scispace - formally typeset
Search or ask a question
Topic

Noble metal

About: Noble metal is a research topic. Over the lifetime, 15113 publications have been published within this topic receiving 337947 citations.


Papers
More filters
Journal ArticleDOI
TL;DR: In this article, a review of the recent achievements and the proposed strategy for addressing the emerging challenges in encapsulated noble metal nanocatalysts is presented, including the types of hybrid nanostructures and successful synthetic strategies.
Abstract: Encapsulation of small noble metal nanoparticles has received attention owing to the resulting highly increased stability and high catalytic activity and selectivity. Among the types of inert metal oxides, CeO2 is unique. It is inexpensive and highly stable, and, more importantly, the unique electronic configuration gives it a strong capability to provide active oxygen. The method of fabricating CeO2-encapsulated noble metal nanocatalysts is determined by the requirements of the application. In this review, we first describe the various types of encapsulated noble metals and then the current developments of synthesis in detail, including the types of hybrid nanostructures and successful synthetic strategies. The following section, concerning catalytic applications, is divided into three topics: anti-sintering capabilities, catalytic activities and selectivities. We hope that this review of the recent achievements and the proposed strategy for addressing the emerging challenges will inspire further developments in this research area.

98 citations

Journal ArticleDOI
TL;DR: The authors report that near-infrared light induces an irreversible accumulated Surface-enhanced Raman scattering (SERS) behavior of a molecule/metal–semiconductor hybrid system and investigate the underlying mechanism and show that it is attributed to crystallinity, charge transfer and reorientation.
Abstract: In recent years, surface-enhanced Raman scattering (SERS) of a molecule/metal–semiconductor hybrid system has attracted considerable interest and regarded as the synergetic contribution of the electromagnetic and chemical enhancements from the incorporation of noble metal into semiconductor nanomaterials. However, the underlying mechanism is still to be revealed in detail. Herein, we report an irreversible accumulated SERS behavior induced by near-infrared (NIR) light irradiating on a 4-mercaptobenzoic acid linked with silver and silver-doped titanium dioxide (4MBA/Ag/Ag-doped TiO2) hybrid system. With increasing irradiation time, the SERS intensity of 4MBA shows an irreversible exponential increase, and the Raman signal of the Ag/Ag-doped TiO2 substrate displays an exponential decrease. A microscopic understanding of the time-dependent SERS behavior is derived based on the microanalysis of the Ag/Ag-doped TiO2 nanostructure and the molecular dynamics, which is attributed to three factors: (1) higher crystallinity of Ag/Ag-doped TiO2 substrate; (2) photo-induced charge transfer; (3) charge-induced molecular reorientation. The authors report that near-infrared light induces an irreversible accumulated Surface-enhanced Raman scattering (SERS) behavior of a molecule/metal–semiconductor hybrid system. They investigate the underlying mechanism and show that it is attributed to crystallinity, charge transfer and reorientation.

98 citations

Journal ArticleDOI
TL;DR: Graphitic carbon nitride (g-C 3 N 4 )/ZnO nanosheets were used for the determination of hydrogen peroxide (H 2 O 2 ).

98 citations

Journal ArticleDOI
TL;DR: The as-engineered IrO2@Ir architecture exhibits extremely high electrocatalytic activity towards the OER, revealing an overpotential of 255 mV at 10 mA cm-2 and Tafel slope of 45 mV dec-1, which is much lower than those observed for the unmodified structure.
Abstract: Noble metal-based catalysts are vital electrocatalysts for the oxygen evolution reaction (OER), which is a half reaction among multiple renewable energy-related reactions. To fully exploit their potential as efficient OER catalysts, we developed a fast one-step strategy to engineer a unique nanostructure for the benchmark catalyst IrO2 utilizing an ultra-fast pulse laser, through which a shell of ultra-small Ir spheres with a diameter of ca. 2 nm is in situ engineered around the IrO2 core. The creation of the Ir sphere shell not only increases the electrochemical surface area, but also improves the electrical conductivity of the electrocatalyst. The as-engineered IrO2@Ir architecture exhibits extremely high electrocatalytic activity towards the OER, revealing an overpotential of 255 mV at 10 mA cm-2 and Tafel slope of 45 mV dec-1. These values are much lower than those observed for the unmodified structure. Furthermore, the catalytic performance is the best among all the noble metal-based OER catalysts. This work may open a new avenue to efficiently improve the catalytic activity of noble metal-based catalysts and significantly advance the development in the energy industry.

98 citations

Book ChapterDOI
TL;DR: The cinnamaldehyde (CAL) hydrogenation into Cinnamyl alcohol (COL) has been performed under 4MPa of H 2 in liquid phase as mentioned in this paper.
Abstract: Noble metal catalysts (Ir, Pt, Ru, Rh Pd) have been prepared with a very homogeneous dispersion on graphite (300 2 m 1 g) and carbon support (1400 m 2 g 1 ). On graphite the particles decorate the edges of the basal planes and there is an electron transfer to the metal. The cinnamaldehyde (CAL) hydrogenation into cinnamyl alcohol (COL) has been performed under 4MPa of H 2 in liquid phase. The factors affecting the selectivity to COL are: (i) the nature of the metal (0=Pd

98 citations


Network Information
Related Topics (5)
Oxide
213.4K papers, 3.6M citations
92% related
Nanoparticle
85.9K papers, 2.6M citations
92% related
Graphene
144.5K papers, 4.9M citations
91% related
Adsorption
226.4K papers, 5.9M citations
91% related
Carbon nanotube
109K papers, 3.6M citations
90% related
Performance
Metrics
No. of papers in the topic in previous years
YearPapers
2023485
2022986
2021622
2020724
2019896
2018767