

NVP Anode-Free Pouch Dry Pouch Cell(Multiple Specs)
$102.00
NVP Anode-Free Sodium-Ion Pouch Dry Cell — lithium-free, cobalt-free anode-free sodium-ion dry pouch cell pairing NVP (Na₃V₂(PO₄)₃) NASICON cathode with carbon-coated aluminum foil current collector — no anode active material. Sodium plates in-situ from cathode during first charge. Higher-voltage NASICON chemistry (3.4 V plateau) combined with anode-free architecture for next-generation high-energy-density sodium-ion battery research.
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Name: NVP Anode-Free Sodium-Ion Pouch Dry Cell (Multiple Specs)
Cell Type: NVP-Anode-Free Pouch Dry Cell
Product Code: XN-NVP-AF
Description:
NVP Anode-Free Sodium-Ion Pouch Dry Cell pairs sodium vanadium phosphate (Na₃V₂(PO₄)₃, NASICON-type) cathode with a carbon-coated aluminum foil current collector — no anode active material — in a fully assembled but unfilled (dry) pouch format. As a result, this configuration combines NVP’s higher operating voltage (3.4 V plateau, 2.5–3.8 V window) and excellent ionic conductivity with the maximum-energy-density anode-free architecture. During the first charge, sodium ions plate directly from the NVP cathode onto the carbon-coated aluminum surface, eliminating the volume and weight overhead of conventional hard carbon anodes. Note that, unlike lithium-ion anode-free cells which use bare copper, sodium-ion anode-free systems require aluminum foil with a thin carbon coating — copper is incompatible with sodium (Cu–Na alloy formation), and the carbon coating is essential to improve sodium nucleation and reduce first-cycle losses. Furthermore, the dry (unfilled) pouch format allows customers to inject their own electrolyte formulations, making this cell ideal for advanced anode-free sodium-ion electrolyte and plating interface research.
Application:
This dry pouch cell serves as a research platform for anode-free sodium-ion battery development based on NASICON-type cathodes, including sodium-ion electrolyte formulation studies for higher-voltage sodium plating, plating/stripping interface research on carbon-coated aluminum, advanced electrolyte additive screening for dendrite suppression and high coulombic efficiency, full-cell prototyping for stationary energy storage and grid-scale storage applications, and academic studies of NVP/anode-free electrochemistry — particularly the comparison between NVP’s 3.4 V voltage plateau and lower-voltage polyanionic chemistries such as NFPP.
Cell Specifications (1 Ah Standard Grade):
| Parameter | Value |
|---|---|
| Cell Type | NVP-Anode-Free Pouch Dry Cell |
| Design Capacity | 1000 mAh (1 Ah) |
| Cell Dimensions | 6090 (60 × 90 mm) |
| Cell Architecture | Stacked (laminated) |
| Recommended Voltage Range | 2.5 – 3.8 V |
| Separator | PE 9+3 (composite) |
| Cathode Sheet Count | 10 |
| Current Collector Sheet Count | 11 |
| Recommended Electrolyte Filling | 5–6 g/Ah |
| Recommended Aging | 45 °C, 24 h rest, 8 kgf/cm² pressure |
| Recommended Formation | 0.1C constant-current charge to 3.8 V (see below) |
| Final Aging | Room temperature, 24 h rest |
Cathode Specifications (NVP):
| Parameter | Value |
|---|---|
| Active Material | NVP (Na₃V₂(PO₄)₃, NASICON-type sodium vanadium phosphate) |
| Active Material Content | 92.0% |
| Specific Capacity | 100 mAh/g |
| Double-Side Areal Density | 30 mg/cm² |
| Electrode Dimensions | 75 × 54 mm |
Current Collector Specifications (Anode-Free):
| Parameter | Value |
|---|---|
| Anode Construction | Carbon-coated aluminum foil — no active material |
| Sodium Source | From cathode during first charge (in-situ plating) |
| Current Collector | Aluminum foil with conductive carbon coating |
| Electrode Dimensions | 77 × 56 mm |
Values measured by Xnergy. Typical values for reference; not guaranteed unless otherwise specified.
Available Capacity Grades:
| Grade | Capacity | Notes |
|---|---|---|
| 1 Ah Standard | 1000 mAh | 6090 dimensions, lab-scale R&D |
| 2 Ah | 2000 mAh | Mid-scale prototyping |
| Single-Layer | — | Single-layer construction for fundamental anode-free studies and SEI characterization |
| Custom Specs | — | Cathode loading, separator, and electrode dimensions customizable; contact sales |
Characteristics:
NASICON NVP cathode: higher voltage plateau (3.4 V) than NFPP
NVP delivers a flat 3.4 V voltage plateau with a 2.5–3.8 V cutoff window — significantly higher than NFPP polyanionic chemistry (which operates at 1.5–3.4 V). As a result, NVP-based anode-free cells deliver higher cell-level energy and provide a useful research platform for studying the voltage-dependence of sodium plating efficiency and SEI stability across different polyanionic cathode systems.
Carbon-coated aluminum: the sodium-compatible current collector
Unlike lithium-ion anode-free systems that use bare copper, sodium-ion anode-free cells must use aluminum foil — copper alloys with sodium and cannot serve as a current collector. Furthermore, a thin conductive carbon coating on the aluminum surface improves sodium nucleation, lowers nucleation overpotential, reduces first-cycle losses, and stabilizes the plating/stripping interface. Therefore, this cell uses carbon-coated aluminum foil as the standard anode-free current collector — a critical materials choice unique to sodium-ion anode-free chemistry.
NASICON 3D ion-conduction framework
The NASICON crystal structure of NVP provides three-dimensional sodium-ion diffusion pathways, resulting in excellent rate capability and high power density. Therefore, this cell is well-suited for high-rate cycling studies and applications requiring fast sodium-ion transport — characteristics that distinguish NVP from olivine-type and layered oxide sodium-ion cathodes.
In-situ sodium plating from NVP cathode
During the first charge, sodium ions migrate from the NVP cathode and plate directly onto the carbon-coated aluminum surface, forming the sodium metal anode in-situ. Therefore, customers can study sodium plating morphology under NVP’s higher-voltage operating window — a regime where dendrite suppression and SEI stability differ from lower-voltage NFPP anode-free systems.
Aging under stack pressure for sodium plating uniformity
The recommended aging protocol applies 8 kgf/cm² stack pressure at 45 °C for 24 h. Consequently, this controlled pressure environment promotes uniform sodium plating during formation, suppresses dendrite formation, and improves cycling stability — a critical practice for anode-free sodium-ion systems.
Dry (unfilled) pouch design for sodium-ion electrolyte studies
The cell ships fully assembled but without electrolyte. Therefore, customers can inject their own sodium-ion electrolyte formulations to study electrolyte effects on sodium plating efficiency at NVP’s 3.4 V plateau, SEI stability, and dendrite suppression — the core challenges of anode-free sodium-ion chemistry that are most strongly influenced by electrolyte design and additive selection.
Multiple capacity grades + single-layer option
Standard 1 Ah and 2 Ah multi-layer grades support full-cell research. Furthermore, the Single-Layer option provides a simplified platform for fundamental anode-free studies — ideal for SEI characterization on carbon-coated aluminum, sodium plating morphology imaging, and one-electrode interface research.
Recommended Activation Protocol:
1. Inject sodium-ion electrolyte at 5–6 g/Ah ratio. 2. Vacuum-seal the pouch under inert atmosphere. 3. Aging: hold at 45 °C for 24 h under 8 kgf/cm² stack pressure (sodium begins plating uniformly across the carbon-coated aluminum surface during formation). 4. Pre-formation rest: 12 h. 5. Formation: charge at 0.1C constant current to 3.8 V (1 cycle, full sodium loading). 6. Final aging: hold at room temperature for 24 h before subsequent cycling tests.
Packaging & Storage:
Cells ship vacuum-sealed under inert atmosphere in moisture-barrier packaging. Therefore, customers should store sealed in a cool, dry environment (15–25 °C, RH < 30 %), protected from moisture and direct sunlight. Open packaging in a dry-room or glovebox environment immediately before electrolyte filling. Note that no sodium metal is present in the cell as shipped — anode-free cells in their pre-formation state are significantly less hazardous than pre-deposited sodium-metal cells, but standard sodium-ion cell handling applies once electrolyte is added and formation begins.
Safety:
For research and industrial use only. Once electrolyte is added and formation initiated, sodium metal is plated onto the carbon-coated aluminum surface — at this point the cell becomes a sodium-metal battery and must be handled accordingly. Activated cells contain flammable electrolyte and reactive sodium metal; handle in glovebox or dry-room conditions during electrolyte filling and formation. Wear full PPE. Never short-circuit, overcharge, overdischarge, puncture, or expose cells to high temperatures (> 60 °C). NVP’s vanadium-based chemistry requires standard sodium-ion handling protocols once activated. Refer to SDS for complete safety information.
Note: Values listed above are typical and for reference only. Performance may vary depending on electrolyte choice, formation protocol, applied stack pressure, cycling conditions, and test environment. Anode-free sodium-ion chemistry is highly sensitive to electrolyte design and current collector surface treatment — consult published literature for guidance on electrolyte formulations targeting high coulombic efficiency on carbon-coated aluminum at NVP’s 3.4 V plateau. See also other dry pouch cells in our catalog: NVP / Hard Carbon, NFPP Polyanionic / Hard Carbon, NFPP Anode-Free, P2 Layered Oxide, Sodium Metal Single-Layer Pouch, LFP Anode-Free, LFP / Artificial Graphite, LFP / Lithium Metal, NCM811 Anode-Free, NCM811 / Artificial Graphite, and LMFP / Artificial Graphite. Browse the full Dry Pouch Cell category for all configurations.
| NVP / Anode-Free | (1ah) |
|---|




