Abstract
We present a technique to nanomechanically vary the distance between a fluorescent source and a mirror, thereby varying the local density of optical states at the source position. Our method can therefore serve to measure the quantum efficiency of fluorophores. Application of our technique to NV defects in diamond nanocrystals shows that their quantum yield can significantly differ from unity. Relying on a lateral scanning mechanism with shear-force probe-sample distance control our technique is straightforwardly implemented in most state-of-the-art near-field microscopes.
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