Laser cooling has given a boost to atomic physics throughout the last 30 years, as it allows one to prepare atoms in motional states, which can only be described by quantum mechanics. Most methods rely, however, on a near-resonant and cyclic coupling between laser light and well-defined internal states, which has remained a challenge for mesoscopic particles. An external cavity may compensate for the lack of internal cycling transitions in dielectric objects and it may provide assistance in the cooling of their centre-of-mass state. Here we demonstrate cavity cooling of the transverse kinetic energy of silicon nanoparticles freely propagating in high vacuum (<10−8 mbar). We create and launch them with longitudinal velocities down to v≤1 m s−1 using laser-induced ablation of a pristine silicon wafer. Their interaction with the light of a high-finesse infrared cavity reduces their transverse kinetic energy by up to a factor of 30.

The de Broglie wave nature of matter is a paradigmatic example of fundamental quantum physics and enables precise measurements of forces, fundamental constants and even material properties. However, even though matter-wave interferometry is nowadays routinely realized in many laboratories, this feat has remained an outstanding challenge for the vast class of native polypeptides, the building blocks of life, which are ubiquitous in biology but fragile and difficult to handle. Here, we demonstrate the quantum wave nature of gramicidin, a natural antibiotic composed of 15 amino acids. Femtosecond laser desorption of a thin biomolecular film with intensities up to 1 TW/cm 2 transfers these molecules into a cold noble gas jet. Even though the peptide's de Broglie wavelength is as tiny as 350 fm, the molecular coherence is delocalized over more than 20 times the molecular size in our all-optical time-domain Talbot-Lau interferometer. We compare the observed interference fringes for two different interference orders with a model that includes both a rigorous treatment of the peptide's quantum wave nature as well as a quantum chemical assessment of its optical properties to distinguish our result from classical predictions. The successful realization of quantum optics with this polypeptide as a prototypical biomolecule paves the way for quantumassisted molecule metrology and in particular the optical spectroscopy of a large class of biologically relevant molecules.The wave-particle duality of massive matter has become an important aspect of modern physics. Atom interferometry [1, 2] enabled new tests from quantum physics [3] to general relativity [4,5], cosmology [6] inertial sensing [7,8] precision measurements of fundamental constants [9] and forces [10]. The de Broglie wave nature has been shown for large molecules, from fullerenes [11] and molecular clusters [12] up to even high-mass particles [13]. Such experiments probe the quantum-toclassical interface and can even be used as a unique tool to characterize neutral molecules in the gas phase [14,15] with the potential for minimally invasive high-precision spectroscopy [16].However until today, quantum optics with massive native biomolecules has remained elusive in particular due to the challenges in forming stable and intense molecular beams which can be detected with high efficiency and selectivity. Measurements on neutral biomolecules in the gas phase will, however, become valuable as they are solvent-free and allow predicting and evaluating biomolecular electronic properties independent of any coupling matrix environments [17]. Here, we present the first realization of matter-wave interferometry of gramicidin A1, a linear antibiotic polypeptide composed of 15 amino acids with a mass m = 1882 amu = 3.13 × 10 −24 kg, naturally produced by the soil bacterium Bacillus brevis. Interference experiments with this biomolecular prototype brings us a step closer towards quantum experiments with living organisms [18].A typical matter-wave experiment requires an efficient so...

Since their first discovery by Louis Dunoyer and Otto Stern, molecular beams have conquered research and technology. However, it has remained an outstanding challenge to isolate and photoionize beams of massive neutral polypeptides. Here we show that femtosecond desorption from a matrix-free sample in high vacuum can produce biomolecular beams at least 25 times more efficiently than nanosecond techniques. While it has also been difficult to photoionize large biomolecules, we find that tailored structures with an abundant exposure of tryptophan residues at their surface can be ionized by vacuum ultraviolet light. The combination of these desorption and ionization techniques allows us to observe molecular beams of neutral polypeptides with a mass exceeding 20,000 amu. They are composed of 50 amino acids-25 tryptophan and 25 lysine residuesand 26 fluorinated alkyl chains. The tools presented here offer a basis for the preparation, control and detection of polypeptide beams.

Modern quantum optics encompasses a wide field of phenomena that are either related to the discrete quantum nature of light, the quantum wave nature of matter or light-matter interactions. We here discuss new perspectives for quantum optics with biological nanoparticles. We focus in particular on the prospects of matter-wave interferometry with amino acids, nucleotides, polypeptides or DNA strands. We motivate the challenge of preparing these objects in a 'biomimetic' environment and argue that hydrated molecular beam sources are promising tools for quantum-assisted metrology. The method exploits the high sensitivity of matter-wave interference fringes to dephasing and shifts in the presence of external perturbations to access and determine molecular properties.

Laser-induced acoustic desorption (LIAD) has recently been established as a tool for analytical chemistry. It is capable of launching intact, neutral, or low charged molecules into a high vacuum environment. This makes it ideally suited to mass spectrometry. LIAD can be used with fragile biomolecules and very massive compounds alike. Here, we apply LIAD time-of-flight mass spectrometry (TOF-MS) to the natural biochromophores chlorophyll, hemin, bilirubin, and biliverdin and to high mass fluoroalkyl-functionalized porphyrins. We characterize the variation in the molecular fragmentation patterns as a function of the desorption and the VUV postionization laser intensity. We find that LIAD can produce molecular beams an order of magnitude slower than matrix-assisted laser desorption (MALD), although this depends on the substrate material. Using titanium foils we observe a most probable velocity of 20 m/s for functionalized molecules with a mass m = 10 000 Da.

Amino acids are essential building blocks of life, and fluorinated derivatives have gained interest in chemistry and medicine. Modern mass spectrometry has enabled the study of oligo‐ and polypeptides as isolated entities in the gas phase, but predominantly as singly or even multiply charged species. While laser desorption of neutral peptides into adiabatically expanding supersonic noble gas jets is possible, UV–VIS spectroscopy, electric or magnetic deflectometry as well as quantum interferometry would profit from the possibility to prepare thermally slow molecular beams. This has typically been precluded by the fragility of the peptide bond and the fact that a peptide would rather ‘fry’, i.e. denature and fragment than ‘fly’. Here, we explore how tailored perfluoroalkyl functionalization can reduce the intermolecular binding and thus increase the volatility of peptides and compare it to previously explored methylation, acylation and amidation of peptides. We show that this strategy is essential and enables the formation of thermal beams of intact neutral tripeptides, whereas only fragments were observed for an extensively fluoroalkyl‐decorated nonapeptide. © 2017 The Authors. Journal of Mass Spectrometry Published by John Wiley & Sons Ltd.

Molecular beam techniques are a key to many experiments in physical chemistry and quantum optics. In particular, advanced matter-wave experiments with high-mass molecules profit from the availability of slow, neutral and mass-selected molecular beams that are sufficiently stable to remain intact during laser heating and photoionization mass spectrometry. We present experiments on the photostability with molecular libraries of tailored oligoporphyrins with masses up to 25 000 Da. We compare two fluoroalkylsulfanyl-functionalized libraries based on two different molecular cores that offer the same number of anchor points for functionalization but differ in their geometry and electronic properties. A pentaporphyrin core stabilizes a library of chemically well-defined molecules with more than 1600 atoms. They can be neutrally desorbed with velocities as low as 20 m/s and efficiently analyzed in photoionization mass spectrometry. Copyright © 2015 John Wiley & Sons, Ltd.

Recent progress in synthetic chemistry and molecular quantum optics has enabled demonstrations of the quantum mechanical wave–particle duality for complex particles, with masses exceeding 10 kDa. Future experiments with even larger objects will require new optical preparation and manipulation methods that shall profit from the possibility to cleave a well-defined molecular tag from a larger parent molecule. Here we present the design and synthesis of two model compounds as well as evidence for the photoinduced beam depletion in high vacuum in one case.