Advanced anode design with PAN-lignin fiber and B, P-co-doped graphitic carbon nitride composites for sustainable lithium-ion battery applications

Abstract This study introduces a sustainable anode material for lithium-ion batteries (LIBs) by integrating boron-phosphorus co-doped graphitic carbon nitride (BPCN) into a polyacrylonitrile-lignin (PAN-Lignin) matrix. The composite leverages lignin’s renewable nature and BPCN’s heteroatom-rich structure to address critical challenges in conventional LIB anodes, such as reliance on fossil-derived materials and limited electrochemical performance. Centrifugal spinning and controlled carbonization (800 °C under argon) yielded hierarchically porous PAN-Lignin/BPCN fibers with expanded interlayer spacing (0.34–0.38 nm), as confirmed by XRD and FTIR. The optimized 75:25 PAN-Lignin/BPCN composite demonstrated exceptional lithium-ion storage, achieving an initial discharge capacity of 522.46 mAh g −1 at 0.5 A/g, 1.4× higher than undoped PAN-Lignin anodes—and retained 72.3% capacity (178 mAh g −1 ) over 50 cycles. Electrochemical analysis revealed synergistic effects: BPCN enhanced electronic conductivity via polarized B–N/P–N bonds, while the lignin-derived carbon framework provided interconnected porosity for efficient ion diffusion. EIS showed low initial interfacial resistance (7.319 Ω) and charge transfer resistance (303 Ω), though post-cycling R ct increased to 710 Ω due to SEI formation. The composite outperformed single-doped analogs (BCN: 467 mAh g −1 ; PCN: 498 mAh g −1 ) and conventional lignin-based carbons, attributed to BPCN’s dual role in stabilizing the SEI layer and introducing active sites. Sustainability was emphasized through lignin’s carbon-negative sourcing and a 200 °C reduction in carbonization temperature compared to graphite anodes. This work advances sustainable LIB technology by replacing >75% fossil-based components with biomass-derived materials while achieving performance metrics rivaling synthetic graphite. The 75:25 PAN-Lignin/BPCN composite sets a benchmark for biomass anodes, aligning with global decarbonization goals. Future efforts should focus on SEI stabilization and full-cell integration to bridge the gap between lab-scale innovation and commercial energy storage systems.

Authors

Institutions

Publication Details

Journal
Materials Research Express
Published
2025-11-01
DOI
https://doi.org/10.1088/2053-1591/ae223e
Citations
1
Primary Topic
Advancements in Battery Materials
Type
article
Field-Weighted Citation Impact
0.73
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Advanced anode design with PAN-lignin fiber and B, P-co-doped graphitic carbon nitride composites for sustainable lithium-ion battery applications

Melih Beşir Arvas, Sibel Yazar, Nihan Aydemi̇r, Osman Eksik et al.
1 citations
Materials Research Express
Advancements in Battery Materials
0.73
article

Advanced anode design with PAN-lignin fiber and B, P-co-doped graphitic carbon nitride composites for sustainable lithium-ion battery applications

Melih Beşir Arvas, Sibel Yazar, Nihan Aydemi̇r, Osman Eksik, Refik Arat, Elanur Kalkan, Korhan Şahin, Ismail O. Koklu
article en
1 citations

Abstract

Abstract This study introduces a sustainable anode material for lithium-ion batteries (LIBs) by integrating boron-phosphorus co-doped graphitic carbon nitride (BPCN) into a polyacrylonitrile-lignin (PAN-Lignin) matrix. The composite leverages lignin’s renewable nature and BPCN’s heteroatom-rich structure to address critical challenges in conventional LIB anodes, such as reliance on fossil-derived materials and limited electrochemical performance. Centrifugal spinning and controlled carbonization (800 °C under argon) yielded hierarchically porous PAN-Lignin/BPCN fibers with expanded interlayer spacing (0.34–0.38 nm), as confirmed by XRD and FTIR. The optimized 75:25 PAN-Lignin/BPCN composite demonstrated exceptional lithium-ion storage, achieving an initial discharge capacity of 522.46 mAh g −1 at 0.5 A/g, 1.4× higher than undoped PAN-Lignin anodes—and retained 72.3% capacity (178 mAh g −1 ) over 50 cycles. Electrochemical analysis revealed synergistic effects: BPCN enhanced electronic conductivity via polarized B–N/P–N bonds, while the lignin-derived carbon framework provided interconnected porosity for efficient ion diffusion. EIS showed low initial interfacial resistance (7.319 Ω) and charge transfer resistance (303 Ω), though post-cycling R ct increased to 710 Ω due to SEI formation. The composite outperformed single-doped analogs (BCN: 467 mAh g −1 ; PCN: 498 mAh g −1 ) and conventional lignin-based carbons, attributed to BPCN’s dual role in stabilizing the SEI layer and introducing active sites. Sustainability was emphasized through lignin’s carbon-negative sourcing and a 200 °C reduction in carbonization temperature compared to graphite anodes. This work advances sustainable LIB technology by replacing >75% fossil-based components with biomass-derived materials while achieving performance metrics rivaling synthetic graphite. The 75:25 PAN-Lignin/BPCN composite sets a benchmark for biomass anodes, aligning with global decarbonization goals. Future efforts should focus on SEI stabilization and full-cell integration to bridge the gap between lab-scale innovation and commercial energy storage systems.

Materials Research ExpressVol. 12(11)
Gebze Technical University (TR), Istanbul University-Cerrahpaşa (TR), Institute of Nanotechnology (GB), Turkish Aerospace Industries (Turkey) (TR), Istanbul Technical University (TR), Istanbul University (TR)
Openalex Percentile: Top 21%
Advancements in Battery Materials
0.73
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.