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Miguel Ceja

Publications and source records attributed to Miguel Ceja.

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Measuring gravity by holding atoms

Despite being the dominant force of nature on large scales, gravity remains relatively elusive to experimental measurement. Many questions remain, such as its behavior at small scales or its role in phenomena ascribed to dark matter and dark energy. Atom interferometers are powerful tools for probing Earth's gravity, the gravitational constant, dark energy theories and general relativity. However, they typically use atoms in free fall, which limits the measurement time to only a few seconds, and to even briefer intervals when measuring the interaction of the atoms with a stationary source mass. Recently, interferometers with atoms suspended for as long as 70 seconds in an optical lattice have been demonstrated. To keep the atoms from falling, however, the optical lattice must apply forces that are billion-fold as strong as the putative signals, so even tiny imperfections reduce sensitivity and generate complex systematic effects. As a result, lattice interferometers have yet to demonstrate precision and accuracy on par with their free fall counterparts and have yet to be used for precision measurement. Here, we optimize the sensitivity of a lattice interferometer and use a system of signal inversions and switches to suppress and quantify systematic effects. This enables us to measure the attraction of a miniature source mass, ruling out the existence of screened dark energy theories over their natural parameter space. More importantly, the combined accuracy of $6.2~\rm{nm/s}^2$ is four times as good as the best similar measurements with freely falling atoms, demonstrating the advantages of lattice interferometry in fundamental physics measurements. Further upgrades may enable measuring forces at sub-millimeter ranges, the gravitational Aharonov-Bohm effect and the gravitational constant, compact gravimetry, and testing whether the gravitational field itself has quantum properties.

physics.atom-ph

Atomic gravimeter robust to environmental effects

Atomic accelerometers and gravimeters are usually based on freely-falling atoms in atomic fountains, which not only limits their size, but also their robustness to environmental factors such as tilts, magnetic fields or vibrations. Such limitations have precluded their broad adoption in the field, for geophysics, geology, and inertial navigation. More recently, atom interferometers based on holding atoms in an optical lattice have been developed. Such gravimeters also suppress the influence of vibrations in the frequency range of ~1 Hz and above by several orders of magnitude relative to conventional atomic gravimeters. Here, we show that such interferometers are robust to tilts of more than 8 mrad with respect to the vertical and can suppress the effect of even strong environmental magnetic fields and field gradients by using atoms in the F=3,4 hyperfine ground states as co-magnetometers, potentially eliminating the need for shielding. We demonstrate gravimeter sensitivity of $0.7~\rm{mGal}/\sqrt{\rm Hz}$ ($1~{\rm mGal}=10~μ\rm{m/s}^2$) in a compact geometry where atoms only travel over mm of space.

physics.atom-ph

Coherence limits in lattice atom interferometry at the one-minute scale

In quantum metrology and quantum simulation, a coherent non-classical state must be manipulated before unwanted interactions with the environment lead to decoherence. In atom interferometry, the non-classical state is a spatial superposition, where each atom coexists in multiple locations as a collection of phase-coherent partial wavepackets. These states enable precise measurements in fundamental physics and inertial sensing. However, atom interferometers usually use atomic fountains, where the available interrogation time is limited to around 3 seconds for a 10 m fountain. Here, we realise an atom interferometer with a spatial superposition state that is maintained for as long as 70 seconds. We analyse the theoretical and experimental limits to coherence arising from collective dephasing of the atomic ensemble. This reveals that the decoherence rate slows down markedly at hold times that exceed tens of seconds. These gains in coherence may enable gravimetry measurements, searches for fifth forces or fundamental probes into the non-classical nature of gravity.

physics.atom-ph

Suppressing chemical corrosions of lithium metal anodes

The lithium (Li) metal anode is essential for next generation high energy density rechargeable Li metal batteries. Although extensive studies have been performed to prolong the cycle life of Li metal batteries, the calendar life, which associates with chemical corrosion of Li metal in liquid electrolytes, has not been quantitatively understood. Here, by combing the Titration Gas Chromatography (TGC) method and Cryogenic Focused Ion Beam (Cryo-FIB), we established a quantitative relationship between the chemical corrosion rate and electrochemically deposited Li morphology in various liquid electrolyte systems. We identified that the corrosion rate is dominated by the porosity of the deposited Li. The larger the porosity of deposited Li has, the faster the corrosion rate will be. We further proposed strategies to mitigate the chemical corrosion on Li thus to extend the calendar life of Li metal batteries. By strictly controlling the stacking pressure during Li plating, Li deposits with ultra-low porosity can be achieved, suppressing the corrosion rate to 0.08% per day compared with 1.71% per day of the high-porosity Li.

cond-mat.mtrl-sci

Quantitatively Designing Porous Copper Current Collectors for Lithium Metal Anode

Lithium metal has been an attractive candidate as a next generation anode material. Despite its popularity, stability issues of lithium in the liquid electrolyte and the formation of lithium whiskers have kept it from practical use. Three-dimensional (3D) current collectors have been proposed as an effective method to mitigate whiskers growth. Although extensive research efforts have been done, the effects of three key parameters of the 3D current collectors, namely the surface area, the tortuosity factor, and the surface chemistry, on the performance of lithium metal batteries remain elusive. Herein, we quantitatively studied the role of these three parameters by synthesizing four types of porous copper networks with different sizes of well-structured micro-channels. X-ray microscale computed tomography (micro-CT) allowed us to assess the surface area, the pore size and the tortuosity factor of the porous copper materials. A metallic Zn coating was also applied to study the influence of surface chemistry on the performance of the 3D current collectors. The effects of these parameters on the performance were studied in detail through Scanning Electron Microscopy (SEM) and Titration Gas Chromatography (TGC). Stochastic simulations further allowed us to interpret the role of the tortuosity factor in lithiation. By understanding these effects, the optimal range of the key parameters is found for the porous copper anodes and their performance is predicted. Using these parameters to inform the design of porous copper anodes for Li deposition, Coulombic efficiencies (CE) of up to 99.56% are achieved, thus paving the way for the design of effective 3D current collector systems.

cond-mat.mtrl-sci

Pressure-tailored lithium deposition and dissolution in lithium metal batteries

A porous electrode resulting from unregulated Li growth is the major cause of the low Coulombic efficiency and potential safety hazards of rechargeable Li metal batteries. Strategies aiming to achieve large granular Li deposits have been extensively explored; yet, the ideal Li deposits, which consist of large Li particles that are seamlessly packed on the electrode and can be reversibly deposited and stripped, have never been achieved. Here, by controlling the uniaxial stack pressure during battery operation, a dense Li deposition (99.49% electrode density) with an ideal columnar structure has been achieved. Using multi-scale characterization and simulation, we elucidated the critical role of stack pressure on Li nucleation, growth and dissolution processes, and developed innovative strategies to maintain the ideal Li morphology during extended cycling. The precision manipulation of Li deposition and dissolution is a critical step to enable fast charging and low temperature operation for Li metal batteries.

physics.app-ph

Quantifying Inactive Lithium in Lithium Metal Batteries

Inactive lithium (Li) formation is the immediate cause of capacity loss and catastrophic failure of Li metal batteries. However, the chemical component and the atomic level structure of inactive Li have rarely been studied due to the lack of effective diagnosis tools to accurately differentiate and quantify Li+ in solid electrolyte interphase (SEI) components and the electrically isolated unreacted metallic Li0, which together comprise the inactive Li. Here, by introducing a new analytical method, Titration Gas Chromatography (TGC), we can accurately quantify the contribution from metallic Li0 to the total amount of inactive Li. We uncover that the Li0, rather than the electrochemically formed SEI, dominates the inactive Li and capacity loss. Using cryogenic electron microscopies to further study the microstructure and nanostructure of inactive Li, we find that the Li0 is surrounded by insulating SEI, losing the electronic conductive pathway to the bulk electrode. Coupling the measurements of the Li0 global content to observations of its local atomic structure, we reveal the formation mechanism of inactive Li in different types of electrolytes, and identify the true underlying cause of low Coulombic efficiency in Li metal deposition and stripping. We ultimately propose strategies to enable the highly efficient Li deposition and stripping to enable Li metal anode for next generation high energy batteries.

cond-mat.mtrl-sci