Wei Zhao

Dr. Wei Zhao

orcid

Research Focus & Metrics

Academic Career Length

21Years (2006-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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12 June 2012 in Advanced Materials
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Journal Article
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FLFeng Liu
Feng Liu
YGYu Gu
Yu Gu
CWCheng Wang
Cheng Wang
Wei ZhaoWei Zhao
Wei Zhao
DCDian Chen
Dian Chen
TRThomas Paul Russell
Thomas Paul Russell

9 August 2011 in Nano Letters
Verified
Journal Article
Closed access
CWCheng Wang
Cheng Wang
DLDong Hyun Lee
Dong Hyun Lee
AHAlexander Hexemer
Alexander Hexemer
MKMyung Im Kim
Myung Im Kim
Wei ZhaoWei Zhao
Wei Zhao
TRThomas Paul Russell
Thomas Paul Russell

9 October 2019 in ACS Sustainable Chemistry & Engineering
Verified
Journal Article
Closed access
BZBoya Zhang
Boya Zhang
Zhen ZhangZhen Zhang
Zhen Zhang
SKSparsh Kapar
Sparsh Kapar
PAParinaz Ataeian
Parinaz Ataeian
JBJuliana da Silva Bernardes
Juliana da Silva Bernardes
KTKam (Michael) Chiu Tam
Kam (Michael) Chiu Tam

17 January 2012 in ACS Nano
Verified
Journal Article
Closed access
DCDian Chen
Dian Chen
Wei ZhaoWei Zhao
Wei Zhao
TRThomas Paul Russell
Thomas Paul Russell

10 May 2024 in Journal of the American Chemical Society
Verified
Journal Article
Open access
GLGuiying Long
Guiying Long
YDYanping Deng
Yanping Deng
Wei ZhaoWei Zhao
Wei Zhao
GZGuofu Zhou
Guofu Zhou
DBDirk Broer
Dirk Broer
Jiawen ChenJiawen Chen
Jiawen Chen
Despite the fascinating developments in design and synthesis of artificial molecular machines operating at the nanoscales, translating molecular motion along multiple length scales and inducing mechanical motion of a three-dimensional macroscopic entity remains an important challenge. The key to addressing this amplification of motion relies on the effective organization of molecular machines in a well-defined environment. By taking advantage of long-range orientational order and hierarchical structures of liquid crystals and unidirectional rotation of light-driven molecular motors, we report here photoresponsive biomimetic functions of liquid crystal elastomers (LCEs) by the repetitive unidirectional rotation of molecular motors using 3D printing. Molecular motors were built in the main chain of liquid crystals oligomers to serve as photoactuators. The oligomers were then used as the ink, and liquid crystal elastomers with different morphologies were printed. The obtained LCEs are able to conduct multiple types of motions including bending, helical coiling, closing of petals, and flipping of wings of a butterfly upon UV illumination, which paves the way for future design of responsive materials with enhanced complex actuating functions.

5 April 2022 in Journal of the American Chemical Society
Verified
Journal Article
Open access
JHJiaxin Hou
Jiaxin Hou
GLGuiying Long
Guiying Long
Wei ZhaoWei Zhao
Wei Zhao
GZGuofu Zhou
Guofu Zhou
DLDanqing Liu
Danqing Liu
Jiawen ChenJiawen Chen
Jiawen Chen
Recent developments in artificial molecular machines have enabled precisely controlled molecular motion, which allows several distinct mechanical operations at the nanoscale. However, harnessing and amplifying molecular motion along multiple length scales to induce macroscopic motion are still major challenges and comprise an important next step toward future actuators and soft robotics. The key to addressing this challenge relies on effective integration of synthetic molecular machines in a hierarchically aligned structure so numerous individual molecular motions can be collected in a cooperative way and amplified to higher length scales and eventually lead to macroscopic motion. Here, we report the complex motion of liquid crystal networks embedded with molecular motors triggered by single-wavelength illumination. By design, both racemic and enantiomerically pure molecular motors are programmably integrated into liquid crystal networks with a defined orientation. The motors have multiple functions acting as cross-linkers, actuators, and chiral dopants inside the network. The collective rotary motion of motors resulted in multiple types of motion of the polymeric film, including bending, wavy motion, fast unidirectional movement on surfaces, and synchronized helical motion with different handedness, paving the way for the future design of responsive materials with enhanced complex functions.