Hot electrons do the impossible: plasmon-induced dissociation of H2 on Au.

نویسندگان

  • Shaunak Mukherjee
  • Florian Libisch
  • Nicolas Large
  • Oara Neumann
  • Lisa V Brown
  • Jin Cheng
  • J Britt Lassiter
  • Emily A Carter
  • Peter Nordlander
  • Naomi J Halas
چکیده

Heterogeneous catalysis is of paramount importance in chemistry and energy applications. Catalysts that couple light energy into chemical reactions in a directed, orbital-specific manner would greatly reduce the energy input requirements of chemical transformations, revolutionizing catalysis-driven chemistry. Here we report the room temperature dissociation of H(2) on gold nanoparticles using visible light. Surface plasmons excited in the Au nanoparticle decay into hot electrons with energies between the vacuum level and the work function of the metal. In this transient state, hot electrons can transfer into a Feshbach resonance of an H(2) molecule adsorbed on the Au nanoparticle surface, triggering dissociation. We probe this process by detecting the formation of HD molecules from the dissociations of H(2) and D(2) and investigate the effect of Au nanoparticle size and wavelength of incident light on the rate of HD formation. This work opens a new pathway for controlling chemical reactions on metallic catalysts.

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

Direct evidence of plasmon enhancement on photocatalytic hydrogen generation over Au/Pt-decorated TiO2 nanofibers.

Direct evidence of plasmon-enhanced H2 generation is observed in photocatalytic water reduction by using TiO2 electrospun nanofibers co-decorated with Au and Pt nanoparticles through dual-beam irradiation. The Au/Pt/TiO2 nanofibers exhibit certain activity for H2 generation under single irradiation at 420 nm that excites the defect/impurity states of TiO2. Significantly, when secondary irradiat...

متن کامل

Hot-electron-transfer enhancement for the efficient energy conversion of visible light.

Great strides have been made in enhancing solar energy conversion by utilizing plasmonic nanostructures in semiconductors. However, current generation with plasmonic nanostructures is still somewhat inefficient owing to the ultrafast decay of plasmon-induced hot electrons. It is now shown that the ultrafast decay of hot electrons across Au nanoparticles can be significantly reduced by strong co...

متن کامل

Gap-plasmon based broadband absorbers for enhanced hot-electron and photocurrent generation

Plasmonic hot-electron generation has recently come into focus as a new scheme for solar energy conversion. So far, however, due to the relatively narrow bandwidth of the surface plasmon resonances and the insufficient resonant light absorption, most of plasmonic photocatalysts show narrow-band spectral responsivities and small solar energy conversion efficiencies. Here we experimentally demons...

متن کامل

Hydrogen sensing by localized surface plasmon resonance in colloidal solutions of Au-WO3-Pd

Nowadays, hydrogen has attracted significant attention as a next generation clean energy source. Hydrogen is highly flammable, so detection of hydrogen gas is required. Gold nanoparticle based localized surface plasmon resonance (LSPR) is an advanced and powerful sensing technique, which is well known for its high sensitivity to surrounding refractive index change in the local environment. We p...

متن کامل

Visible-light photodecomposition of acetaldehyde by TiO2-coated gold nanocages: plasmon-mediated hot electron transport via defect states.

Skeletal gold nanocages (Au NCs) are synthesized and coated with TiO2 layers (TiO2-Au NCs). The TiO2-Au NCs exhibit enhanced photodecomposition activity toward acetaldehyde under visible light (>400 nm) illumination because hot electrons are generated over the Au NCs by local surface plasmon resonance (LSPR) and efficiently transported across the metal/semiconductor interface via the defect sta...

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:
  • Nano letters

دوره 13 1  شماره 

صفحات  -

تاریخ انتشار 2013