Hao Shen

Prof. Hao Shen

orcid

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

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18 May 2017 in Chemical Reviews
Verified
Journal Article
Closed access
HSHao Shen
Hao Shen
LTLawrence J. Tauzin
Lawrence J. Tauzin
RBRashad Baiyasi
Rashad Baiyasi
WWWenxiao Wang
Wenxiao Wang
NMNicholas Moringo
Nicholas Moringo
CLChristy F. Landes
Christy F. Landes

4 June 2018 in ACS Nano
Verified
Journal Article
Closed access
NZNingmu Zou
Ningmu Zou
GCGuanqun Chen
Guanqun Chen
XMXianwen Mao
Xianwen Mao
HSHao Shen
Hao Shen
ECEric Choudhary
Eric Choudhary
PCPeng Chen
Peng Chen

16 February 2023 in Journal of the American Chemical Society
Verified
Journal Article
Closed access
LZLi Zuo
Li Zuo
KRKehao Ren
Kehao Ren
XGXianming Guo
Xianming Guo
PPPravin Pokhrel
Pravin Pokhrel
BPBishal Pokhrel
Bishal Pokhrel
HSHao Shen
Hao Shen

10 November 2023 in Chemical & Biomedical Imaging
Verified
Journal Article
Open access
LZLi Zuo
Li Zuo
HKHallie King
Hallie King
MHMohammad Akter Hossain
Mohammad Akter Hossain
FFFatiha Farhana
Fatiha Farhana
MKMadelyn M. Kist
Madelyn M. Kist
HSHao Shen
Hao Shen
Gold nanoparticles are frequently employed as nanozyme materials due to their capacity to catalyze various enzymatic reactions. Given their plasmonic nature, gold nanoparticles have also found extensive utility in chemical and photochemical catalysis owing to their ability to generate excitons upon exposure to light. However, their potential for plasmon-assisted catalytic enhancement as nanozymes has remained largely unexplored due to the inherent challenge of rapid charge recombination. In this study, we have developed a strategy involving the encapsulation of gold nanorods (AuNRs) within a titanium dioxide (TiO2) shell to facilitate the efficient separation of hot electron/hole pairs, thereby enhancing nanozyme reactivity. Our investigations have revealed a remarkable 10-fold enhancement in reactivity when subjected to 530 nm light excitation following the introduction of a TiO2 shell. Leveraging single-molecule kinetic analyses, we discovered that the presence of the TiO2 shell not only amplifies catalytic reactivity by prolonging charge relaxation times but also engenders additional reactive sites within the nanozyme's intricate structure. We anticipate that further enhancements in nanozyme performance can be achieved by optimizing interfacial interactions between plasmonic metals and semiconductors.

12 September 2019 in Journal of Materials Chemistry A
Verified
Journal Article
Closed access
PDF file
ADArosha C. Dassanayake
Arosha C. Dassanayake
NWNilantha P. Wickramaratne
Nilantha P. Wickramaratne
MHMohammad Akter Hossain
Mohammad Akter Hossain
VPVindya S. Perera
Vindya S. Perera
JJJacob Jeskey
Jacob Jeskey
MJMietek Jaroniec
Mietek Jaroniec
Synthesis of nitrogen doped mesoporous graphitic carbon spheres with dispersed metal oxide nanoparticles using a single temperature treatment step serves as one of the big challenges in materials research. To date only a few reports have been published on the soft-templating synthesis of mesoporous graphitic carbons. The preparation of graphitic carbons with dispersed Fe2O3 using a single carbonization step at relatively low temperatures is yet to be explored. The first phase of this work shows the potential of graphitization of polyvinylpyrrolidine (PVP) stabilized cubic Prussian blue nanoparticles (CPB) in phenolic resin spheres to produce graphitic carbon spheres through a facile Stöber-like method. In the second phase, the Pluronic F127 soft template was used along with PVP stabilized Prussian blue nanoparticles (PB) in carbon spheres to generate mesopores and graphitic domains with uniformly dispersed Fe2O3 nanoparticles in these spheres. Due to the presence of graphitic layers, doped N species and Fe2O3 nanoparticles in the carbon matrix, the yielded carbon spheres feature a high surface area and magnetic properties. Moreover, these graphitic spheres exhibited excellent capacitive behavior with rectangular cyclic voltammetry (CV) profiles and large capacitance up to 247 F g−1 at 1 mV s−1 scan rate in 6 M KOH solution.

3 June 2025 in Journal of the American Chemical Society
Verified
Journal Article
Closed access
ASArpit Sharma
Arpit Sharma
WJWjdan Jogadi
Wjdan Jogadi
MKMan Kshetri
Man Kshetri
SASuha Alqarni
Suha Alqarni
AAAl Amin
Al Amin
YZyaorong zheng
yaorong zheng