TY  - JOUR
A1  - Jia, He
A1  - Gao, Haitao
A1  - Mei, Shilin
A1  - Kneer, Janosch
A1  - Lin, Xianzhong
A1  - Ran, Qidi
A1  - Wang, Fuxian
A1  - Palzer, Stefan
A1  - Lu, Yan
T1  - Cu2O@PNIPAM core-shell microgels as novel inkjet materials for the preparation of CuO hollow porous nanocubes gas sensing layers
JF  - Journal of materials chemistry : C, Materials for optical and electronic devices
N2  - There has been long-standing interest in developing metal oxide-based sensors with high sensitivity, selectivity, fast response and low material consumption. Here we report for the first time the utilization of Cu2O@PNIPAM core-shell microgels with a nanocube-shaped core structure for construction of novel CuO gas sensing layers. The hybrid microgels show significant improvement in colloidal stability as compared to native Cu2O nanocubes. Consequently, a homogeneous thin film of Cu2O@PNIPAM nanoparticles can be engineered in a quite low solid content (1.5 wt%) by inkjet printing of the dispersion at an optimized viscosity and surface tension. Most importantly, thermal treatment of the Cu2O@PNIPAM microgels forms porous CuO nanocubes, which show much faster response to relevant trace NO2 gases than sensors produced from bare Cu2O nanocubes. This outcome is due to the fact that the PNIPAM shell can successfully hinder the aggregation of CuO nanoparticles during pyrolysis, which enables full utilization of the sensor layers and better access of the gas to active sites. These results point out great potential of such an innovative system as gas sensors with low cost, fast response and high sensitivity.
Y1  - 2018
U6  - https://doi.org/10.1039/c8tc01995a
SN  - 2050-7526
SN  - 2050-7534
VL  - 6
IS  - 27
SP  - 7249
EP  - 7256
PB  - Royal Society of Chemistry
CY  - Cambridge
ER  - 
TY  - JOUR
A1  - Yang, Guang
A1  - Hu, Rongting
A1  - Ding, Hong-ming
A1  - Kochovski, Zdravko
A1  - Mei, Shilin
A1  - Lu, Yan
A1  - Ma, Yu-qiang
A1  - Chen, Guosong
A1  - Jiang, Ming
T1  - CO2-switchable response of protein microtubules
BT  - behaviour and mechanism
JF  - Materials chemistry frontiers
N2  - Recently, we proposed a small molecular inducing ligand strategy to assemble proteins into highly-ordered structures via dual non-covalent interactions, i.e. carbohydrate-protein interaction and dimerization of Rhodamine B. Using this approach, artificial protein microtubules were successfully constructed. In this study, we find that these microtubules exhibit a perfect CO2 responsiveness; assembly and disassembly of these microtubules were nicely controlled by the alternative passage of CO2 and N-2. Upon the injection of CO2, a negative net-charged SBA turns into a neutral or positive net-charged SBA, which elongated, to some extent, the effective distance between SBA and Rhodamine B, resulting in the disassociation of the Rhodamine B dimer. Further experimental and simulation results reveal that the CO2-responsive mechanism differs from that of solubility change of the previously reported CO2-responsive synthetic materials.
Y1  - 2018
U6  - https://doi.org/10.1039/c8qm00245b
SN  - 2052-1537
VL  - 2
IS  - 9
SP  - 1642
EP  - 1646
PB  - Royal Society of Chemistry
CY  - Cambridge
ER  -