A 1-V, 100-MHz, 10-mW cache using a separated bit-line memoryhierarchy architecture and domino tag comparators

A 1-V 16-KB (L2) 2-KB (L1) four-way set-associative cache was fabricated using a 0.25-μm CMOS technology for future low-power high-speed microprocessors. Effective latency of 6.9 ns and power consumption of 10 mW at 100 MHz are obtained at a supply voltage of 1 V. This performance is achieved by using a new separated bit-line memory hierarchy architecture (SBMHA) that speeds up latency and reduces power consumption, and domino tag comparators (DTC's) that reduce the power dissipation of tag comparisons     

Gas permeability and permselectivity of polyimides with large aromatic rings

Polyimides with large aromatic rings were prepared from 3,6-diaminocarbazole (CDA), N-ethyl-3,6-diaminocarbazole (ECDA), 2,7-diaminofluorene (DAF), 2,7-diaminofluorenon (DAFO), and dimethyl-3,7-diaminodibenzothiophene-5,5-dioxide (DDBT) with 2-bis(2,4-dicarboxyphenyl) hexafluoropropane dianhydride (6FDA) and 3,3′,4,4′-biphenyltetracarboxylic dianhydride (BPDA). Their physical properties, including gas permeability and permselectivity, were investigated in comparison with those of the related polyimides from 1,3-phenylenediamine (mPD). Glass transition temperatures of the polyimides with large aromatic rings were much higher than those of the mPD-based polyimides as a result of increased rigidity of the former polymer chains. With changing diamine from mPD to the large aromatic diamines, charge transfer (CT) interaction between the moieties of acid anhydride and diamine seems to be enhanced, judging from the red shift of absorption edge of the polyimide films and the red shift of CT excitation band of the 6FDA-based polyimides in solution. Fraction of free space (V_F) was a little smaller for the polyimides with large aromatic rings except DDBT than for the mPD-based polyimides, probably because of enhancement in polymer chain-chain interactions as a result of the increased CT interaction. The DDBT-based polyimides had large V_F than the mPD-based polyimides because of the nonplanar structure of neighboring dibenzothiophene-5,5-dioxide and imide rings. For the 6FDA-based polyimides, permeability coefficients to H₂, O₂, N₂, CO₂, and CH₄ were in the order, DAFO < mPD ～ DAF < CDA < ECDA < DDBT. As for the membrane performance for H₂/CH₄, CO₂/CH₄, and O₂/N₂ systems, it is significant to change diamine from mPD to DDBT or CDA, but not to DAF or DAFO. The DDBT-based polyimides were excellent for H₂/CH₄ and CO₂/CH₄ separations. © 1995 John Wiley & Sons, Inc.     

Hydrogen-induced Sulfur Vacancies on the MoS2 Basal Plane Studied by Ambient Pressure XPS and DFT Calculations

Sulfur vacancy on an MoS₂ basal plane plays a crucial role in device performance and catalytic activity; thus, an understanding of the electronic states of sulfur vacancies is still an important issue. We investigate the electronic states on an MoS₂ basal plane by ambient-pressure X-ray photoelectron spectroscopy (AP-XPS) and density functional theory calculations while heating the system in hydrogen. The AP-XPS results show a decrease in the intensity ratio of S 2p to Mo 3d, indicating that sulfur vacancies are formed. Furthermore, low-energy components are observed in Mo 3d and S 2p spectra. To understand the changes in the electronic states induced by sulfur vacancy formation at the atomic scale, we calculate the core-level binding energies for the model vacancy surfaces. The calculated shifts for Mo 3d and S 2p with the formation of sulfur vacancy are consistent with the experimentally observed binding energy shifts. Mulliken charge analysis indicates that this is caused by an increase in the electronic density associated with the Mo and S atoms around the sulfur vacancy as compared to the pristine surface. The present investigation provides a guideline for sulfur vacancy engineering.     

Mild and efficient pentafluorophenylammonium triflate (PFPAT)-catalyzed C-acylations of enol silyl ethers or ketene silyl (Thio)acetals with acid chlorides

A pentafluorophenylammonium triflate (PFPAT) catalyst (5 mol %) successfully promoted C-acylation of enol silyl ethers with acid chloride to produce various beta-diketones (12 examples; 62-92% yield). Similarly, C-acylation of ketene silyl acetals or ketene silyl thioacetals (i.e., crossed Claisen condensation) proceeded smoothly to provide not only alpha-monoalkylated beta-keto (thio)esters but also thermodynamically unfavorable (less accessible) alpha,alpha-dialkylated beta-keto (thio)esters in good to excellent yield (38 examples; 60-92% yield).     

Enhanced velocity of surfactant binding after the volume collapse of an oppositely charged gel

This paper is a kinetic study of the interaction between an ionic surfactant and an oppositely charged polymer gel. The volume collapse of the gel enhances substantially the velocity of surfactant uptake, despite the decreased free volume for diffusion. This indicates that the increased charge density of the polymer network accelerates the surfactant binding.     

AgI/Ag Heterojunction Nanowires: Facile Electrochemical Synthesis,Photoluminescence, and Enhanced Ionic Conductivity

The construction of an electronic‐conductor/ionic‐conductor heterojunction in a well‐defined nanostructure is the basis of studying interfacial and bulk transport and the reactions of ions and electrons at the nanoscale level. An ionic‐conductor/metal (AgI/Ag) heterostructured nanowire array is easily fabricated by a template‐confined, step‐electrochemical technique. The structural and morphological evolution of the AgI/Ag heterostructure before and after its release from the anodic aluminum oxide (AAO) membrane is characterized by scanning electron microscopy, X‐ray diffraction, and optical spectroscopy. The structural disordering of released AgI is suggested by the appearance of a broad photoluminescence emission band at longer wavelengths and a short‐range‐order‐like Raman peak. The ionic conductivity of the AgI nanowire embedded inside the insulating AAO membrane is measured as being on the order of 10^–3 S cm^–1, which is an enhancement by two to three orders of magnitude compared with that of bulk polycrystalline AgI at room temperature. This electrochemical method could be useful in fabricating other pure and mixed ionic conductors in heterojunction nanostructures.     

Hydrothermal contraction–dilation of polymer networks by reversible complexation with a complementary macromolecule

A mechanochemical system which works by complexation between a poly(methacrylic acid) (PMAA) network and poly(ethylene glycol) (PEG) was studied. A PMAA membrane swollen with an aqueous PEG solution, to which a load 100 times the weight of the membrane was attached, contracts by over 90% of its length when heated from 10°C to 60°C. The work per contraction was 5 × 10^?3 cal/g of membrane. The temperature at which the mechanochemical system undergoes a specified contraction can be regulated by the PEG concentration of the swelling fluid. The sign of the temperature coefficient of the membrane dimension can be reversed by addition of a small amount of ethanol to the swelling solution of PEG. A simple method for calculating the stability constant and thermodynamic parameters for the complexation is outlined.     

Umwandlung der mechanochemischen Energie in einer Polymermembran durch thermo-reversible Polymer-Polymer-Wechselwirkungen

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