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<p>Extending the π-conjugated bridge in donor–π–acceptor dyes improves light harvesting but systematically erodes interfacial charge-transfer performance. Here, density functional theory (DFT) and time-dependent DFT (TD-DFT) were used to investigate triphenylamine–cyanoacrylic acid dyes with one to four thiophene bridge units (T1–T4) alongside a site-specific alkyl-chain engineering strategy on the tetra-thiophene scaffold. Bridge extension progressively red-shifts the absorption maximum from 445&#xa0;nm (T1) to 508&#xa0;nm (T4) but simultaneously delocalizes excited-state electron density over the π-bridge, reducing effective electron density at the acceptor–TiO₂ interface and weakening adsorption stability, dye regeneration thermodynamics, and injection efficiency. Site-specific alkyl substitution addresses this conflict: the alternating a, d-substitution pattern constructs a bilateral steric fence that suppresses face-to-face π–π stacking and relocates dye–electrolyte interactions away from the conjugated core, thereby suppressing charge recombination. Lorentzian fitting of projected density-of-states profiles confirms that all alkylated variants retain ultrafast electron injection and near-unity injection efficiency, demonstrating that the steric modification is electronically decoupled from the injection channel. These results establish site-specific alkyl-chain engineering as an effective strategy for mitigating the trade-off inherent to long-bridge dye design.</p>

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Addressing the Trade-off in Long π-Bridge Dyes: Performance Optimization by Site-Specific Alkyl Chain Engineering

  • 期刊论文

  • 发表日期：

    2026年6月22日

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  • Haiping Li,
  • Zongxue Wang,
  • Xing Hu,
  • Hancheng Zhu,
  • Ji Zhang,
  • Xinzhao Zhang

摘要

Extending the π-conjugated bridge in donor–π–acceptor dyes improves light harvesting but systematically erodes interfacial charge-transfer performance. Here, density functional theory (DFT) and time-dependent DFT (TD-DFT) were used to investigate triphenylamine–cyanoacrylic acid dyes with one to four thiophene bridge units (T1–T4) alongside a site-specific alkyl-chain engineering strategy on the tetra-thiophene scaffold. Bridge extension progressively red-shifts the absorption maximum from 445 nm (T1) to 508 nm (T4) but simultaneously delocalizes excited-state electron density over the π-bridge, reducing effective electron density at the acceptor–TiO₂ interface and weakening adsorption stability, dye regeneration thermodynamics, and injection efficiency. Site-specific alkyl substitution addresses this conflict: the alternating a, d-substitution pattern constructs a bilateral steric fence that suppresses face-to-face π–π stacking and relocates dye–electrolyte interactions away from the conjugated core, thereby suppressing charge recombination. Lorentzian fitting of projected density-of-states profiles confirms that all alkylated variants retain ultrafast electron injection and near-unity injection efficiency, demonstrating that the steric modification is electronically decoupled from the injection channel. These results establish site-specific alkyl-chain engineering as an effective strategy for mitigating the trade-off inherent to long-bridge dye design.