News Release

Self‑regulated bilateral anchoring enables efficient charge transport pathways for high‑performance rigid and flexible perovskite solar cells

Peer-Reviewed Publication

Shanghai Jiao Tong University Journal Center

Self-Regulated Bilateral Anchoring Enables Efficient Charge Transport Pathways for High-Performance Rigid and Flexible Perovskite Solar Cells

image: 

  • Robust interface molecular bridge was constructed by employing self-transforming squaric acid (SA) to reduce residual stress and passivate defects at the buried interface.
  • Attributing to the efficient charge transport pathways, the SA-modified perovskite solar cells demonstrate high photovoltaic performance with power conversion efficiency up to 25.50% (rigid) and 24.92% (flexible).
  • The SA-modified devices demonstrate excellent stability under various environmental stress conditions, including humidity, thermal aging, light irradiation, and bending.
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Credit: Haiying Zheng, Guozhen Liu, Xinhe Dong, Feifan Chen, Chao Wang, Hongbo Yu, Zhihua Zhang, Xu Pan.

As perovskite solar cells (PSCs) approach commercialization, the buried electron-transport interface remains a hidden source of efficiency loss and long-term instability. Now researchers from Dalian Jiaotong University, Dalian University of Technology and CAS Hefei Institutes, led by Prof. Guozhen Liu, Prof. Zhihua Zhang and Prof. Xu Pan, introduce a one-molecule, self-regulated “bilateral anchoring” strategy that turns this buried weakness into a performance booster. Their work, published in Nano-Micro Letters, delivers record efficiencies for both rigid and flexible PSCs while extending device lifetime under real-world stress.

Why the Buried Interface Matters

  • Defect Hot-Spot: Oxygen vacancies in SnO2 and under-coordinated Pb2+/halide defects at the perovskite side trap carriers and lower open-circuit voltage.
  • Energy-Level Mis-Match: Poor band alignment impedes electron extraction and invites recombination.
  • Mechanical Stress: Residual tensile stress accelerates crack formation when devices are heated or bent.
  • Solvent Instability: Conventional modifiers dissolve during perovskite casting, losing activity before the film even dries.

Innovative Design and Features

  • Squaric Acid (SA) Molecular Bridge: A four-membered, self-transforming ring delivers two carboxylic acid sites that simultaneously H-bond to SnO₂ and coordinate Pb2+, creating a solvent-proof, dual-sided anchor.
  • Dynamic Stress Release: SA’s quasi-aromatic backbone expands/contracts during thermal processing, converting 24.6 MPa tensile stress into −17 MPa beneficial compression in the perovskite lattice.
  • Defect-Healing & Mobility Boost: DFT shows formation energies of VFA, VI, VPb and VO rise by 0.1–1.2 eV after SA bonding; SCLC mobility climbs from 3.22 × 10-3 to 5.88 × 10-3 cm2 V-1 s-1.
  • Universal Applicability: Process is compatible with spin, blade or slot-die coating on glass, PEN or stainless-steel foils.

Applications and Future Outlook

  • High-Efficiency Devices: Champion rigid cells deliver 25.50 % PCE (Voc 1.19 V, Jsc 25.47 mA cm-2, FF 84.3 %); flexible cells reach 24.92 % with only 1.57 % hysteresis.
  • Large-Area Viability: 1 cm2 rigid modules still yield 24.01 %, proving scalability.
  • Multistress Stability: Un-encapsulated films retain >90 % of peak output after 3840 h at 45 ± 5 % RH, 88 % after 528 h at 85 °C, and 88 % after 1700 h continuous 1-sun MPP tracking; flexible devices survive 10 000 bends at 5 mm radius with <10 % loss.
  • Industrial Roadmap: Team is transferring the SA interlayer to roll-to-roll PEN lines and 30 × 30 cm2 minimodules, targeting IEC 61215 certification within two years.

This work establishes squaric acid as a commercially viable, single-component modifier that unites defect passivation, stress management and energy-level tuning—offering a clear pathway toward >25 % stable PSCs on any substrate. Stay tuned for pilot-line results from Prof. Liu, Prof. Zhang and Prof. Pan’s joint laboratories!


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