We investigated the photon emission spectra on Ag(111)surface excited by tunneling electrons using a low temperature scanning tunneling microscope in ultrahigh vacuum.Characteristic plasmon modes were illustrated as a...We investigated the photon emission spectra on Ag(111)surface excited by tunneling electrons using a low temperature scanning tunneling microscope in ultrahigh vacuum.Characteristic plasmon modes were illustrated as a function of the bias voltage.The one electron excitation process was revealed by the linear relationship between the luminescence intensity and the tunneling current.Luminescence enhancement is observed in the tunneling regime for the relatively high bias voltages,as well as at the field emission resonance with bias voltage increased up to 9 V.Presence of a silver(Ag)nanoparticle in the tunneling junction results in an abnormally strong photon emission at the high field emission resonances,which is explained by the further enhancement due to coupling between the localized surface plasmon and the vacuum.The results are of potential value for applications where ultimate enhancement of photon emission is desired.展开更多
The key to fully understanding water-solid interfaces relies on the microscopic nature of hydrogen bond networks,including their atomic structures, interfacial interactions, and dynamic behaviors. Here, we report the ...The key to fully understanding water-solid interfaces relies on the microscopic nature of hydrogen bond networks,including their atomic structures, interfacial interactions, and dynamic behaviors. Here, we report the observation of two types of simplest water chains on Au(111) surface which is expected unstable according to the rules of hydrogen network on noble metal surfaces. A common feature at the end of chain structures is revealed in high resolution scanning tunneling microscopy images. To explain the stability in observed hydrogen bond networks,we propose a structure model of the water chains terminated with a hydroxyl group. The model is consistent with detailed image analysis and molecular manipulation. The observation of simplest water chains suggests a new platform for exploring fundamental physics in hydrogen bond networks on surfaces.展开更多
The orientation switching of a single azobenzene molecule on Au(111)surface excited by tunneling electrons and/or photons has been demonstrated in recent experiments.Here we investigate the rotation behavior of this m...The orientation switching of a single azobenzene molecule on Au(111)surface excited by tunneling electrons and/or photons has been demonstrated in recent experiments.Here we investigate the rotation behavior of this molecular rotor by first-principles density functional theory(DFT)calculation.The anchor phenyl ring prefers adsorption on top of the fcc hollow site,simulated by a benzene molecule on close packed atomic surface.The adsorption energy for an azobenzene molecule on Au(111)surface is calculated to be about 1.76 eV.The rotational energy profile has been mapped with one of the phenyl rings pivots around the fcc hollow site,illustrating a potential barrier about 50 meV.The results are consistent with experimental observations and valuable for exploring a broad spectrum of molecules on this noble metal surface.展开更多
基金Project supported by the National Natural Science Foundation of China(Grant Nos.21961142021,11774395,and 11727902)the Strategic Priority Research Program(B)of the Chinese Academy of Sciences(Grant No.XDB30201000)the Beijing Natural Science Foundation,China(Grant No.4181003)。
文摘We investigated the photon emission spectra on Ag(111)surface excited by tunneling electrons using a low temperature scanning tunneling microscope in ultrahigh vacuum.Characteristic plasmon modes were illustrated as a function of the bias voltage.The one electron excitation process was revealed by the linear relationship between the luminescence intensity and the tunneling current.Luminescence enhancement is observed in the tunneling regime for the relatively high bias voltages,as well as at the field emission resonance with bias voltage increased up to 9 V.Presence of a silver(Ag)nanoparticle in the tunneling junction results in an abnormally strong photon emission at the high field emission resonances,which is explained by the further enhancement due to coupling between the localized surface plasmon and the vacuum.The results are of potential value for applications where ultimate enhancement of photon emission is desired.
基金Supported by the National Natural Science Foundation of China under Grant Nos 11774395 and 91753136the Beijing Natural Science Foundation under Grant No 4181003the Strategic Priority Research Program(B)of the Chinese Academy of Sciences under Grant Nos XDB30201000 and XDB28000000
文摘The key to fully understanding water-solid interfaces relies on the microscopic nature of hydrogen bond networks,including their atomic structures, interfacial interactions, and dynamic behaviors. Here, we report the observation of two types of simplest water chains on Au(111) surface which is expected unstable according to the rules of hydrogen network on noble metal surfaces. A common feature at the end of chain structures is revealed in high resolution scanning tunneling microscopy images. To explain the stability in observed hydrogen bond networks,we propose a structure model of the water chains terminated with a hydroxyl group. The model is consistent with detailed image analysis and molecular manipulation. The observation of simplest water chains suggests a new platform for exploring fundamental physics in hydrogen bond networks on surfaces.
基金Project supported by the National Natural Science Foundation of China(Grant Nos.21961142021,11774395,91753136,and 11727902)the Beijing Natural Science Foundation,China(Grant No.4181003)the Strategic Priority Research Program(B)of the Chinese Academy of Sciences(Grant Nos.XDB30201000 and XDB28000000).
文摘The orientation switching of a single azobenzene molecule on Au(111)surface excited by tunneling electrons and/or photons has been demonstrated in recent experiments.Here we investigate the rotation behavior of this molecular rotor by first-principles density functional theory(DFT)calculation.The anchor phenyl ring prefers adsorption on top of the fcc hollow site,simulated by a benzene molecule on close packed atomic surface.The adsorption energy for an azobenzene molecule on Au(111)surface is calculated to be about 1.76 eV.The rotational energy profile has been mapped with one of the phenyl rings pivots around the fcc hollow site,illustrating a potential barrier about 50 meV.The results are consistent with experimental observations and valuable for exploring a broad spectrum of molecules on this noble metal surface.
