All forty-one right modes
Each row is a separately normalized right eigenmode, not a simultaneous particle population. Brightness is square-root probability, fixed from zero to 0.7. Selecting a row prepares that mode anew.
NON-HERMITIAN SKIN EFFECT
Close a 41-site loop, cut one link, and watch its right eigenmodes concentrate at a boundary. Reverse the hopping bias, inspect the complex spectrum, or release a central wave packet.
CONDITIONAL WEIGHT IN FIVE EDGE SITES
EVOLUTION TIME
EVERY OUTCOME COUNTS
Each row is a separately normalized right eigenmode, not a simultaneous particle population. Brightness is square-root probability, fixed from zero to 0.7. Selecting a row prepares that mode anew.
Cyan ellipse: closed-loop energies. Amber segment: open-chain energies. The highlighted point belongs to the selected boundary and mode. The imaginary axis includes the passive loss shift.
INDEPENDENT SIMULATED PREPARATIONS
Each of 1,024 fresh preparations produces one outcome: lost, or detected at a site. The event grid uses amber for loss and cyan for survival. The histogram counts only those recorded surviving sites.
Ideal loss-or-position readout, with no detector inefficiency. Time and display-scale changes preserve the record. A new preparation clears it. Export includes every loss and every site, plus a separately labelled model reference.
The hopping energy sets the units. Site number increases from left to right in the data plots. The three-dimensional layout is schematic; no physical length or calibrated apparatus is assigned.
The directional couplings require an effective open-system construction. With the stated uniform shift, the anti-Hermitian loss matrix is positive semidefinite, so an absorbing-vacuum loss-channel realization exists. This does not model independent local decay at every site or a particular experimental circuit.
Open modes carry an exponential envelope multiplying a standing wave; ring modes are plane waves. The index labels each spectrum separately, rather than identifying a mode followed adiabatically through a boundary change. The displayed map is the right-mode probability, not a biorthogonal density.
The propagator uses fourth-order Runge–Kutta with a step no larger than 0.01. It never renormalizes the evolving state. A separately integrated loss rate checks the probability balance. The bright conditional display divides by survival; raw acquisition always includes lost trials. No gain, many-body statistics or continuously observed particle paths are claimed.
These sources establish the physical context. This Lab uses a stated linear model and illustrative parameters, not a reproduction of their experimental data.
Physics tutorial
BackgroundClose a 41-site loop, cut one link, and watch its right eigenmodes concentrate at a boundary. Reverse the hopping bias, inspect the complex spectrum, or release a central wave packet.
Why it mattersLearn to distinguish a changing wave shape from the probability that anything remains.
Start with the essentials
Time is measured in inverse hopping units. The propagation is not renormalized.
Here site indices run from zero to forty. Reversing the bias reverses the exponential envelope.
Typical misconceptionThe wave gets brighter, so probability must have been created.
Better mental modelThe display scale and conditioning are stated explicitly. The dynamics is passive; total survival never grows.
Typical misconceptionThis is a calibrated apparatus or an interacting many-body experiment.
Better mental modelA passive, uniformly loss-shifted Hatano–Nelson model of one excitation. Bright conditional shapes can coexist with very small survival. Changing controls prepares a new experiment; it is not a mid-run boundary quench or a many-body skin measurement.
Compare the first two presets at the same time.
What to observe: Every control change prepares a new state with the selected boundary. Cutting the link is not applied during this run.Switch between all trials and surviving trials. Keep an eye on the survival meter.
What to observe: The conditional shape sums to one even when very few trials survive.Acquire 1,024 independent preparations. Export lost outcomes as well as measured sites.
What to observe: A bright conditional image does not increase the number of detected events. The snapshot stays frozen when time moves.