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Ling Zheng,Zhiliang Qiu,Shiyong Sun,Weitao Pan,Ya Gao,Zhiyi Zhang 한국통신학회 2018 Journal of communications and networks Vol.20 No.6
The network switches and routers require both highspeedand large-capacity packet buffers. However, existing packetbuffer architectures have the problems of speed scaling and flownumber scaling limitations. To address the two problems simultaneously,this paper proposes a parallel hybrid SRAM/DRAMarchitecture for per-flow buffering in high-speed switches androuters. Tail SRAM and head SRAM are used to apply per-flowbuffering for packet aggregation, so that the middle DRAM is accessedin a larger granularity and the DRAM’s bandwidth utilizationis improved. To mitigate the flow number scaling limitation,a dynamic memory allocation with hard timeout (DMA-HT) memorymanagement algorithm is designed. The key idea of DMA-HTis that the memory space is dynamically allocated for the newly arrivedflows, and a hard timeout is assigned for each queue. Aftera specific period of time, the memory space is freed, so that theSRAM space is efficiently utilized by the most recently active flows. A queuing system is used to model the proposed method, and theoreticalanalysis is performed to optimize the timeout value. Withthe derived formulas, multiple performance parameters are quantitativelyanalyzed, and the optimal timeout can be obtained. Bothnumerical results and simulations show that the proposed architecturecan and reduce packet loss rate and average delay significantlycompared with previous solutions with the same SRAM capacity.
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ULTRAFINE AU NANODOTS ON GRAPHENE OXIDE FOR CATALYTIC REDUCTION OF 4-NITROPHENOL
JIANLI CHEN,GANG CHENG,ZHUANGNAN LI,FUJUN MIAO,XIAOQIANG CUI,WEITAO ZHENG 성균관대학교(자연과학캠퍼스) 성균나노과학기술원 2013 NANO Vol.8 No.3
Graphene oxide nanosheet is an ideal platform to capture nanoparticles for highly efficient catalysis, electrochemical sensing and biosensing. In this work, we have described a simple synthesis method for preparation graphene oxide–Au nanohybrid. Au nanodots with an average size of 1.6 nm uniformly dispersed on the surface of graphene oxide. The well-defined nanostructure has been characterized by transmission electron microscopy (TEM) and atomic force microscopy (AFM). The nanohybrid also exhibits enhanced catalytic activity toward the reduction of 4-nitrophenol by NaBH4. Comparing with pure Au nanodots and graphene oxide, graphene oxide–Au nanohybrid shows the highest catalytic activity. This approach not only suggests a wide potential application of graphene oxide nanosheet as a host material for supporting a variety of nanoparticles, but also provides a new approach for the fabrication of graphene-based nanohybrids with multiple physical and chemical properties.
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Xuedong Gao,Lulu Liu,Qiyu Wang,Kun Qi,Zhao Jin,WEITAO ZHENG,XIAOQIANG CUI 성균관대학교(자연과학캠퍼스) 성균나노과학기술원 2017 NANO Vol.12 No.2
Nanodendritic Pt-based bimetallic alloys are one promising catalyst with three-dimensional (3D) networks structure composed of integrating branches for electrochemical catalytic reaction. We successfully synthesized dendrites Pt6Ir4 alloy with small size of 20 nm in oleylamine. The dendritic Pt6Ir4 alloy are characterized by high-resolution transmission electron microscopy (HRTEM), X-ray diffraction (XRD) and X-ray photoelectron spectroscopy (XPS). The electrochemical tests suggest that the as-prepared dendritic Pt6Ir4 alloy exhibits greatly enhanced ethylene glycol oxidation reaction (EGOR) activity than commercial Pt/C with high EGOR mass activity, anti-poisoning and stability.
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Wang, Dong,Zhang, Wei,Drewett, Nicholas E.,Liu, Xiaofei,Yoo, Seung Jo,Lee, Sang-Gil,Kim, Jin-Gyu,Deng, Ting,Zhang, Xiaoyu,Shi, Xiaoyuan,Zheng, Weitao American Chemical Society 2018 ACS central science Vol.4 No.1
<▼1><P/><P>Graphitic carbon anodes have long been used in Li ion batteries due to their combination of attractive properties, such as low cost, high gravimetric energy density, and good rate capability. However, one significant challenge is controlling, and optimizing, the nature and formation of the solid electrolyte interphase (SEI). Here it is demonstrated that carbon coating via chemical vapor deposition (CVD) facilitates high electrochemical performance of carbon anodes. We examine and characterize the substrate/vertical graphene interface (multilayer graphene nanowalls coated onto carbon paper via plasma enhanced CVD), revealing that these low-tortuosity and high-selection graphene nanowalls act as fast Li ion transport channels. Moreover, we determine that the hitherto neglected parallel layer acts as a protective surface at the interface, enhancing the anode performance. In summary, these findings not only clarify the synergistic role of the parallel functional interface when combined with vertical graphene nanowalls but also have facilitated the development of design principles for future high rate, high performance batteries.</P></▼1><▼2><P>We explored an anti-T-shaped graphene surface-coating concept which offers a low-tortuosity, sieve-like interface that may be exploited for optimized Li-based anodes.</P></▼2>
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Zhang, Xinxin,Cheng, Shiyang,Zhang, Wei,Zhang, Cai,Drewett, Nicholas E.,Wang, Xiyang,Wang, Dong,Yoo, Seung Jo,Kim, Jin-Gyu,Zheng, Weitao American Chemical Society 2017 INDUSTRIAL & ENGINEERING CHEMISTRY RESEARCH - Vol.56 No.39
<P>Ag/Pr<SUB>6</SUB>O<SUB>11</SUB> catalysts supported by either Pr<SUB>6</SUB>O<SUB>11</SUB> nanorods (Pr<SUB>6</SUB>O<SUB>11</SUB>-NRs) or nanoparticles (Pr<SUB>6</SUB>O<SUB>11</SUB>-NPs) were prepared by conventional incipient wetness impregnation. The nanocomposite of Ag/Pr<SUB>6</SUB>O<SUB>11</SUB>-NRs demonstrated a higher catalytic activity for CO oxidation than Ag/Pr<SUB>6</SUB>O<SUB>11</SUB>-NPs at lower temperatures. This improved performance may be ascribed to the mesoporous features and resultant oxygen vacancies of the Pr<SUB>6</SUB>O<SUB>11</SUB> nanorods support, as well as the large surface area and homogeneous loading of Ag species. As a result, 98.7 and 100% CO conversions were achieved at 210 and 240 °C for Ag/Pr<SUB>6</SUB>O<SUB>11</SUB>-NRs, while Ag/Pr<SUB>6</SUB>O<SUB>11</SUB>-NPs require a temperature of 320 °C to obtain the 100% CO conversion rate. These findings reveal that Pr<SUB>6</SUB>O<SUB>11</SUB>-NRs is the preferable support, comparative to Pr<SUB>6</SUB>O<SUB>11</SUB>-NPs, for Ag/Pr<SUB>6</SUB>O<SUB>11</SUB> catalysts, for CO oxidation.</P><P><B>Graphic Abstract</B> <IMG SRC='http://pubs.acs.org/appl/literatum/publisher/achs/journals/content/iecred/2017/iecred.2017.56.issue-39/acs.iecr.7b02530/production/images/medium/ie-2017-02530c_0006.gif'></P><P><A href='http://pubs.acs.org/doi/suppl/10.1021/ie7b02530'>ACS Electronic Supporting Info</A></P>
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