Electronics is based on the manipulation of electrons, possibly enhanced by exploiting internal structure associated with spin (spintronics). Atomtronics seeks do the same with neutral atoms. The more complex internal structure of atoms makes the possibilities of such an architecture far richer than its electronic analog. Recently, persistent currents of superfluid neutral atoms have been created in ring circuits, which are close analogs to superconducting circuits1. There have also been efforts towards developing analogs to active electronic circuit elements such as diodes and transistors2. Any usable neutral atom circuit, however, will need analogs to the most basic electronic elements – resistors (R), capacitors (C) and inductors (L). Using a two-dimensional (2D) optical dipole potential3 to generate what we call free-space atom chips, we have created and characterized a neutral-atom RLC circuit. We show that the resistance is analogous to ballistic (Sharvin4) resistance in metals, the inductance is analogous to kinetic inductance in superconductors5 and the capacitance is analogous to the quantum capacitance in nanoscale devices6,7.

A 2D neutral atom analog to an electronic RLC circuit can be realized with a classical ideal gas using two containers of areas A1 and A2 connected by a channel. In an electronic capacitor, a charge imbalance (Q) between two conductors produces a potential difference (ΔV). When a resistor connects the two conductors, electrons flow to eliminate the charge imbalance, causing ΔV to vanish. In our system, a number imbalance (N) between the two containers produces a chemical potential difference (Δμ). When a channel connects the two containers, atoms flow to eliminate the number imbalance, causing Δμ to vanish. To complete this analogy, we define a chemical capacitance,

with SI units of 1/J and with the same form as the electronic capacitance C = QV.

The chemical potential of a 2D ideal gas is the change in free energy associated with changing the number of particles in the system8,

where k is Boltzmann's constant, h Planck's constant, T the temperature, n the 2D number density and m the mass of a particle in the gas. To determine the capacitance, we start by assuming the two chambers to be in equilibrium, with equal temperatures and equal densities, N1e/A1 = N2e/A2 = ne. Moving a small number of particles N from A1 to A2 leads to an imbalance in the densities so that n1 = (N1eN)/A1 and n2 = (N2e + N)/A2. Subtracting equation (2) with n1 from equation (2) with n2 leads to

This linear approximation is valid for N N1e and N2e. The experiment we describe below is within this limit. Combining equations (1) and (4) leads to an expression for the neutral-atom chemical capacitance,

where is the harmonic mean of A1 and A2 and εT is the thermal energy of the gas.

When a channel is opened between the chambers, it acts as a resistor and an inductor. To determine the values of R and L, we examine the flow dynamics of the system. In a 2D ideal gas, the effusion rate F of atoms out of either container is given by

where Ai is the area of the container and w is the width of the channel. The total rate of change in atom number in container 1 can then be written as

where the second term on the right hand side of the equation, representing the rate that atoms enter container 1 due to leaving container 2, is evaluated at a time Δt earlier. This delay is due to the finite velocity of the atoms traversing the channel. We approximate this delay time using the average transverse velocity of an atom in the channel,

where l is the length of the channel. When we combine equations (58) and linearly expand the terms in equation (7) involving Δt, the result is analogous to Kirchhoff's law applied to a series RLC circuit,

with chemical resistance and inductance given by

with SI units of J · s and J · s2 respectively. Here,

is the average 2D momentum of the particles in one container. We dropped a second term in the resistance that is only significant when the channel represents a large portion of the entire area of the system. At this point the small N approximation breaks down, thus the second term is negligible when equation (9) is valid.

The chemical capacitance, resistance and inductance each have specific electronic analogs. Our capacitance results from the shift in chemical potential due to transfer of particles, the same effect that causes the quantum capacitance in nanostructures6,7. For 2D quantum dots with areas A1 and A2, the quantum capacitance is given by

where εF is the Fermi energy of the gas. This is similar to equation (5), with an electrical factor of e2 and the thermal energy replaced by the 2D Fermi energy. It is interesting to note that taking in equation (12) does not yield the correct classical limit of the quantum capacitance, which is equation (5).

In electronics, a point junction smaller than the mean free path of the electrons creates what is known as the Sharvin resistance. This arises purely from the ballistic motion of the electrons because there is no scattering of electrons in the point junction itself. For a 2D electronic system the Sharvin resistance is given by9

where is the Fermi momentum. This has the same form as our chemical resistance in equation (10), differing by a factor of e2 and a numerical factor because the Sharvin resistance is derived for a 2D, charged, T = 0 Fermi gas, which has a different velocity distribution than our neutral, classical gas.

There is an inductance in electronic systems, the kinetic inductance5, that arises due to the kinetic energy associated with current flow in a wire,

Again, this shares the same form as our chemical inductance, differing by a factor of e2 and a numerical factor.

The methods that we used to calculate the capacitance and resistance of classical ideal gas circuit elements can be extended to other atomic systems such as degenerate Fermi gases and Bose-Einstein condensates. To define the chemical capacitance, all that is needed is the dependence of the chemical potential on atom number. The momentum distribution of the sample determines the effusion rate, which leads directly to the chemical resistance. Table 1 summarizes these results for 2D and 3D non-interacting classical gases, non-interacting degenerate Fermi gases and BECs. The BEC cases are derived using the Gross-Pitaevskii (GP) equations for hard-wall containers in the Thomas-Fermi limit. In this case it is not sufficient to describe the system as consisting of point particles with classical trajectories, which is needed to derive the resistance, thus this is omitted. The 2D Fermi gas capacitance formula is exact. The classical gas and the 3D Fermi gas capacitances are all the first-order terms in Taylor series expansions.

Table 1 Summary of chemical capacitances and resistances for various systems. In the 2D systems, is the harmonic mean of the two container areas, w is the cross-sectional width of the channel, the average classical 2D momentum is and the 2D Fermi momentum is . In the 3D systems, is the harmonic mean of the two container volumes, a is the cross-sectional area of the channel, the average classical 3D momentum is and the 3D Fermi momentum is


To realize a classical ideal gas neutral atom capacitor, we begin with a sample of 87Rb atoms, cooled and confined using a magneto-optical trap10 (MOT). This MOT is created inside of a free-space atom chip that consists of two circular containers separated by a rectangular channel. The method used for creating this potential is discussed in the methods section. At time t = 0, the atoms are released from the MOT after a final cooling stage and allowed to flow between the containers for a variable amount of time, after which a fluorescence image is taken of the atoms. We directly image the gas flow between the containers with this setup. The evolution of this system can be seen in figure 1. We point out that the arrangement employed is similar to that used in atom-optics billiards where a circular potential is known to lead to ”regular” dynamics, which would affect the effusion rate in our experiment11. In our case however, the container walls are not smooth, as discussed in the methods. Because of this the atom-wall collisions are not always specular, leading to ergodic dynamics, thus our use of equation (6) is valid. Figure 2 shows the decay of the normalized number imbalance N/Ne as a function of time for several channel widths, as well as the solution to the RLC differential equation for the parameters used. The only fit parameter for the RLC solution is the initial atom number imbalance.

Figure 1
figure 1

Capacitor Discharge.

Images of a discharging atom capacitor with a channel width of 340 μm. The atoms are loaded into the right container and released from the MOT at t = 0 ms. The images are snapshots at 5 ms intervals, starting at t = 5 ms (viewed left to right, top to bottom). Each frame is the average of eight individual experimental runs and is scaled independently of the other frames.

Figure 2
figure 2

Comparison of experimental data to analytic solution.

The points indicate the experimental data and the solid lines represent the relevant RLC solution. The black line is for a channel width of 240 μm, the red 384 μm and the green 576 μm. From equations (5,10), the RC time constant, , can be calculated for each of these systems to be 34, 21 and 14 ms respectively. The diameter of each container is 600 μm. For each experimental data point, 8 individual runs were averaged. The error bars are the standard deviation of the mean.


For channels up to approximately half the width of the containers, the data and theory agree well. For channels that approach the width of the containers (green plot in figure 2), the assumption of local equilibrium is no longer valid and good agreement is not expected and indeed is not seen. The nature of the disagreement appears to be inductive, showing a significant overshoot. This however, is not the inductance we derive, which is too small to account for this phenomenon.

We have experimentally demonstrated atomtronic capacitors and resistors and shown how to construct an atomtronic inductor, all on a free-space atom chip defined using 2D optical dipole potentials. These basic linear devices are necessary for biasing active devices and are also essential for constructing oscillators and filters. Integration into systems such as loops containing BECs1, atomtronic Josephson junctions based on BECs, BEC analogs of SQUIDs12 and atomtronic batteries, diodes and transistors2, is made much more simple through the flexibility of our atom-chip technique.


To create the trap geometry that was necessary to carry out this experiment, we used what we call free-space atom chips, which are a type of crossed optical dipole trap. We use a sheet dipole trap to confine the atoms to a 2D plane. On top of this, we project an arbitrary 2D optical dipole potential to create the geometry necessary for the experiment. In this particular experiment, the sheet trap was a blue-detuned, repulsive beam confining the atoms from below, with gravity confining them from above.

In the plane, we create our arbitrary 2D pattern using a generalized phase contrast approach13. This scheme is shown in figure 3 a). A phase pattern is imprinted onto an input TEM00 beam and sent through a 4-f imaging system. We used a 2D spatial light modulator (SLM) to imprint the pattern. At the Fourier plane, there is a phase-contrast filter that shifts the phase of the lowest spatial frequencies, which exist near the optical axis, by π relative to the remaining spatial frequencies of the beam. The two parts of the beam interfere in the output plane to produce an intensity profile that mirrors the input phase mask. This plane is imaged onto the sheet potential, effectively etching the sheet to create our free-space atom chip. The intensity profile for one of our capacitor potentials is shown in figure 3 b). This method, with the use of the computer-addressable SLM, allows us to create and easily modify the confining potential used in the experiment. This ability was integral to this experiment as it allowed us to easily adjust the channel width. Because of the pixelazation of our SLM, the walls of our containers are rough on the order of 10 μm.

Figure 3
figure 3

Phase-Contrast imaging system with typical output.

a) A basic phase-contrast imaging system with input phase mask, phase-contrast filter and 4-f lens arrangement and b) a typical output pattern used to create blue-detuned optical dipole potentials for an atom capacitor. The blue (white) areas correspond to light (absence of light).

In the experiment, the atoms start with a temperature of approximately 40 μK. The potential height of the container walls is approximately 60 μK. Since there is a significant population of atoms in the thermal distribution with an energy that can escape the trap, there is a truncated velocity distribution in the sample. The number density of the atoms in this experiment is not high enough for rethermalization to occur. Time-of-flight expansion experiments have shown that the truncated distribution is well approximated by a thermal distribution at a temperature of about 20 μK, which is the temperature used in the analytical RLC plots in figure 3. The potential height of the sheet below the atoms is approximately 500 μK, which is effectively infinite when compared to our atom temperatures.

The images were taken by switching on the original near-resonant MOT light for 100 μs and collecting the light scattered by the atoms using a single lens, one-to-one imaging system with the image plane on the sensor of our camera. A background image was then subtracted to obtain the final image for any one shot. Eight individual runs were then averaged together for each frame of figure 1. To count the atom number difference plotted in figure 2, each imaged was masked off to count the number of atoms in either the left or right container. The error bars in this plot are the standard deviation in the mean for this measurement for the eight runs. Each image was taken after a short (2 ms) time-of-flight for technical reasons.