密度泛函理论
离域电子
材料科学
超极化率
石墨烯
空位缺陷
兴奋剂
化学物理
光电子学
吸收光谱法
带隙
分子物理学
激发
吸收(声学)
计算化学
纳米技术
凝聚态物理
化学
非线性光学
非线性系统
光学
物理
复合材料
有机化学
量子力学
作者
Jyotirmoy Deb,Pratim Kumar Chattaraj
出处
期刊:Chemistry
[Multidisciplinary Digital Publishing Institute]
日期:2025-08-07
卷期号:7 (4): 126-126
标识
DOI:10.3390/chemistry7040126
摘要
This study investigates the influence of vacancy engineering and nitrogen doping on the structural, electronic, and optical properties of T-graphene fragments (TFs) using density functional theory (DFT) and time-dependent DFT (TD-DFT). A central vacancy and five pyridinic nitrogen doping configurations are explored to modulate the optoelectronic behavior. All systems are thermodynamically stable, exhibiting tunable HOMO–LUMO gaps, orbital distributions, and charge transfer characteristics. Optical absorption spectra show redshifts and enhanced oscillator strengths in doped variants, notably v-NTF2 and v-NTF4. Nonlinear optical (NLO) analysis reveals significant enhancement in both static and frequency-dependent responses. v-NTF2 displays an exceptionally high first-order hyperpolarizability (⟨β⟩ = 1228.05 au), along with a strong electro-optic Pockels effect (β (−ω; ω, 0)) and second harmonic generation (β (−2ω; ω, ω)). Its third-order response, γ (−2ω; ω, ω, 0), also exceeds 1.2 × 105 au under visible excitation. Conceptual DFT descriptors and energy decomposition analysis further supports the observed trends in reactivity, charge delocalization, and stability. These findings demonstrate that strategic nitrogen doping in vacancy-engineered TFs is a powerful route to tailor electronic excitation, optical absorption, and nonlinear susceptibility. The results offer valuable insight into the rational design of next-generation carbon-based materials for optoelectronic, photonic, and NLO device applications.
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