3 research outputs found
Zero-Valent Iron Nanoparticles with Unique Spherical 3D Architectures Encode Superior Efficiency in Copper Entrapment
The
large-scale preparation of spherical condensed-type superstructures
of zero-valent iron (nZVI), obtained by controlled solid-state reaction
through a morphologically conserved transformation of a magnetite
precursor, is herein reported. The formed 3D nanoarchitectures (S-nZVI)
exhibit enhanced entrapment efficiency of heavy metal pollutants,
such as copper, compared to all previously tested materials reported
in the literature, thus unveiling the relevance in the material’s
design of the morphological variable. The superior removal efficiency
of these mesoporous S-nZVI superstructures is linked to their extraordinary
ability to couple effectively processes such as reduction and sorption
of the metal pollutant
Templated Dewetting–Alloying of NiCu Bilayers on TiO<sub>2</sub> Nanotubes Enables Efficient Noble-Metal-Free Photocatalytic H<sub>2</sub> Evolution
Photocatalytic
H<sub>2</sub> evolution reactions on pristine TiO<sub>2</sub> is characterized
by low efficiencies that are due to trapping
and recombination of charge carriers and due to a sluggish kinetics
of electron transfer. Noble-metal (mainly Pt, Pd, Au) nanoparticles
are typically decorated as co-catalysts on the TiO<sub>2</sub> surface
to reach reasonable photocatalytic yields. However, because of the
high cost of noble metals, alternative metal co-catalysts are being
developed. Here, we introduce an approach to fabricate an efficient
noble-metal-free photocatalytic platform for H<sub>2</sub> evolution
based on alloyed NiCu co-catalytic nanoparticles at the surface of
anodic TiO<sub>2</sub> nanotube arrays. NiCu bilayers are deposited
onto the TiO<sub>2</sub> nanotubes by plasma sputtering. A subsequent
thermal treatment is carried out that leads to dewetting, that is,
because of surface diffusion, the Ni- and Cu-sputtered layers simultaneously
mix with each other while
splitting into NiCu nanoparticles at the nanotube surface. The approach
allows for a full control over key features of the alloyed nanoparticles,
such as their composition, work function, and co-catalytic ability
toward H<sub>2</sub> generation. Dewetted–alloyed co-catalytic
nanoparticles composed of equal Ni and Cu amounts not only are significantly
more reactive than pure Ni or Cu nanoparticles, but also lead to H<sub>2</sub> generation rates that can be comparable to those obtained
by conventional noble-metal (Pt) decoration of TiO<sub>2</sub> nanotube
arrays
Functional Nanosheet Synthons by Covalent Modification of Transition-Metal Dichalcogenides
We report on the
facile preparation of versatile MoS<sub>2</sub>–thiobarbituric
acid conjugates, which, in addition to excellent
electrochemical behavior, can serve as nanosheet platforms for further
functionalization in a multitude of applications. We show that chemically
exfoliated MoS<sub>2</sub> was extensively modified with up to 50%
surface coverage, while maintaining its metallic character, and that
the strategy can be extended to MoSe<sub>2</sub>, WS<sub>2</sub>,
and WSe<sub>2</sub>. The covalent functionalization endowed the materials
not only with good aqueous dispersibility, but also with improved
hydrogen evolution reaction (HER) activity, as well as promise in
the oxidative detection of DNA nucleobases in solution