Topic
Electron paramagnetic resonance
About: Electron paramagnetic resonance is a research topic. Over the lifetime, 39904 publications have been published within this topic receiving 779300 citations. The topic is also known as: EPR & ESR.
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01 Jan 1963
TL;DR: In this article, the effect of changing the precession frequency of the magnetic field has been studied using NMR to study rate properties. But the effect is limited to the case of double and double resonance.
Abstract: 1. Elements of Resonance.- 2 Basic Theory.- 3. Magnetic Dipolar Broadening of Rigid Lattices.- 4. Magnetic Interactions of Nuclei with Electrons.- 5. Spin-Lattice Relaxation and Motional Narrowing of Resonance Lines.- 6. Spin Temperature in Magnetism and in Magnetic Resonance.- 7. Double Resonance.- 8. Advanced Concepts in Pulsed Magnetic Resonance.- 9. Multiple Quantum Coherence.- 10. Electric Quadrupole Effects.- 11. Electron Spin Resonance.- 12. Summary.- Problems.- Appendixes.- A. A Theorem About Exponential Operators.- B. Some Further Expressions for the Susceptibility.- D. A Theorem from Perturbation Theory.- E. The High Temperature Approximation.- F. The Effects of Changing the Precession Frequency - Using NMR to Study Rate Phenomena.- G. Diffusion in an Inhomogeneous Magnetic Field.- H. The Equivalence of Three Quantum Mechanics Problems.- I. Powder Patterns.- J. Time-Dependent Hamiltonians.- K. Correction Terms in Average Hamiltonian Theory - The Magnus Expansion.- Selected Bibliography.- References.- Author Index.
4,860 citations
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TL;DR: Because the photoluminescence in the conducting polymer is quenched by interaction with C60, the data imply that charge transfer from the excited state occurs on a picosecond time scale.
Abstract: Evidence for photoinduced electron transfer from the excited state of a conducting polymer onto buckminsterfullerene, C(60), is reported. After photo-excitation of the conjugated polymer with light of energy greater than the pi-pi* gap, an electron transfer to the C(60) molecule is initiated. Photoinduced optical absorption studies demonstrate a different excitation spectrum for the composite as compared to the separate components, consistent with photo-excited charge transfer. A photoinduced electron spin resonance signal exhibits signatures of both the conducting polymer cation and the C(60) anion. Because the photoluminescence in the conducting polymer is quenched by interaction with C(60), the data imply that charge transfer from the excited state occurs on a picosecond time scale. The charge-separated state in composite films is metastable at low temperatures.
3,902 citations
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TL;DR: By combining electron paramagnetic resonance (EPR), optical absorption, and photoluminescence (PL) spectroscopy, a strong correlation is observed between the green 510 nm emission, the free-carrier concentration, and the density of singly ionized oxygen vacancies in commercial ZnO phosphor powders as mentioned in this paper.
Abstract: By combining electron paramagnetic resonance (EPR), optical absorption, and photoluminescence (PL) spectroscopy, a strong correlation is observed between the green 510 nm emission, the free‐carrier concentration, and the density of singly ionized oxygen vacancies in commercial ZnO phosphor powders. From these results, we demonstrate that free‐carrier depletion at the particle surface, and its effect on the ionization state of the oxygen vacancy, can strongly impact the green emission intensity. The relevance of these observations with respect to low‐voltage field emission displays is discussed.
1,815 citations
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TL;DR: In this article, the electron spin resonance hyperfine splitting constants of spin adducts of interest in this area are tabulated and a brief comment on the source of the radical trapped is given.
Abstract: Spin trapping has become a valuable tool for the study of free radicals in biology and medicine. The electron spin resonance hyperfine splitting constants of spin adducts of interest in this area are tabulated. The entries also contain a brief comment on the source of the radical trapped.
1,361 citations