Jingjing Wang

Jingjing Wang

orcid

Research Focus & Metrics

Academic Career Length

3Years (2024-Present)

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

Representative Publications

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6 January 2025 in Journal of Colloid and Interface Science
Verified
Journal Article
Closed access
YXYu-Jia Xiao
Yu-Jia Xiao
SCShi Chen
Shi Chen
PLPing Li
Ping Li
DZDong Zhang
Dong Zhang
JWJingjing Wang
Jingjing Wang
YHYan-Rong He
Yan-Rong He

30 September 2024 in Journal of Hazardous Materials
Verified
Journal Article
Closed access
LLLinshuai Liu
Linshuai Liu
NWNannan Wang
Nannan Wang
CHChunlin He
Chunlin He
YWYuezhou Wei
Yuezhou Wei
JWJingjing Wang
Jingjing Wang
Xinpeng WangXinpeng Wang
Xinpeng Wang

1 August 2026 in Nano Research
Verified
Journal Article
Open access
PDF file
THTeng He
Teng He
YJYanxin Jiang
Yanxin Jiang
WWWei Wang
Wei Wang
JWJingjing Wang
Jingjing Wang
PLPeng Liu
Peng Liu
QFQiaohui Fan
Qiaohui Fan
Photocatalytic separation of uranium presents a promising approach for resource recovery, yet its efficiency remains limited by severe carrier recombination. Integrating piezocatalysis with photocatalysis provides an attractive pathway to overcome this barrier. Herein, a type-II scheme CdS@BaTiO3 heterojunction was fabricated by growing CdS nanoparticles onto a BaTiO3 matrix, which enables efficient piezo-photocatalytic uranium extraction. The built-in electric field of the heterojunction, reinforced by the stirring-induced piezoelectric polarization of CdS@BaTiO3, drives directional charge migration and greatly enhances carrier separation. As a result, CdS@BaTiO3 achieved 98% uranium removal within 10 mins under stirring and light irradiation, being 2.5 times and 8.3 times higher than that of photocatalysis and piezocatalysis alone, respectively. The composite also delivers a high uranium separation capacity of 1893.2 mg g-1, exceeding most previously reported piezo-photocatalytic uranium extraction systems. Mechanistic investigations identify superoxide radicals (•O2⁻) as the dominant reactive species responsible for U(VI) reduction and immobilization. This work demonstrates a promising water-flow-driven energy coupling strategy for uranium extraction.