Kim Joong Hee Lee 《Liver Transplantation》2020,10(8)
A novel hybrid of small core@shell structured CoSx@Cu2MoS4 uniformly hybridizing with a molybdenum dichalcogenide/N,S‐codoped graphene hetero‐network (CoSx@Cu2MoS4‐MoS2/NSG) is prepared by a facile route. It shows excellent performance toward the oxygen reduction reaction (ORR), oxygen evolution reaction (OER), and hydrogen evolution reaction (HER) in alkaline medium. The hybrid exhibits rapid kinetics for ORR with high electron transfer number of ≈3.97 and exciting durability superior to commercial Pt/C. It also demonstrates great potential with remarkable stability for HER and OER, requiring low overpotential of 118.1 and 351.4 mV, respectively, to reach a current density of 10 mA cm?2. An electrolyzer based on CoSx@Cu2MoS4‐MoS2/NSG produces low cell voltage of 1.60 V and long‐term stability, surpassing a device of Pt/C + RuO2/C. In addition, a Zn‐air battery using cathodic CoSx@Cu2MoS4‐MoS2/NSG catalyst delivers a high cell voltage of ≈1.44 V and a power density of 40 mW cm?2 at 58 mA cm?2, better than the state‐of‐the‐art Pt/C catalyst. These achievements are due to the rational combination of highly active core@shell CoSx@Cu2MoS4 with large‐area and high‐porosity MoS2/NSG to produce unique physicochemical properties with multi‐integrated active centers and synergistic effects. The outperformances of such catalyst suggest an advanced candidate for multielectrocatalysis applications in metal‐air batteries and hydrogen production. 相似文献
12.
Low‐Temperature Solution‐Based Phosphorization Reaction Route to Sn4P3/Reduced Graphene Oxide Nanohybrids as Anodes for Sodium Ion Batteries
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Qun Li Zhaoqiang Li Zhiwei Zhang Caixia Li Jingyun Ma Chengxiang Wang Xiaoli Ge Shihua Dong Longwei Yin 《Liver Transplantation》2016,6(15)
Different from previously reported mechanical alloying route to synthesize Sn x P3, novel Sn4P3/reduced graphene oxide (RGO) hybrids are synthesized for the first time through an in situ low‐temperature solution‐based phosphorization reaction route from Sn/RGO. Sn4P3 nanoparticles combining with advantages of high conductivity of Sn and high capacity of P are homogenously loaded on the RGO nanosheets, interconnecting to form 3D mesoporous architecture nanostructures. The Sn4P3/RGO hybrid architecture materials exhibit significantly improved electrochemical performance of high reversible capacity, high‐rate capability, and excellent cycling performance as sodium ion batteries (SIBs) anode materials, showing an excellent reversible capacity of 656 mA h g?1 at a current density of 100 mA g?1 over 100 cycles, demonstrating a greatly enhanced rate capability of a reversible capacity of 391 mA h g?1 even at a high current density of 2.0 A g?1. Moreover, Sn4P3/RGO SIBs anodes exhibit a superior long cycling life, delivering a high capacity of 362 mA h g?1 after 1500 cycles at a high current density of 1.0 A g?1. The outstanding cycling performance and rate capability of these porous hierarchical Sn4P3/RGO hybrid anodes can be attributed to the advantage of porous structure, and the synergistic effect between Sn4P3 nanoparticles and RGO nanosheets. 相似文献
13.
Hierarchical Zn–Co–S Nanowires as Advanced Electrodes for All Solid State Asymmetric Supercapacitors
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A facile two‐step strategy is developed to design the large‐scale synthesis of hierarchical, unique porous architecture of ternary metal hydroxide nanowires grown on porous 3D Ni foam and subsequent effective sulfurization. The hierarchical Zn–Co–S nanowires (NWs) arrays are directly employed as an electrode for supercapacitors application. The as‐synthesized Zn–Co–S NWs deliver an ultrahigh areal capacity of 0.9 mA h cm?2 (specific capacity of 366.7 mA h g?1) at a current density of 3 mA cm?2, with an exceptional rate capability (≈227.6 mA h g?1 at a very high current density of 40 mA cm?2) and outstanding cycling stability (≈93.2% of capacity retention after 10 000 cycles). Most significantly, the assembled Zn–Co–S NWs//Fe2O3@reduced graphene oxide asymmetric supercapacitors with a wide operating potential window of ≈1.6 V yield an ultrahigh volumetric capacity of ≈1.98 mA h cm?3 at a current density of 3 mA cm?2, excellent energy density of ≈81.6 W h kg?1 at a power density of ≈559.2 W kg?1, and exceptional cycling performance (≈92.1% of capacity retention after 10 000 cycles). This general strategy provides an alternative to design the other ternary metal sulfides, making it facile, free‐standing, binder‐free, and cost‐effective ternary metal sulfide‐based electrodes for large‐scale applications in modern electronics. 相似文献
14.
Hai‐Ning Fan Xing‐Yong Wang Hai‐Bo Yu Qin‐Fen Gu Shan‐Liang Chen Zheng Liu Xiao‐Hua Chen Wen‐Bin Luo Hua‐Kun Liu 《Liver Transplantation》2020,10(21)
The strategy of inducing interlayer anionic ligands in 2D MoS1.5Se0.5 nanosheets is employed to consolidate the interlayer band gap and optimize the electronic structure for the potassium ion battery. It combines complementary advantages from two kinds of anionic ligands with high conductivity and good affinity with potassium ions. The potassium ion diffusion rate is accelerated as well by an optimized lower energy barrier for ion diffusion pathways, with the formation of highly reversible KMo3Se3 crystal other than K0.4MoS2/K2MoS4, which encounters a much slower electro/ion diffusion rate upon discharging. These advances deliver enhanced potassium storage properties with excellent cycling stability, with retained specific capacity of 531.6 mAh g?1 at a current density of 200 mA g?1 even after 1000 cycles, and high rate capability with specific capacity of 270.1 mAh g?1 at 5 A g?1. The insertion and conversion mechanism are also elucidated by a combination of density functional theory computations and in situ synchrotron measurements. 相似文献
15.
Mesoporous MoS2 as a Transition Metal Dichalcogenide Exhibiting Pseudocapacitive Li and Na‐Ion Charge Storage
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John B. Cook Hyung‐Seok Kim Yan Yan Jesse S. Ko Shauna Robbennolt Bruce Dunn Sarah H. Tolbert 《Liver Transplantation》2016,6(9)
The ion insertion properties of MoS2 continue to be of widespread interest for energy storage. While much of the current work on MoS2 has been focused on the high capacity four‐electron reduction reaction, this process is prone to poor reversibility. Traditional ion intercalation reactions are highlighted and it is demonstrated that ordered mesoporous thin films of MoS2 can be utilized as a pseudocapacitive energy storage material with a specific capacity of 173 mAh g?1 for Li‐ions and 118 mAh g?1 for Na‐ions at 1 mV s?1. Utilizing synchrotron grazing incidence X‐ray diffraction techniques, fast electrochemical kinetics are correlated with the ordered porous structure and with an iso‐oriented crystal structure. When Li‐ions are utilized, the material can be charged and discharged in 20 seconds while still achieving a specific capacity of 140 mAh g?1. Moreover, the nanoscale architecture of mesoporous MoS2 retains this level of lithium capacity for 10 000 cycles. A detailed electrochemical kinetic analysis indicates that energy storage for both ions in MoS2 is due to a pseudocapacitive mechanism. 相似文献
16.
A Robust Approach for Efficient Sodium Storage of GeS2 Hybrid Anode by Electrochemically Driven Amorphization
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Sodium ion batteries (NIBs) have become attractive promising alternatives to lithium ion batteries in a broad field of future energy storage applications. The development of high‐performance anode materials has become an essential factor and a great challenge toward satisfying the requirements for NIBs, advancement. This work is the first report on GeS2 nanocomposites uniformly distributed on reduced graphene oxide (rGO) as promising anode materials for NIBs prepared via a facile hydrothermal synthesis and a unique carbo‐thermal annealing. The results show that the GeS2/rGO hybrid anode yields a high reversible specific capacity of 805 mA h g?1 beyond the theoretical capacity, an excellent rate capability of 616 mA h g?1 at 5 A g?1, and a cycle retention of 89.4% after 100 cycles. A combined ex situ characterization study reveals that the electrochemically driven amorphization plays a key role in achieving efficient sodium storage by accommodating excess sodium ions in the electrode materials. Understanding the sequential conversion‐alloying reaction mechanism for GeS2/rGO hybrid anodes provides a new approach for developing high‐performance energy storage applications. 相似文献
17.
Edney Geraldo da Silveira Firmiano Adriano C. Rabelo Cleocir J. Dalmaschio Antonio N. Pinheiro Ernesto C. Pereira Wido H. Schreiner Edson Robeto Leite 《Liver Transplantation》2014,4(6)
Layered molybdenum disulfide (MoS2) is deposited by microwave heating on a reduced graphene oxide (RGO). Three concentrations of MoS2 are loaded on RGO, and the structure and morphology are characterized. The first layers of MoS2 are detected as being directly bonded with the oxygen of the RGO by covalent chemical bonds (Mo‐O‐C). Electrochemical characterizations indicate that this electroactive material can be cycled reversibly between 0.25 and 0.8 V in 1 m HClO4 solution for hybrids with low concentrations of MoS2 layers (LCMoS2/RGO) and between 0.25 and 0.65 V for medium (MCMoS2/RGO) and high concentrations (HCMoS2/RGO) of MoS2 layers on graphene. The specific capacitance measured values at 10 mV s?1 are 128, 265, and 148 Fg?1 for the MoS2/RGO with low, medium, and high concentrations of MoS2, respectively, and the calculated energy density is 63 W h kg?1 for the LCMoS2/RGO hybrid. This supercapacitor electrode also exhibits superior cyclic stability with 92% of the specific capacitance retained after 1000 cycles. 相似文献
18.
Dual‐Functional N Dopants in Edges and Basal Plane of MoS2 Nanosheets Toward Efficient and Durable Hydrogen Evolution
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Wen Xiao Peitao Liu Jingyan Zhang Wendong Song Yuan Ping Feng Daqiang Gao Jun Ding 《Liver Transplantation》2017,7(7)
Herein, the authors explicitly reveal the dual‐functions of N dopants in molybdenum disulfide (MoS2) catalyst through a combined experimental and first‐principles approach. The authors achieve an economical, ecofriendly, and most efficient MoS2‐based hydrogen evolution reaction (HER) catalyst of N‐doped MoS2 nanosheets, exhibiting an onset overpotential of 35 mV, an overpotential of 121 mV at 100 mA cm?2 and a Tafel slope of 41 mV dec?1. The dual‐functions of N dopants are (1) activating the HER catalytic activity of MoS2 S‐edge and (2) enhancing the conductivity of MoS2 basal plane to promote rapid charge transfer. Comprehensive electrochemical measurements prove that both the amount of active HER sites and the conductivity of N‐doped MoS2 increase as a result of doping N. Systematic first‐principles calculations identify the active HER sites in N‐doped MoS2 edges and also illustrate the conducting charges spreading over N‐doped basal plane induced by strong Mo 3d –S 2p –N 2p hybridizations at Fermi level. The experimental and theoretical research on the efficient HER catalysis of N‐doped MoS2 nanosheets possesses great potential for future sustainable hydrogen production via water electrolysis and will stimulate further development on nonmetal‐doped MoS2 systems to bring about novel high‐performance HER catalysts. 相似文献
19.
Xinxin Cao Anqiang Pan Sainan Liu Jiang Zhou Site Li Guozhong Cao Jun Liu Shuquan Liang 《Liver Transplantation》2017,7(20)
Sodium (Na) super ion conductor structured Na3V2(PO4)3 (NVP) is extensively explored as cathode material for sodium‐ion batteries (SIBs) due to its large interstitial channels for Na+ migration. The synthesis of 3D graphene‐like structure coated on NVP nanoflakes arrays via a one‐pot, solid‐state reaction in molten hydrocarbon is reported. The NVP nanoflakes are uniformly coated by the in situ generated 3D graphene‐like layers with the thickness of 3 nm. As a cathode material, graphene covered NVP nanoflakes exhibit excellent electrochemical performances, including close to theoretical reversible capacity (115.2 mA h g?1 at 1 C), superior rate capability (75.9 mA h g?1 at 200 C), and excellent cyclic stability (62.5% of capacity retention over 30000 cycles at 50 C). Furthermore, the 3D graphene‐like cages after removing NVP also serve as a good anode material and deliver a specific capacity of 242.5 mA h g?1 at 0.1 A g?1. The full SIB using these two cathode and anode materials delivers a high specific capacity (109.2 mA h g?1 at 0.1 A g?1) and good cycling stability (77.1% capacity retention over 200 cycles at 0.1 A g?1). 相似文献
20.
Jia‐Zhao Wang Lin Lu Mustafa Lotya Jonathan N. Coleman Shu‐Lei Chou Hua‐Kun Liu Andrew I. Minett Jun Chen 《Liver Transplantation》2013,3(6):798-805
Layered MoS2 prepared by liquid‐phase exfoliation has been blended with single‐walled carbon nanotubes (SWNTs) to form novel composite thin films for lithium battery applications. The films were formed by vacuum filtration of blended dispersions onto nitrocellulose membranes. The resulting composite films were transferred onto Cu foil electrodes via a facile filtration/wet transfer technique from nitrocellulose membranes. The morphology of the film was characterised by field emission scanning electron microscopy, which suggests that the MoS2‐SWNT composite film shows good adherence to the Cu foil substrate. The MoS2‐SWNT composite thin films show strong electrochemical performance at different charge‐discharge rates. The capacity of a MoS2‐SWNT composite film with thickness of 1 μm is approximately 992 mAh g?1 after 100 cycles. The morphology study showed that the MoS2‐SWNT thin film retains structural integrity after 100 cycles, while the MoS2 thin film without SWNTs displays significant cracking. In addition, the novel composite thin film preparation and transfer protocols developed in this study could be extended to the preparation of various layered‐material‐based composite films, with the potential for new device designs for energy applications. 相似文献