Q
Qiang Zheng
Researcher at SLAC National Accelerator Laboratory
Publications - 16
Citations - 881
Qiang Zheng is an academic researcher from SLAC National Accelerator Laboratory. The author has contributed to research in topics: Ultrafast electron diffraction & Nanoporous. The author has an hindex of 11, co-authored 16 publications receiving 635 citations. Previous affiliations of Qiang Zheng include Shanghai Jiao Tong University.
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Journal ArticleDOI
Imaging CF3I conical intersection and photodissociation dynamics with ultrafast electron diffraction
Jie Yang,Xiaolei Zhu,Xiaolei Zhu,Thomas J. A. Wolf,Zheng Li,Zheng Li,Zheng Li,J. Pedro F. Nunes,Ryan Coffee,Ryan Coffee,James P. Cryan,Markus Gühr,Markus Gühr,Kareem Hegazy,Kareem Hegazy,Tony F. Heinz,Tony F. Heinz,Keith Jobe,Renkai Li,Xiaozhe Shen,Theodore Veccione,Stephen Weathersby,Kyle J. Wilkin,Charles Yoneda,Qiang Zheng,Todd J. Martínez,Todd J. Martínez,Martin Centurion,Xijie Wang +28 more
TL;DR: This work presents the simultaneous experimental characterization of one-photon and two- photon excitation channels in isolated CF3I molecules using ultrafast gas-phase electron diffraction and mapped out the real-space trajectories of a coherent nuclear wave packet, which bifurcates onto two potential energy surfaces when passing through a conical intersection.
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Light-induced picosecond rotational disordering of the inorganic sublattice in hybrid perovskites
Xiaoxi Wu,Liang Z. Tan,Xiaozhe Shen,Te Hu,Kiyoshi Miyata,M. Tuan Trinh,Renkai Li,Ryan Coffee,Shi Liu,David Egger,Igor Makasyuk,Qiang Zheng,Alan Fry,Joseph Robinson,Matthew D. Smith,Burak Guzelturk,Hemamala I. Karunadasa,Xijie Wang,Xiaoyang Zhu,Leeor Kronik,Andrew M. Rappe,Aaron M. Lindenberg,Aaron M. Lindenberg +22 more
TL;DR: The important role of light-induced structural deformations within the inorganic sublattice in elucidating the unique optoelectronic functionality exhibited by hybrid perovskites is shown and new understanding of hot carrier—lattices interactions, which fundamentally determine solar cell efficiencies is provided.
Journal ArticleDOI
Imaging the Photochemical Ring-Opening of 1,3-Cyclohexadiene by Ultrafast Electron Diffraction
Thomas J. A. Wolf,D. M. Sanchez,Jie Yang,Robert M. Parrish,J. P. F. Nunes,Martin Centurion,R. Coffee,James P. Cryan,Markus Gühr,Kareem Hegazy,Adam Kirrander,Renkai Li,Jennifer M. Ruddock,Xiaozhe Shen,Theodore Veccione,S. P. Weathersby,Peter M. Weber,Kyle J. Wilkin,Haiwang Yong,Qiang Zheng,Xijie Wang,Michael P. Minitti,Todd J. Martínez +22 more
TL;DR: In this paper, the authors observed a substantial acceleration of the ring-opening motion after internal conversion to the ground state due to steepening of the electronic potential gradient towards the product minima and demonstrated the potential of megaelectronvolt ultrafast electron diffraction to elucidate photochemical reaction paths in organic chemistry.
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Heterogeneous to homogeneous melting transition visualized with ultrafast electron diffraction
Mianzhen Mo,Zhijiang Chen,Renkai Li,M. Dunning,B. B. L. Witte,B. B. L. Witte,Jon K. Baldwin,Luke Fletcher,J. B. Kim,Andrew Ng,Ronald Redmer,Alexander H. Reid,Prashant Shekhar,Xiaozhe Shen,M. Shen,Klaus Sokolowski-Tinten,Ying Y. Tsui,Yongqiang Wang,Qiang Zheng,Xijie Wang,Siegfried Glenzer +20 more
TL;DR: The results constrain the electron-ion coupling rate, determine the Debye temperature, and reveal the melting sensitivity to nucleation seeds, which shows evidence for the heterogeneous coexistence of solid and liquid.
Journal ArticleDOI
The photochemical ring-opening of 1,3-cyclohexadiene imaged by ultrafast electron diffraction.
Thomas J. A. Wolf,D. M. Sanchez,D. M. Sanchez,Jie Yang,Robert M. Parrish,Robert M. Parrish,J. P. F. Nunes,J. P. F. Nunes,Martin Centurion,Ryan Coffee,James P. Cryan,Markus Gühr,Markus Gühr,Kareem Hegazy,Kareem Hegazy,Adam Kirrander,Renkai Li,Jennifer M. Ruddock,Xiaozhe Shen,Theodore Vecchione,Stephen Weathersby,Peter M. Weber,Kyle J. Wilkin,Haiwang Yong,Qiang Zheng,Xijie Wang,Michael P. Minitti,Todd J. Martínez,Todd J. Martínez +28 more
TL;DR: The photochemical electrocyclic ring-opening of 1,3-cyclohexadiene is a textbook organic chemistry reaction that is resolved on the level of atomic distances and on its natural femtosecond timescale using megaelectronvolt ultrafast electron diffraction.