arXiv subjects

Haifeng Pan

Publications and source records attributed to Haifeng Pan.

6 recordsLinked to original sources

arXiv2026

In-Situ Polarimetry in Collimated Magneto-Infrared Spectroscopy System

Magneto-infrared spectroscopy under strong magnetic fields provides a powerful probe of Landau quantization and field-induced collective excitations, yet its full potential has long been constrained by the lack of in-situ polarization control, because the highly divergent infrared beam propagating through narrow light tubes undergoes multiple wall reflections, leading to severe polarization degradation. Here we report a collimated magneto-infrared spectroscopy system that integrates continuous in-situ polarimetry. The system employs incident and exit collimation chambers forming a Kepler type optical architecture, which converts the large-aperture FTIR output into a low-divergence beam and strongly suppresses multi-reflection trajectories inside long gold-plated light tubes, thereby enhancing both optical throughput and polarization fidelity. A remotely controlled polarization module, consisting of an automated linear polarizer and a switchable Fresnel rhomb positioned entirely outside the high-field region, enables continuous in-situ tuning between linear, circular, and arbitrary elliptical polarization states without thermal cycling, manual realignment, or breaking vacuum. Interchangeable compact focusing modules further support Faraday and Voigt geometries in both transmission and reflection experiments within a 50 mm magnet bore, providing efficient beam focusing and signal collection while maintaining polarization fidelity. The setup achieves a minimum root-mean-square noise of 0.0033%, an average noise of 0.0082%, and a linear polarization extinction ratio up to 40:1. We demonstrate the capability through continuous in-situ linear polarimetry and broadband circular polarimetry in the magneto-infrared spectroscopy of various single crystals. This platform establishes a robust experimental framework for in-situ polarization-resolved magneto-infrared spectroscopy.

physics.ins-det↗

arXiv2025

A High-Flux and High-Efficiency Setup for Magneto-Infrared Spectroscopy

We report the design and implementation of a high-flux, high-efficiency magneto-infrared spectroscopy system optimized for broadband measurements in high magnetic fields. The setup integrates a Fourier transform infrared spectrometer, a 12 T cryogen-free superconducting magnet, precision-polished and gold-plated light tubes, custom-designed reflective focusing modules for Faraday and Voigt geometries, and an external multi-detector chamber with motorized selection. Optical throughput is maximized by reducing light tube loss from 65.5%/m to 22.0%/m via abrasive flow and mechanical polishing followed by gold electroplating, and by adopting a single-on-axis parabolic-mirror Faraday module that increases the effective numerical aperture from 0.14 to 0.36, enhancing collection efficiency by nearly an order of magnitude. An eight-position motorized sample stage and fully automated control over magnetic field, temperature, optical path, and detector choice enable high-throughput measurements without repeated warm-ups. The optimized configuration achieves a root-mean-square noise level of 0.0061% in a 2-minute integration for a 40% reflectivity sample, corresponding to a signal-to-noise ratio exceeding 16000. System capabilities are demonstrated by resolving weak replica bands in EuCd2As2 and faint Landau level transitions in LaAlSi.

cond-mat.mtrl-sci↗

arXiv2023

The discovery of three-dimensional Van Hove singularity

Arising from the extreme/saddle point in electronic bands, Van Hove singularity (VHS) manifests divergent density of states (DOS) and induces various new states of matter such as unconventional superconductivity. VHS is believed to exist in one and two dimensions, but rarely found in three dimension (3D). Here, we report the discovery of 3D VHS in a topological magnet EuCd2As2 by magneto-infrared spectroscopy. External magnetic fields effectively control the exchange interaction in EuCd2As2, and shift 3D Weyl bands continuously, leading to the modification of Fermi velocity and energy dispersion. Above the critical field, the 3D VHS forms and is evidenced by the abrupt emergence of inter-band transitions, which can be quantitatively described by the minimal model of Weyl semimetals. Three additional optical transitions are further predicted theoretically and verified in magneto-near-infrared spectra. Our results pave the way to exploring VHS in 3D systems and uncovering the coordination between electronic correlation and the topological phase.

cond-mat.mtrl-sci↗

arXiv2016

Disentangling the role of laser coupling in directional breaking of molecules

The directional control of molecular dissociation with the laser electric field waveform is a paradigm and was demonstrated for a variety of molecules. In most cases, the directional control occurs via a dissociative ionization pathway. The role of laser-induced coupling of electronic states in the dissociating ion versus selective ionization of oriented neutral molecules, however, could not be distinguished for even small heteronuclear molecules such as CO. Here, we introduce a technique, using elliptically polarized pump and linearly polarized two-color probe pulses that unambiguously distinguishes the roles of laser-induced state coupling and selective ionization. The measured photoelectron momentum distributions governed by the light polarizations allow us to coincidently identify the ionization and dissociation from the pump and probe pulses. Directional dissociation of CO+ as a function of the relative phase of the linearly polarized two-color pulse is observed for both parallel and orthogonally oriented molecules. We find that the laser-induced coupling of various electronic states of CO+ plays an important role for the observed directional bond breaking, which is verified by quantum calculations.

physics.optics↗

arXiv2014

Visualizing molecular unidirectional rotation

A molecule can be optically accelerated to rotate unidirectionally at a frequency of a few terahertzes which is many orders higher than the classical mechanical rotor. Such a photon-induced ultrafast molecular unidirectional rotation has been well explored as a controllable spin of the molecular nuclear wave packet. Although it has been observed for more than 10 years, a complete imaging of the unidirectional rotating nuclear wave packet is still missing, which is essentially the cornerstone of all the exploring applications. Here, for the first time, we experimentally visualize the time-dependent evolution of the double-pulse excited molecular unidirectional rotation by Coulomb explosion imaging the rotational nuclear wave packet. Our results reveal comprehensive details undiscovered in pioneering measurements, which exhibits as a joint of the quantum revival of the impulsively aligned rotational wave packet and its unidirectional rotation following the angular momentum conservation. The numerical simulations well reproduce the experimental observations and intuitively revivify the thoroughgoing evolution of the rotational wave packet.

physics.optics↗

arXiv2010

THz generation by dual-color pulse in prealigned molecules

We demonstrate that the THz generation in air from a dual-color pulse, composed of the fundamental and second-harmonic waves, can be coherently controlled by field-free molecular alignment. By tuning its time delay to properly match various molecular alignment revivals, the THz generation from the dual-color pulse can be promoted or decreased due to the spatial cross-(de)focusing effect and the alignment-dependent ionization probabilities of the prealigned diatomic molecules of air. For the dual-color pulse of orthogonally polarized fundamental and second-harmonic waves, the polarization of the generated THz radiation can be controlled by the field-free molecular alignment, which functions as a transient dynamic wave-plate for the dual-color pulse with different phase velocities for the orthogonally polarized field components. The plasma effect on the THz generation of the dual-color pulse is also observed, leading to additional intensity and polarization control of the THz radiation.

physics.optics↗