Ultraviolet Free-electron Laser Research Articles

Effects of NOx and NH3 on the secondary organic aerosol formation from α-pinene photooxidation

Understanding the effects of mixed anthropogenic pollutants on the photooxidation of volatile organic compounds (VOCs) is essential for unraveling the formation pathways of secondary organic aerosols (SOA). Yet, it remains a highly challenging experimental target owing to the complexities in the precise measurement of molecular compositions of products and number/mass concentrations of particles as a function of pollutant concentration in the ambient atmosphere. Here, a series of well-defined chamber experiments were performed to explore the effects of NOx and NH3 on the SOA formation from photooxidation of the most abundant monoterpene, α-pinene. The results indicate that the suppression effect of NO and NO2 on the α-pinene photooxidation shows monotonous and parabolic trends, respectively. The presence of NH3 enhances particle number concentrations during the α-pinene + NOx photooxidation by participating in reactions with organic acids. New compounds, including organic peroxides, esters, organic nitrates, and peroxyacyl nitrates, are observed at molecular weight (MW) = 166, 173, 217, 231, 280, 282, 304, and 410 through threshold photoionization making use of a recently constructed vacuum ultraviolet free electron laser in positive ion mode. The molecular structures and formation paths of these species are speculated, which advance the category of VOC oxidation products. Our study provides significant understanding of the influence of NOx and NH3 on the VOC photooxidation, which can be utilized to establish predictive SOA formation networks and to improve atmospheric models.

Comparative studies of the NOx impacts on the photooxidation mechanisms of isomeric monoterpenes of β-pinene and limonene

It is highly challenging to precisely compare the impacts of anthropogenic pollutants on the photooxidation of isomeric volatile organic compounds with respect to molecular compositions and particle number/mass concentrations of secondary organic aerosols (SOAs). In this study, we conducted a series of well-defined indoor chamber experiments to compare the effects of NOx (NO and NO2) on the photooxidation of isomeric monoterpenes of β-pinene and limonene. For the photooxidation of β-pinene with NOx, the increase of the initial concentrations of NO ([NO]0) shows a monotonous suppression of the particle mass concentration, whereas the increase of [NO2]0 shows a monotonous enhancement of the particle mass concentration. For the photooxidation of limonene with NOx, the increase of [NO]0 exhibits a monotonous suppression of the particle mass concentration, whereas the increase of [NO2]0 shows a parabolic trend of the particle mass concentration. Utilizing a newly developed vacuum ultraviolet free electron laser (VUV-FEL), the online threshold photoionization mass spectrometry reveals a series of novel compounds at molecular weight (MW) = 232 and 306 for the β-pinene + NOx system and MW = 187, 261, 280, and 306 for the limonene + NOx system. The molecular structures and formation pathways of these species were inferred, which led to the prediction of the diversity and difference of SOA products (i.e., ester and peroxide accretion products) formed from different monoterpene precursors. To improve the predictions of future air quality, it is recommended that climate models should incorporate the NOx-driven diurnal photooxidation of monoterpenes for SOA formation mechanisms.

Multi-functional gas cell in the vacuum ultraviolet free-electron laser beamline.

A long gas cell, filled with noble gas, is typically positioned between the undulator and the first mirror in the free-electron laser (FEL) beamline to attenuate the laser power as required by the end-stations. In addition to attenuation, the gas cell also serves important functions in various applications, such as spectrometer calibration, resolving power evaluation during beamline commissioning, and filtering of third harmonic in FEL operations. These functions of the gas cell have been successfully tested and implemented at the Dalian Coherent Light Source, a vacuum ultraviolet FEL facility located in Dalian, China. The resolving power of higher than 5000 has been obtained, and accurate calibration has been completed using the gas cell. During operation, the third harmonic of the FEL was attenuated by approximately one order of magnitude with almost the same power of the fundamental. This greatly improved the signal-to-noise ratio at the end-stations.

Size-Specific Infrared Spectroscopy of Neutral Hydrated Clusters Based on a Vacuum Ultraviolet Free Electron Laser.

Spectroscopic study of neutral hydrated clusters provides microscopic insights into the local structures and dynamics of complex systems but is very challenging because of the difficulty in size discrimination. Recently, we developed infrared (IR) spectroscopy based on threshold ionization using a tunable vacuum ultraviolet free electron laser (VUV-FEL). This experimental method allows for size-specific IR spectroscopic measurement of numerous neutral clusters without confinement, such as messenger tags, ultraviolet chromophores, and host matrix. This Perspective aims to highlight the latest advances in VUV-FEL-based IR spectroscopic studies on the confinement-free neutral amine-water, sulfur dioxide-water, and metal-water clusters. Fruitful collaborations with high-level quantum chemical calculations are reviewed. Future research directions with relevance to the atmosphere, biology, and catalysis are proposed.

An experimental application of machine learning algorithms to optimize the FEL lasing via beam trajectory tuning at Dalian Coherent Light Source

The lasing optimization of Free-Electron Laser (FEL) facilities is a time-consuming and challenging task. Instead of operating manually by experienced operators, implementation of machine learning algorithms offers a rapid and adaptable approach for FEL lasing optimization. Recently, such an experiment has been conducted at the vacuum ultraviolet FEL facility - Dalian Coherent Light Source (DCLS). Four algorithms, namely the standard and the neural network-based genetic algorithms, the deep deterministic policy gradient and the soft actor critic reinforcement learning algorithms, have been employed to enhance the FEL intensity by optimizing the electron beam trajectory. These algorithms have shown notable efficacy in enhancing the FEL lasing, especially the reinforcement learning ones which achieved convergence within only approximately 400 iterations. This study demonstrates the validity of machine learning algorithms for FEL lasing optimization, providing a forward-looking perspective on the automatic operation of DCLS.

Spectroscopic and Theoretical Identifications of Two Structural Motifs of (H2O)10 Cluster.

Precise characterization of archetypal systems of aqueous hydrogen-bonding networks is essential for developing accurate potential functions and universal models of water. The structures of water clusters (H2O)n (n = 2-9) have been verified recently through size-specific infrared spectroscopy with a vacuum ultraviolet free electron laser (VUV-FEL) and quantum chemical studies. For (H2O)10, the pentagonal prism and butterfly motifs were proposed to be important building blocks and were observed in previous experiments. Here we report the size-specific infrared spectra of (H2O)10 via a joint experimental and theoretical study. Well-resolved spectra provide a unique signature for the coexistence of pentagonal prism and butterfly motifs. These (H2O)10 motifs develop from the dominant structures of (H2O)n (n = 8, 9) clusters. This work provides an intriguing prelude to the diverse structure of liquid water and opens avenues for size-dependent measurement of larger systems to understand the stepwise formation mechanism of hydrogen-bonding networks.

Effects of isoprene on the ozonolysis of Δ3-carene and β-caryophyllene: Mechanisms of secondary organic aerosol formation and cross-dimerization

Elucidating the mutual effects between the different volatile organic compounds (VOCs) is crucial for comprehending the formation mechanism of atmospheric secondary organic aerosols (SOA). Here, the mixed VOCs experiments of isoprene and Δ3-carene/β-caryophyllene were carried out in the presence of O3 using an indoor smog chamber. The suppression effect of isoprene was recognized by the scanning mobility particle sizer spectrometer, online vacuum ultraviolet free electron laser (VUV-FEL) photoionization aerosol mass spectrometry, and quantum chemical calculations. The results indicate that the suppression effect of isoprene on the ozonolysis of Δ3-carene and β-caryophyllene shows fluctuating and monotonous trends, respectively. The carbon content of the precursor could be the main factor for regulating the strength of the suppression effect. Plausible structures and formation mechanisms of several new products generated from the single VOC precursor and VOC-cross-reaction are proposed, which enrich the category of VOC oxidation products. Meanwhile, a new dimerization mechanism of the RO2 + R'O2 reaction is suggested, which offers an intriguing perspective on the gas phase formation process of particle phase accretion products. The present findings provide valuable insights into clarifying the pivotal roles played by isoprene in the interplay between different VOCs and understanding of SOA formation mechanisms of VOC mixtures, especially nearby the emission origins.

Effects of NO and SO2 on the secondary organic aerosol formation from isoprene photooxidation

Investigation of the effects of anthropogenic pollutants on the mass concentrations, particle number concentrations, and chemical compositions of secondary organic aerosol (SOA) formation is essential in understanding the photooxidation mechanism of volatile organic compounds but has been proven to be a very challenging experimental target because of their complex processes. Here, the effects of NO and SO2 on SOA formation from isoprene photooxidation were studied by a number of laboratory studies. The results indicate the accumulated O3 upon the NO conversion triggers the main oxidation reaction, by which the oxidants (i.e., OH and SO4−) are derived. The SOA mass concentrations and particle number concentrations are enhanced by NO under low NO concentrations but suppressed by NO under high NO concentrations, which are consistent with previous studies (Kroll et al., 2005, 2006). This could be rationalized that the large amount of accumulated O3 inhibit the multi-step isoprene oxidation and a large number of less oxidized products (m/z < 130) absorb or condense on the surface of existing particles, which decelerate the SOA nucleation and growth. The presence of SO2 accelerates the conversion of NO and the accumulation of O3, which promotes the main oxidation reaction of isoprene. New compounds are observed at m/z = 134, 137, 150, 152, and 179 measured by threshold photoionization (positive ion mode) with a tunable vacuum ultraviolet free electron laser and are found to be mainly formed from the isoprene oxidization by O3 and OH. The present findings provide both macroscopic and microscopic information to advance understanding of atmospheric components affected by the anthropogenic-biogenic interactions in the neighborhood of emission origins.

Wakefields in superconducting rf cavities and the impact on vacuum ultraviolet free-electron laser oscillator performance

Wakefields in superconducting rf cavities and the impact on vacuum ultraviolet free-electron laser oscillator performance

Exploring the vacuum ultraviolet photochemistry of astrochemically important triatomic molecules.

The recently constructed vacuum ultraviolet (VUV) free electron laser (FEL) at the Dalian Coherent Light Source (DCLS) is yielding a wealth of new and exquisitely detailed information about the photofragmentation dynamics of many small gas-phase molecules. This Review focuses particular attention on five triatomic molecules-H2O, H2S, CO2, OCS and CS2. Each shows excitation wavelength-dependent dissociation dynamics, yielding photofragments that populate a range of electronic and (in the case of diatomic fragments) vibrational and rotational quantum states, which can be characterized by different translational spectroscopy methods. The photodissociation of an isolated molecule from a well-defined initial quantum state provides a lens through which one can investigate how and why chemical reactions occur, and provides numerous opportunities for fruitful, synergistic collaborations with high-level ab initio quantum chemists. The chosen molecules, their photofragments and the subsequent chemical reaction networks to which they can contribute are all crucial in planetary atmospheres and in interstellar and circumstellar environments. The aims of this Review are 3-fold: to highlight new photochemical insights enabled by the VUV-FEL at the DCLS, notably the recently recognized central atom elimination process that is shown to contribute in all of these triatomic molecules; to highlight some of the potential implications of this rich photochemistry to our understanding of interstellar chemistry and molecular evolution within the universe; and to highlight other and future research directions in areas related to chemical reaction dynamics and astrochemistry that will be enabled by increased access to VUV-FEL sources.

Ultrafast Roaming Mechanisms in Ethanol Probed by Intense Extreme Ultraviolet Free-Electron Laser Radiation: Electron Transfer versus Proton Transfer

Ultrafast H2+ and H3+ formation from ethanol is studied using pump-probe spectroscopy with an extreme ultraviolet (XUV) free-electron laser. The first pulse creates a dication, triggering H2 roaming that leads to H2+ and H3+ formation, which is disruptively probed by a second pulse. At photon energies of 28 and 32 eV, the ratio of H2+ to H3+ increases with time delay, while it is flat at a photon energy of 70 eV. The delay-dependent effect is ascribed to a competition between electron and proton transfer. High-level quantum chemistry calculations show a flat potential energy surface for H2 formation, indicating that the intermediate state may have a long lifetime. The ab initio molecular dynamics simulation confirms that, in addition to the direct emission, a small portion of H2 undergoes a roaming mechanism that leads to two competing pathways: electron transfer from H2 to C2H4O2+ and proton transfer from C2H4O2+ to H2.

Spectroscopic snapshot for neutral water nonamer (H2O)9: Adding a H2O onto a hydrogen bond-unbroken edge of (H2O)8.

Structural characterization of neutral water clusters is crucial to understanding the structures and properties of water, but it has been proven to be a challenging experimental target due to the difficulty in size selection. Here, we report the size-specific infrared spectra of confinement-free neutral water nonamer (H2O)9 based on threshold photoionization, using a tunable vacuum ultraviolet free-electron laser. Distinct OH stretch vibrational fundamentals in the 3200-3350cm-1 region are observed, providing unique spectral signatures for the formation of an unprecedented (H2O)9 structure evolved by adding a ninth water molecule onto a hydrogen bond-unbroken edge of the (H2O)8 octamer with D2d symmetry. This nonamer structure coexists with the five previously identified structures that can be viewed as derived by inserting a ninth water molecule into a hydrogen bond-broken edge of the D2d/S4 octamer. These findings provide key microscopic information for systematic understanding of the formation and growth mechanism of dynamical hydrogen-bonding networks that are responsible for the structure and properties of condensed-phase water.

Infrared Spectroscopy of Stepwise Hydration Motifs of Sulfur Dioxide.

Experimental characterization of microscopic events and behaviors of SO2-H2O interactions is crucial to understanding SO2 atmospheric chemistry but has been proven to be very challenging due to the difficulty in size selection. Here, size-dependent development of SO2 hydrate structure and cluster growth in the SO2(H2O)n (n = 1-16) complexes was probed by infrared spectroscopy based on threshold photoionization using a tunable vacuum ultraviolet free electron laser. Spectral changes with cluster size demonstrate that the sandwich structure initially formed at n = 1 develops into cycle structures with the sulfur and oxygen atoms in a two-dimensional plane (n = 2 and 3) and then into three-dimensional cage structures (n ≥ 4). SO2 is favorably bound to the surface of larger water clusters. These stepwise features of SO2 hydration on various sized water clusters contribute to understanding the reactive sites and electrophilicity of SO2 on cloud droplets, which may have important atmospheric implications for studying the SO2-containing aerosol systems.

Infrared spectroscopic signature of the structural diversity of the water heptamer

As a key species in understanding the hydrogen-bonding network transitions between liquid water and ice, the neutral water heptamer is a challenging experimental target, owing to the richness of low-lying isomers. Here, we report the size-specific infrared spectra of confinement-free, neutral water heptamer (H2O)7 based on threshold photoionization using a tunable vacuum ultraviolet free electron laser. The complexity of the observed spectra indicates that many nearly isoenergetic isomers are present at finite temperatures. Two classes of prism- and cage-like structures are identified in a high-pressure pulsed supersonic expansion of water heptamer, in which the former is favored energetically at low temperatures and serves as a major contributor to the experimental spectrum. These findings provide key information for filling the gap between well-studied water hexamer and octamer.

Application of a modified chirp-taper scheme for generation of attosecond pulses in extreme ultraviolet and soft x-ray free electron lasers

Typically, in Self-Amplified Spontaneous Emission Free Electron Laser (SASE FEL) based short-pulse schemes, pulse duration is limited by FEL coherence time. For hard X-ray FELs, coherence time is in a few hundred attosecond range while for XUV and soft X-ray FELs it is in the femtosecond regime. In this paper the modification of so-called chirp-taper scheme is developed that allows to overcome the coherence time barrier. Numerical simulations for XUV and soft X-ray FEL user facility FLASH demonstrate that one can generate a few hundred attosecond long pulses in the wavelength range 2 - 10 nm with peak power reaching hundreds of megawatts. With several thousand pulses per second this can be a unique source for attosecond science.

Compact LWFA-Based Extreme Ultraviolet Free Electron Laser: Design Constraints

The combination of advanced high-power laser technology, new acceleration methods and achievements in undulator development offers the opportunity to build compact, high-brilliance free electron lasers driven by a laser wakefield accelerator. Here, we present a simulation study outlining the main requirements for the laser–plasma-based extreme ultraviolet free electron laser setup with the aim to reach saturation of the photon pulse energy in a single unit of a commercially available undulator with the deflection parameter K0 in the range of 1–1.5. A dedicated electron beam transport strategy that allows control of the electron beam slice parameters, including collective effects, required by the self-amplified spontaneous emission regime is proposed. Finally, a set of coherent photon radiation parameters achievable in the undulator section utilizing the best experimentally demonstrated electron beam parameters are analyzed. As a result, we demonstrate that the ultra-short, few-fs-level pulse of the photon radiation with the wavelength in the extreme ultraviolet range can be obtained with the peak brilliance of ∼7×1028 photons/pulse/mm2/mrad2/0.1%bw.

Aerosol mass spectrometry of neutral species based on a tunable vacuum ultraviolet free electron laser.

A vacuum ultraviolet free electron laser (VUV-FEL) photoionization aerosol mass spectrometer (AMS) has been developed for online measurement of neutral compounds in laboratory environments. The aerosol apparatus is mainly composed of a smog chamber and a reflectron time-of-flight mass spectrometer (TOF-MS). The indoor smog chamber had a 2 m3 fluorinated ethylene propylene film reactor placed in a temperature- and humidity-controlled room, which was used to generate the aerosols. The aerosols were sampled via an inlet system consisting of a 100 μm orifice nozzle and aerodynamic lenses. The application of this VUV-FEL AMS to the α-pinene ozonolysis under different concentrations reveals two new compounds, for which the formation mechanisms are proposed. The present findings contribute to the mechanistic understanding of the α-pinene ozonolysis in the neighborhood of emission origins of α-pinene. The VUV-FEL AMS method has the potential for chemical analysis of neutral aerosol species during the new particle formation processes.

Vacuum ultraviolet free-electron laser photoionization mass spectrometry of alpha-pinene ozonolysis

α-pinene is the most abundant monoterpene that represents an important family of volatile organic compounds. Molecular identification of key transient compounds during the α-pinene ozonolysis has been proven to be a challenging experimental target because of a large number of intermediates and products involved. Here we exploit the recently developed hybrid instruments that integrate aerosol mass spectrometry with a vacuum ultraviolet free-electron laser to study the α-pinene ozonolysis. The experiments of α-pinene ozonolysis are performed in an indoor smog chamber, with reactor having a volume of 2 m3 which is made of fluorinated ethylene propylene film. Distinct mass spectral peaks provide direct experimental signatures of previously unseen compounds produced from the reaction of α-pinene with O3. With the aid of quantum chemical calculations, plausible mechanisms for the formation of these new compounds are proposed. These findings provide crucial information on fundamental understanding of the initial steps of α-pinene oxidation and the subsequent processes of new particle formation.

Enhancement of Above Threshold Ionization in Resonantly Excited Helium Nanodroplets.

Clusters and nanodroplets hold the promise of enhancing high-order nonlinear optical effects due to their high local density. However, only moderate enhancement has been demonstrated to date. Here, we report the observation of energetic electrons generated by above-threshold ionization (ATI) of helium (He) nanodroplets which are resonantly excited by ultrashort extreme ultraviolet (XUV) free-electron laser pulses and subsequently ionized by near-infrared (NIR) or near-ultraviolet (UV) pulses. The electron emission due to high-order ATI is enhanced by several orders of magnitude compared with He atoms. The crucial dependence of the ATI intensities with the number of excitations in the droplets suggests a local collective enhancement effect.

Flexible ptychography platform to expand the potential of imaging at free electron lasers.

Ptychography, a scanning coherent diffraction imaging method, can produce a high-resolution reconstruction of a sample and, at the same time, of the illuminating beam. The emergence of vacuum ultraviolet and X-ray free electron lasers (FELs) has brought sources with unprecedented characteristics that enable X-ray ptychography with highly intense and ultra-fast short-wavelength pulses. However, the shot-to-shot pulse fluctuations typical for FEL pulses and particularly the partial spatial coherence of self-amplified spontaneous emission (SASE) FELs lead to numerical complexities in the ptychographic algorithms and ultimately restrict the application of ptychography at FELs. We present a general adaptive forward model for ptychography based on automatic differentiation, which is able to perform reconstructions even under these conditions. We applied this model to the first ptychography experiment at FLASH, the Free electron LASer in Hamburg, and obtained a high-resolution reconstruction of the sample as well as the complex wavefronts of individual FLASH pulses together with their coherence properties. This is not possible with more common ptychography algorithms.