RESUMO
Lithium (Li) metal batteries (LMBs) provide superior energy densities far beyond current Li-ion batteries (LIBs) but practical applications are hindered by uncontrolled dendrite formation and the build-up of dead Li in "hostless" Li metal anodes. To circumvent these issues, we created a 3D framework of a carbon paper (CP) substrate decorated with lithiophilic nanowires (silicon (Si), germanium (Ge), and SiGe alloy NWs) that provides a robust host for efficient stripping/plating of Li metal. The lithiophilic Li22 Si5 , Li22 (Si0.5 Ge0.5 )5, and Li22 Ge5 formed during rapid Li melt infiltration prevented the formation of dead Li and dendrites. Li22 Ge5 /Li covered CP hosts delivered the best performance, with the lowest overpotentials of 40 mV (three times lower than pristine Li) when cycled at 1 mA cm-2 /1 mAh cm-2 for 1000 h and at 3 mA cm-2 /3 mAh cm-2 for 500 h. Ex situ analysis confirmed the ability of the lithiophilic Li22 Ge5 decorated samples to facilitate uniform Li deposition. When paired with sulfur, LiFePO4, and NMC811 cathodes, the CP-LiGe/Li anodes delivered 200 cycles with 82%, 93%, and 90% capacity retention, respectively. The discovery of the highly stable, lithiophilic NW decorated CP hosts is a promising route toward stable cycling LMBs and provides a new design motif for hosted Li metal anodes.
RESUMO
Herein, we demonstrate the ability of Zn to catalyze the growth of Si nanowires via reaction temperature determined, vapour-liquid-solid (VLS) or vapour-solid-solid (VSS) growth mechanisms. This is the first reported use of a type B catalyst to grow Si nanowires via the VSS mechanism to our knowledge whereby the highly faceted Zn seeds resulted in an increased NW diameter. This was used to induce diameter variations along the axial length of individual nanowires by transitioning between VLS and VSS growth.
Assuntos
Nanofios/química , Silício/química , Zinco/química , Catálise , Transição de Fase , TemperaturaRESUMO
The electrochemical performance of Ge, an alloying anode in the form of directly grown nanowires (NWs), in Li-ion full cells (vs LiCoO2) was analyzed over a wide temperature range (-40 to 40 °C). LiCoO2||Ge cells in a standard electrolyte exhibited specific capacities 30× and 50× those of LiCoO2||C cells at -20 and -40 °C, respectively. We further show that propylene carbonate addition further improved the low-temperature performance of LiCoO2||Ge cells, achieving a specific capacity of 1091 mA h g-1 after 400 cycles when charged/discharged at -20 °C. At 40 °C, an additive mixture of ethyl methyl carbonate and lithium bis(oxalato)borate stabilized the capacity fade from 0.22 to 0.07% cycle-1. Similar electrolyte additives in LiCoO2||C cells did not allow for any gains in performance. Interestingly, the capacity retention of LiCoO2||Ge improved at low temperatures due to delayed amorphization of crystalline NWs, suppressing complete lithiation and high-order Li15Ge4 phase formation. The results show that alloying anodes in suitably configured electrolytes can deliver high performance at the extremes of temperature ranges where electric vehicles operate, conditions that are currently not viable for commercial batteries without energy-inefficient temperature regulation.
RESUMO
High loading (>1.6 mg cm-2 ) of Si nanowires (NWs) is achieved by seeding the growth from a dense array of Cu15 Si4 NWs using tin seeds. A one-pot synthetic approach involves the direct growth of CuSi NWs on Cu foil that acts as a textured surface for Sn adhesion and Si NW nucleation. The high achievable Si NW loading is enabled by the high surface area of CuSi NWs and bolstered by secondary growth of Si NWs as branches from both Si and CuSi NW stems, forming a dense Si active layer, interconnected with an electrically conducting CuSi array (denoted Si/CuSi). When employed as Li-ion battery anodes, the Si/CuSi nest structure demonstrates impressive rate performance, reaching 4.1 mAh cm-2 at C/20, 3.1 mAh cm-2 at C/5, and 0.8 mAh cm-2 at 6C. Also, Si/CuSi shows remarkable long-term stability, delivering a stable areal capacity of 2.2 mAh cm-2 after 300 cycles. Overall, complete anode fabrication is achieved within a single reaction by employing an inexpensive Sn powder approach.
RESUMO
A scalable and cost-effective process is used to electroplate metallic Zn seeds on stainless steel substrates. Si and Ge nanowires (NWs) are subsequently grown by placing the electroplated substrates in the solution phase of a refluxing organic solvent at temperatures >430 °C and injecting the respective liquid precursors. The native oxide layer formed on reactive metals such as Zn can obstruct NW growth and is removed in situ by injecting the reducing agent LiBH4 . The findings show that the use of Zn as a catalyst produces defect-rich Si NWs that can be extended to the synthesis of Si-Ge axial heterostructure NWs with an atomically abrupt Si-Ge interface. As an anode material, the as grown Zn seeded Si NWs yield an initial discharge capacity of 1772 mAh g-1 and a high capacity retention of 85% after 100 cycles with the active participation of both Si and Zn during cycling. Notably, the Zn seeds actively participate in the Li-cycling activities by incorporating into the Si NWs body via a Li-assisted welding process, resulting in restructuring the NWs into a highly porous network structure that maintains a stable cycling performance.