Jizhuang Wang

Jizhuang Wang


Research Focus & Metrics

Academic Career Length

15Years (2012-Present)

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

Representative Publications

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17 October 2016 in Nature Nanotechnology
Verified
Journal Article
Closed access
BDBaohu Dai
Baohu Dai
Jizhuang WangJizhuang Wang
Jizhuang Wang
Ze XiongZe Xiong
Ze Xiong
XZXiaojun Zhan
Xiaojun Zhan
WDWei Dai
Wei Dai
JTJinyao Tang
Jinyao Tang

4 September 2018 in Accounts of Chemical Research
Verified
Journal Article
Closed access
Jizhuang WangJizhuang Wang
Jizhuang Wang
Ze XiongZe Xiong
Ze Xiong
JZJing Zheng
Jing Zheng
XZXiaojun Zhan
Xiaojun Zhan
JTJinyao Tang
Jinyao Tang

17 July 2012 in Nanoscale
Verified
Journal Article
Closed access
PDF file
CAChanghua An
Changhua An
Jizhuang WangJizhuang Wang
Jizhuang Wang
WJWen Jiang
Wen Jiang
MZMeiyu Zhang
Meiyu Zhang
XMXijuan Ming
Xijuan Ming
QZQinhui Zhang
Qinhui Zhang
Plasmonic shaped AgX:Ag (X = Cl, Br) nanoparticles have been synthesized by a facile and versatile glycerol-mediated solution route. The as-prepared AgX:Ag nanoparticles exhibit regular shapes, i.e., cube-tetrapod-like AgCl:Ag nanoparticles and AgBr:Ag nanoplates. Compared with the pristine AgX, AgX:Ag nanocomposites display stronger absorption in the visible region due to the surface plasmon resonance of silver nanoparticles. The calculation of bandgaps and band positions indicates the as-achieved AgX:Ag nanoparticles can be used as a class of potential photocatalyst for the reduction of CO2. For example, reduction of CO2 under visible light irradiation with the assistance of the anisotropic AgX:Ag nanoparticles yields as much as 100 μmol methanol in the products. Furthermore, the AgX:Ag nanoparticles can maintain its structure and activity after 3 runs of reactions. Therefore, the present route opens an avenue to acquire plasmonic photocatalysts for conversion of CO2 into useful organic compounds.

9 June 2017 in Advanced Materials
Verified
Journal Article
Closed access
PDF file
Jizhuang WangJizhuang Wang
Jizhuang Wang
Ze XiongZe Xiong
Ze Xiong
XZXiaojun Zhan
Xiaojun Zhan
BDBaohu Dai
Baohu Dai
JZJing Zheng
Jing Zheng
JTJinyao Tang
Jinyao Tang

11 November 2022 in Science Advances
Verified
Journal Article
Closed access
WLWanyuan Li
Wanyuan Li
CWChangjin Wu
Changjin Wu
Ze XiongZe Xiong
Ze Xiong
CLChaowei Liang
Chaowei Liang
ZLZiyi Li
Ziyi Li
DLDan Li
Dan Li
Micro/nanoplastic (MNP) contamination in nonmarine waters has evolved into a notable ecotoxicological threat to the global ecosystem. However, existing strategies for MNP removal are typically limited to chemical flocculation or physical filtering that often fails to decontaminate plastic particulates with ultrasmall sizes or ultralow concentrations. Here, we report a self-driven magnetorobot comprising magnetizable ion-exchange resin sphere that can be used to dynamically remove or separate MNPs from nonmarine waters. As a result of the long-range electrophoretic attraction established by recyclable ion-exchange resin, the magnetorobot shows sustainable removal efficiency of >90% over 100 treatment cycles, with verified broad applicability to varying plastic compositions, sizes, and shapes as well as nonmarine water samples. Our work may facilitate industry-scale MNP removal with affordable cost and minimal secondary pollution and suggests an appealing strategy based on self-propelled micro/nanorobots to sample and assess nanoplastics in aqueous environment.

10 November 2017 in Nature Communications
Verified
Journal Article
Open access
PDF file
JZJing Zheng
Jing Zheng
BDBaohu Dai
Baohu Dai
Jizhuang WangJizhuang Wang
Jizhuang Wang
Ze XiongZe Xiong
Ze Xiong
YYYa Yang
Ya Yang
JTJinyao Tang
Jinyao Tang
Nano/microswimmers represent the persistent endeavors of generations of scientists towards the ultimate tiny machinery for device manufacturing, targeted drug delivery, and noninvasive surgery. In many of these envisioned applications, multiple microswimmers need to be controlled independently and work cooperatively to perform a complex task. However, this multiple channel actuation remains a challenge as the controlling signal, usually a magnetic or electric field, is applied globally over all microswimmers, which makes it difficult to decouple the responses of multiple microswimmers. Here, we demonstrate that a photoelectrochemically driven nanotree microswimmer can be easily coded with a distinct spectral response by loading it with dyes. By using different dyes, an individual microswimmer can be controlled and navigated independently of other microswimmers in a group. This development demonstrates the excellent flexibility of the light navigation method and paves the way for the development of more functional nanobots for applications that require high-level controllability.