Abstract:A novel and cost-effective synthesis of silicon nanocrystallites (<10 nm) sealed in hollow carbon spheres (nc-Si@HCS) is developed as a promising anode material for high-performance Li-ion batteries (LIBs). The preparation method involves dichlorosilane (H2SiCl2) as widely available feedstock, to form a hydrogen-rich polysiloxane as a precursor for the production of large quantities of silicon nanoparticles. The final electrode material is composed of agglomerated 5 nm sized silicon nanoparticles encapsulated … Show more
“…Figure presents the plots of the areal capacity against the active materials areal mass loading (the detailed data is shown in Table S2). These plots display the recent studies of alloy anode materials (data taken from refs , , , , , , , and − ), which achieve or overpass the areal mass loading level of commercial graphite, indicating that the stacked Ge/Cu nanowire laminate electrode reaches a new level of areal mass loading of 14.8 mg cm –2 , being 1.5 times higher than that of the second place. Moreover, stacked Ge/Cu nanowire laminate electrode with 14.8 mg cm –2 provided a reversible capacity of 16 mA h per unit area that utilized Ge of approximately 80%, ranking first place among all of the alloy anodes reported in the literature.…”
Section: Resultsmentioning
confidence: 68%
“…Comparison of stacked Ge/Cu nanowire laminate electrode and reported Ge, Si, Sn anodes at the rate of around 0.1 C. Data taken from refs , , , , , , , and − . The detailed data is shown in Table S1.…”
Herein, a stacked Ge/Cu nanowire (NW) laminate made by stacking several Ge/Cu nanowire laminates accompanied by the conductive glue adhesives is used to achieve high capacity output per unit area (>10 mA h cm −2 ). The combination of Cu NWs and conductive adhesives constructs a tough and conducting network through the electrode, and the stacked Ge/ Cu nanowire laminate electrodes can load an ultrahigh mass of 14.8 mg Ge per unit area and provide an areal capacity output over 16 mA h cm −2 . A fullcell with an areal capacity of 11 mA h cm −2 built by stacked Ge/Cu nanowire laminate anode and Li(Ni 0.5 Co 0.3 Mn 0.2 )O 2 cathode was prepared and used to supply electricity for electronic devices, demonstrating their potential to be a candidate anode for high areal capacity Li-ion microbatteries that can be used for high-tech and integrated microsystems with limited space.
“…Figure presents the plots of the areal capacity against the active materials areal mass loading (the detailed data is shown in Table S2). These plots display the recent studies of alloy anode materials (data taken from refs , , , , , , , and − ), which achieve or overpass the areal mass loading level of commercial graphite, indicating that the stacked Ge/Cu nanowire laminate electrode reaches a new level of areal mass loading of 14.8 mg cm –2 , being 1.5 times higher than that of the second place. Moreover, stacked Ge/Cu nanowire laminate electrode with 14.8 mg cm –2 provided a reversible capacity of 16 mA h per unit area that utilized Ge of approximately 80%, ranking first place among all of the alloy anodes reported in the literature.…”
Section: Resultsmentioning
confidence: 68%
“…Comparison of stacked Ge/Cu nanowire laminate electrode and reported Ge, Si, Sn anodes at the rate of around 0.1 C. Data taken from refs , , , , , , , and − . The detailed data is shown in Table S1.…”
Herein, a stacked Ge/Cu nanowire (NW) laminate made by stacking several Ge/Cu nanowire laminates accompanied by the conductive glue adhesives is used to achieve high capacity output per unit area (>10 mA h cm −2 ). The combination of Cu NWs and conductive adhesives constructs a tough and conducting network through the electrode, and the stacked Ge/ Cu nanowire laminate electrodes can load an ultrahigh mass of 14.8 mg Ge per unit area and provide an areal capacity output over 16 mA h cm −2 . A fullcell with an areal capacity of 11 mA h cm −2 built by stacked Ge/Cu nanowire laminate anode and Li(Ni 0.5 Co 0.3 Mn 0.2 )O 2 cathode was prepared and used to supply electricity for electronic devices, demonstrating their potential to be a candidate anode for high areal capacity Li-ion microbatteries that can be used for high-tech and integrated microsystems with limited space.
“…To evaluate the practical application capability of our designed anode material, − the electrochemical performance of the HPRP-36 electrode with active material loading of about 2.0 mg cm –2 at 0.05 A g –1 was also tested. It can deliver an areal capacity of 3.3 mA h cm –2 in the second cycle and remains at 2.0 mA h cm –2 after 50 cycles.…”
Large-volume-expansion-induced material pulverization severely limits the electrochemical performance of high-capacity red phosphorus (RP) in alkali-ion batteries. Honeycomb-like porous materials can effectively solve the issues due to their abundant interconnected pore structures. Nevertheless, it is difficult and greatly challenging to fabricate a honeycomb-like porous RP that has not yet been fabricated via chemical synthesis. Herein, we successfully fabricate a honeycomb-like porous micron-sized red phosphorus (HPRP) with a controlled pore structure via a large-scale green and templateless hydrothermal strategy. It is demonstrated that dissolved oxygen in the solution can accelerate the destruction of P9 cages of RP, thus forming abundant active defects with a faster reaction rate, so the fast corrosion forms the honeycomb-like porous structure. Owing to the free volume, interconnected porous structure, and strong robustness, the optimized HPRP-36 can mitigate drastic volume variation and prevent pulverization during cycling resulting in tiny particle-level outward expansion, demonstrated by in situ TEM and ex situ SEM analysis. Thus, the HPRP-36 anode delivers a large reversible capacity (2587.4 mAh g −1 at 0.05 A g −1 ) and long-cycling stability with over 500 cycles (∼81.9% capacity retention at 0.5 A g −1 ) in lithium-ion batteries. This generally scalable, green strategy and deep insights provide a good entry point in designing honeycomb-like porous micron-sized materials for highperformance electrochemical energy storage and conversion.
“…Zheng's group 15 reported optimal thickness (~5 nm) of the coating layer for Si particles with a particle size of ~30 nm in terms of Li‐ion kinetics and mechanical stability at the interface. Synergistic effects originating from different Si valances in SiO x are gradually becoming a vitally important strategy for high‐performance Si‐based materials, in which Si valance can be mediated via self‐oxidation, 15 dismutate reaction, 16,17 or silicon reagents 18 …”
Section: Introductionmentioning
confidence: 99%
“…18 In fact, a series of intermediate states of SiO x (0 < x < 2) inevitably form on the surface or inside the particle undergoing high-temperature calcination, and the oxygen vacancy content of SiO x has a profound effect on electrochemical performances. 8,19 The larger oxygen vacancy content in SiO x reflects the high valence state of the Si element. SiO x with different oxygen content demonstrates nonlinear phenomena in volume expansion, internal stress/strain, and SEI-film evolution upon performing a lithiated process.…”
Relieving the stress or strain associated with volume change is highly desirable for high-performance SiO x anodes in terms of stable solid electrolyte interphase (SEI)-film growth. Herein, a Si-valence gradient is optimized in SiO x composites to circumvent the large volume strain accompanied by lithium insertion/extraction. SiO x @C annealed at 850°C has a gentle Si-valence gradient along the radial direction and excellent electrochemical performances, delivering a high capacity of 506.9 mAh g −1 at 1.0 A g −1 with a high Coulombic efficiency of ~99.8% over 400 cycles. Combined with the theoretical prediction, the obtained results indicate that the gentle Si-valence gradient in SiO x @C is useful for suppressing plastic deformation and maintaining the inner connection integrity within the SiO x @C particle. Moreover, a gentle Si-valence gradient is expected to form a stress gradient and affect the distribution of dangling bonds, resulting in local stress relief during the lithiation/delithiation process and enhanced Li-ion kinetic diffusion. Furthermore, the lowest interfacial stress variation ensures a stable SEI film at the interface and consequently increases cycling stability. Therefore, rational design of a Si-valence gradient in SiO x can provide further insights into achieving high-performance SiO x anodes with large-scale production.
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