The S_(1) state decay dynamics of 2-hydroxypyridine following UV excitation at a wavelength range of 276.9-250.0 nm is investigated using femtosecond time-resolved photoelectron imaging technique.Based on pump wavelen...The S_(1) state decay dynamics of 2-hydroxypyridine following UV excitation at a wavelength range of 276.9-250.0 nm is investigated using femtosecond time-resolved photoelectron imaging technique.Based on pump wavelength dependence of the decay dynamics,a refined decay picture is proposed.At pump wavelength of 276.9 nm,the S_(1) state is depopulated through intersystem crossing to lower triplet state(s).At 264.0 nm,both intersystem crossing to lower triplet state(s)and internal conversion to the ground state are in operation.At 250.0 nm,internal conversion to the ground state becomes dominated.展开更多
N-ethylpyrrole is one of ethylsubstituted derivatives of pyrrole and its excited-state decay dynamics has never been explored.In this work,we investigate ultrafast decay dynamics of N-ethylpyrrole excited to the S_(1)...N-ethylpyrrole is one of ethylsubstituted derivatives of pyrrole and its excited-state decay dynamics has never been explored.In this work,we investigate ultrafast decay dynamics of N-ethylpyrrole excited to the S_(1)electronic state using a femtosecond time-resolved photoelectron imaging method.Two pump wavelengths of 241.9 and 237.7 nm are employed.At 241.9 nm,three time constants,5.0±0.7 ps,66.4±15.6 ps and 1.3±0.1 ns,are derived.For 237.7 nm,two time constants of 2.1±0.1 ps and 13.1±1.2 ps are derived.We assign all these time constants to be associated with different vibrational states in the S_(1)state.The possible decay mechanisms of different S_(1)vibrational states are briefly discussed.展开更多
The ultrafast dynamics of water molecules excited to the two F states is studied by combining two-photon excitation and time-resolved photoelectron imaging techniques. The lifetimes of the F1A1 and F1B1 states of H2O ...The ultrafast dynamics of water molecules excited to the two F states is studied by combining two-photon excitation and time-resolved photoelectron imaging techniques. The lifetimes of the F1A1 and F1B1 states of H2O (D2O) were derived to be 1.0±0.3 (1.9±0.4) and 10±3 (30±10) ps, respectively. We propose that the F1A1 state mainly decays through the D state, due to the nonadiabatic coupling between them, while the F1B1 state decays through the F1A1 state via Coriolis interaction.展开更多
基金supported by the National Natural Science Foundation of China(No.21833003)the Strategic Priority Research Program of the Chinese Academy of Sciences(No.XDB17000000)the Key Technology Team of the Chinese Academy of Sciences(GJJSTD20190002)。
文摘The S_(1) state decay dynamics of 2-hydroxypyridine following UV excitation at a wavelength range of 276.9-250.0 nm is investigated using femtosecond time-resolved photoelectron imaging technique.Based on pump wavelength dependence of the decay dynamics,a refined decay picture is proposed.At pump wavelength of 276.9 nm,the S_(1) state is depopulated through intersystem crossing to lower triplet state(s).At 264.0 nm,both intersystem crossing to lower triplet state(s)and internal conversion to the ground state are in operation.At 250.0 nm,internal conversion to the ground state becomes dominated.
基金This work was supported by the National Natural Science Foundation of China(No.21833003 and No.21773213)the Strategic Priority Research Program of the Chinese Academy of Sciences(No.XDB17000000)Chinese Academy of Sciences(GJJSTD20190002).
文摘N-ethylpyrrole is one of ethylsubstituted derivatives of pyrrole and its excited-state decay dynamics has never been explored.In this work,we investigate ultrafast decay dynamics of N-ethylpyrrole excited to the S_(1)electronic state using a femtosecond time-resolved photoelectron imaging method.Two pump wavelengths of 241.9 and 237.7 nm are employed.At 241.9 nm,three time constants,5.0±0.7 ps,66.4±15.6 ps and 1.3±0.1 ns,are derived.For 237.7 nm,two time constants of 2.1±0.1 ps and 13.1±1.2 ps are derived.We assign all these time constants to be associated with different vibrational states in the S_(1)state.The possible decay mechanisms of different S_(1)vibrational states are briefly discussed.
基金supported by the National Natural Science Foundation of China (No.21573228, No.21833003, No.21673232, and No.21773236)the Strategic Priority Research Program of the Chinese Academy of Sciences (No.XDB17000000)
文摘The ultrafast dynamics of water molecules excited to the two F states is studied by combining two-photon excitation and time-resolved photoelectron imaging techniques. The lifetimes of the F1A1 and F1B1 states of H2O (D2O) were derived to be 1.0±0.3 (1.9±0.4) and 10±3 (30±10) ps, respectively. We propose that the F1A1 state mainly decays through the D state, due to the nonadiabatic coupling between them, while the F1B1 state decays through the F1A1 state via Coriolis interaction.
