Pd nanomaterials can be cheaper alternative catalysts for the electrocatalytic formic acid oxidation reaction (FAOR) in fuel cells. The size and shape of the nanoparticles and crystal engineering can play a crucial role in enhancing the catalytic activities of Pd nanostructures. A systematic study on the effect of varying the morphology of Pd nanostructures on their catalytic activities for FAOR is reported here. Palladium nanoparticles (Pd), nanowires (Pd) and nanosheets (Pd) could be synthesized by using swollen liquid crystals as 'soft' templates. Swollen liquid crystals are lyotropic liquid crystals that are formed from a quaternary mixture of a surfactant, cosurfactant, brine and Pd salt dissolved in oil. Pd nanostructures exhibited 2.7 and 19 fold higher current density than Pd and Pd nanostructures in the FAOR. The Pd nanostructure possess higher electrochemically active surface area (ECSA), better catalytic activity, stability, and lower impedance to charge transfer when compared to the Pd and Pd nanostructures. The presence of relatively higher amounts of crystal defects and enriched (100) crystal facets in the Pd nanostructure were found to be the reasons for their enhanced catalytic activities.

Download full-text PDF

Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9418200PMC
http://dx.doi.org/10.1039/d0na00798fDOI Listing

Publication Analysis

Top Keywords

catalytic activities
12
liquid crystals
12
formic acid
8
acid oxidation
8
swollen liquid
8
nanostructures
6
engineering morphology
4
morphology palladium
4
palladium nanostructures
4
nanostructures tune
4

Similar Publications

Ce1-xMnxVO4 with Improved Activity for Low-Temperature Catalytic Reduction of NO with NH3.

Chem Asian J

January 2025

Fudan University, Department of Environmental Science and Engineering, Shanghai Handan Road 220, 200433, Shanghai, CHINA.

Novel Ce1-xMnxVO4 catalysts prepared via modified hydrothermal synthesis were used in selective catalytic reduction of NO using NH3 (NH3-SCR). The Ce1-xMnxVO4 catalysts displayed optimum NO removal efficiency at 250 oC. Physicochemical properties including crystal type, morphology, particle size, elemental composition, BET surface area, chemical bond, and valence state were studied by XRD, TEM, EDS, N2 adsorption-desorption, Raman spectroscopy, and XPS.

View Article and Find Full Text PDF

Cyclic diguanosine monophosphate (c-di-GMP) is a ubiquitous bacterial secondary messenger with diverse functions. A previous Escherichia coli proteome microarray identified that c-di-GMP binds to the 23S rRNA methyltransferases RlmI and RlmE. Here we show that c-di-GMP inhibits RlmI activity in rRNA methylation assays, and that it modulates ribosome assembly in the presence of kanamycin.

View Article and Find Full Text PDF

In this study, a novel hybrid nanostructure consisting of acid-decorated chitosan and magnetic AlFeO nanoparticles was fabricated. The acid-decorated chitosan provided a stable and biocompatible matrix for the magnetic AlFeO nanoparticles. Various techniques including Fourier transform infrared spectroscopy (FT-IR), X-ray diffraction patterns (XRD), thermogravimetric analysis (TGA), vibrating sample magnetometry (VSM), specific surface area (BET), scanning electron microscopy (SEM), and energy-dispersive X-ray spectroscopy (EDS) were used to characterize and confirm the successful synthesis of the hybrid nanostructure.

View Article and Find Full Text PDF

Piezoelectric catalysis possesses the potential to convert ocean wave energy into and holds broad prospects for extracting uranium from seawater. Herein, the Z-type ZnO@COF heterostructure composite with excellent piezoelectric properties was synthesized through in situ growth of covalent organic frameworks (COFs) on the surface of ZnO and used for efficient uranium extraction. The designed COFs shell enables ZnO with stability, abundant active sites and high-speed electron transport channels.

View Article and Find Full Text PDF

Electron donor-acceptor complexes are commonly employed to facilitate photoinduced radical-mediated organic reactions. However, achieving these photochemical processes with catalytic amounts of donors or acceptors can be challenging, especially when aiming to reduce catalyst loadings. Herein, we have unveiled a framework-based heterogenization approach that significantly enhances the photoredox activity of perylene diimide species in radical addition reactions with alkyl silicates by promoting faster and more efficient electron donor-acceptor complex formation.

View Article and Find Full Text PDF

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!