A fundamental limit to existing optical techniques for measurement and manipulation of spin degrees of freedom is set by diffraction, which does not allow spins separated by less than about a quarter of a micrometre to be resolved using conventional far-field optics. Here, we report an efficient far-field optical technique that overcomes the limiting role of diffraction, allowing individual electronic spins to be detected, imaged and manipulated coherently with nanoscale resolution. The technique involves selective flipping of the orientation of individual spins, associated with nitrogen-vacancy centres in room-temperature diamond, using a focused beam of light with intensity vanishing at a controllable location, which enables simultaneous single-spin imaging and magnetometry at the nanoscale with considerably less power than conventional techniques. Furthermore, by inhibiting spin transitions away from the laser intensity null, selective coherent rotation of individual spins is realized. This technique can be extended to subnanometre dimensions, thus enabling applications in diverse areas ranging from quantum information science to bioimaging.O ptical techniques constitute powerful tools for spin detection and manipulation that enable applications ranging from atomic clocks 1,2 and magnetometers 3 to quantum information processors [4][5][6][7] and new sensors and imaging modalities for the biological and life sciences [8][9][10][11][12][13] . Several promising methods for fluorescence imaging have recently been developed to surpass the diffraction limit and are already being applied to important problems in biology and neuroscience [14][15][16] as well as subwavelength optical lithography [17][18][19] . For example, subdiffraction imaging of fluorophores can be obtained by stimulated emission depletion (STED) microscopy and related methods based on reversible saturable optical linear fluorescence transitions 20-23 (RESOLFT). Using optical fields with intensity zeros and steep spatial gradients, such as those provided by doughnut-shaped beams, one can transiently switch the fluorophores to a different state everywhere except for a small region near the vanishing optical intensity. In this case the emitters from that small region can be separated from neighbours closer than the diffraction limit. As the emitters are switched to the designated (on or off) state provided the optical stimulation rate exceeds that of the spontaneous decay rate of that state, the ultimate resolution is, in principle, limited only by the applicable optical power 23 .
The concept of subdiffraction spin detection and controlOur new approach to subdiffraction spin detection and manipulation is outlined in Fig. 1. We consider an electronic spin system, such as the nitrogen-vacancy (NV) centre in diamond, which can be polarized by optical pumping, coherently manipulated with resonant microwave radiation and read-out with spin-state-dependent fluorescence. Improved spatial resolution is achieved by illuminating the sample with a doughnut-sha...