Abstract:A novel composite consisting of hollow carbon spheres with encapsulated germanium (Ge@HCS) was synthesized by introducing a germanium precursor into the porous-structured hollow carbon spheres. The carbon spheres not only function as a scaffold to hold the germanium and thus maintain the structural integrity of the composite, but also increase the electrical conductivity. The voids and vacancies that are formed after the reduction of germanium dioxide to germanium provide free space for accommodating the volum… Show more
“…Structural design with surface coating modification: a) Schematic illustration of self-assembled germanium/carbon nanostructures and TEM images of the nanostructures corresponding to each synthetic step. [23] Copyright 2014, Royal Society of Chemistry. [22] Copyright 2012, John Wiley and Sons.…”
Section: Surface Coating Modificationmentioning
confidence: 99%
“…To alleviate or eliminate the adverse influence of these problems, some strategies have been applied to optimize the electrochemical properties, including structural modification, [11,[13][14][15][16][17][18][19][20] modification by surface coating, [21][22][23][24] forming germaniumbased alloys, [25][26][27] and forming binary [28][29][30][31][32][33] or ternary [34][35][36] germanium-based composites. Based on our previous studies and experience, we found that the complete and effectively surface coating on nanostructures with high structural robustness is vital to achieving good electrochemical performance in terms of high specific capacity, superior long-term cyclability, and good rate capability.…”
Germaniumâbased materials are arousing increasing interest as anodes for lithiumâion batteries, stemming from the intrinsic physical and chemical advantages of germanium. This progress report provides a brief review on the current development of germaniumâbased materials in lithium storage. The stateâofâtheâart strategies to achieve enhanced electrochemical properties are highlighted, with their main aim being to resolve the trickiest issue: vast volume changes in germanium during cycling. These strategies include structural modification, modification by surface coating, forming germaniumâbased alloys, and forming binary or ternary germaniumâbased composites. The recent work on a novel composite of germanium and tin particles encapsulated in doubleâconcentric carbon hollow spheres is also presented here, with an emphasis on the relationship between structural design and improved performance.
“…Structural design with surface coating modification: a) Schematic illustration of self-assembled germanium/carbon nanostructures and TEM images of the nanostructures corresponding to each synthetic step. [23] Copyright 2014, Royal Society of Chemistry. [22] Copyright 2012, John Wiley and Sons.…”
Section: Surface Coating Modificationmentioning
confidence: 99%
“…To alleviate or eliminate the adverse influence of these problems, some strategies have been applied to optimize the electrochemical properties, including structural modification, [11,[13][14][15][16][17][18][19][20] modification by surface coating, [21][22][23][24] forming germaniumbased alloys, [25][26][27] and forming binary [28][29][30][31][32][33] or ternary [34][35][36] germanium-based composites. Based on our previous studies and experience, we found that the complete and effectively surface coating on nanostructures with high structural robustness is vital to achieving good electrochemical performance in terms of high specific capacity, superior long-term cyclability, and good rate capability.…”
Germaniumâbased materials are arousing increasing interest as anodes for lithiumâion batteries, stemming from the intrinsic physical and chemical advantages of germanium. This progress report provides a brief review on the current development of germaniumâbased materials in lithium storage. The stateâofâtheâart strategies to achieve enhanced electrochemical properties are highlighted, with their main aim being to resolve the trickiest issue: vast volume changes in germanium during cycling. These strategies include structural modification, modification by surface coating, forming germaniumâbased alloys, and forming binary or ternary germaniumâbased composites. The recent work on a novel composite of germanium and tin particles encapsulated in doubleâconcentric carbon hollow spheres is also presented here, with an emphasis on the relationship between structural design and improved performance.
“…The rate capability and the capacity are becoming more important than ever in battery technology for application in hybrid or pure electric vehicles, which require higher specifications of energy density and power density. Among the lithium alloybased anode materials, Si has the highest specific capacity of 4200 mAh g -1 for Li 22 Si 5 , but the poorest electrical conductivity and lithium diffusivity. Accordingly, the Si anode only can cycle at a rather slow rate.…”
Electrode materials with three-dimensional (3D) mesoporous structures possess superior features, such as shortened solid-phase lithium diffusion distance, large pore volume, full lithium ion accessibility, and a high specific area, which can facilitate fast lithium ion transport and electron transfer between solid/electrolyte interfaces. In this work, we introduce a facile synthesis route for the preparation of a 3D nanoarchitecture of Ge coated with carbon (3D-Ge/C) via a carbothermal reduction method in an inert atmosphere. The 3D-Ge/C showed excellent cyclability: almost 86.8% capacity retention, corresponding to a charge capacity of 1216 mAh g -1 even after 1000 cycles at a 2 C-rate. Surprisingly, the high average reversible capacity of 1122 mAh g -1 was maintained at a high charge rate of 100 C (160 A g -1 ). Even at an ultrahigh charge rate of 400 C (640 A g -1 ), an average capacity of 429 mAh g -1 was attained. Further, the full cell composed of 3D-Ge/C anode and LiCoO2 cathode exhibited excellent rate capability and cyclability with 94.7% capacity retention over 50 cycles. 3D-Ge/C, which offers a high energy density like batteries as well as a high power density like supercapacitors, is expected to be used in a wide range of electrochemical devices.A novel, facile synthetic route has been proposed to prepare a 3D nanoarchitecture Ge coated with carbon (3D-Ge/C) via a carbothermal reduction. The GeO 2 /PVP composite was carbonized in an argon atmosphere at 775 °C for 1 h to carbonize the PVP. During carbonization, the carbothermal reduction of GeO 2 occurred and simultaneously formed Ge within a 3D structure.
“…A high reversible capacity of 745 mA h g â1 at C/5 was shown by carbonâcoated Fe 3 O 4 nanospindles, and this was attributed to the facts that the carbon coating layers improved the electronic conductivity and protected the electrode materials from cracking and aggregation . The polymerization of resorcinolâformaldehyde (RF) prepared by a simple procedure with precise control has drawn attention in surface coating, as it can be further transformed into a carbon coating, as in Si@C, hollow carbon spheres with encapsulated germanium (Ge@HCS), and pitayaâlike Sn@C nanocomposites . These composite materials showed enhanced performance.…”
Transitionâmetal oxides are considered promising anode materials for lithiumâion batteries (LIBs). However, their application is limited because of huge volume changes and poor conductivity during the discharge/charge process. To this end, integration of different active components into an assemblage poses a potential solution. To gain better structural and synthetic control, the integration should be executed in a stepwise manner. In this paper, a versatile strategy to obtain C@Fe3O4@C hollow sandwiched composite structures was explored. Starting from Fe2O3 nanotubes, a RF (resorcinolâformaldehyde resins) layer was sequentially applied outside to form RF@Fe2O3@RF structures, which were calcined to realize carbonization and finalize the C@Fe3O4@C sandwiched structures. To the best of our knowledge, this is the first study on the preparation of a novel Fe3O4/carbonâbased nanocomposite. Upon using as an anode material for LIBs, the C@Fe3O4@C hollow sandwiched structures displayed high reversible capacity and good rate performance. The discharge capacity was maintained at 593 mAâhâgâ1 after 350 cycles at a current density of 1000 mAâgâ1, which is better than that of Fe2O3 nanotubes (discharge capacity of 140 mAâhâgâ1 after 80 cycles at 500 mAâgâ1). The improved electrochemical performance was attributed to the unique hollow sandwiched composite structure and good electrical conductivity.
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