Observation of large water-cluster anions with surface-bound excess electrons.

نویسندگان

  • J R R Verlet
  • A E Bragg
  • A Kammrath
  • O Cheshnovsky
  • D M Neumark
چکیده

Anionic water clusters have long been studied to infer properties of the bulk hydrated electron. We used photoelectron imaging to characterize a class of (H2O)n- and (D2O)n- cluster anions (n </= 200 molecules) with vertical binding energies that are significantly lower than those previously recorded. The data are consistent with a structure in which the excess electron is bound to the surface of the cluster. This result implies that the excess electron in previously observed water-cluster anions, with higher vertical binding energies, was internally solvated. Thus, the properties of those clusters could be extrapolated to those of the bulk hydrated electron.

برای دانلود رایگان متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

منابع مشابه

Characterization of excess electrons in water-cluster anions by quantum simulations.

Water-cluster anions can serve as a bridge to understand the transition from gaseous species to the bulk hydrated electron. However, debate continues regarding how the excess electron is bound in (H2O)-n, as an interior, bulklike, or surface electronic state. To address the uncertainty, the properties of (H2O)-n clusters with 20 to 200 water molecules have been evaluated by mixed quantum-classi...

متن کامل

Comment on "Characterization of excess electrons in water-cluster anions by quantum simulations".

The conclusion by Turi et al. (Reports, 5 August 2005, p. 914) that all experimental spectral and energetic data on water-cluster anions point toward surface-bound electrons is overstated. Comparison of experimental vertical detachment energies with their calculated values for (H2O)n- clusters with surface-bound and internalized electrons supports previous arguments that both types of clusters ...

متن کامل

Electron solvation in water clusters following charge transfer from iodide.

The dynamics following charge transfer to solvent from iodide to a water cluster are studied using time-resolved photoelectron imaging of I-(H2O)n and I-(D2O)n clusters with n< or =28. The results show spontaneous conversion, on a time scale of approximately 1 ps, from water cluster anions with surface-bound electrons to structures in which the excess electron is more strongly bound and possibl...

متن کامل

Interior- and surface-bound excess electron states in large water cluster anions.

We present the results of mixed quantum/classical simulations on relaxed thermal nanoscale water cluster anions, (H(2)O)(n)(-), with n=200, 500, 1000, and 8000. By using initial equilibration with constraints, we investigate stable/metastable negatively charged water clusters with both surface-bound and interior-bound excess electron states. Characterization of these states is performed in term...

متن کامل

Analysis of localization sites for an excess electron in neutral methanol clusters using approximate pseudopotential quantum-mechanical calculations.

We have used a recently developed electron-methanol molecule pseudopotential in approximate quantum mechanical calculations to evaluate and statistically analyze the physical properties of an excess electron in the field of equilibrated neutral methanol clusters ((CH(3)OH)(n), n=50-500). The methanol clusters were generated in classical molecular dynamics simulations at nominal 100 and 200 K te...

متن کامل

ذخیره در منابع من


  با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید

عنوان ژورنال:
  • Science

دوره 307 5706  شماره 

صفحات  -

تاریخ انتشار 2005