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Ma, Haiqing,Mahadik, Mahadeo A.,Park, Jin Woo,Kumar, Manish,Chung, Hee Suk,Chae, Weon Sik,Kong, Gi Won,Lee, Hyun Hwi,Choi, Sun Hee,Jang, Jum Suk The Royal Society of Chemistry 2018 Nanoscale Vol.10 No.47
<P>In this study, we present an advanced strategy of low-temperature hydrogen annealing combined with high- temperature quenching in air for activating α-Fe2O3 nanorod photoanodes to boost the photoelectrochemical performance. We report that various low-temperature annealing conditions (340, 360, 380, and 400 °C) under hydrogen gas flow convert β-FeOOH into magnetite (Fe3O4) as well as introduce Sn<SUP>4+</SUP> diffusion from FTO substrates to its surface. Furthermore, high-temperature quenching (800 °C) resulted in the phase change of magnetite (Fe3O4) into hematite (α-Fe2O3) and self Sn<SUP>4+</SUP> doping into the hematite lattice. Thus, the hydrogen-assisted thermally activated hematite photoanode achieved a photocurrent density of 1.35 mA cm<SUP>−2</SUP> at 1.23 V <I>vs.</I> RHE and 1.91 mA cm<SUP>−2</SUP> at 1.4 V <I>vs.</I> RHE, which is 70% and 80% higher than that of directly quenched hematite at 800 °C. These combined two step strategies provide new insight into high Sn-self doping for α-Fe2O3 photoanodes and allow for further development of more efficient solar water oxidation systems.</P>
KAI-GUO MA,JIN-YI BAI,TAN FANG,Haiqing Guo 성균관대학교(자연과학캠퍼스) 성균나노과학기술원 2013 NANO Vol.8 No.5
4-Mercaptovaleric acid (4MVA) and 3-mercaptovaleric acid (3MVA), two branched isomers of 5-mercaptovaleric acid (MVA), were designed and synthesized. They were used as capping agents in the aqueous synthesis of CdTe quantum dots (QDs) by a modified hydrothermal method with sodium tellurite as Te source. Compared with MVA-CdTe, either 4MVA-QDs or 3MVA-QDs exhibited higher fluorescent quantum yield (QY) and sharper absorption peak, which confirmed the superiority of using branched mercapto acids in the aqueous synthesis of QDs for improved optical properties. The fluorescence of QDs capped with 4MVA was higher than that of QDs capped with 4-mercaptobutyric acid (MBA) but lower than that of QDs capped with 3-mercaptobutyric acid (3MBA), which further confirmed the advantage of designing methyl side group rather than methylene group in the main chain for desired optical properties. However, the lower fluorescence, less sharp absorption peak and faster growth rate of 3MVA-QDs than that of 3MBA-QDs indicated adverse effect of side group on the aqueous synthesis of QDs if the size of side group is very bulky. Our results are helpful for selecting and designing appropriate capping agents for QDs with excellent properties.
Huanhuan Sun,Haiqing Ma,Guangyao He,Jiashu Chen,Pengxin Qiu,Guangmei Yan 대한약학회 2010 Archives of Pharmacal Research Vol.33 No.7
FIa, a factor X activator, was isolated from the venom of Daboia russellii siamensis (Myanmar) after a series of chromatographic separations. FIa displayed procoagulant activity by shortening plasma recalcification time and converted human factor X (FX) to activated human factor X (FXa) by cleaving the heavy FX chain, possibly at the Arg51-Ile52 peptide. FIa was positive in a glycoprotein staining test, demonstrating that it is a glycoprotein. Optimal temperature and pH values were important for FIa procoagulant activity. Procoagulant activity was maintained above 85% of the initial activity at pH 7.0~8.0, and showed equally maximum activity at temperatures ranging from 30 to 50oC. In addition, FIa procoagulant activity was completely inhibited by EDTA (5 mM), but not by PMSF (10 mM), suggesting that it is a metalloproteinase.