Weidong Jiang

Dr. Weidong Jiang


Research Focus & Metrics

Academic Career Length

19Years (2008-Present)

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

Representative Publications

View All Publications
31 January 2020 in ACS Applied Materials & Interfaces
Verified
Journal Article
Closed access
XZXianwen Zhang
Xianwen Zhang
QZQin Zhang
Qin Zhang
BXBin Xu
Bin Xu
XLXiaoqiang Liu
Xiaoqiang Liu
KZKaiming Zhang
Kaiming Zhang
WJWeidong Jiang
Weidong Jiang

13 May 2022 in Analytica Chimica Acta
Verified
Journal Article
Closed access
JTJiyu Tang
Jiyu Tang
FLFuling Li
Fuling Li
CLChang Liu
Chang Liu
JSJun Shu
Jun Shu
JYJian Yue
Jian Yue
WJWeidong Jiang
Weidong Jiang

2 March 2018 in Nanomaterials
Verified
Journal Article
Open access
PDF file
GFGuangyin Fan
Guangyin Fan
XLXiaojing Li
Xiaojing Li
CXCaili Xu
Caili Xu
WJWeidong Jiang
Weidong Jiang
YZYun Zhang
Yun Zhang
YWYi Wang
Yi Wang
Developing highly efficient and recyclable catalysts for the transformation of toxic organic contaminates still remains a challenge. Herein, Titanium Carbide (Ti3C2) MXene modified by alkali treatment process was selected as a support (designated as alk-Ti3C2X2, where X represents the surface terminations) for the synthesis of Pd/alk-Ti3C2X2. Results show that the alkali treatment leads to the increase of surface area and surface oxygen-containing groups of Ti3C2X2, thereby facilitating the dispersion and stabilization of Pd species on the surface of alk-Ti3C2X2. The Pd/alk-Ti3C2X2 catalyst shows excellent catalytic activity for the hydrodechlorination of 4-chlorophenol and the hydrogenation of 4-nitrophenol in aqueous solution at 25 °C and hydrogen balloon pressure. High initial reaction rates of 216.6 and 126.3 min−1· g pd − 1 are observed for the hydrodechlorination of 4-chlorophenol and hydrogenation of 4-nitrophenol, respectively. Most importantly, Pd/alk-Ti3C2X2 exhibits excellent stability and recyclability in both reactions without any promoters. The superior property of Pd/alk-Ti3C2X2 makes it as a potential material for practical applications.

7 October 2020 in Organic Letters
Verified
Journal Article
Closed access
WLWenjing Li
Wenjing Li
JTJuan Tang
Juan Tang
SLShun Li
Shun Li
XZXueli Zheng
Xueli Zheng
MYMaolin Yuan
Maolin Yuan
HCHua Chen
Hua Chen

1 June 2016 in Applied Catalysis A: General
Verified
Journal Article
Closed access
WJWeidong Jiang
Weidong Jiang
BXBin Xu
Bin Xu
ZXZhen Xiang
Zhen Xiang
XLXiaoqiang Liu
Xiaoqiang Liu
FLFuan Liu
Fuan Liu

26 April 2018 in Nanomaterials
Verified
Journal Article
Open access
PDF file
QWQi Wang
Qi Wang
CXCaili Xu
Caili Xu
MMMei Ming
Mei Ming
YYYingchun Yang
Yingchun Yang
WJWeidong Jiang
Weidong Jiang
GFGuangyin Fan
Guangyin Fan
The development of highly-efficient heterogeneous supported catalysts for catalytic hydrolysis of ammonia borane to yield hydrogen is of significant importance considering the versatile usages of hydrogen. Herein, we reported the in situ synthesis of AgCo bimetallic nanoparticles supported on g-C3N4 and concomitant hydrolysis of ammonia borane for hydrogen evolution at room temperature. The as-synthesized Ag0.1Co0.9/g-C3N4 catalysts displayed the highest turnover frequency (TOF) value of 249.02 mol H2·(molAg·min)−1 for hydrogen evolution from the hydrolysis of ammonia borane, which was higher than many other reported values. Furthermore, the Ag0.1Co0.9/g-C3N4 catalyst could be recycled during five consecutive runs. The study proves that Ag0.1Co0.9/g-C3N4 is a potential catalytic material toward the hydrolysis of ammonia borane for hydrogen production.