skip to main content
US FlagAn official website of the United States government
dot gov icon
Official websites use .gov
A .gov website belongs to an official government organization in the United States.
https lock icon
Secure .gov websites use HTTPS
A lock ( lock ) or https:// means you've safely connected to the .gov website. Share sensitive information only on official, secure websites.

Explore Research Products in the PAR
It may take a few hours for recently added research products to appear in PAR search results.


Title: Silicon carbide (SiC) derived from agricultural waste potentially competitive with silicon anodes
Biomass-derived materials offer low carbon approaches to energy storage. High surface area SiC w/wo 13 wt% hard carbon (SiC/HC, SiC/O), derived from carbothermal reduction of silica depleted rice hull ash (SDRHA), can function as Li+ battery anodes. Galvanostatic cycling of SiC/HC and SiC/O shows capacity increases eventually to >950 mA h g−1 (Li1.2–1.4SiC) and >740 mA h g−1 (Li1.1SiC), respectively, after 600 cycles. Post-mortem investigation via XRD and 29Si MAS NMR reveals partial phase transformation from 3C- to 6H-SiC, with no significant changes in unit cell size. SEMs show cycled electrodes maintain their integrity, implying almost no volume expansion on lithiation/delithiation, contrasting with >300% volume changes in Si anodes on lithiation. Significant void space is needed to compensate for these volume changes with Si in contrast to SiC anodes suggesting nearly competitive capacities. 6Li MAS NMR and XPS show no evidence of LixSi, with Li preferring all-C environments supported by computational modeling. Modeling also supports deviation from the 3C phase at high Li contents with minimal volume changes.  more » « less
Award ID(s):
1926199
PAR ID:
10357012
Author(s) / Creator(s):
; ; ; ;
Date Published:
Journal Name:
Green chemistry
Volume:
24
ISSN:
1463-9262
Page Range / eLocation ID:
4061-4070
Format(s):
Medium: X
Sponsoring Org:
National Science Foundation
More Like this
  1. ; ; ; ; (, Electrochimica acta)
    Utilizing silicon as an anode material for Li-ion batteries has been the subject of many studies. However, due to the huge volume change of silicon during lithiation, the electrochemical performance of silicon is poor. Here, we have investigated a novel yet simple approach to synthesize nanostructured silicon/graphite composites with a carbon coating and engineered voids. High-energy ball mill is employed to convert micrometer-sized silicon and graphite to nanostructured silicon/graphite composite building blocks, while a thin carbon coating is applied to encapsulate these composite agglomerates, followed by partial etching of silicon to create engineered voids inside the composite agglomerates. The batteries made with this tailored nanostructure exhibit improved electrochemical performance over the counterparts made with silicon nanoparticles and exhibited a specific capacity of ~1800 mA h g-1 discharge capacity at the first cycle, 580 mA h g-1 after 40 cycles, and 350 mA h g-1 after 300 cycles. This study has established a novel method scalable at industry environment and capable of producing low cost Si anodes and clearly shown that the cycle stability of the tailored nanostructure improves with increasing engineered voids in the range we have investigated. 
    more » « less
  2. ; ; ; ; ; ; ; ; (, Advanced Functional Materials)
    Abstract Si‐based anodes with a stiff diamond structure usually suffer from sluggish lithiation/delithiation reaction due to low Li‐ion and electronic conductivity. Here, a novel ternary compound ZnSi2P3with a cation‐disordered sphalerite structure, prepared by a facile mechanochemical method, is reported, demonstrating faster Li‐ion and electron transport and greater tolerance to volume change during cycling than the existing Si‐based anodes. A composite electrode consisting of ZnSi2P3and carbon achieves a high initial Coulombic efficiency (92%) and excellent rate capability (950 mAh g−1at 10 A g−1) while maintaining superior cycling stability (1955 mAh g−1after 500 cycles at 300 mA g−1), surpassing the performance of most Si‐ and P‐based anodes ever reported. The remarkable electrochemical performance is attributed to the sphalerite structure that allows fast ion and electron transport and the reversible Li‐storage mechanism involving intercalation and conversion reactions. Moreover, the cation‐disordered sphalerite structure is flexible to ionic substitutions, allowing extension to a family of Zn(Cu)Si2+xP3solid solution anodes (x= 0, 2, 5, 10) with large capacity, high initial Coulombic efficiency, and tunable working potentials, representing attractive anode candidates for next‐generation, high‐performance, and low‐cost Li‐ion batteries. 
    more » « less
  3. ; ; ; ; (, ACS applied energy materials)
    Applications of silicon as a high-performance anode material has been impeded by its low intrinsic conductivity and huge volume expansion (> 300%) during lithiation. To address these problems, nano-Si particles along with conductive coatings and engineered voids are often employed, but this results in high cost anodes. Here, we report a scalable synthesis method that can realize high specific capacity (~800 mAh g-1), ultrafast charge/discharge (at 8 A g-1 Si) and high initial Coulombic efficiency (~90%) with long cycle life (1000 cycles) at the same time. To achieve 1000 cycle stability, micron-sized Si particles are subjected to high-energy ball milling to create nanostructured Si building blocks with nano-channel shaped voids encapsulated inside a nitrogen (N)-doped carbon shell (termed as Si micro-reactor). The nano-channel voids inside a Si micro-reactor not only offer the space to accommodate the volume expansion of Si, but also provide fast pathways for Li ion diffusion into the center of the nanostructured Si core and thus ultrafast charge/discharge capability. The porous N-doped carbon shell helps to improve the conductivity while allowing fast Li ion transport and confining the volume expansion within the Si micro-reactor. Submicron-sized Si micro-reactors with limited specific surface area (35 m2 g-1) afford sufficient electrode/electrolyte interfacial area for fast lithiation/delithiation, leading to the specific capacity ranging from ~800 to 420 mAh g-1 under ultrafast charging conditions (8 A g-1), but not too much interfacial area for surface side reactions and thus high initial coulombic efficiency (~90%). Since Si micro-reactors with superior electrochemical properties are synthesized via an industrially scalable and eco-friendly method, they have the potential for practical applications in the future. 
    more » « less
  4. ; ; ; (, physica status solidi (a))
    Germanium (Ge) is deemed as one of the most promising alloying anodes for rechargeable lithium‐ion batteries (LIBs) due to its large theoretical capacity, high electrical conductivity, fast lithium‐ion diffusivity, and mechanical robustness. However, Ge‐based anodes suffer from large volume changes during lithiation and delithiation, which can deteriorate their electrochemical performance rapidly. Herein, the large volume change issue is effectively addressed using an asymmetric membrane structure that is prepared using a phase‐inversion method in combination with hydrogen peroxide etching and surface coating. The asymmetric Ge membrane etched by ≈30 wt% H2O2at 90 °C for 30 s demonstrates a capacity retention higher than 80% in 50 cycles at 160 mA g−1. Coating the H2O2‐etched Ge membrane with carbonaceous membranes can further improve the retention up to 95% in 50 cycles at 160 mA g−1, whereas ≈100% capacity of 700 mAh g−1can be maintained in 170 cycles at 400 mA g−1. A combination of electron microscopy, spectrophotometry, and X‐ray analyses confirms the electrochemical performance of asymmetric Ge membranes as the LIB anode can be significantly affected by membrane geometry, the duration of hydrogen peroxide etching, carbonaceous membrane coating, and Ge concentration. 
    more » « less
  5. ; ; ; (, Journal of Materials Chemistry A)
    Nickel phosphide (Ni 5 P 4 ) nanosheets are synthesized using in situ chemical vapor deposition of P on Ni foam. The thickness of the as-synthesized Ni 5 P 4 film is determined to be ∼5 nm, using atomic force microscopy (AFM). The small thickness shortens the diffusion path of Li ions and results in fast ion transport. In addition, the 2D Ni 5 P 4 nanosheets seamlessly connect to the Ni foam, which facilitates electron transfer between Ni 5 P 4 and the Ni current collector. Therefore, the binder/carbon free-nickel supported Ni 5 P 4 shows fast rate performance as an anode for lithium-ion batteries (LIBs). The specific capacity of 2D Ni 5 P 4 is obtained as 600 mA h g −1 at a cycling rate of 0.1C, approaching the theoretical capacity of 768 mA h g −1 . Even at a rate of 0.5C, the capacity remains as 450 mA h g −1 over 100 cycles. A capacity >100 mA h g −1 is retained at a very high rate of 20C. Ni 5 P 4 also exhibits a low voltage of ∼0.5 V with respect to Li metal, which makes it a suitable negative electrode for LIBs. In operando 31 P NMR and 7 Li NMR are employed to probe the lithiation and de-lithiation mechanisms upon electrochemical cycling. 
    more » « less
  • Citation Formats
  • MLA
  • APA
  • Chicago
  • BibTeX
  • Save / Share this Record
  • Send to Email