We investigate the dissociation of H_{2}^{+} into a proton and a H^{0} after single ionization with photons of an energy close to the threshold. We find that the p^{+} and the H^{0} do not emerge symmetrically in the case of the H_{2}^{+} dissociating along the 1sσ_{g} ground state. Instead, a preference for the ejection of the p^{+} in the direction of the escaping photoelectron can be observed. This symmetry breaking is strongest for very small electron energies. Our experiment is consistent with a recent prediction by Serov and Kheifets [Phys. Rev. A 89, 031402 (2014)]. In their model, which treats the photoelectron classically, the symmetry breaking is induced by the retroaction of the long-range Coulomb potential onto the dissociating H_{2}^{+}.
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http://dx.doi.org/10.1103/PhysRevLett.116.043001 | DOI Listing |
J Am Chem Soc
January 2025
National Center for Nanoscience and Technology, No. 11 ZhongGuanCun BeiYiTiao, Beijing 100190, China.
The development of highly active and stable cathodes in alkaline solutions is crucial for promoting the commercialization of anion exchange membrane (AEM) electrolyzers, yet it remains a significant challenge. Herein, we synthesized atomically dispersed CoP moieties (CoP-SSC) immobilized on ultrathin carbon nanosheets via a phosphidation exfoliation strategy at medium temperature. The thermodynamic formation process of the Co-P moieties was elucidated using X-ray absorption spectroscopy (XAS) and theoretical calculations.
View Article and Find Full Text PDFMolecules
January 2025
The Joint Graduate School of Energy and Environment, CHE Center for Energy Technology and Environment, King Mongkut's University of Technology Thonburi, 126 Pracha Uthit Rd., Bang Mod, Thung Khru, Bangkok 10140, Thailand.
A single-bed and dual-bed catalyst system was studied to maximize H production from the combination of partial oxidation of CH and water gas shift reaction. In addition, the different types of catalysts, including Ni, Cu, Ni-Re, and Cu-Re supported on gadolinium-doped ceria (GDC) were investigated under different operating conditions of temperature (400-650 °C). Over Ni-based catalysts, methane can easily dissociate on a Ni surface to give hydrogen and carbon species.
View Article and Find Full Text PDFNat Commun
January 2025
Department of Physics, Stockholm University, 10691, Stockholm, Sweden.
The surface chemistry of the Fischer-Tropsch catalytic reaction over Co has still several unknows. Here, we report an in-situ X-ray photoelectron spectroscopy study of Co and Co( ), and in-situ high energy surface X-ray diffraction of Co during the Fischer-Tropsch reaction at 0.15 bar - 1 bar and 406 K - 548 K in a H/CO gas mixture.
View Article and Find Full Text PDFJ Colloid Interface Sci
January 2025
Key Lab of Organic Optoelectronics & Molecular Engineering, Tsinghua University, Beijing 100084, PR China. Electronic address:
Exploring suitable dual active site and metal-substrate interface effect is essential for designing efficient and robust electrocatalysts across a wide pH range for the hydrogen evolution reaction (HER). Herein, alloyed platinum-ruthenium clusters supported on nanosheet-assembled molybdenum carbide microflowers (PtRu/MoC) are reported as efficient pH-universal electrocatalysts for HER. Due to dual active site and metal-substrate interface effect, the optimized PtRu/MoC electrocatalyst exhibits extremely low overpotentials (η) of 9, 19, and 33 mV to deliver 10 mA cm in 0.
View Article and Find Full Text PDFJ Hazard Mater
January 2025
School of Materials Science and Engineering, South China University of Technology, Guangzhou 510641, PR China. Electronic address:
Catalytic oxidation of formaldehyde (HCHO) is a highly effective method for indoor HCHO removal. However, many aspects of the catalytic mechanism remain unclear, making the optimization of catalysts largely empirical. Herein, we report a coupled experimental and computational study of Pt/TiO catalysts, with special focus on the functional roles of surface oxygen vacancies and hydroxyl groups in the catalytic oxidation of HCHO.
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