Dicyandiamide-Driven Tailoring of the n-Value Distribution and Interface Dynamics for High-Performance ACI 2D Perovskite Solar Cells

Published in Materials

Dicyandiamide-Driven Tailoring of the n-Value Distribution and Interface Dynamics for High-Performance ACI 2D Perovskite Solar Cells
Like

Share this post

Choose a social network to share with, or copy the URL to share elsewhere

This is a representation of how your post may appear on social media. The actual post will vary between social networks

Explore the Research

SpringerLink
SpringerLink SpringerLink

Dicyandiamide-Driven Tailoring of the n-Value Distribution and Interface Dynamics for High-Performance ACI 2D Perovskite Solar Cells - Nano-Micro Letters

Organic–inorganic hybrid perovskite solar cells achieve remarkable efficiencies (> 26%) yet face stability challenges. Quasi-2D alternating-cation-interlayer perovskites offer enhanced stability through hydrophobic spacer cations but suffer from vertical phase segregation and buried interface defects. Herein, we introduce dicyanodiamide (DCD) to simultaneously address these dual limitations in GA(MA)nPbnI3n+1 perovskites. The guanidine group in DCD passivates undercoordinated Pb2+ and MA+ vacancies at the perovskite/TiO2 interface, while cyano groups eliminate oxygen vacancies in TiO2 via Ti4+–CN coordination, reducing interfacial trap density by 73% with respect to the control sample. In addition, DCD regulates crystallization kinetics, suppressing low-n-phase aggregation and promoting vertical alignment of high-n phases, which benefit for carrier transport. This dual-functional modification enhances charge transport and stabilizes energy-level alignment. The optimized devices achieve a record power conversion efficiency of 21.54% (vs. 19.05% control) and retain 94% initial efficiency after 1200 h, outperforming unmodified counterparts (84% retention). Combining defect passivation with phase homogenization, this work establishes a molecular bridge strategy to decouple stability-efficiency trade-offs in low-dimensional perovskites, providing a universal framework for interface engineering in high-performance optoelectronics.

A research team led by Professors Pengwei Li, Yanlin Song, and Yiqiang Zhang has advanced quasi-2D alternating-cation-interlayer (ACI) perovskite solar cells by introducing a dicyandiamide (DCD)-based molecular bridge strategy. Their work, published in Nano-Micro Letters, demonstrates a dual-functional interface engineering approach that simultaneously passivates defects and regulates phase distribution, enabling record efficiencies and enhanced stability for 2D perovskite photovoltaics.

Why This Strategy Matters

  • Efficiency Boost: DCD-modified devices achieve a power conversion efficiency (PCE) of 54%, compared to 19.05%in control samples.
  • Reduced Defects: DCD lowers interfacial trap density by 73%, accelerating charge transport and suppressing recombination.
  • Stability: Devices retain 94% of initial efficiency after 1200 h, significantly outperforming unmodified PSCs (84% retention).

Design Strategy

The innovation lies in leveraging the multifunctional guanidine and cyano groups of DCD:

  • Interface Passivation: The guanidine group binds undercoordinated Pb2+ and fills cation/iodide vacancies at the perovskite buried interface.
  • ETL Engineering: The cyano group coordinates with Ti4+ in TiO2, eliminating oxygen vacancies and improving perovskite/ETL contact.
  • Phase Regulation: DCD suppresses low-n phase aggregation while promoting high-n phase vertical alignment, leading to uniform charge transport channels.

Mechanistic Insights

Spectroscopic and theoretical analyses confirm that:

  • XPS and FTIR validate DCD–Ti and DCD–Pb interactions, while reduced oxygen vacancy ratios (from 48% to 33%) highlight defect mitigation.
  • Transient absorption (TA) and PL studies reveal more homogeneous phase distribution, minimizing energy transfer losses.
  • DFT calculations confirm strong –CN–Ti bonding, explaining suppressed trap formation.

Performance Highlights

  • Device Metrics: VOC of 172 V, JSC of 23.08 mA cm-2, FF of 79.6%.
  • Carrier Dynamics: Trap densities decreased by more than threefold; recombination resistance increased to 68 kΩ, confirming efficient charge extraction.
  • Operational Stability: DCD-modified devices sustain performance under continuous 400 h illumination and withstand 1200 h of thermal and environmental stress.

Future Outlook

This study establishes a molecular bridge strategy that integrates defect passivation and phase homogenization, effectively decoupling the long-standing efficiency–stability trade-off in quasi-2D perovskites. Beyond solar cells, this versatile approach provides a universal platform for interface engineering in perovskite-based optoelectronics, including light-emitting diodes and photodetectors.

By uniting materials chemistry, interfacial physics, and device optimization, Professors Li, Song, and Zhang deliver a clear blueprint for the scalable development of efficient and durable next-generation perovskite photovoltaics.

Please sign in or register for FREE

If you are a registered user on Research Communities by Springer Nature, please sign in

Follow the Topic

Solar Cells
Physical Sciences > Materials Science > Materials for Devices > Photonic Devices > Solar Cells
Perovskites
Physical Sciences > Materials Science > Materials for Energy and Catalysis > Perovskites
Surfaces, Interfaces and Thin Film
Physical Sciences > Materials Science > Surfaces, Interfaces and Thin Film
Two-dimensional Materials
Physical Sciences > Materials Science > Surfaces, Interfaces and Thin Film > Two-dimensional Materials
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.