Cryogenic scanning photocurrent spectroscopy for materials responses to structured optical fields

Fuente: arXiv
Gespeichert in:
Bibliographische Detailangaben
Hauptverfasser: Hao, Duxing, Lu, Chun-I, Sun, Ziqi, Chang, Yu-Chen, Chang, Wen-Hao, Chen, Ye-Ru, Park, Akiyoshi, Rao, Beining, Qiu, Siyuan, Lan, Yann-Wen, Lu, Ting-Hua, Yeh, Nai-Chang
Format: Preprint
Veröffentlicht: 2025
Schlagworte:
Online-Zugang:
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
_version_ 1866918040311955456
author Hao, Duxing
Lu, Chun-I
Sun, Ziqi
Chang, Yu-Chen
Chang, Wen-Hao
Chen, Ye-Ru
Park, Akiyoshi
Rao, Beining
Qiu, Siyuan
Lan, Yann-Wen
Lu, Ting-Hua
Yeh, Nai-Chang
author_facet Hao, Duxing
Lu, Chun-I
Sun, Ziqi
Chang, Yu-Chen
Chang, Wen-Hao
Chen, Ye-Ru
Park, Akiyoshi
Rao, Beining
Qiu, Siyuan
Lan, Yann-Wen
Lu, Ting-Hua
Yeh, Nai-Chang
contents Circular dichroism spectroscopy is known to provide important insights into the interplay of different degrees of freedom in quantum materials, and yet spectroscopic study of the optoelectronic responses of quantum materials to structured optical fields, such as light with finite spin and orbital angular momentum, has not yet been widely explored, particularly at cryogenic temperature. Here we demonstrate the design and application of a novel instrument that integrates scanning spectroscopic photocurrent measurements with structured light of controlled spin and orbital angular momentum. For structured photons with wavelengths between 500 nm to 700 nm, this instrument can perform spatially resolved photocurrent measurements of two-dimensional materials or thin crystals under magnetic fields up to $\pm$ 14 Tesla, at temperatures from 300 K down to 3 K, with either spin angular momentum $\pm \hbar$ ororbital angular momentum $\pm \ell \hbar$ (where $\ell$=1,2,3... is the topological charge), and over a (35 $\times$ 25) $μm^2$ area with ~ 1 $μm$ spatial resolution. These capabilities of the instrument are exemplified by magneto-photocurrent spectroscopic measurements of monolayer 2H-$MoS_2$ field-effect transistors, which not only reveal the excitonic spectra but also demonstrate monotonically increasing photocurrents with increasing |$\ell $| as well as excitonic Zeeman splitting and an enhanced Landé g-factor due to the enhanced formation of intervalley dark excitons under magnetic field. These studies thus demonstrate the versatility of the scanning photocurrent spectrometry for investigating excitonic physics, optical selection rules, and optoelectronic responses of novel quantum materials and engineered quantum devices to structured light.
format Preprint
id arxiv_https___arxiv_org_abs_2505_24833
institution arXiv
publishDate 2025
record_format arxiv
spellingShingle Cryogenic scanning photocurrent spectroscopy for materials responses to structured optical fields
Hao, Duxing
Lu, Chun-I
Sun, Ziqi
Chang, Yu-Chen
Chang, Wen-Hao
Chen, Ye-Ru
Park, Akiyoshi
Rao, Beining
Qiu, Siyuan
Lan, Yann-Wen
Lu, Ting-Hua
Yeh, Nai-Chang
Other Condensed Matter
Instrumentation and Detectors
Circular dichroism spectroscopy is known to provide important insights into the interplay of different degrees of freedom in quantum materials, and yet spectroscopic study of the optoelectronic responses of quantum materials to structured optical fields, such as light with finite spin and orbital angular momentum, has not yet been widely explored, particularly at cryogenic temperature. Here we demonstrate the design and application of a novel instrument that integrates scanning spectroscopic photocurrent measurements with structured light of controlled spin and orbital angular momentum. For structured photons with wavelengths between 500 nm to 700 nm, this instrument can perform spatially resolved photocurrent measurements of two-dimensional materials or thin crystals under magnetic fields up to $\pm$ 14 Tesla, at temperatures from 300 K down to 3 K, with either spin angular momentum $\pm \hbar$ ororbital angular momentum $\pm \ell \hbar$ (where $\ell$=1,2,3... is the topological charge), and over a (35 $\times$ 25) $μm^2$ area with ~ 1 $μm$ spatial resolution. These capabilities of the instrument are exemplified by magneto-photocurrent spectroscopic measurements of monolayer 2H-$MoS_2$ field-effect transistors, which not only reveal the excitonic spectra but also demonstrate monotonically increasing photocurrents with increasing |$\ell $| as well as excitonic Zeeman splitting and an enhanced Landé g-factor due to the enhanced formation of intervalley dark excitons under magnetic field. These studies thus demonstrate the versatility of the scanning photocurrent spectrometry for investigating excitonic physics, optical selection rules, and optoelectronic responses of novel quantum materials and engineered quantum devices to structured light.
title Cryogenic scanning photocurrent spectroscopy for materials responses to structured optical fields
topic Other Condensed Matter
Instrumentation and Detectors
url https://arxiv.org/abs/2505.24833