Ion Concentration and Voltage Imaging with Fluorescent Nanodiamonds
Patrick Voorhoeve, Hiroshi Abe, Takeshi Ohshima, Qiang Sun, Anita Quigley, Rob Kapsa, Nikolai Dontschuk, Philipp Reineck

TL;DR
This paper demonstrates reversible charge state switching in fluorescent nanodiamonds and uses this to achieve sensitive, all-optical imaging of voltage and ion concentration at the nanoscale.
Contribution
It introduces a reliable method for controlling NV charge states in nanodiamonds and applies this to voltage and ion concentration imaging with high sensitivity.
Findings
Reversible switching between NV$^0$ and NV$^+$ states achieved in sub-30 nm FNDs.
Voltage imaging sensitivity up to 16 mV Hz$^{-1/2}$ demonstrated.
Ion concentration imaging sensitivity up to 1.8% per millimolar NaCl achieved.
Abstract
The nitrogen-vacancy (NV) center in diamond exists in different charge states with distinct photoluminescence properties, which are sensitive to the nanoscale electrochemical environment. Hence, the NV charge state is emerging as a powerful all-optical platform for nanoscale sensing and imaging. Although significant progress has been made in engineering near-surface NV centers in bulk diamond, controlling the NV charge state in fluorescent nanodiamonds (FNDs) has proven challenging, limiting the sensitivity and reliability of FND-based charge state sensing. Here, we demonstrate reliable, reversible switching between the fluorescent NV and non-fluorescent NV charge states in sub-30 nm FNDs via surface oxidation and hydrogenation, respectively, for single particles and particle powder. In aqueous electrochemical cells, we demonstrate voltage and ion concentration imaging based on…
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