Single-particle longitudinal motion and pairwise lateral motion was investigated while the particles were excited by an oscillating electric field directed normally to an electrode proximate to the particles. The electrode was polarized over a range of potential insufficient to drive electrochemical reactions, a range called the "ideally polarizable region". The particles' motion was qualitatively dependent on the choice of electrolyte despite the absence of electrochemical reactions. As when electrochemical reactions were not explicitly excluded, the phase angle θ between particle height and electric field correlated with the particles' separation or aggregation during excitation. A simple harmonic oscillator model of the particles' response, including colloidal and hydrodynamic forces and including the Basset force not previously cited in this context, showed how θ can increase from 0° at low frequencies, cross 90° at ∼100 Hz, and then increase to 180° as frequency was increased. The model captured the essence of experimental observations discussed here and in earlier works. This is the first a priori prediction of θ for this problem.
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http://dx.doi.org/10.1021/la2017038 | DOI Listing |
Angew Chem Int Ed Engl
January 2025
Beijing Institute of Technology, Research Center of Materials Science, School of Materials Science and Engineering, No.5 South Street of Zhongguancun, Haidian District, 100081, Beijing, CHINA.
Copper (Cu)-based catalysts exhibit distinctive performance in the electrochemical CO2 reduction reaction (CO2RR) with complex mechanism and sophisticated types of products. The management of key intermediates *CO and *H is a necessary factor for achieving high product selectivity, but lack of efficient and versatile strategies. Herein, we designed Pt modified Cu catalysts to effectively modulate the competitive coverage of those intermediates.
View Article and Find Full Text PDFSmall
January 2025
College of Materials Science and Engineering, Sichuan University, Chengdu, 610065, China.
The transition metal single atoms (SAs)-based catalysts with M-N coordination environment have shown excellent performance in electrocatalytic reduction of CO, and they have received extensive attention in recent years. However, the presence of SAs makes it very difficult to efficiently improve the coordination environment. In this paper, a method of direct high-temperature pyrolysis carbonization of ZIF-8 adsorbed with Ni and Fe ions is reported for the synthesis of Ni SAs and FeN nanoparticles (NPs) supported by the N-doped carbon (NC) hollow nanododecahedras (HNDs) with nanotubes (NTs) on the surface (Ni SAs/FeN NPs@NC-HNDs-NTs).
View Article and Find Full Text PDFJ Am Chem Soc
January 2025
CAS Key Laboratory of Nanosystem and Hierarchical Fabrication, National Center for Nanoscience and Technology (NCNST), Beijing 100190, China.
The mechanical effects on carbon-based metal-free catalysts (C-MFCs) have rarely been explored, despite the global interest in C-MFCs as substitutes for noble metal catalysts. Stress is ubiquitous, whereas its dedicated study is severely restricted due to its frequent entanglement with other structural variables, such as dopants, defects, and interfaces in catalysis. Herein, we report a proof-of-concept study by establishing a platform to continuously apply strain to a highly oriented pyrolytic graphite (HOPG) lamina, simultaneously collecting electrochemical signals.
View Article and Find Full Text PDFChem Commun (Camb)
January 2025
State Key Laboratory of Pulp and Paper Engineering, South China University of Technology, 510640 Guangzhou, P. R. China.
Herein, we report a novel electrochemical hydrogenolysis method for β-O-4 bond cleavage by using carbon foam as the cathode and waste aluminum as the anode. The reaction takes place at the cathode, producing ketones and phenolic compounds. Employing waste aluminum as the anode could avoid anodic excessive oxidation of phenols.
View Article and Find Full Text PDFInorg Chem
January 2025
State Key Laboratory of Nuclear Resources and Environment, East China University of Technology, Nanchang, Jiangxi 330013, China.
Extracting uranium from nuclear wastewater is vital for environmental and human health protection. However, despite progress in uranium extraction, there remains a demand for an optimized adsorbent with improved capability, efficiency, and selectivity. To bridge this gap, 1,2,3,4-butane tetracarboxylic acid (BTCA)-modified MIL-101 was synthesized through a simple hydrothermal reaction between amino-modified MIL-101 (MIL-101-NH) and BTCA.
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