synthesis-of-hierarchical-znocdsse-heterostructure-nanotrees

Synthesis of Hierarchical ZnO/CdSSe Heterostructure Nanotrees

A two-step chemical vapor deposition procedure is here employed to prepare tree-like hierarchical ZnO/CdSSe hetero-nanostructures. The structures are ...

University of Delaware

Ultrafast time-resolved measurements were performed on a novel pentafluorophenyl substituted 5,5-dimethyl phlorin derivative in solution and when attached to TiO2 colloidal films. The complex excited state dynamics of this porphyrinoid after S1 and S2 excitation was compared at different wavelengths and can be assigned to several subsequent relaxation mechanisms. The difference between excited state dynamics in the free molecule and when attached to an electron accepting electrode was measured. For both cases the dynamics was compared after excitation to the S1 and the S2 state. For the free molecule in solution an intermediate relaxation step was identified and assigned to a buckling motion of the tetrapyrrole ring. On the electrode, heterogeneous electron transfer (HET) times from both states were very similar and around 50 fs. Surprisingly, the large difference in the density of acceptor states that are resonant with the respective donor level of the molecule does not significantly influence HET dynamics. This result indicates that HET proceeds into intermediate transition states that are different from steady state surface states obtained from experiments or computations. The density of states (DOS) of these transient acceptor states appears not to be directly related to the corresponding surface or bulk DOS.

Electronic state dependence of heterogeneous electron transfer: injection from the S1 and S2 state of phlorin into TiO2.

This Perspective discusses recent developments in ultrafast electron transfer dynamics at interfaces between organic and inorganic materials. Heterogeneous electron transfer (HET) is a key process in important fields like catalysis and solar energy conversion. Furthermore, the solid state nature of the systems gives control over relevant parameters and allows for investigating excited state dynamics and electron transfer processes in unprecedented detail. Progress in synthesis, sample preparation, and instrumentation makes it possible to provide experimental proof of recent prediction from theory concerning the adiabaticity of the reaction and the influence of coherence. A short recapitulation of the field is followed by a discussion of recent experimental efforts that allowed for studying HET, particularly focusing on the influence of energetics and vibrational dynamics.

Photoinduced Ultrafast Heterogeneous Electron Transfer at Molecule-Semiconductor Interfaces.

A new tree-like ZnO/CdSSe nanocomposite with CdSSe branches grown on ZnO nanowires prepared via a two-step chemical vapor deposition is presented. The nanotrees (NTs) are vertically aligned on a substrate. The CdSSe branches result in strong visible light absorption and form a type-II heterojunction with the ZnO stem that facilitates efficient electron transfer. A combination of photoluminescence spectroscopy and lifetime measurements indicates that the NTs are promising materials for applications that benefit from a Z-scheme charge transfer mechanism. Vertically aligned branched ZnO nanowires can provide direct electron transport pathways to substrates and allow for efficient charge separation. These advantages of nanoscale hierarchical heterostructures make ZnO/CdSSe NTs a promising semiconductor material for solar cells, and other opto-electronic devices.

Efficient Z-scheme charge separation in novel vertically aligned ZnO/CdSSe nanotrees.

A Kerr-gated microscope capable of imaging ultraviolet luminescence with femtosecond time resolution has been developed. The system allows the spatial, spectral, and temporal measurement of UV-emitting samples. The instrumentation was optimized for emission collection in the UV, resulting in sub 90 fs time resolution of gated signals. ZnO nanowires were used to demonstrate the performance of the instrument. The evolution of the emission from a single nanowire was tracked via ultrafast transient spectroscopy and through sequential imaging. Transient dynamics were extracted from a region of intense emission on a single ZnO nanowire. This technique is a powerful tool capable of contactless ultrafast measurements of charge carrier dynamics in single nanoparticles.

Ultraviolet femtosecond Kerr-gated wide-field fluorescence microscopy.

Cyclic tetrapyrroles are the active core of compounds with crucial roles in living systems, such as hemoglobin and chlorophyll, and in technology as photocatalysts and light absorbers for solar energy conversion. Zinc-tetraphenylporphyrin (Zn-TPP) is a prototypical cyclic tetrapyrrole that has been intensely studied in past decades. Because of its importance for photochemical processes the optical properties are of particular interest, and, accordingly, numerous studies have focused on light absorption and excited-state dynamics of Zn-TPP. Relaxation after photoexcitation in the Soret band involves internal conversion that is preceded by an ultrafast process. This relaxation process has been observed by several groups. Hitherto, it has not been established if it involves a higher lying "dark" state or vibrational relaxation in the excited S2 state. Here we combine high time resolution electronic and vibrational spectroscopy to show that this process constitutes vibrational relaxation in the anharmonic S2 potential.

Jesus Nieto-Pescador

Department of Chemistry & Biochemistry,
Department of Physics & Astronomy

University of Delaware

Synthesis of Hierarchical ZnO/CdSSe Heterostructure Nanotrees

Jesus Nieto-Pescador

.css-o250i3{font-size:18px;font-family:Open Sans,sans-serif;line-height:21.6px;}Department of Chemistry & Biochemistry,Department of Physics & Astronomy

University of Delaware

Synthesis of Hierarchical ZnO/CdSSe Heterostructure Nanotrees

Department of Chemistry & Biochemistry,
Department of Physics & Astronomy