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Quantum sensors emerged among quantum technologies as the ones with promising potential applications in the near future. This perspective reviews two leading quantum sensing platforms and their advancements toward biological applications: quantum light sources and color centers in diamonds. Quantum light, including squeezed states and N00N states, allows enhanced phase measurements by surpassing the classical shot noise limits. This advantage can be exploited in several contexts, enabling improved resolution and sensitivity, which are particularly valuable in biological contexts where traditional high-intensity illumination could damage or alter delicate samples. In parallel, color centers in diamonds, specifically nitrogen-vacancy and silicon-vacancy centers, also emerged as promising for sensing applications due to their high sensitivity and biocompatibility. These sensors enable detailed intracellular measurements, such as temperature detection, and show potential for measuring magnetic fields of biological origin. Despite these advancements, significant challenges remain in translating these technologies from a controlled laboratory environment to practical, widely applicable devices for diverse biological applications. Overcoming these challenges is crucial for unlocking the full potential of quantum sensors in the biological field.

Abstract Recent demonstrations of optically active telecom emitters show that silicon is a compelling candidate for solid-state quantum photonic platforms. In particular, the fabrication of a defect known as the G center has been shown in carbon-rich silicon upon conventional thermal annealing. However, the high-yield controlled fabrication of these emitters at the wafer scale still requires the identification of a suitable thermodynamic pathway enabling its activation following ion implantation. Here we demonstrate the activation of G centers in high-purity silicon substrates upon nanosecond pulsed laser annealing. The proposed method enables non-invasive, localized activation of G centers by the supply of short non-stationary pulses, thus overcoming the limitations of conventional rapid thermal annealing related to the structural metastability of the emitters. A finite-element analysis highlights the strong non-stationarity of the technique, offering radically different defect-engineering capabilities with respect to conventional longer thermal treatments, paving the way to the direct and controlled fabrication of emitters embedded in integrated photonic circuits and waveguides.

Abstract Temperature is one of the most relevant parameters for the regulation of intracellular processes. Measuring localized subcellular temperature gradients is fundamental for a deeper understanding of cell function, such as the genesis of action potentials, and cell metabolism. Notwithstanding several proposed techniques, at the moment detection of temperature fluctuations at the subcellular level still represents an ongoing challenge. Here, for the first time, temperature variations (1 °C) associated with potentiation and inhibition of neuronal firing is detected, by exploiting a nanoscale thermometer based on optically detected magnetic resonance in nanodiamonds. The results demonstrate that nitrogen‐vacancy centers in nanodiamonds provide a tool for assessing various levels of neuronal spiking activity, since they are suitable for monitoring different temperature variations, respectively, associated with the spontaneous firing of hippocampal neurons, the disinhibition of GABAergic transmission and the silencing of the network. Conjugated with the high sensitivity of this technique (in perspective sensitive to < 0.1 °C variations), nanodiamonds pave the way to a systematic study of the generation of localized temperature gradients under physiological and pathological conditions. Furthermore, they prompt further studies explaining in detail the physiological mechanism originating this effect.