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LY
Verified CAS / Academic Author2 Decoded Studies

Prof. LIU Yuqi

Beijing Normal University

Co-Affiliations:Tianjin University

Research Publications & English Decoded Briefs

Showing 2 publications
SCIENCE CHINA Materials2026DOI: 10.1007/s40843-025-3793-9

High-efficiency hybrid planar/bulk heterojunction organic solar cells

Organic solar cells (OSCs) require both a high donor/acceptor (D/A) interfacial area for efficient exciton dissociation and a vertically phase-separated morphology for efficient charge transport. Traditional bulk heterojunctions (BHJs) provide large interfacial areas but lack vertical phase separation, while quasi-planar heterojunctions (QPHJs) achieve vertical separation at the cost of reduced interfacial contact. Here, we introduce an in situ pore-forming strategy for polymer thin films. By incorporating an excess of additives as pore-forming agents into the donor layer, a nanoporous film with a fibrous nano-network is generated. Subsequent deposition of acceptor molecules fills these nanopores, creating a hybrid planar/bulk heterojunction (HP/BHJ) that synergizes the strengths of both architectures. This design enhances performance by: (1) increasing the D/A interfacial area via nanopores, forming a three-dimensional network that accelerates exciton dissociation; (2) promoting close molecular packing that minimizes carrier recombination and establishes low-defect charge transport channels; and (3) fostering vertical phase separation through layer-by-layer deposition. Binary OSCs fabricated with this strategy achieve a power conversion efficiency (PCE) of 20.0%, surpassing conventional BHJ and QPHJ devices by a significant margin. The approach demonstrates general applicability, with analogous improvements observed in D18/BTP-eC9-4F and PM6/L8-BO systems, underscoring its potential for advancing OSC performance.

SCIENCE CHINA Materials2025DOI: 10.1007/s40843-025-3394-6

Improving the Initial Coulombic Efficiency of Phenolic Resin-Derived Hard Carbon Anodes for Sodium-Ion Batteries by Pore-Forming

Hard carbon (HC) is a leading anode candidate for sodium-ion batteries (SIBs) due to its disordered structure and expanded interlayer spacing (3.4–4 Å), which facilitate sodium-ion intercalation. However, the poor initial Coulombic efficiency (ICE) of HC remains a critical barrier to commercial viability. Phenolic resin (PF) precursors offer high carbon yield and good reversible capacity, yet the relationship between PF solid content and ICE is not fully understood. This study investigates four commercial PF-based hard carbons with varying solid contents, then modifies them via pore-forming agents, cross-linking curing, and ball-milling. The optimized U-HC sample, derived from the highest solid-content PF, achieves an ICE of 89.84% and a specific discharge capacity of 354.18 mAh g⁻¹ at 35 mA g⁻¹. Baseline PF-derived HCs typically exhibit ICE values below 82%, as reported for resorcinol-formaldehyde resin (82%) and PTCDA-modified PF (77.9%). The pore-forming strategy enhances ICE beyond 86% across modified samples, with U-HC reaching 89.84%. This improvement is attributed to optimized pore architecture that reduces irreversible sodium trapping and SEI formation. The findings provide a rational design pathway for high-ICE PF-derived hard carbon anodes, addressing a key bottleneck in SIB commercialization.