Hot adsorbate-induced retardation of the internal thermalization of nonequilibrium electrons in adsorbate-covered metal nanoparticles.

نویسندگان

  • Christophe Bauer
  • Jean-Pierre Abid
  • Hubert H Girault
چکیده

Femtosecond transient absorption spectroscopy has been used to investigate the electron-electron scattering dynamics in sulfate-covered gold nanoparticles of 2.5 and 9.2 nm in diameter. We observe an unexpected retardation of the absolute internal thermalization time compared to bulk gold, which is attributed to a negative feedback by the vibrationally excited sulfate molecules. These hot adsorbates, acting as a transient energy reservoir, result from the back and forth inelastic scattering of metal nonequilibrium electrons into the pi orbital of the sulfate. The vibrationally excited adsorbates temporarily govern the dynamical behavior of nonequilibrium electrons in the metal by re-emitting hot electrons. In other terms, metal electrons reabsorb the energy deposited in the hot sulfates by a mechanism involving the charge resonance between the sulfate molecules and the gold NPs. The higher surface-to-volume ratio of sulfate-covered gold nanoparticles of 2.5 nm leads to a stronger inhibition of the internal thermalization. Interestingly, we also note an analogy between the mechanism described here for the slow-down of electron-electron scattering in metal nanoparticles by the hot adsorbates and the hot phonon-induced retardation of hot charge carriers cooling in semiconductors.

منابع مشابه

Supporting Information Hot adsorbate-induced retardation of the internal thermalization of nonequilibrium electrons in adsorbate-covered metal nanoparticles

We use "soft" surface science approach to prepare the samples, that permit the investigation of the metal/molecule interface by transient absorption spectroscopy. The overall structure of the sample consists of a mesoporous nanostructured metal oxide film, that acts as a host for the adsorbate-covered metal nanoparticles (see Fig. S1). The three dimensional nanostructured samples were prepared ...

متن کامل

Photochemistry on metal nanoparticles.

The photochemistry of small molecules on well-defined metal surfaces has been the subject of intense research for more than three decades.1 This field is of interest because it rests on the superposition of two influences. On one hand, new reaction channels can become possible by electronic excitation, which are usually not accessible by thermal activation. On the other hand, compared to molecu...

متن کامل

Time-resolved IR laser-assisted XUV photoelectron spectroscopy of metal surfaces

Photoemission of localized and delocalized electrons from an (adsorbate-covered) metal surface by an XUV pulse of length τX into the field of a delayed IR laser pulse with carrier period TL allows for the time-resolved observation of surface and adsorbate electronic processes. For τX ¿ TL, the energy of the emitted photoelectrons (PEs) oscillates with period TL as a function of the XUV-IR pulse...

متن کامل

Adsorbate diffusion on transition metal nanoparticles.

Diffusion of adsorbates on transition metal nanoparticles is a precursor process for heterogeneously catalyzed reactions, and as a result, an atomistic understanding of the diffusion mechanism is very important. We systematically studied adsorption and diffusion of atomic and diatomic species (H, C, N, O, CO, and NO) on nanometer-sized Pt and Cu nanoparticles with different sizes and shapes usi...

متن کامل

Role of adsorbates on dynamics of hot-electron (type I and II) thermalization within gold nanoparticles

Early stages of hot-electron thermalization in small gold nanoparticles wrapped in an adsorbates shell have been investigated by femtosecond transient absorption spectroscopy. Type-I hot electrons thermalize in 800 fs (to form type-II hot electron) either by scattering with cold conduction band electrons or by chemical interface scattering with adsorbates shell. Type-II hot electrons redistribu...

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

متن کامل
عنوان ژورنال:
  • The journal of physical chemistry. B

دوره 110 10  شماره 

صفحات  -

تاریخ انتشار 2006