A time crystal is a time dependent physical system that does not reach a standstill, even in state of minimum energy. Here we show that the stability of a time crystal can be enhanced by its topology. For this we simulate time crystals made of chainlike ensembles of mutually interacting point particles. When we tie the chain into a knot we find that its timecrystalline qualities improve. The theoretical models we consider are widely used in coarse grained descriptions of linear polymers. Thus we expect that physical realizations of time crystals can be found in terms of knotted molecules.
A time crystal is a time dependent physical system that does not reach a standstill, even in state of minimum energy. Here we show that the stability of a time crystal can be enhanced by its topology. For this we simulate time crystals made of chainlike ensembles of mutually interacting point particles. When we tie the chain into a knot we find that its timecrystalline qualities improve. The theoretical models we consider are widely used in coarse grained descriptions of linear polymers. Thus we expect that physical realizations of time crystals can be found in terms of knotted molecules.
We show that topology is a very effective tool, to construct classical Hamiltonian time crystals. For this we numerically analyze a general class of time crystalline Hamiltonians that are designed to model the dynamics of molecular closed strings. We demonstrate how the time crystalline qualities of a closed string are greatly enhanced when the string becomes knotted. The Hamiltonians that we investigate include a generalized Kratky-Porod wormlike chain model in combination with long range Coulomb and Lennard-Jones interactions. Such energy functions are commonplace in coarse grained molecular modeling. Thus we expect that physical realizations of Hamiltonian time crystals can be constructed in terms of knotted ring molecules.
Time crystals are nonequilibrium phases of matter characterized by the emergence of temporal ordering, in which an interacting many-body system develops robust structure in its time evolution that is not trivially dictated by the external driving or environment. While related phenomena have long been studied in classical nonlinear systems, their realization in entangled quantum matter represents a distinct frontier. The theoretical understanding of discrete time crystals has substantially advanced, yet recent experiments using modern quantum devices and quantum processors reveal regimes beyond established paradigms. These developments call for an extended classification of time-crystalline phases according to both their stabilization mechanisms and their physical character, including discrete and continuous, closed and open, critical, topological, quasiperiodic, and controlled realizations. We review recent implementations of time crystals on quantum platforms and propose such a classification framework, identifying promising directions for the discovery of novel time-crystalline phases of matter.
Time crystals are quantum many-body systems that, due to interactions between particles, are able to spontaneously self-organize their motion in a periodic way in time by analogy with the formation of crystalline structures in space in condensed matter physics. In solid state physics properties of space crystals are often investigated with the help of external potentials that are spatially periodic and reflect various crystalline structures. A similar approach can be applied for time crystals, as periodically driven systems constitute counterparts of spatially periodic systems, but in the time domain. Here we show that condensed matter problems ranging from single particles in potentials of quasicrystal structure to many-body systems with exotic long-range interactions can be realized in the time domain with an appropriate periodic driving. Moreover, it is possible to create molecules where atoms are bound together due to destructive interference if the atomic scattering length is modulated in time.
Recently, Wilczek proposed a fascinating new concept of time crystals, which spontaneously break the continuous time translation symmetry, in analogy with ordinary crystals which break the continuous spatial translation symmetry. Li et al. soon followed with a concrete proposal for an experimental realization and observation of a (space-)time crystal using trapped ions in a ring threaded by an Aharonov-Bohm flux. However, the very existence, even as a matter of principle, of time crystals is rather controversial. Bruno proved a no-go theorem for time crystals for a specific class of Hamiltonians, which covers the original proposal. A similar observation was made for a charge density wave in a superconducting ring by Nozieres. However, since these arguments were not fully general, several new realizations of time crystals, which avoid these no-go arguments, were proposed. In fact, a part of the confusion can be attributed to the lack of a precise mathematical definition of time crystals. Here, we first propose a definition of time crystals in the equilibrium, which is a natural generalization of that of ordinary crystals and can be formulated precisely also for time crystals. We then prove generally the absence of time crystals defined as such, in the ground state of an arbitrary Hamiltonian which consists only of short-range interactions. While the nature of the time crystal is less understood, it is natural to expect that time crystals would be most easily realized, if at all, at zero temperature, as in the case of ordinary crystals. Thus, we focus on the question whether time crystals can exist as the ground state, as in Wilczek’s original proposal. Naively, time crystals would be defined in terms of the ground-state expectation value of an observable O(t). If it exhibits a periodic time dependence, the system may be regarded as a time crystal. However, the very definition of the ground state Ĥ|0〉 = E0|0〉 immediately implies that the expectation value of any Heisenberg operator O(t) ≡ eiĤtO(0)e−iĤt is time-independent. Yet it is too early to reject the idea of time crystals just from this observation, since a similar argument would preclude ordinary (spatial) crystals. One might naively define crystals from a spatially modulating expectation value of the density operator ρ(~x) = e−i ~ P ·~xρ(~0)ei ~ P ·~x. The unique ground state of the Hamiltonian in a finite box is nevertheless symmetric and hence ~ P |0〉 = 0, implying that 〈0|ρ(~x)|0〉 is constant over space.
In analogy with crystalline solids around us, Wilczek recently proposed the idea of "time crystals" as phases that spontaneously break the continuous time translation into a discrete subgroup. The proposal stimulated further studies and vigorous debates whether it can be realized in a physical system. However, a precise definition of the time crystal is needed to resolve the issue. Here we first present a definition of time crystals based on the time-dependent correlation functions of the order parameter. We then prove a no-go theorem that rules out the possibility of time crystals defined as such, in the ground state or in the canonical ensemble of a general Hamiltonian, which consists of not-too-long-range interactions.
This paper investigates the application of quantum algorithms to enhance the prediction of topological knot topology. Traditional methods often struggle with the inherent complexity of these structures, particularly in their intricate knot configurations. We propose a novel 'Quantum Topological Knot Reconstruction' algorithm, leveraging quantum superposition to effectively reconstruct the knot structure. The core claim is that this algorithm, when implemented with suitable quantum hardware, will significantly improve the accuracy and speed of predicting topological knot properties, potentially unlocking new discoveries in materials science and theoretical physics. The paper details the algorithm's design, explores its potential benefits, and discusses the challenges and future directions of this research.