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			<titleStmt><title level='a'>Two-Dimensional Programmable Tweezer Arrays of Fermions</title></titleStmt>
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				<publisher></publisher>
				<date>09/01/2022</date>
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				<bibl> 
					<idno type="par_id">10438795</idno>
					<idno type="doi">10.1103/PhysRevLett.129.123201</idno>
					<title level='j'>Physical Review Letters</title>
<idno>0031-9007</idno>
<biblScope unit="volume">129</biblScope>
<biblScope unit="issue">12</biblScope>					

					<author>Zoe Z. Yan</author><author>Benjamin M. Spar</author><author>Max L. Prichard</author><author>Sungjae Chi</author><author>Hao-Tian Wei</author><author>Eduardo Ibarra-García-Padilla</author><author>Kaden R.A. Hazzard</author><author>Waseem S. Bakr</author>
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			<abstract><ab><![CDATA[We prepare high-filling two-component arrays of tens of fermionic 6 Li atoms in optical tweezers, with the atoms in the ground motional state of each tweezer. Using a stroboscopic technique, we configure the arrays in various two-dimensional geometries with negligible Floquet heating. A full spin-and densityresolved readout of individual sites allows us to postselect near-zero entropy initial states for fermionic quantum simulation. We prepare a correlated state in a two-by-two tunnel-coupled Hubbard plaquette, demonstrating all the building blocks for realizing a programmable fermionic quantum simulator.]]></ab></abstract>
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<div xmlns="http://www.tei-c.org/ns/1.0"><p>Ultracold atoms in optical tweezer arrays have become a popular platform for quantum simulation, computation, and metrology <ref type="bibr">[1]</ref>. The tweezer platform has recently witnessed rapid breakthroughs, ranging from the development of precise optical clocks <ref type="bibr">[2,</ref><ref type="bibr">3]</ref> to the demonstration of entangling operations <ref type="bibr">[4]</ref><ref type="bibr">[5]</ref><ref type="bibr">[6]</ref><ref type="bibr">[7]</ref>. The realization of defect-free arbitrary geometries <ref type="bibr">[8,</ref><ref type="bibr">9]</ref>, in particular in two dimensions, has paved the way for studying rich quantum many-body physics with localized Rydberg atoms, including frustrated spin models on a triangular lattice <ref type="bibr">[10,</ref><ref type="bibr">11]</ref>, topological phases in a zig-zag chain <ref type="bibr">[12]</ref>, and quantum spin liquids with atoms placed on the links of a kagome lattice <ref type="bibr">[13]</ref>.</p><p>The versatility of tweezer arrays has also been extended to systems of itinerant atoms where quantum statistics play a role <ref type="bibr">[14]</ref><ref type="bibr">[15]</ref><ref type="bibr">[16]</ref><ref type="bibr">[17]</ref><ref type="bibr">[18]</ref><ref type="bibr">[19]</ref>. In particular, tunnel-coupled arrays have been realized for small systems of bosonic <ref type="bibr">[14]</ref> and fermionic <ref type="bibr">[15]</ref><ref type="bibr">[16]</ref><ref type="bibr">[17]</ref><ref type="bibr">[18]</ref> atoms in one-dimensional arrays. If these experiments can be scaled, they would constitute a bottom-up approach toward quantum simulation that complements optical lattice experiments with quantum gas microscopes, which currently lie at the forefront of studying one-and two-dimensional Hubbard models <ref type="bibr">[20]</ref><ref type="bibr">[21]</ref><ref type="bibr">[22]</ref><ref type="bibr">[23]</ref><ref type="bibr">[24]</ref><ref type="bibr">[25]</ref><ref type="bibr">[26]</ref><ref type="bibr">[27]</ref><ref type="bibr">[28]</ref><ref type="bibr">[29]</ref>. The difficulty of reconfiguring microscope experiments has led to an almost exclusive focus on physics in square lattices (Ref. <ref type="bibr">[30]</ref> is a recent exception). Programmable Hubbard tweezer arrays would allow the extension of siteresolved studies to arbitrary lattice geometries that bring additional ingredients into play, including frustration, topology, and flat-band physics.</p><p>Hubbard tweezer arrays may also provide a route to address another major challenge for optical lattice experiments: the preparation of low-entropy phases of fermions. In optical lattice experiments, the entropy of the gas is limited by evaporative cooling, which is hindered by poor efficiencies at low temperatures. Entropy redistribution schemes relying on the flow of entropy away from gapped phases have been proposed <ref type="bibr">[31,</ref><ref type="bibr">32]</ref> and experimentally explored <ref type="bibr">[33]</ref>, but they have not resulted in significant reduction of achieved temperatures for correlated phases.</p><p>Here we show that stroboscopic optical tweezer arrays can be used to prepare fermionic systems with arbitrary two-dimensional (2D) geometry and entropies comparable to those achieved in optical lattices, with the additional advantage of being able to further reduce the entropy through postselection. This is possible due to several features particular to this platform. First, in loading a tweezer from a degenerate Fermi gas, the tweezer acts as a "dimple trap," wherein the local Fermi temperature (T F ) is significantly higher than in the bulk gas. Since the fraction of atoms loaded into the tweezers is low, the temperature of the system remains approximately fixed to the bulk gas's temperature, but the tweezers' phase space density is enhanced. Furthermore, the occupancy of the lowest level of each tweezer (given by the Fermi-Dirac distribution) is close to unity. This enables the preparation of a state with two atoms in the ground motional state (one per spin state) on every tweezer with high fidelity, as first demonstrated in Ref. <ref type="bibr">[34]</ref>. Second, the system can be evolved from the band insulator into a correlated state via an adiabatic ramp on of additional sites, taking advantage of independent tunability of each lattice site. We have previously shown that this technique can be used to prepare a state with antiferromagnetic correlations in an eight-site Fermi Hubbard chain <ref type="bibr">[18]</ref>. We extend this approach to 2D and show that any preramp entropy in the system can be effectively eliminated by postselection on the atom number in each spin state. Postselection is enabled by spin-and density-resolved readout <ref type="bibr">[22,</ref><ref type="bibr">35]</ref>, which we implement in a bilayer imaging scheme.</p><p>The experimental cycle, including tweezer loading, is the same as detailed in Ref. <ref type="bibr">[18]</ref>. Tweezers are loaded from a bulk Fermi gas at T=T F &#8776; 0.2 that is a balanced mixture of the lowest and third lowest hyperfine ground states (j&#8593;i, j&#8595;i, respectively). Our scheme for generating 2D arrays uses two crossed acousto-optical modulators (AOMs) [Fig. <ref type="figure">1(a)</ref>]. The tweezers are produced using light with a wavelength of 780 nm, and their waist at the atoms is 1000 &#254;180 -140 nm. Radiofrequency tones for both AOMs are generated by a two-channel arbitrary waveform generator, with a tone separation of 8 MHz corresponding to a tweezer spacing of 1350 nm in the atom plane. The aperture size and bandwidth of the modulators currently limit us to &#8764;9 tweezers in each direction. The beat frequency of neighboring tweezers is &gt; 100 times larger than typical tweezer depths, leading to negligible parametric heating.</p><p>Homogenizing the tweezer depths is particularly challenging for 2D arrays generated using crossed AOMs. A common approach used in Rydberg tweezer experiments is to apply a static set of frequencies consisting of n x and n y tones for the x-and y-directional AOMs, respectively. This generates a rectangular array of n x n y sites; however, the n x &#254; n y degrees of freedom from the signal strength of each tone are insufficient to independently tune the depth of each tweezer. Better homogeneity can be achieved by tuning the relative phases of the tones, but the typical resultant inhomogeneity still exceeds 1%. Tunnel-coupled arrays have more stringent requirements for homogeneity, since the energy offsets in tweezers of a typical depth of &#8764;h &#215; 50 kHz must be controlled to within tunneling energies of &#8764;h &#215; 250 Hz, or better than 0.5%.</p><p>To homogenize arrays to within this precision and produce arrays with nearly arbitrary geometry (limited by the optical resolution of our objective), we introduce a stroboscopic tweezer technique. We generate the array one column at a time, with different y-directional tones applied in every time step [Fig. <ref type="figure">1(b)</ref>]. Effectively, the atoms experience a time-averaged potential of concatenated 1D arrays, as long as the strobe rate f s far exceeds the tweezers' harmonic trap frequencies. As the typical axial (radial) trap frequencies are around 2.5 (15) kHz, we need strobe rates over an order of magnitude higher to avoid significant Floquet heating of the atoms.</p><p>We verify that the stroboscopic scheme is compatible with long lifetimes in the tweezer ground vibrational state with the following study. We measure the dependence of the lifetime in the lowest vibrational state on f s in a two-site strobed array, varying the strobe rate from 163 to 1083 kHz, as shown in the Supplemental Material <ref type="bibr">[36]</ref>. Higher frequencies are inaccessible due to limitations on the AOM response rate, set by the speed of sound and beam size in the crystal. We also compare the lifetimes to that of a static (nonstrobed) tweezer, which is limited by background gas collisions and off-resonant photon scattering due to the trapping light. Consistent with expectations, the lowest strobe rates give the shortest lifetimes in the ground state [Fig. <ref type="figure">1(d)</ref>]. Measurements and numerics using a discrete variable representation method <ref type="bibr">[36,</ref><ref type="bibr">44,</ref><ref type="bibr">45]</ref> both indicate that Floquet heating decreases exponentially with increasing f s and is negligible for f s &#8819; 250 kHz, although the numerics underestimate the threshold frequency range below which severe heating occurs by &#8764;18%.</p><p>We demonstrate loading the arrays with band insulators of fermions with high fidelity using the stroboscopic method. These band insulators serve as low-entropy initial states for fermionic quantum simulation. As proofs of principle, we implement a rectangular 5 &#215; 5 array, 21-site Lieb plaquette, triangular 4 &#215; 5 array, and an eight-site octagonal ring (Fig. <ref type="figure">2</ref>) <ref type="bibr">[36]</ref>. The tweezers are homogenized using a density balancing algorithm where the number of required experimental shots is almost independent of the array size <ref type="bibr">[18]</ref>. In these examples, the sites are not tunnelcoupled due to the large separations. Readout is accomplished by transferring the atoms into a 2D lattice of 752 nm spacing, which oversamples the tweezer array by a factor of 2 or more, and performing Raman sideband cooling on the j&#8593;i atoms after removal of the j&#8595;i atoms <ref type="bibr">[18,</ref><ref type="bibr">23]</ref> with a detection fidelity of 98.5%. Throughout these different geometries, the loading fidelity of a single spin averages to 92%/site, corrected for imaging infidelity, indicating a low entropy of loading in the array. As in previous work <ref type="bibr">[18,</ref><ref type="bibr">34]</ref>, the tweezer depths are chosen so the predominant type of defect in each tweezer is a missing particle rather than an extra one in a higher motional state. In these data, we only measure one of the spin states in a given experimental shot, due to the problem of lightassisted collisions, which necessitates the removal of the other spin state before imaging <ref type="bibr">[46]</ref>.</p><p>To circumvent this problem and obtain full density resolution and spin resolution, we adopt a high-fidelity bilayer imaging scheme <ref type="bibr">[35,</ref><ref type="bibr">[47]</ref><ref type="bibr">[48]</ref><ref type="bibr">[49]</ref>, which also allows the reduction of entropy upon postselection. A bilayer density readout and spin readout was first accomplished in fermionic quantum gas microscope experiments in a superlattice charge-pumping scheme <ref type="bibr">[35]</ref>. Our method is conceptually similar but involves no superlattice (Fig. <ref type="figure">3</ref>). Starting with tweezer-trapped atoms, we adiabatically turn off the tweezer and turn on a 2D lattice of 1064 nm to 60 E R and a vertical trap frequency of 1.2 kHz in 5 ms.</p><p>The magnetic field is brought to 572 G, where we perform a spin flip of j&#8593;i to the second-lowest hyperfine state j &#8593;i, with an efficiency exceeding 99%, and then decrease the field to near 0 G. Atoms in j &#8593;i and j&#8595;i have a greater differential magnetic moment than those in j&#8593;i, enabling the Stern-Gerlach separation of these populations to &#8764;9 &#956;m using a z-magnetic gradient of 168 G=cm in the 2D lattice at a depth of 280 E R . We turn on two lightsheet potentials <ref type="bibr">[23]</ref>-highly anisotropic beams, each with z-directional trap frequencies of 26 kHz-and linearly ramp their vertical separation to 25 &#956;m for imaging. We measure a combined transport and spin identification fidelity of  98.7%. Finally, we image the atoms using Raman sideband cooling simultaneously in both layers, with the 2D lattice depth at 2500 E R and the two lightsheet z-trap frequencies at 70 kHz. Resulting fluorescence is collected by a high numerical aperture objective with atoms in the two planes focused onto two different active areas of a CCD camera. Imaging fidelity is 98% (97%) for the layer of j &#8593;i (j&#8595;i) atoms.</p><p>Bilayer imaging enables reduction of the effective entropy associated with the initial state of the tweezer array (the band insulator) through postselection. The initial entropy per particle of the tweezer ensemble, assuming independent tweezers and single-band occupation, is given by</p><p>where p is the probability to load one spin on a site. With a typical loading efficiency of p &#188; 0.907&#240;3&#222;, the array starts with 0.34(1) k B per particle, with entropy entering from microstates with undesired holes. By selecting only images with the population per spin state equal to the number of loading tweezers, we can effectively choose a subsample with S &#188; 0. Importantly, this postselection criterion eliminates the initial state entropy even after changing the filling of the system (by introducing additional tweezers) to prepare a correlated state. The postselection criterion can be relaxed to use more images from the experiment at the cost of introducing additional initial state entropy. This trade-off is illustrated in Figs. 3(g)-3(h) for a 3 &#215; 5 array in which j&#8593;i and j&#8595;i had average p &#188; 0.914&#240;3&#222; and 0.900(3), respectively (not accounting for imaging fidelity). Out of 972 images, 12% had perfect filling of 15 fermions of each species. However, even keeping images with up to two holes, or over 50% of shots, still results in a low entropy of 0.17(1) k B per particle, which is favorable compared with state-of-the-art optical lattice experiments that range from 0.25 to 0.5 k B per particle <ref type="bibr">[25,</ref><ref type="bibr">33,</ref><ref type="bibr">50,</ref><ref type="bibr">51]</ref>. While postselection can be used to reduce the effective entropy of the initial state to near zero, subsequent ramps to correlated states will inevitably introduce additional entropy. Numerical simulations of the dynamical ramps in small systems indicate this extra entropy should be low for defect-free initial configurations. For example, for the ramp used in our previous work with an eight-site chain <ref type="bibr">[18]</ref>, the ramp is expected to have introduced an additional entropy of 0.04 k B per particle when starting with a defectfree state, but the presence of even a single localized hole would lead to a significant entropy increase of 0.2-0.3 k B per particle depending on the position of the hole. The entropy reported in Fig. <ref type="figure">3</ref>(h) should therefore be treated only as a lower bound for future experiments.</p><p>Postselection on spin and density in this context should be distinguished from the context of optical lattice-based quantum gas microscopy measurements. For example, in a recent study with a fermionic microscopes <ref type="bibr">[51]</ref>, spin readout and density readout enabled postselection of half filled systems with zero total magnetization, keeping &#8764; 9% of data. However, postselection there did not eliminate the finite spin temperature in the initial state. Furthermore, our postselection approach is difficult to implement in optical lattice systems where it has proven challenging to engineer arrays with sharp boundaries and a well-defined number of sites <ref type="bibr">[33]</ref>.</p><p>Equipped with the ability to load near-zero-entropy band insulators after postselection, we implement the simplest building block of a two-dimensional Fermi-Hubbard model: a tunnel-coupled 2 &#215; 2 plaquette. The single-band Hamiltonian is</p><p>where &#265; &#8224; i&#963; is the fermionic creation operator of spin &#963; at site i, ni&#963; is the number operator, t x&#240;y&#222; is the tunneling matrix element in the x&#240;y&#222; direction, &#916; is the energy offset, and U is on site interaction between opposite spin states. We start by loading two diagonal sites in a rectangular array with vertical (horizontal) spacing of 1520 ( <ref type="formula">1690</ref> adiabatically ramping on the two opposing diagonal sites in 50 ms <ref type="bibr">[18]</ref>, with tunnelings of t x &#189;t y &#188; h &#215; 140&#240;5&#222;&#189;220&#240;5&#222; Hz in the final configuration <ref type="bibr">[36]</ref>. We also ramp U= t from 0 to 3.4(2) in the same time using the Feshbach resonance. Here, t &#188;&#240;t x &#254; t y &#222;=2.</p><p>The resulting spin-spin correlations are shown in Fig. <ref type="figure">4</ref>(c), which depicts C ij &#188;hS z;i S z;j i -hS z;i ihS z;j i, where S z;i &#8801; 1 2 &#240;n &#8593;;i -n &#8595;;i &#222;. Here, data were postselected to include only images that contained two j&#8593;i and two j&#8595;i atoms, for a total of 673 experimental cycles. With full spin readout and density readout, we are able to reconstruct the diagonals of the density matrix &#961; &#188;j&#936;ih&#936;j in the basis of allowed number states (with Hilbert space size &#240; 4  2 &#222; 2 &#188; 36), and compare data with theory. In Fig. <ref type="figure">4(d)</ref>, we plot the experimental population in each microstate together with the populations expected theoretically for the plaquette ground state, which are consistent within error bars. Here, we reduce our statistical errors by taking advantage of the spin symmetry of the Hubbard Hamiltonian to average the probabilities for spin-reversed microstates. Furthermore, we fit the temperature of the canonical ensemble to best reproduce the distribution of microstates. The fit gives an upper bound for the temperature of k B T &#8764; 0.3 t (with the fit losing sensitivity below that temperature). This corresponds to an entropy in the range [0,0.09] k B per particle, which is consistent with the prediction from simulating the ramp dynamics (entropy gain of 0.02 k B per particle).</p><p>In conclusion, we have realized a 2D tweezer array of fermions with software-programmable geometry using a novel stroboscopic technique that allows independent control over all tweezer depths and positions. We have realized the building blocks to implement programmable 2D Fermi-Hubbard models, and demonstrated these on a small scale. Future work will focus on increasing the system size of the tunnel-coupled arrays. A natural target for future work will be few-leg ladder systems. For example, two-leg triangular ladder systems can be used to explore the J 1 -J 2 model, including the special case of the Majumdar-Ghosh model and its valence-bond solid ground states <ref type="bibr">[52]</ref>. Furthermore, upon introducing spin imbalance and hole doping, a triangular two-leg ladder is predicted to host magnon-hole binding at energy scales set by the tunneling, rather than the superexchange <ref type="bibr">[53]</ref>. Multileg triangular ladders may potentially host other exotic states such as a chiral spin liquid at half filling and intermediate U=t that evolves to a 120&#176;-antiferromagnetic order at strong U=t <ref type="bibr">[54]</ref>. Ultimately, fully 2D tunnel-coupled arrays with arbitrary geometry will be a rich playground for exploring novel phases of correlated fermions.</p></div></body>
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