Bio
I am a postdoctoral researcher at Stanford University in the Zong/Hwang group. I received my undergraduate and doctoral degrees from Shanghai Jiao Tong University (SJTU), where I specialized in pulsed laser deposition, the synthesis of complex oxide materials and MeV ultrafast electron diffraction (UED).
My research focuses on ultrafast structural dynamics in quantum materials using techniques such as MeV-UED, ultrafast electron microscopy (UEM), time-resolved X-ray diffraction, and pump–probe optical spectroscopy. These time-resolved probes are integrated with advanced and highly tunable sample environments, including in situ strain engineering and electrostatic gating, to actively control competing electronic, structural, and ferroic orders. This capability enables the design, discovery, and quantitative understanding of nonequilibrium phases, transient orders, and metastable states in quantum materials.
All Publications
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Comment on "Photoinduced Dynamics and Momentum Distribution of Chiral Charge Density Waves in 1T-TiSe<sub>2</sub>"
PHYSICAL REVIEW LETTERS
2026; 137 (2)
View details for DOI 10.1103/p5d8-548h
View details for Web of Science ID 001824444300004
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Comment on "Photoinduced Dynamics and Momentum Distribution of Chiral Charge Density Waves in 1T-TiSe_{2}".
Physical review letters
2026; 137 (2): 029601
View details for DOI 10.1103/p5d8-548h
View details for PubMedID 42503136
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Structural Contribution to Light-Induced Gap Suppression in Ta_{2}NiSe_{5}.
Physical review letters
2025; 135 (9): 096901
Abstract
An excitonic insulator is a material that hosts an exotic ground state, where an energy gap opens due to spontaneous condensation of bound electron-hole pairs. Ta_{2}NiSe_{5} is a promising candidate for this type of material, but the coexistence of a structural phase transition with the gap opening has led to a long-standing debate regarding the origin of the insulating gap. Here we employ MeV ultrafast electron diffraction to obtain quantitative insights into the atomic displacements in Ta_{2}NiSe_{5} following photoexcitation, which has been overlooked in previous time-resolved spectroscopy studies. In conjunction with first-principles calculations using the measured atomic displacements, we find that the structural change can largely account for the photoinduced reduction in the energy gap without considering excitonic effects. Our Letter illustrates the importance of a quantitative reconstruction of individual atomic pathways during nonequilibrium phase transitions, paving the way for a mechanistic understanding of a diverse array of phase transitions in correlated materials where lattice dynamics can play a pivotal role.
View details for DOI 10.1103/1kzk-sz7g
View details for PubMedID 40952197
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Structural Contribution to Light-Induced Gap Suppression in Ta2NiSe5
PHYSICAL REVIEW LETTERS
2025; 135 (9)
View details for DOI 10.1103/1kzk-sz7g
View details for Web of Science ID 001563968300001
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Giant electrocaloric effect in high-polar-entropy perovskite oxides
NATURE
2025; 640 (8060): 924-930
Abstract
Materials with a high electrocaloric effect (ECE)1,2 tend to favour a disordered yet easily tunable polar structure. Perovskite ferroelectrics3 stand out as ideal candidates owing to their high dielectric responses and reasonable thermal conductivity. The introduction of multielement atomic distortions induces a high-polar-entropy state4 that notably increases the ECE by effectively overcoming the constraints imposed by highly ordered, polar-correlated perovskite structures. Here we developed a lead-free relaxor ferroelectric with strong polar disorder through targeted multielement substitution at both the A and B sites of the perovskite, effectively distorting the lattice structure and inducing a variety of nanoscale polar configurations, polymorphic polar variants and non-polar regions. A combination of these multielement-induced features led to an increased density of interfaces, significantly enhancing the polar entropy. Remarkably, a high ECE for an entropy change of about 15 J kg-1 K-1 under a 10 MV m-1 field is observed for the material across a broad temperature range exceeding 60 °C. The formation of ultrafine, dispersed, multiphase lattice configurations leads to high-polar-entropy ferroelectric oxides with a high ECE and a long lifetime of over 1 million cycles that are suitable for manufacturing multilayer ceramic capacitors for practical electrocaloric refrigeration applications.
View details for DOI 10.1038/s41586-025-08768-8
View details for Web of Science ID 001462520400001
View details for PubMedID 40205056
View details for PubMedCentralID 10957880
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Time-domain study of coupled collective excitations in quantum materials
NPJ QUANTUM MATERIALS
2025; 10 (1)
View details for DOI 10.1038/s41535-025-00726-x
View details for Web of Science ID 001421278900002
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Transient dynamics of the phase transition in VO<sub>2</sub> revealed by mega-electron-volt ultrafast electron diffraction
NATURE COMMUNICATIONS
2023; 14 (1): 1265
Abstract
Vanadium dioxide (VO2) exhibits an insulator-to-metal transition accompanied by a structural transition near room temperature. This transition can be triggered by an ultrafast laser pulse. Exotic transient states, such as a metallic state without structural transition, were also proposed. These unique characteristics let VO2 have great potential in thermal switchable devices and photonic applications. Although great efforts have been made, the atomic pathway during the photoinduced phase transition is still not clear. Here, we synthesize freestanding quasi-single-crystal VO2 films and examine their photoinduced structural phase transition with mega-electron-volt ultrafast electron diffraction. Leveraging the high signal-to-noise ratio and high temporal resolution, we observe that the disappearance of vanadium dimers and zigzag chains does not coincide with the transformation of crystal symmetry. After photoexcitation, the initial structure is strongly modified within 200 femtoseconds, resulting in a transient monoclinic structure without vanadium dimers and zigzag chains. Then, it continues to evolve to the final tetragonal structure in approximately 5 picoseconds. In addition, only one laser fluence threshold instead of two thresholds suggested in polycrystalline samples is observed in our quasi-single-crystal samples. Our findings provide essential information for a comprehensive understanding of the photoinduced ultrafast phase transition in VO2.
View details for DOI 10.1038/s41467-023-37000-2
View details for Web of Science ID 000957599200004
View details for PubMedID 36882433
View details for PubMedCentralID PMC9992676
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Manipulating the magneto-resistance of Bi<sub>2</sub>Se<sub>3</sub> thin films by strontium doping
JOURNAL OF APPLIED PHYSICS
2022; 132 (9)
View details for DOI 10.1063/5.0092075
View details for Web of Science ID 000978622900004
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Coexistence of Ferroelectriclike Polarization and Dirac-like Surface State in TaNiTe<sub>5</sub>
PHYSICAL REVIEW LETTERS
2022; 128 (10): 106802
Abstract
By combining angle-resolved photoemission spectroscopy, scanning tunneling microscopy, atomic force microscope based piezoresponse force microscopy and first-principles calculations, we have studied the low-energy band structure, atomic structure, and charge polarization on the surface of a topological semimetal candidate TaNiTe_{5}. Dirac-like surface states were observed on the (010) surface by angle-resolved photoemission spectroscopy, consistent with the first-principles calculations. On the other hand, piezoresponse force microscopy reveals a switchable ferroelectriclike polarization on the same surface. We propose that the noncentrosymmetric surface relaxation observed by scanning tunneling microscopy could be the origin of the observed ferroelectriclike state in this novel material. Our findings provide a new platform with the coexistence of a ferroelectriclike surface charge distribution and novel surface states.
View details for DOI 10.1103/PhysRevLett.128.106802
View details for Web of Science ID 000767685400005
View details for PubMedID 35333064
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Magnetic properties of the quasi two-dimensional centered honeycomb antiferromagnet GdInO<sub>3</sub>
PHYSICAL REVIEW B
2021; 104 (13)
View details for DOI 10.1103/PhysRevB.104.134432
View details for Web of Science ID 000747136300005
https://orcid.org/0000-0003-1610-3568