Proton-coupled electron transfer (PCET) has been significant in understanding the reactions in solution. In a solid-gas interface, it remains a challenge to identify electron transfer or proton transfer intermediates. Here, in a Au/N interface, we regulated and characterized the PCET from -aminothiophenol (PATP) to -nitrothiophenol (PNTP) in the plasmon-mediated conversion to ,-dimercaptoazobenzene by variable-temperature surface-enhanced Raman spectroscopy. The Raman bands of PATP and PNTP characteristically blue shifted and red shifted as the laser wavelength- and power density-regulated PCET from PATP to PNTP, respectively. These characteristic Raman band shifts were well reproduced by the density functional theoretical simulations of positively charged PATP and negatively charged PNTP, which explicitly evidenced the electron transfer intermediates of PATP or PNTP on the Au surface. PCET did not occur in the temperature cycle between 100 and 370 K without laser illumination. These results demonstrated a characteristic local PCET loop composed of electron transfer between PATP/PNTP and Au followed by intermolecular proton transfer between PATP and PNTP and the significance of conducting electron transfer on Au.
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http://dx.doi.org/10.1021/acs.analchem.4c04579 | DOI Listing |
Phys Rev Lett
December 2024
Lawrence Berkeley National Laboratory, Berkeley, California 94720, USA.
We measure the high-intensity laser propagation throughout meter-scale, channel-guided laser-plasma accelerators by adjusting the length of the plasma channel on a shot-by-shot basis, showing high-quality guiding of 500 TW laser pulses over 30 cm in a hydrogen plasma of density n_{0}≈1×10^{17} cm^{-3}. We observed transverse energy transport of higher-order modes in the first ≈12 cm of the plasma channel, followed by quasimatched propagation, and the gradual, dark-current-free depletion of laser energy to the wake. We quantify the laser-to-wake transfer efficiency limitations of currently available petawatt-class lasers and demonstrate via simulation how control over the laser mode can significantly improve beam parameters.
View Article and Find Full Text PDFPhys Rev Lett
December 2024
Collaborative Innovation Center of Advanced Microstructures, National Laboratory of Solid State Microstructures, College of Engineering and Applied Sciences, Nanjing University, No. 22 Hankou Road, Nanjing, Jiangsu 210093, People's Republic of China.
Water electrolysis suffers from electron transfer barriers during oxygen evolution reactions, which are spin-related for magnetic materials. Here, the electron transfer at the Fe_{64}Ni_{36}-FeNiO_{x}H_{y} interface is effectively accelerated when the electrode is heated to trigger the Invar effect in Fe_{64}Ni_{36} Invar alloy, providing more unoccupied orbitals as electron transfer channels without pairing energy. As a result of thermally stimulated changes in electronic states, Fe_{64}Ni_{36}/FeNiO_{x}H_{y} achieved a cascaded oxidation of the catalytic center and water.
View Article and Find Full Text PDFACS Nano
January 2025
State Key Laboratory of Inorganic Synthesis and Preparative Chemistry, College of Chemistry, Jilin University, 2699 Qianjin Street, Changchun 130012, China.
Despite the potential of sonodynamic therapy (SDT) in treating malignant tumors, the lack of effective sonosensitizers has limited its clinical implementation. In this study, we explored the relationship between the heteroatom doping concentration in metal-organic frameworks and interface formation after pyrolysis by regulating the addition of manganese sources and successfully derived Z-scheme heterojunctions MnO/(A/R)TiO (MTO) in situ from MIL-125-NH (Ti/Mn). The electron transfer pathway introduced by interfacial contact promoted carrier separation and greatly preserved the effective redox components, significantly influencing the performance of reactive oxygen species generation.
View Article and Find Full Text PDFJ Am Chem Soc
January 2025
Department of Mechanical Engineering & Materials Science and Engineering Program, State University of New York at Binghamton, Binghamton, New York 13902, United States.
In contrast to the traditional perspective that thermal fluctuations are insignificant in surface dynamics, here we report their influence on surface reaction dynamics. Using real-time low-energy electron microscopy imaging of NiAl(100) under both vacuum and O atmospheres, we demonstrate that transient temperature variations substantially alter the direction of atom diffusion between the surface and bulk, leading to markedly different oxidation outcomes. During heating, substantial outward diffusion of atoms from the bulk to the surface results in step growth.
View Article and Find Full Text PDFProc Natl Acad Sci U S A
January 2025
Division of Biology and Biological Engineering, California Institute of Technology, Pasadena, CA 91125.
Microbial metabolism is impressively flexible, enabling growth even when available nutrients differ greatly from biomass in redox state. , for example, rearranges its physiology to grow on reduced and oxidized carbon sources through several forms of fermentation and respiration. To understand the limits on and evolutionary consequences of this metabolic flexibility, we developed a coarse-grained mathematical framework coupling redox chemistry with principles of cellular resource allocation.
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