Nitrogen-vacancy centers in diamond allow for coherent spin state manipulation at room temperature, which could bring dramatic advances to nanoscale sensing and quantum information technology. We introduce a novel method for the optical measurement of the spin contrast in dense nitrogen-vacancy (NV) ensembles. This method brings a new insight into the interplay between the spin contrast and fluorescence lifetime. We show that for improving the spin readout sensitivity in NV ensembles, one should aim at modifying the far field radiation pattern rather than enhancing the emission rate.Nitrogen-vacancy color centers (NV) in diamond are fluorescent lattice defects resulting from a vacancy and an adjacent nitrogen substitution [1,2]. These color centers have proven to be excellent testbeds for novel nanoscale optical devices.Ultrasensitive electromagnetic field [3][4][5][6][7][8], strain [9,10], pressure [11], and temperature [12,13] sensors as well as integrated quantum information processors [14][15][16] operating at ambient conditions have been prototyped using NVs. These capabilities are in large part due to the unique properties of the NV's electron spin, which may be optically initialized and manipulated by microwave signals [17,18]. The NV exhibits a spin-dependent fluorescence rate, which can be used for optical spin state readout [19]. We have calibrated the laser power using saturation measurements to ensure that both nanodiamonds on sapphire and TiN experience a similar optical excitation rate opt 1.5 MHz k [51]. For larger pump powers, we found that the contrast 1 T C drops and almost completely vanishes in strong saturation [51]. The origin of this effect, which is still under investigation, can be attributed to the charge exchange processes involving proximal NV centers and/or nitrogen impurities. Such dynamics may be especially pronounced in dense ensembles like ours, e.g. due to Auger-type effects. This effect makes it impractical to work in the saturation regime and limits the observable spin contrast values.Before rigorously investigating the observed dependence of spin contrast on fluorescence lifetime, we present a qualitative explanation, based on the NV level structure (Figure 4(a)). For simplicity, in this discussion we assume that the optical excitation rate is much lower than all the level decay rates. Following the absorption of a photon, both the excited state (ES) and the singlet levels relax into the ground state (GS) levels before the next photon is absorbed. The excited states (ES) of the s 0 m and s 1 m subsystems (i.e. levels 0e and 1e respectively) have equal radiative decay rates ( rad k ) into their respective ground states (GS) 0g and 1g . However, the fluorescence rate of the s 0 m subsystem is higher, because the non-radiative decay of 0e through the singlet state s is less probable than that of 1e ( Here,is the rate of spin-conserving direct ES decay, opt k is the optical pumping rate, () cross i k are the intersystem crossing rates from 0e and 1e to the singlet state...