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- ECE PhD Thesis Defense: Danchen Jia11:00 am
- Ni de Aquí, Ni de Allá (Not From Here, Not From There) Exhibition11:00 am
- How Setting Up Informational Interviews NOW will Advance Your Career LATER12:00 pm
- ECE PhD Prospectus Defense: Zeynep Ece Kizilates2:00 pm
- ECE PhD Thesis Defense: Daniel Shahar2:00 pm
- Employee Commuter Benefit Party4:00 pm
- Pre-Law Basics for Freshmen4:00 pm
- [UMich] ROMS Postdoc Fellowship 2025 Virtual Information Session4:00 pm
- The Limits of "Mixedness": Ethno-National Conflicts in post-1948 Israel’s “Mixed Cities”4:30 pm
- Winter Movie Night5:00 pm
- 2025 Springboard Series7:00 pm
- Tuesday Night Lecture Series: Jennifer Roberts7:00 pm
- Directors' Project7:30 pm
- Crossing the Finish Line: Finalizing Your End-of-Semester Gradebook10:00 am
- Seminar Series: Theodore Greene (Bowdin College)12:00 pm
- CFA Holiday Celebration2:00 pm
- Education Policy Seminar Series: Melissa "Mimi" Arnold Lyon3:00 pm
- Fall Educational Policy Seminar: Melissa "Mimi" Arnold Lyon3:00 pm
- BUCSA Holiday Get-Together4:00 pm
- Counseling (EdM) Information Session6:00 pm
- BU Tanglewood Institute Monthly Chamber Music Reading Party6:30 pm
- Boston University Jazz Festival7:30 pm
ECE PhD Thesis Defense: Danchen Jia
ECE PhD Thesis Defense: Danchen Jia
Title: Mid-Infrared Photothermal Imaging: from Cellular Volumes to Nanostructured Interfaces
Presenter: Danchen Jia
Advisor: Professor Ji-Xin Cheng
Chair: TBA
Committee: Professor Ji-Xin Cheng, Professor Siddharth Ramachandran, Professor Jerome Mertz, Professor Lei Tian
Google Scholar Link: https://scholar.google.com/citations?user=LnNn-oYAAAAJ&hl=en
Abstract: Mid-infrared photothermal (MIP) microscopy enables subcellular chemical imaging of key metabolites in life science. However, three-dimensional (3D) chemical imaging speed is not sufficient for live cell studies. This dissertation developed two methods for volumetric chemical imaging at video rates. Firstly, by exploiting thermo-sensitive fluorescence, we demonstrate fluorescence-detected mid-infrared photothermal Fourier light field (FMIP-FLF) microscopy, achieving double-shot 3D chemical imaging. FMIP-FLF visualized protein in bacteria and revealed altered lipid metabolism in drug-resistant pancreatic cancer cells. Secondly, we present photothermal relaxation intensity diffraction tomography (PRIDT) that encodes IR-induced refractive index changes through photothermal relaxation and reconstructs them via intensity diffraction tomography. PRIDT achieves 15 Hz volumetric chemical imaging, enabling label-free, video-rate visualization of lipid and protein metabolism in live cells.
Beyond imaging speed, MIP sensitivity is limited by the weak interaction between IR photons and molecules. To address this, two ultrasensitive infrared photothermal spectroscopy methods were developed. We first report mid-infrared encoded plasmonic scattering (MIREPS) spectroscopy, which leverages a nanoparticle-on-film cavity as a spectroscopic sensor for the analyte molecules inside the nanogap to detect nitrile or nitro groups in ~130 molecules. Next, we introduce metasurface-enhanced infrared photothermal (MEIP) microscope, which achieved a detection limit as low as 0.24 monolayer surface coverage of bovine serum albumin with mid-infrared-resonant metasurface.
Together, these strategies for high-speed, high-throughput, high-sensitivity and 3D-resolved infrared photothermal imaging open pathways for quantitative chemical analysis of low-abundance molecules in living systems.
| When | 11:00 am - 1:00 pm on 9 December 2025 |
|---|---|
| Building | PHO 339 |