RYRunqing Yu

Runqing Yu

*This is an algorithmically generated author record based on publicly available information.

Current Organizations / Institutes

The organizations/institutes from the scholar's latest article

Previous Organizations / Institutes

The organizations / institutes from the scholar's other articles in the past ten years


Runqing Yu has a total of 10 co-authors. Here are the top co-authors by number of shared publications:

  • Bian Wu

    Chinese Acad Sci, Anhui Inst Opt & Fine Mech, Hefei Inst Phys Sci, Anhui Prov Key Lab Photon Devices & Mat, Hefei 230031, Peoples R China

    2 shared publications
  • Hua Xia

    Chinese Acad Sci, Anhui Inst Opt & Fine Mech, Hefei Inst Phys Sci, Anhui Prov Key Lab Photon Devices & Mat, Hefei 230031, Peoples R China

    2 shared publications
  • Sun Pengshuai

    Chinese Acad Sci, Anhui Inst Opt & Fine Mech, Hefei Inst Phys Sci, Anhui Prov Key Lab Photon Devices & Mat, Hefei 230031, Peoples R China

    2 shared publications
  • Zhirong Zhang

    Anhui Provincial Key Laboratory of Photonic Devices and Materials, Anhui Institute of Optics and Fine Mechanics, Chinese Academy of Sciences, Hefei 230031, China

    2 shared publications
  • Feng-Zhong Dong

    Anhui Provincial Key Laboratory of Photonic Devices and Materials, Anhui Institute of Optics and Fine Mechanics, Chinese Academy of Sciences, Hefei, China

    1 shared publication
  • Pang Tao

    Chinese Acad Sci, Anhui Inst Opt & Fine Mech, Hefei Inst Phys Sci, Anhui Prov Key Lab Photon Devices & Mat, Hefei 230031, Peoples R China

    1 shared publication

Latest Publications

  • Open Access

    Development of a Rapid Measurement Method for Analysis of the NOx Conversion Process Based on Quantum Cascade Laser Absorption Spectroscopy

    by Xi Yang, Zhirong Zhang, Shuang Yang, Pengshuai Sun, Bian Wu, Hua Xia, Runqing Yu

    In this study, a method for double-beam quantum cascade laser absorption spectroscopy (DB-QCLAS) was developed. Two mid-infrared distributed feedback quantum cascade laser beams were coupled in an optical cavity for the monitoring of NO and NO2 (NO at 5.26 μm; NO2 at 6.13 μm). Appropriate lines in the absorption spectra were selected, and the influence of common gases in the atmosphere, such as H2O and CO2, was avoided. By analyzing the spectral lines under different pressure conditions, the appropriate measurement pressure of 111 mbar was selected. Under this pressure, the interference between adjacent spectral lines could be effectively distinguished. The experimental results show that the standard deviations for NO and NO2 were 1.57 ppm and 2.67 ppm, respectively. Moreover, in order to improve the feasibility of this technology for detecting chemical reactions between NO and O2, the standard gases of NO and O2 were used to fill the cavity. A chemical reaction instantaneously began, and the concentrations of the two gases were immediately changed. Through this experiment, we hope to develop new ideas for the accurate and rapid analysis of the process of NOx conversion and to lay a foundation for a deeper understanding of the chemical changes in atmospheric environments.


  • Development of a Quantum Cascade Laser-Based Sensor for Environmental HONO Monitoring in the Mid-Infrared at 8 μm

    by Xiao-Juan Cui, Runqing Yu, Wei-Dong Chen, Zhi-Rong Zhang, Tao Pang, Peng-Shuai Sun, Hua Xia, Bian Wu, Feng-Zhong Dong

    The development of a fast in situ optical sensor based on a continuous-wave (cw) quantum cascade laser (QCL) operating at 8 μm for measurement of environmental gaseous nitrous acid (HONO) is reported. A strong absorption line at 1252.2109 cm $^{-1}$ is found to be free of interferences and used for the first time for ambient HONO detection. Loss of HONO on the wall of the gas sample absorption cell is evaluated. The resulting 1-s detection limit for HONO is 110 pptv with a folded path length of 172 m. Continuous monitoring of HONO and NO2 mixing ratios variations along with the basic meteorological parameters were performed during a field campaign of several days. Typical photochemical reactions of HONO have been observed on sunny and snowy days. Atmospheric HONO mixing ratios observed in this study indicate that direct emission from traffic exhausts and local heterogeneous reactions are potentially important sources of HONO.