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Non-invasive measurement of absolute temperature is important for proper characterization of various pathologies and for evaluation of thermal dose during interventional procedures. The proton (hydrogen nucleus) magnetic resonance (MR) frequency shift method can be used to map relative temperature changes. However, spatiotemporal variations in the main magnetic field and the lack of local internal frequency reference challenge the determination of absolute temperature. Here, we introduce a multinuclear method for absolute MR thermometry, based on the fact that the hydrogen and sodium nuclei exhibit a unique and distinct characteristic frequency dependence with temperature and with electrolyte concentration. A one-to-one mapping between the precession frequency difference of the two nuclei and absolute temperature is demonstrated. Proof-of-concept experiments were conducted in aqueous solutions with different NaCl concentrations, in agarose gel samples, and in freshly excised ex vivo mouse tissues. One-dimensional chemical shift imaging experiments also demonstrated excellent agreement with infrared measurements.

 

Sensitive and accurate diagnostic technologies with magnetic sensors are of great importance for identifying and localizing defects of rechargeable solid batteries using noninvasive detection. We demonstrate a microwave-free alternating current (AC) magnetometry method with negatively charged NV centers in diamond based on a cross-relaxation feature between nitrogen-vacancy (NV) centers and individual substitutional nitrogen (P1) centers occurring at 51.2 mT. We apply the technique to non-destructively image solid-state batteries. By detecting the eddy-current-induced magnetic field of the battery, we distinguish a defect on the external electrode and identify structural anomalies within the battery body. The achieved spatial resolution is μμμ360μm. The maximum magnetic field and phase shift generated by the battery at the modulation frequency of 5 kHz are estimated as 0.04 mT and 0.03 rad respectively. 

Solid-state battery technology is motivated by the desire to deliver flexible power storage in a safe and efficient manner. The increasingly widespread use of batteries from mass production facilities highlights the need for a rapid and sensitive diagnostic tool for identifying battery defects. We demonstrate the use of atomic magnetometry to measure the magnetic fields around miniature solid-state battery cells. These fields encode information about battery manufacturing defects, state of charge, and impurities, and they can provide important insights into battery aging processes. Compared with SQUID-based magnetometry, the availability of atomic magnetometers, however, highlights the possibility of constructing a low-cost, portable, and flexible implementation of battery quality control and characterization technology. 

The ever-increasing demand for high-capacity rechargeable batteries highlights the need for sensitive and accurate diagnostic technology for determining the state of a cell, for identifying and localizing defects, and for sensing capacity loss mechanisms. Here, we leverage atomic magnetometry to map the weak induced magnetic fields around Li-ion battery cells in a magnetically shielded environment. The ability to rapidly measure cells nondestructively allows testing even commercial cells in their actual operating conditions, as a function of state of charge. These measurements provide maps of the magnetic susceptibility of the cell, which follow trends characteristic for the battery materials under study upon discharge. In particular, hot spots of charge storage are identified. In addition, the measurements reveal the capability to measure transient internal current effects, at a level of μA, which are shown to be dependent upon the state of charge. These effects highlight noncontact battery characterization opportunities. The diagnostic power of this technique could be used for the assessment of cells in research, quality control, or during operation, and could help uncover details of charge storage and failure processes in cells.