Ultrafast Sulfur Redox Dynamics Enabled by a PPy@N‑TiO2 Z‑Scheme Heterojunction Photoelectrode for Photo‑Assisted Lithium–Sulfur Batteries

Published in Chemistry and Materials

Ultrafast Sulfur Redox Dynamics Enabled by a PPy@N‑TiO2 Z‑Scheme Heterojunction Photoelectrode for Photo‑Assisted Lithium–Sulfur Batteries
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Ultrafast Sulfur Redox Dynamics Enabled by a PPy@N-TiO2 Z-Scheme Heterojunction Photoelectrode for Photo-Assisted Lithium–Sulfur Batteries - Nano-Micro Letters

Photo-assisted lithium–sulfur batteries (PALSBs) offer an eco-friendly solution to address the issue of sluggish reaction kinetics of conventional LSBs. However, designing an efficient photoelectrode for practical implementation remains a significant challenge. Herein, we construct a free-standing polymer–inorganic hybrid photoelectrode with a direct Z-scheme heterostructure to develop high-efficiency PALSBs. Specifically, polypyrrole (PPy) is in situ vapor-phase polymerized on the surface of N-doped TiO2 nanorods supported on carbon cloth (N-TiO2/CC), thereby forming a well-defined p–n heterojunction. This architecture efficiently facilitates the carrier separation of photo-generated electron–hole pairs and significantly enhances carrier transport by creating a built-in electric field. Thus, the PPy@N-TiO2/CC can simultaneously act as a photocatalyst and an electrocatalyst to accelerate the reduction and evolution of sulfur, enabling ultrafast sulfur redox dynamics, as convincingly validated by both theoretical simulations and experimental results. Consequently, the PPy@N-TiO2/CC PALSB achieves a high discharge capacity of 1653 mAh g−1, reaching 98.7% of the theoretical value. Furthermore, 5 h of photo-charging without external voltage enables the PALSB to deliver a discharge capacity of 333 mAh g−1, achieving dual-mode energy harvesting capabilities. This work successfully integrates solar energy conversion and storage within a rechargeable battery system, providing a promising strategy for sustainable energy storage technologies.

While lithium–sulfur batteries (LSBs) promise 2600 Wh kg⁻¹, the sluggish liquid-solid conversion of polysulfides keeps practical capacities far below theory. Now, researchers at Northwestern Polytechnical University, led by Prof. Yibo He, report a free-standing PPy@N-TiO2/Carbon-Cloth photocathode that harvests sunlight to co-drive sulfur redox, delivering 1 653 mAh g-1 (98.7 % of theory) and 333 mAh g-1 after 5 h of pure photo-charging. Published in Nano-Micro Letters, the work realizes dual-mode energy harvesting in a single cell.

Why Photo-Assisted Strategy Matters

  • Polysulfide Bottleneck: Long-chain Li2S6/8 species shuttle and precipitate as electrically insulating Li2S, wasting active mass.
  • External-Field Boost: Optical fields lower activation energy via photocatalysis, yet single-semiconductor electrodes suffer wide band-gaps and fast carrier recombination.
  • Sun-in-Sulfur Vision: Integrating solar conversion and storage slashes grid demand during charging, ideal for high-altitude or off-grid devices.

Innovative Heterojunction Design

  • Z-Scheme p–n Junction: Vapor-phase polymerized polypyrrole (p-type) coats N-doped TiO2 nanorods (n-type), building an internal electric field that separates e-/h+ pairs.
  • Band-Engineered Alignment: narrowed gap (2.17 eV) extends visible harvest; CB electrons reduce S8→Li2S while VB holes oxidize Li2S→S8, closing a catalytic loop.
  • Free-standing Architecture: 3-D carbon cloth offers 599 mAh g-1 at 4 C and 3.3 mAh cm⁻² under 3 mg cm-2 sulfur, mitigating volume swing and blocking shuttle.

Performance Breakthroughs

  • Ultrafast Redox: Tafel slopes drop from 122 → 48 mV dec-1; Li2S nucleation time shortens from 3600 → 3010 s with 17 % higher capacity.
  • Dual-Mode Harvesting: 0.33 % solar-to-output efficiency; coin cell powers toy car 288 cm under light vs 212 cm in dark, then 77 cm after 2 h re-charge under ambient sunlight.
  • Long-term Stability: 61.7 % retention over 328 cycles at 0.5 C; DRT analysis shows illuminated cell maintains lower RSEI and RPS, suppressing parasitic reactions.

Future Outlook
The plug-and-play photocathode design is scalable through roll-to-roll vapor coating, pointing toward solar-assisted EV packs and stratospheric drones where every photon counts.

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Batteries
Physical Sciences > Materials Science > Materials for Energy and Catalysis > Batteries
Electrochemistry
Physical Sciences > Chemistry > Physical Chemistry > Electrochemistry
Photocatalysis
Physical Sciences > Chemistry > Physical Chemistry > Catalysis > Photocatalysis
Electrocatalysis
Physical Sciences > Chemistry > Physical Chemistry > Catalysis > Electrocatalysis
Nanoscale Design, Synthesis and Processing
Physical Sciences > Materials Science > Nanotechnology > Nanoscale Design, Synthesis and Processing
  • Nano-Micro Letters Nano-Micro Letters

    Nano-Micro Letters is a peer-reviewed, international, interdisciplinary and open-access journal that focus on science, experiments, engineering, technologies and applications of nano- or microscale structure and system in physics, chemistry, biology, material science, and pharmacy.