Friction between ordered, atomically smooth surfaces at the nanoscale (nanofriction) is often governed by stick-slip processes. To test long-standing atomistic models of such processes, we implemented a synthetic nanofriction interface between a laser-cooled Coulomb crystal of individually addressable ions as the moving object and a periodic light-field potential as the substrate. We show that stick-slip friction can be tuned from maximal to nearly frictionless via arrangement of the ions relative to the substrate. By varying the ion number, we also show that this strong dependence of friction on the structural mismatch, as predicted by many-particle models, already emerges at the level of two or three atoms. This model system enables a microscopic and systematic investigation of friction, potentially even into the quantum many-body regime.

Solid-state quantum emitters that couple coherent optical transitions to long-lived spin states are essential for quantum networks. Here we report on the spin and optical properties of single tin-vacancy (SnV) centers in diamond nanostructures. Through magneto-optical spectroscopy at 4 K, we verify the inversion-symmetric electronic structure of the SnV, identify spin-conserving and spin-flipping transitions, characterize transition linewidths, and measure electron spin lifetimes. We find that the optical transitions are consistent with the radiative lifetime limit and that the spin lifetimes are longer than for other inversion-symmetric color centers under similar conditions. These properties indicate that the SnV is a promising candidate for quantum optics and quantum networking applications.A central goal of quantum information processing is the development of quantum networks consisting of stationary, long-lived matter qubits coupled to flying photonic qubits [1,2], with applications in quantum computing, provably secure cryptography, and quantumenhanced metrology [3]. Among matter qubits, quantum emitters in wide-bandgap semiconductors [4,5] have emerged as leading systems as their coherent, spinselective optical transitions act as an interface between quantum information stored in their spin degrees of freedom and emitted photons. While most work has so far focused on the nitrogen-vacancy (NV) center in diamond [6-8], its relatively poor optical properties, including a low percentage of emission into the coherent zero-phonon-line (ZPL) [9] and large spectral diffusion when located near surfaces [10,11], have fueled the investigation of alternative emitters. These include the group-IV color centers in diamond [12], comprising the silicon-vacancy (SiV) [13][14][15][16], germanium-vacancy (GeV) [17,18], and the recently observed lead-vacancy (PbV) [19] centers. These centers have a large fraction of emission into the ZPL and a crystallographic inversion symmetry that limits spectral diffusion and inhomogeneous broadening [20,21]. Unlike the NV center, however, the electronic spin coherence of SiV and GeV centers is limited by phonon scattering to an upperlying ground-state orbital [22,23], requiring operation at dilution-refrigerator temperatures (∼ 100 mK) [24,25], or controllably induced strain [26] to achieve long coherence times.The tin-vacancy (SnV) center in diamond [27, 28] is a group-IV color center that promises favorable optical properties and long spin coherence time at readily achievable temperatures (liquid helium, ∼ 4 K). DFT calculations predict that the SnV has the same symmetry as the SiV and GeV[9], while experimental measurement of a large ground-state orbital splitting indicates that single-phonon scattering, the dominant spin dephasing mechanism of SiV and GeV centers at liquid helium temperatures, should be suppressed significantly [27]. In this work, we report spectroscopic measurements that are consistent with the conjectured electronic structure of the SnV, demonstrate that its optical...

Coherent excitation of an ensemble of quantum objects underpins quantum many-body phenomena, and offers the opportunity to realize a quantum memory to store information from a qubit. Thus far, a deterministic and coherent interface between a single quantum system, e.g. a qubit, and such an ensemble has remained elusive. We first use an electron to cool the mesoscopic nuclear-spin ensemble of a semiconductor quantum dot to the nuclear sidebandresolved regime. We then implement an all-optical approach to access these individual quantized electronic-nuclear spin transitions. Finally, we perform coherent optical rotations of a single collective nuclear spin excitation corresponding to a spin wave called a nuclear magnon. These results constitute the building blocks of a dedicated local memory per quantum-dot spin qubit and promise a solid-state platform for quantum-state engineering of isolated many-body systems.

The highly nonlinear many-body physics of a chain of mutually interacting atoms in contact with a periodic substrate gives rise to complex static and dynamical phenomena, such as structural phase transitions and friction. In the limit of an infinite chain incommensurate with the substrate, Aubry predicted a transition with increasing substrate potential, from the chain's intrinsic arrangement free to slide on the substrate, to a pinned arrangement favouring the substrate pattern. So far, the Aubry transition has not been observed. Here, using spatially resolved position and friction measurements of cold trapped ions in an optical lattice, we observed a finite version of the Aubry transition and the onset of its hallmark fractal atomic arrangement. Notably, the observed critical lattice depth for few-ion chains agrees well with the infinite-chain prediction. Our results elucidate the connection between competing ordering patterns and superlubricity in nanocontacts-the elementary building blocks of friction.