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sob老师、各位老师好,
我最近在做非生色团簇发光相关的模拟,目前在算小分子的发光机制,文献中说这些非生色基团的发光一般在S1->S0。
但我在计算某些二聚体和小分子时(使用b3lyp//6-311g**步骤为opt、freq 然后opt td),会出现S1的发射波长为1000多nm的情况,而且极难收敛,而S2的发射波长与我预测的波长类似。我看了sob老师关于势能面交叉的博文,但即使使用maxstep=3,notrust和root=2,nstates=5,此时S2才是1000多nm,而S1又与预测值相近。
感谢大家的解惑,祝大家研运昌隆!
以下是极端情况S1、S2都过高,是一个二聚体的td opt。
Excitation energies and oscillator strengths:
Excited State 1: Singlet-A 0.0089 eV 140021.62 nm f=0.0000 <S**2>=0.000
87 -> 89 -0.14474
88 -> 89 -1.86643
88 -> 90 0.18347
87 <- 89 0.12757
88 <- 89 1.72960
88 <- 90 -0.17675
This state for optimization and/or second-order correction.
Total Energy, E(TD-HF/TD-DFT) = -1152.34107803
Copying the excited state density for this state as the 1-particle RhoCI density.
Excited State 2: Singlet-A 1.4387 eV 861.76 nm f=0.0301 <S**2>=0.000
87 -> 89 -0.70169
87 -> 90 -0.21444
87 <- 89 0.22039
Excited State 3: Singlet-A 2.3566 eV 526.12 nm f=0.0048 <S**2>=0.000
86 -> 89 0.17390
87 -> 90 0.13050
88 -> 90 -0.66731
SavETr: write IOETrn= 770 NScale= 10 NData= 16 NLR=1 NState= 3 LETran= 64.
The selected state is a singlet.
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