TY - JOUR A1 - Xie, Y. A1 - Cui, Y. A1 - Wu, Dejian A1 - Zeng, Y. A1 - Sun, L. T1 - Economic analysis of hydrogen-powered data center N2 - The data center needs more and more electricity due to the explosive growth of IT servers and it could cause electricity power shortage and huge carbon emission. It is an attractive and promising solution to power the data center with hydrogen energy source. The present work aims to conduct an economic analysis on the hydrogen-powered data center. Configurations of hydrogen-powered and traditional data centers are compared and the differences focus on backup power system, converter/inverter, fuel cell subsystem, carbon emission, hydrogen and electricity consumptions. Economic analysis is conducted to evaluate the feasibility to power the data center with hydrogen energy source. Results show that electricity price increasing rate and hydrogen cost are the main factors to influence economic feasibility of hydrogen-powered data center. When the electricity price keeps constant in the coming two decades, the critical hydrogen price is about 2.8 U.S. dollar per kilogram. If the electricity price could increase 5% annually due to explosive growth of electric vehicles and economy, critical hydrogen price will become 6.4 U.S. dollar per kilogram. Hydrogen sources and transportation determine the hydrogen price together. Hydrogen production cost varies greatly with hydrogen sources and production technologies. Hydrogen transport cost is greatly influenced by distances and H2 consumptions to consumers. It could be summarized that the hydrogen-powered data center is economic if hydrogen could be produced from natural gas or H2-rich industrial waste streams in chemical plant and data center could not be built too far away from hydrogen sources. In addition, large-scale hydrogen-powered data center is more likely to be economic. Solar hydrogen powered data center has entered into a critical stage in the economic feasibility. Solar hydrogen production cost has restrained the H2 utilization in data center power systems now, since it could be competitive only when more strict carbon emission regulation is employed, hydrogen production cost reduces greatly and electricity price is increasing greatly in the future. However, it could be expected solar hydrogen-powered system will be adopted as the power source of data centers in the next few years. KW - Hydrogen KW - Date center KW - Economic analysis PY - 2021 DO - https://doi.org/10.1016/j.ijhydene.2021.06.048 SN - 0360-3199 VL - 46 IS - 55 SP - 27841 EP - 27850 PB - Elsevier Ltd. AN - OPUS4-53658 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Yao, Dongxu A1 - Xia, Y. A1 - Zuo, K.-h. A1 - Jiang, D. A1 - Günster, Jens A1 - Zeng, Y.-P. A1 - Heinrich, J.G. T1 - Porous Si3N4 ceramics prepared via partial nitridation and SHS N2 - Porous Si3N4 ceramics were prepared via partial nitridation and self-propagating high temperature synthesis (SHS) process. Raw Si and additive Y2O3 were mixed and molded under 10 MPa into a compact, the compact was partial nitridation at 1300 °C to form a porous Si/Si3N4, and then it was buried in a Si/Si3N4 bed for SHS to obtain porous Si3N4 with rod-like β-Si3N4 morphology. The processing combined the advantages of the nitridation of Si and SHS with low cost, low shrinkage and time saving. Porous Si3N4 with a porosity of 47%, a strength of 143 MPa were obtained by this method. KW - Si3N4 KW - Strength KW - Porosity PY - 2013 DO - https://doi.org/10.1016/j.jeurceramsoc.2012.08.033 SN - 0955-2219 SN - 1873-619X VL - 33 IS - 2 SP - 371 EP - 374 PB - Elsevier CY - Oxford AN - OPUS4-31282 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Yao, Dongxu A1 - Xia, Y. A1 - Zuo, K.-h. A1 - Jiang, D. A1 - Günster, Jens A1 - Zeng, Y.-P. A1 - Heinrich, J.G. T1 - The effect of fabrication parameters on the mechanical properties of sintered reaction bonded porous Si3N4 ceramics N2 - Porous silicon nitride ceramics were prepared via sintered reaction bonded silicon nitride at 1680 °C. The grain size of nitrided Si3N4 and diameter of post-sintered ß-Si3N4 are controlled by size of raw Si. Porosity of 42.14–46.54% and flexural strength from 141 MPa to 165 MPa were obtained. During post-sintering with nano Y2O3 as sintering additive, nano Y2O3 can promote the formation of small ß-Si3N4 nuclei, but the large amount of ß-Si3N4 (>20%) after nitridation also works as nuclei site for precipitation, in consequence the growth of fine ß-Si3N4 grains is restrained, the length is shortened, and the improvement on flexural strength is minimized. The effect of nano SiC on the refinement of the ß-Si3N4 grains is notable because of the pinning effect, while the effect of nano C on the refinement of the ß-Si3N4 grains is not remarkable due to the carbothermal reaction and increase in viscosity of the liquid phase. KW - Porous ceramics KW - Silicon nitride KW - Reaction bonding KW - Anisotropic grain growth KW - Ceramic PY - 2014 DO - https://doi.org/10.1016/j.jeurceramsoc.2014.06.018 SN - 0955-2219 SN - 1873-619X VL - 34 IS - 15 SP - 3461 EP - 3467 PB - Elsevier CY - Oxford AN - OPUS4-32542 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Yao, Dongxu A1 - Xia, Y. A1 - Zuo, K.-h. A1 - Zeng, Y.-P. A1 - Jiang, D. A1 - Günster, Jens A1 - Heinrich, J.G. T1 - Gradient porous silicon nitride prepared via vacuum foaming and freeze drying N2 - Gradient porous silicon nitride (Si3N4) was fabricated by a novel vacuum foaming and freeze drying process. Aqueous Si3N4 slurries were foamed at vacuum pressure of 50–90 kPa, the green body was obtained by the freeze drying process, a gradient pore structure with porosities of 72–90% was achieved after pressureless sintering at 1680 °C. The porosity was increased with decreasing vacuum pressure. The pore structure consists of large pores (~100 μm) on top, medium pores (~45 μm) on the wall of the large pores, and small pores (~0.7 μm) in the matrix. Such gradient porous Si3N4 with macro- and micro-pores has potential application as high temperature filters. KW - Silicon nitride KW - Graded PY - 2015 DO - https://doi.org/10.1016/j.matlet.2014.11.067 SN - 0167-577x SN - 1873-4979 VL - 141 SP - 138 EP - 140 PB - Elsevier B.V. CY - Amsterdam AN - OPUS4-35177 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Hu, H.-L. A1 - Zeng, Y.-P. A1 - Zuo, K.-H. A1 - Xia, Y. A1 - Yao, Dongxu A1 - Günster, Jens A1 - Heinrich, J. A1 - Li, S. T1 - Synthesis of porous Si3N4/SiC ceramics with rapid nitridation of silicon N2 - Porous Si3N4/SiC ceramics were prepared with Si and SiC as raw materials, Y2O3 as sintering additive and ZrO2 as nitrided catalyst through a rapid nitration process. The nitriding rate as a function of temperature and duration was investigated. The porous Si3N4/SiC ceramics with 8 wt% monoclinic ZrO2 addition that was nitrided at 1400 °C for 2 h exhibited the highest nitridation degree of 95%. The experimental results also demonstrated that the reciprocal formation of ZrO2 and ZrN can effectively enhance the level of nitridation by suppressing the melting of silicon in micro-regions. The effects of nitriding time on the mechanical properties of the specimens with ZrO2 as a catalyst was also studied. After nitrided at 1400 °C for various durations from 2 to 8 h, the porous Si3N4/SiC ceramics with the properties of a porosity over 39.8%, a flexural strength over 88.9 MPa and a linear shrinkage lower than 0.6% were achieved. The systematic investigation reveals the catalytic mechanism of ZrO2 in the synthesis of Si3N4/SiC ceramics. KW - Si3N4 PY - 2015 DO - https://doi.org/10.1016/j.jeurceramsoc.2015.06.028 SN - 0955-2219 SN - 1873-619X VL - 35 IS - 14 SP - 3781 EP - 3787 PB - Elsevier Ltd. CY - Oxford AN - OPUS4-34956 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Hu, H.-L. A1 - Zeng, Y.-P. A1 - Xia, Y. A1 - Yao, Dongxu A1 - Zuo, K.-H. A1 - Günster, Jens A1 - Heinrich, J.G. T1 - Rapid fabrication of porous Si3N4/SiC ceramics via nitridation of silicon powder with ZrO2 as catalyst N2 - Porous Si3N4/SiC ceramics were rapidly prepared with Y2O3 as sintering additive and ZrO2 as nitrided catalyst, using Si and SiC as starting powders. Porous Si3N4/SiC ceramics with 5 wt% ZrO2 addition showed a complete nitridation and good mechanical properties (with a high porosity of 34.96%, flexural strength of 150±4.2 MPa, linear shrinkage of 0.02%). It was revealed that the reciprocal formation of ZrO2 and ZrN effectively enhanced nitridation by inhibiting the melting of silicon in micro-regions. KW - D. ZrO2 KW - Rapid nitridation KW - Si3N4/SiC porous ceramics PY - 2014 DO - https://doi.org/10.1016/j.ceramint.2013.11.098 SN - 0272-8842 SN - 1873-3956 VL - 40 IS - 5 SP - 7579 EP - 7582 PB - Ceramurgia CY - Faenza AN - OPUS4-30295 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Zeng, Y. A1 - Grandner, S. A1 - Oliveira, C.L.P. A1 - Thünemann, Andreas A1 - Paris, O. A1 - Pedersen, J.S. A1 - Klapp, S.H.L. A1 - von Klitzing, R. T1 - Effect of particle size and Debye length on order parameters of colloidal silica suspensions under confinement N2 - Using atomic force microscopy (AFM) and small angle X-ray scattering (SAXS), we show a full comparison between structuring of nanoparticles in confinement and in bulk in order to explain the effect of confinement on characteristic lengths and the scaling law of the characteristic lengths. Three different-sized particle suspensions are used to check the generalization and the correlation between the characteristic lengths and the system parameters, like particle diameter and Debye length. The two characteristic lengths obtained from AFM force curves, the oscillatory wavelength λ, which is related to the average particle distance, and the decay length ξ, which measures how far particle correlates to obtain periodic oscillations, are in good agreement with the mean particle distance 2π/qmax and the correlation length 2/Δq in bulk, respectively, obtained from the structure peaks of SAXS diagrams. Although confinement causes layering of nanoparticles parallel to the confining surfaces, the characteristic lengths in the direction perpendicular to the confining surfaces follow the bulk behavior. The wavelength scales as ρ-1/3 with the particle number density ρ irrespective of the particle size and the ionic strength and shows a pure volume effect. Upon comparing with literature results, the λ = ρ-1/3 scaling law can be applied more generally for charged particles, as long as the repulsive interaction is sufficiently long-ranged, than the previous expression of λ = 2(R + κ-1), which only approaches the value of average particle distance under specific conditions. The decay length ξ is controlled both by the particle size and the ionic strength of the suspensions, and ξ = R + κ-1 is proposed in the paper. In addition, the interaction strength, the force amplitude and maximum scattering intensity, increases linearly with particle concentration. On the other hand, the Monte Carlo (MC) simulations and approximate hypernetted chain (HNC) closure calculation based on Derjaguin-Landau-Verwey-Overbeek (DLVO) potential are employed to study the characteristic lengths from the theoretical point of view. The experimental wavelengths are in good agreement with the theoretical counterparts and the experimental decay lengths show the same qualitative behavior as theoretical ones on the particle size and ionic strength. KW - Nanoparticle PY - 2011 DO - https://doi.org/10.1039/c1sm05971h SN - 1744-683X VL - 7 IS - 22 SP - 10899 EP - 10909 PB - RSC Publ. CY - Cambridge AN - OPUS4-24660 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Bates, J. S. A1 - Martinez, J. J. A1 - Hall, M. N. A1 - Al-Omari, A. A. A1 - Murphy, E. A1 - Zeng, Y. A1 - Luo, F. A1 - Primbs, M. A1 - Menga, D. A1 - Bibent, N. A1 - Sougrati, M. T. A1 - Wagner, F. E. A1 - Atanassov, P. A1 - Wu, G. A1 - Strasser, P. A1 - Fellinger, Tim-Patrick A1 - Jaouen, F. A1 - Root, T. W. A1 - Stahl, S. S. T1 - Chemical Kinetic Method for Active-Site Quantification in Fe-N‑C Catalysts and Correlation with Molecular Probe and Spectroscopic Site-Counting Methods N2 - Mononuclear Fe ions ligated by nitrogen (FeNx) dispersed on nitrogen-doped carbon (Fe-N-C) serve as active centers for electrocatalytic O2 reduction and thermocatalytic aerobic oxidations. Despite their promise as replacements for precious metals in a variety of practical applications, such as fuel cells, the discovery of new Fe-N-C catalysts has relied primarily on empirical approaches. In this context, the development of quantitative structure−reactivity relationships and benchmarking of catalysts prepared by different synthetic routes and by different laboratories would be facilitated by the broader adoption of methods to quantify atomically dispersed FeNx active centers. In this study, we develop a kinetic probe reaction method that uses the aerobic oxidation of a model hydroquinone substrate to quantify the density of FeNx centers in Fe-N-C catalysts. The kinetic method is compared with low-temperature Mössbauer spectroscopy, CO pulse chemisorption, and electrochemical reductive stripping of NO derived from NO2 − on a suite of Fe-N-C catalysts prepared by diverse routes and featuring either the exclusive presence of Fe as FeNx sites or the coexistence of aggregated Fe species in addition to FeNx. The FeNx site densities derived from the kinetic method correlate well with those obtained from CO pulse chemisorption and Mössbauer spectroscopy. The broad survey of Fe-N-C materials also reveals the presence of outliers and challenges associated with each site quantification approach. The kinetic method developed here does not require pretreatments that may alter active-site distributions or specialized equipment beyond reaction vessels and standard analytical instrumentation. KW - Active-Site Quantification PY - 2023 DO - https://doi.org/10.1021/jacs.3c08790 SP - 1 EP - 16 PB - ACS Publications AN - OPUS4-58889 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Yao, Dongxu A1 - Wirth, Cynthia A1 - Zeng, Y.-P. A1 - Jiang, D. A1 - Günster, Jens A1 - Heinrich, J. T1 - Near zero shrinkage porous Al2O3 prepared via 3D-printing and reaction bonding N2 - Porous Al2O3 with high porosity (~45%), remarkable flexural strength (~70 MPa), and low dimensional change (~1–2%), was produced by indirect 3D printing and reaction bonding. Coarse Al with good flowability was carried out printing green body. The green body was heat treated to get fully oxidized, volume expansion during oxidation simultaneously formed strong neck bonding, not only brought good strength, but also restricted shrinkage. Porous Al2O3 with architecture of macro pores designed by 3D printing and micro pores in the strut formed by packing of particles was obtained. The near zero shrinkage can facilitate precise design of product with complex shape. KW - Al2O3 reaction bonding PY - 2015 DO - https://doi.org/10.1016/j.matlet.2015.02.037 SN - 0167-577x SN - 1873-4979 VL - 147 SP - 116 EP - 118 PB - North-Holland Publ. Co. CY - Amsterdam AN - OPUS4-34960 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER -