arXiv2012
Electron paramagnetic resonance (EPR) spectroscopy interrogates unpaired electron spins in solids and liquids to reveal local structure and dynamics; for example, EPR has elucidated parts of the structure of protein complexes that have resisted all other techniques in structural biology. EPR can also probe the interplay of light and electricity in organic solar cells and light-emitting diodes, and the origin of decoherence in condensed matter, which is of fundamental importance to the development of quantum information processors. Like nuclear magnetic resonance (NMR), EPR spectroscopy becomes more powerful at high magnetic fields and frequencies, and with excitation by coherent pulses rather than continuous waves. However, the difficulty of generating sequences of powerful pulses at frequencies above 100 GHz has, until now, confined high-power pulsed EPR to magnetic fields of 3.5 T and below. Here we demonstrate that ~1 kW pulses from a free-electron laser (FEL) can power a pulsed EPR spectrometer at 240 GHz (8.5 T), providing transformative enhancements over the alternative, a state-of-the-art ~30 mW solid state source. Using the UC Santa Barbara FEL as a source, our 240 GHz spectrometer can rotate spin-1/2 electrons through pi/2 in only 6 ns (vs. 300 ns with the solid state source). Fourier transform EPR on nitrogen impurities in diamond demonstrates excitation and detection of EPR lines separated by ~200 MHz. Decoherence times for spin-1/2 systems as short as 63 ns are measured, enabling measurement of the decoherence time in a frozen solution of nitroxide free-radicals at temperatures as high as 190 K. Both FELs and the quasi-optical technology developed for the spectrometer are scalable to frequencies well in excess of 1 THz, opening the possibility of high-power pulsed EPR spectroscopy up to the highest static magnetic fields on earth.