
Yu Ding
· Anderson-Interface Chair ProfessorVerifiedGeorgia Institute of Technology · Industrial and Systems Engineering
Active 1998–2026
About
Dr. Yu Ding is the Anderson-Interface Chair and Professor in the H. Milton Stewart School of Industrial and Systems Engineering at Georgia Tech. Prior to joining Georgia Tech in 2023, he was the Mike and Sugar Barnes Professor of Industrial and Systems Engineering at Texas A&M University.
Research topics
- Metallurgy
- Materials science
- Chemistry
- Chemical engineering
- Organic chemistry
- Nanotechnology
- Composite material
- Inorganic chemistry
- Environmental science
- Engineering
- Physical chemistry
- Business
Selected publications
2026-03-22
articleThis work presents a unified framework for large-scale characterization and statistical modeling of hot-carrier-induced (HCI) variability in 55 nm CMOS technology. A 16 × 16 nMOSFET testing array enables high-throughput HCI evaluation, while a compact virtual-source model (VSM) is employed to extract and analyze key transport parameters. The study identifies the HCI-induced traps are the dominant physical mechanisms responsible for aggravated parameter variation after stress. The degradation statistics of multiple parameters can be well described by Exponential-Poisson distribution, and strong inter-parameter correlations are identified and modeled. A variation-aware aging model incorporating parameter correlation is development and implemented in Verilog-A for circuit-level reliability simulation. The proposed framework provides a systematic and efficient approach for investigating HCI-induced variability and supports reliability-aware circuit design.
Synthesis of Pd–Ag Alloy Nanoframes Comprised of Hollow Ridges by Templating With Ag Nanocubes
ChemNanoMat · 2026-04-01
articleOpen accessNoble‐metal nanoframes are attractive for catalytic applications due to their open structures and large specific surface areas. However, traditional nanoframes are known to suffer from poor structural robustness because of their ultrathin ridges. Here, we address this issue by developing a new class of nanoframes characterized by relatively thick but hollow ridges. Our demonstration is based upon Pd and a typical synthesis involves the one‐shot injection of PdBr 2 powder suspension into an aqueous mixture containing Ag nanocubes, ascorbic acid, poly(vinyl pyrrolidone), and KBr held at 75°C. The poor solubility of PdBr 2 in water enables slow release of Pd (II) and thus a steady reduction rate for controlling the deposition of Pd atoms. During the synthesis, the side faces of Ag nanocubes are continuously carved away through galvanic replacement, accompanied by the deposition of Pd atoms on the corners and edges for the generation of cage cubes—cubes with through holes across the opposite faces. At a later stage, the Ag remaining in the ridges is etched away, leading to the formation of hollow ridges with a final composition of Pd 1 Ag 2 . The Pd–Ag alloy nanoframes exhibited good structural robustness during 1 h of chronoamperometric test toward formic acid oxidation reaction.
Unveiling the high-activity origins of BiVO4-Zn tandems for CO2 photoreduction
Journal of Energy Chemistry · 2025-09-10
articleResearch Square · 2025-08-08
preprintOpen accessAdvanced Energy Materials · 2025-09-15 · 9 citations
articleAbstract Self‐assembled monolayers (SAMs) have emerged as highly promising hole transport layers for inverted perovskite solar cells, owing to their low parasitic absorption and effective charge extraction. However, their inherent strong hydrophobicity often inhibits the quality and uniformity of perovskite films and induces defects at the buried interface. In this study, a chlorine‐substituted all‐hydrophilic molecule is introduced to modify the buried interface. Such decoration transforms the hydrophobic SAM into a super‐hydrophilic surface, significantly enhancing the quality and uniformity of perovskite films. This chlorine‐substituted molecule exhibits a strong coordination with lead ions and effectively passivates defects at the buried interface of perovskite films. As a result, the single‐junction wide‐bandgap (1.67 eV) perovskite solar cell achieves a power conversion efficiency of 23.97%, the highest value achieved for MeO‐2PACz‐based devices. Furthermore, the perovskite‐silicon tandem solar cell reaches an efficiency of 31.12%. Additionally, the applicability of chlorine‐functionalized all‐hydrophilic molecule at the buried interface modification is demonstrated to various SAMs (4PADCB, 2PACz and Me‐4PACz) and narrower‐ or wider‐bandgap (1.61, 1.68, and 1.72 eV) perovskite solar cells. This work presents a promising strategy to overcome the challenges associated with SAM‐based perovskite solar cells, paving the way for further performance advancement.
Water Air & Soil Pollution · 2025-06-07
articleParallel Imaging Using Virtual Conjugate Coils and Spatial Nulling Maps (VCC-SNMs)
Proceedings on CD-ROM - International Society for Magnetic Resonance in Medicine. Scientific Meeting and Exhibition/Proceedings of the International Society for Magnetic Resonance in Medicine, Scientific Meeting and Exhibition · 2025-09-16
articleMotivation: One of the key challenges in parallel imaging (PI) reconstruction is the amplification of noise. Effectively minimizing the noise is essential for achieving high-quality images. Goal(s): Implementation of highly robust and efficient PI reconstruction method with reduced noise amplification. Approach: The recent SNMs method has shown its robustness and efficiency as one hybrid-domain PI reconstruction method. Phase constraint was incorporated in the SNMs method by employing virtual conjugate coils (VCC-SNMs). Results: The VCC-SNMs method was successfully developed in the study, and it was shown to be effective in achieving less amplified noise, in comparison with VCC-GRAPPA, VCC-ESPIRiT, and the original SNMs method. Impact: A VCC-SNMs method leveraging the priori knowledge of the image phase constraint was successfully implemented for efficient and robust parallel imaging reconstruction with reduced noise amplification.
Journal of the American Chemical Society · 2025-11-24 · 4 citations
articleAccelerating the hydrogen evolution reaction (HER) is essential for improving water electrolysis efficiency with renewable energy, ensuring a sustainable hydrogen economy. Heterostructure catalysts show promise in significantly enhancing alkaline HER by facilitating both water dissociation and hydrogen generation, but the rational design and synthesis of robust and active heterostructures remains challenging. Here, we correlate the bias-driven dynamic surface reconstruction of ruthenate perovskites with their O 2p band center to design exsolved Ru/perovskite heterostructures for highly efficient alkaline HER. BaRuO3 is used as a model because its O 2p band center is closest to the Fermi level, allowing facile surface reconstruction under HER conditions. This results in exsolved Ru on BaRuO3 with rich oxygen vacancies, as confirmed by microscopy and spectroscopy, including in situ Ru exsolution over time under transmission electron microscopy observation. The target heterostructure shows approximately 120-fold enhancement in HER activity after surface reconstruction, with a mass activity of ∼ 1.68 times higher than commercial Pt/C at an overpotential of 80 mV. We reveal that perovskite oxides facilitate water dissociation and the exsolved Ru promotes hydrogen generation. Moreover, this bias-driven dynamic reconstruction strategy is applicable to other perovskite oxides. These findings provide guidelines for the rational design of efficient heterostructure electrocatalysts and identify the electronic structure descriptor for oxide catalyst exsolution behavior.
Journal of the American Chemical Society · 2025-07-10 · 4 citations
articleOpen access. This method should be extendible to the fabrication of other core-shell nanocatalysts with desired monolayer shells for various catalytic reactions.
ACS Nano · 2025-12-03 · 3 citations
articleOpen accessThis work demonstrates an effective method for directly exchanging the toxic cetyltrimethylammonium bromide/chloride (CTAB/C) on Au nanocrystals with tri-citrate. Our experimental and computational studies indicate that counterion plays a vital role in the exchange process. Specifically, when citrate species bind to Au surface, they all evolve into tri-citrate with different counterions. In the case of three H+ counterions, tri-citrate could readily replace the CTAB/C due to a strong binding of the carboxylate group with the Au surface. The substitution of H+ counterion by Na+ or K+ weakens the binding strength and thus compromises the exchange. Additionally, our quantitative measurements and theoretical calculations indicate that Au nanospheres encased by high-index facets are advantageous over their counterparts enclosed by {111} and/or {100} facets for the exchange owing to the difference in binding strength. The mechanistic insights and experimental control should be extendable to other combinations of surface ligands and metal nanocrystals.
Recent grants
Piezotronic Effect on Ultrasensitive Chemical and Biochemical Sensors
NSF · $400k · 2015–2019
NSF · $450k · 2019–2022
Frequent coauthors
- 375 shared
Zhong Lin Wang
Georgia Institute of Technology
- 65 shared
Meilin Liu
Guangdong Pharmaceutical University
- 45 shared
Xiangdong Feng
- 45 shared
Dean C. Sayle
University of Kent
- 45 shared
Thi X. T. Sayle
University of Kent
- 40 shared
Xudong Wang
- 37 shared
Bote Zhao
South China University of Technology
- 36 shared
Brian Santora
Ferro (United States)
Labs
Yu Ding LabPI
Education
Ph.D., Industrial and Systems Engineering
Georgia Institute of Technology
M.S., Industrial and Systems Engineering
Texas A&M University
B.S., Automation
University of Science and Technology of China
Awards & honors
- INFORMS Impact Prize (2022)
- IISE Energy Systems Division's Career Achievement Award (202…
- ASME Blackall Machine Tool and Gage Award (2024)
- Society of Manufacturing Engineers (SME) S. M. Wu Research I…
- IISE Fellow (2025)
- Resume-aware match score
- Save to shortlist
- AI-drafted outreach
See your match with Yu Ding
PhdFit ranks faculty by your research interests, methods, and publications — grounded in their actual work, not templates.
- Free to start
- No credit card
- 30-second signup