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Texture Plus Depth Video Coding Using Camera Global Motion Information
Cheng, Fei,Tillo, Tammam,Xiao, Jimin,Jeon, Byeungwoo IEEE 2017 IEEE transactions on multimedia Vol.19 No.11
<P>In video coding, traditional motion estimation methods work well for videos with camera translational motion, but their efficiency drops for other motions, such as rotational and dolly motions. In this paper, a motion-information-based three-dimensional (3D) video coding method is proposed for texture plus depth 3D video. The synchronized global motion information of the camera is obtained to assist the encoder improve its rate-distortion performance by projecting the temporal neighboring texture and depth frames into the position of the current frame, using the depth and camera motion information. Then, the projected frames are added into the reference buffer list as virtual reference frames. As these virtual reference frames could be more similar to the current to-be-encoded frame than the conventional reference frames, the required bits to represent the residual will be reduced. The experimental results demonstrate that the proposed scheme enhances the coding performance for all camera motion types and for various scene settings and resolutions using H.264 and HEVC standards, respectively. With the computer graphic sequences, for H.264, the average gain of texture and depth coding are up to 2 dB and 1 dB, respectively. For HEVC and HD resolution sequences, the gain of texture coding reaches 0.4 dB. For realistic sequences, up to 0.5 dB gain (H.264) is achieved for the texture video, while up to 0.7 dB gain is achieved for the depth sequences.</P>
Du, Jimin,Wang, Huiming,Yang, Mengke,Zhang, Fangfang,Wu, Haoran,Cheng, Xuechun,Yuan, Sijie,Zhang, Bing,Li, Kaidi,Wang, Yina,Lee, Hyoyoung Elsevier 2018 International journal of hydrogen energy Vol.43 No.19
<P><B>Abstract</B></P> <P>Efficient production of hydrogen through visible-light-driven water splitting mechanism using semiconductor-based composites has been identified as a promising strategy for converting light into clean H<SUB>2</SUB> fuel. However, researchers are facing lots of challenges such as light absorption and electron-hole pair recombination and so on. Here, new sheet-shaped MoS<SUB>2</SUB> and pyramid-shaped CdS <I>in-situ</I> co-grown on porous TiO<SUB>2</SUB> photocatalysts (MoS<SUB>2</SUB> CdSTiO<SUB>2</SUB>) are successfully obtained <I>via</I> mild sulfuration of MoO<SUB>3</SUB> and CdO coexisted inside porous TiO<SUB>2</SUB> monolith by a hydrothermal route. The scanning electron microscopy and transmission electron microscopy results exhibit that the MoS<SUB>2</SUB> CdSTiO<SUB>2</SUB> composites have average pore size about 500 nm. The 3%MoS<SUB>2</SUB> 10%CdSTiO<SUB>2</SUB> demonstrated excellent photocatalytic activity and high stability for a hydrogen production with a high H<SUB>2</SUB>-generation rate of 4146 μmol h<SUP>−1</SUP> g<SUP>−1</SUP> under visible light irradiation even without noble-metal co-catalysts. The super photocatalytic performance of the visible-light-driven hydrogen evolution is predominantly attributed to the synergistic effect. The conduction band of MoS<SUB>2</SUB> facilitates in transporting excited electrons from visible-light on CdS to the porous TiO<SUB>2</SUB> for catalytic hydrogen production, and holes to MoS<SUB>2</SUB> for inhibiting the photocorrosion of CdS, respectively, leading to enhancing the efficient separation of electrons and holes.</P> <P><B>Highlights</B></P> <P> <UL> <LI> MoS<SUB>2</SUB>-CT photocatalysts have been successfully synthesized by two-step method. </LI> <LI> The porous structure can enhance photogenerated electron-hole pairs separation. </LI> <LI> The 3% MoS<SUB>2</SUB>-CT shows an excellent H<SUB>2</SUB> evolution rate of 4146 μmol h<SUP>−1</SUP> g<SUP>−1</SUP>. </LI> </UL> </P> <P><B>Graphical abstract</B></P> <P>[DISPLAY OMISSION]</P>
Du, Jimin,Yang, Mengke,Zhang, Fangfang,Cheng, Xuechun,Wu, Haoran,Qin, Huichuang,Jian, Qingsong,Lin, Xialing,Li, Kaidi,Kang, Dae Joon Elsevier 2018 CERAMICS INTERNATIONAL Vol.44 No.3
<P><B>Abstract</B></P> <P>Photoelectrochemical (PEC) water splitting using high-performance catalysts shows considerable promise in generating environment-friendly hydrogen energy. Its practical applications, however, suffer from several shortcomings, such as low photocurrent density, large onset-voltage value, and poor durability. In this study, CuS and CdS quantum-dot-cosensitized porous TiO<SUB>2</SUB>-based PEC catalysts (CuS-CT) have been successfully synthesized via in situ sulfuration of CuO and CdO coexisting inside a porous TiO<SUB>2</SUB> monolith by a hydrothermal method. Compared to porous TiO<SUB>2</SUB>, CuS-sensitized porous TiO<SUB>2</SUB> (CuS-TiO<SUB>2</SUB>), and CdS-sensitized porous TiO<SUB>2</SUB> (CdS-TiO<SUB>2</SUB>) in terms of PEC performance, the CuS-CT photoanode exhibited a significantly high anodic photocurrent for water splitting under simulated sunlight radiation. The photocurrent produced by the optimized sample of 7% CuS-5% CdS-TiO<SUB>2</SUB> (7% CuS-CT) was nearly 2.7 times higher than that of pure porous TiO<SUB>2</SUB> at 1.0V versus a reversible hydrogen electrode (RHE). Porous TiO<SUB>2</SUB> possesses large surface areas that can drive fast electrolyte transport and afford more surface reaction active sites. On the other hand, CuS and CdS quantum dots not only broaden the visible light absorption range, but also improve photoinduced electron-hole separation efficiency. The co-sensitized multi-nanostructures photoanodes lead to a remarkable and promising application in PEC water splitting reactions.</P>
A SERS-based lateral flow assay biosensor for highly sensitive detection of HIV-1 DNA
Fu, Xiuli,Cheng, Ziyi,Yu, Jimin,Choo, Priscilla,Chen, Lingxin,Choo, Jaebum Elsevier Applied Science 2016 Biosensors & bioelectronics Vol. No.
<P><B>Abstract</B></P> <P>User-friendly lateral flow (LF) strips have been extensively used for point-of-care (POC) self-diagnostics, but they have some limitations in their detection sensitivity and quantitative analysis because they only identify the high cut-off value of a biomarker by utilizing color changes that are detected with the naked eye. To resolve these problems associated with LF strips, we developed a novel surface-enhanced Raman scattering (SERS)-based LF assay for the quantitative analysis of a specific biomarker in the low concentration range. Herein, human immunodeficiency virus type 1 (HIV-1) DNA was chosen as the specific biomarker. Raman reporter-labeled gold nanoparticles (AuNPs) were employed as SERS nano tags for targeting and detecting the HIV-1 DNA marker, as opposed to using bare AuNPs in LF strips. It was possible to quantitatively analyze HIV-1 DNA with high sensitivity by monitoring the characteristic Raman peak intensity of the DNA-conjugated AuNPs. Under optimized conditions, the detection limit of our SERS-based lateral flow assay was 0.24pg/mL, which was at least 1000 times more sensitive compared to colorimetric or fluorescent detection methods. These results demonstrate the potential feasibility of the proposed SERS-based lateral flow assay to quantitatively detect a broad range of genetic diseases with high sensitivity.</P> <P><B>Highlights</B></P> <P> <UL> <LI> We report a SERS-based lateral flow biosensor for the detection of HIV-1 DNA. </LI> <LI> Quantitative analysis of HIV-1 DNA is possible using this SERS platform. </LI> <LI> This approach provides new insights into the early diagnosis of a HIV-1 disease. </LI> </UL> </P>
Minqiang He,Min Chen,Aixia Pan,Jimin Xie,Huamin Li,Xinhua Yuan,Xiaonong Cheng 한국화학공학회 2012 Korean Journal of Chemical Engineering Vol.29 No.10
A novel one-pot catalytic synthesis of 1-benzoylpyrene through acylation of pyrene with benzoic anhydride catalyzed by several heteropoly acids (HPAs) was investigated. Pure 1-benzoylpyrene was obtained and its structure was identified by GC/MS, FT-IR and 1H NMR spectra. Silica-supported phosphotungstic heteropoly acid (PW/SiO2)was found to be the most active catalyst in the acylation. The yield and the selectivity of 1-benzoylpyrene were up to 62.5% and 100%, respectively. The effects of experimental parameters on the catalytic acylation reaction, and the possibility of reusability of PW/SiO2 catalyst were studied. PW/SiO2 catalyst is easily separable from the reaction mixture and reusable without loss of its activity.