26 research outputs found

    Optimization of the Phase Change Random Access Memory Employing Phase Change Materials

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    Phase-change random access memory (PCRAM) is a semiconductor device based on phase change material (PCM). The SET speed is the bottleneck of limiting the speed of PCRAM. Extract the electrical parameters of the SET operation of the PCRAM test chip and analyze the process of the SET operations. It is found that adding a high and narrow pulse before a single pulse (SP) benefits the SET resistance reduction and the SET speed improvement. A dual pulses SET (D-SET) method is proposed and optimized. The mechanism of D-SET is that the first pulse forms a large optimum temperature field cover over all regions of the PCM material. When the first pulse is converted to the second pulse, the optimum temperature field shrinks and causes the amorphous regions to rapidly crystallize from the edge to the center. On the 40 nm PCRAM test chip, the SET time of D-SET method is under 300 ns. Compared with the conventional SET method such as SP and staircase down pulses (SCD), the D-SET method is optimal for SET performance such as SET resistance distribution, SET speed, and the anti-drift ability

    A Phase Change Memory Chip Based on TiSbTe Alloy in 40-nm Standard CMOS Technology

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    In this letter, a phase change random access memory (PCRAM) chip based on Ti0.4Sb2Te3 alloy material was fabricated in a 40-nm 4-metal level complementary metal-oxide semiconductor (CMOS) technology. The phase change resistor was then integrated after CMOS logic fabrication. The PCRAM was successfully embedded without changing any logic device and process, in which 1.1 V negative-channel metal-oxide semiconductor device was used as the memory cell selector. The currents and the time of SET and RESET operations were found to be 0.2 and 0.5 mA, 100 and 10 ns, respectively. The high speed performance of this chip may highlight the design advantages in many embedded applications

    Correction: 12-state multi-level cell storage implemented in a 128 Mb phase change memory chip.

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    Correction for '12-state multi-level cell storage implemented in a 128 Mb phase change memory chip' by Zhitang Song et al., Nanoscale, 2021, DOI: 10.1039/d1nr00100k

    A 130nm 1Mb Embedded Phase Change Memory with 500kb/s Single Channel Write Throughput

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    Abstract A 130 nm 1Mb embedded phase change memory (PCM) has been achieved, requiring only three additional masks for phase change storage element, featuring 500 kb/s single channel write throughput and > 10 8 endurance. The prepare process has been optimized to reduce the cost and power. An 80 nm heat electrode has been prepared with 130 nm process. The optimal Read/Write circuit module is designed to realize the load/store function for PCM. The critical operation parameter is Reset/70 ns/2.5 mA and Set/1500 ns/1 mA, which means that the signal channel write throughput arrives to 500 kb/s

    Molecular mechanisms of cell death: recommendations of the Nomenclature Committee on Cell Death 2018.

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    Over the past decade, the Nomenclature Committee on Cell Death (NCCD) has formulated guidelines for the definition and interpretation of cell death from morphological, biochemical, and functional perspectives. Since the field continues to expand and novel mechanisms that orchestrate multiple cell death pathways are unveiled, we propose an updated classification of cell death subroutines focusing on mechanistic and essential (as opposed to correlative and dispensable) aspects of the process. As we provide molecularly oriented definitions of terms including intrinsic apoptosis, extrinsic apoptosis, mitochondrial permeability transition (MPT)-driven necrosis, necroptosis, ferroptosis, pyroptosis, parthanatos, entotic cell death, NETotic cell death, lysosome-dependent cell death, autophagy-dependent cell death, immunogenic cell death, cellular senescence, and mitotic catastrophe, we discuss the utility of neologisms that refer to highly specialized instances of these processes. The mission of the NCCD is to provide a widely accepted nomenclature on cell death in support of the continued development of the field
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