期刊文献+

一款带POR的可校正低功耗电压基准源 被引量:2

A Correctable Low-power Voltage Reference with POR
下载PDF
导出
摘要 为了解决低功耗、深亚微米工艺条件下基准源的精度问题,本文通过引入工作在亚阈值区MOS管和数字微调技术,提出一种带POR的可校正超低功耗电压基准源,并采用TSMC 90nm COMS工艺对其进行仿真验证。仿真结果表明:该基准源总电流仅为0.876μA,温度系数为24.4 10-6/℃,微调电压步进为25mV。本文提出的基准源与传统基准源比,具有低温漂、可校正、低功耗等优点,适用于便携式低功耗电子产品。 In order to solve the problem of accuracy problem of voltage reference in low power and deep sub-micron process,a correctable ultra low power voltage reference with power on reset(POR)is proposed,by introducing the MOS tube working in the sub-threshold region and digital trimming technology.The voltage reference is simulated by Spectre in TSMC90 nm COMS technology.Simulation results show that,the designen reference achieve total current of only 0.876μA,temperature drift coefficient of 24.4 10-6/℃ and tunable voltage with 25 mV steps.Compared with traditional voltage reference,the proposed voltage reference has the advantages of low temperature drift coefficient,easy correction and low power consumption,and can be applied to low-power and portable electronic devices.
出处 《广西师范大学学报(自然科学版)》 CAS 北大核心 2016年第1期26-31,共6页 Journal of Guangxi Normal University:Natural Science Edition
基金 国家自然科学基金资助项目(61361011) 广西高校优秀青年骨干教师培养计划项目(GXQG022014002) 广西自然科学基金资助项目(2014jjAA70058) 广西高校科学技术研究项目(LX2014032)
关键词 基准源 低功耗 校正 POR voltage reference low-power correction POR
  • 相关文献

参考文献13

  • 1MAGNELLI L,CRUPI F,CORSONELLO P,et al. A 2.6 nW, 0.45 V temperature-compensated subthreshold CMOSvoltage referenced[J].IEEE Journal of Solid-State Circuits,2011,46(2) . 465-474.
  • 2凡东东,宋树祥,蒋品群,岑明灿.新型高增益CMOS跨导运算放大器[J].广西师范大学学报(自然科学版),2014,32(4):6-10. 被引量:7
  • 3LEE S,LEE H?WOO J K.Low-voltage bandgap reference with output-regulated current mirror in 90 nm CMOS[J].Electronics Letters,2010,46(14) : 976-977.
  • 4LAM Y H, KI W H. CMOS bandgap references with self-biased symmetrically matched current-voltage mirror andextension of sub-l-V design[J]. IEEE Transactions on, Very Large Scale Integration Systems,2010,18(6) : 857-865.
  • 5IVANOV V,BREDERLOW R,GERBER J. An ultra low power bandgap operational at supply from 0.75 V[J]. IEEEJournal of Solid-State Circuits, 2012,47(7) : 1515-1523.
  • 6HE J ,CHEN D, GEIGER R. Systematic characterization of subthreshold-MOSFETs-based voltage references for ultralow power low voltage applications [C]// 53rd IEEE International Midwest Symposium on Circuits and Systems.IEEE, 2010: 280-283.
  • 7LEUNG K N,MOK P K T,LEUNG C Y. A 2-V 23-pA 5.3-ppm/C curvature-compensated CMOS bandgap voltagereference[J]. IEEE Journal of Solid-State Circuits,2003,38(3) : 561-564.
  • 8LUO Hao, HAN Yan, ZHANG Zesong, et al. Subthreshold CMOS voltage reference circuit with body biascompensation for process variation[J]. IET Circuits,Devices and Systems,2012,6(3) : 198-203.
  • 9ANDREOU C M, KOUDOUNAS S, GEORGIOU J. A novel wide-temperature-range 3. 9 ppm/oC CMOS bandgapreference circuit[J]. IEEE Journal of Solid-State Circuits,2012,47(2) : 574-581.
  • 10王会杰,王春华,何海珍,李湛.一种基于MOS亚阈值特性的低功耗电压基准源[J].微电子学,2011,41(5):654-657. 被引量:7

二级参考文献36

  • 1周耀,汪西川,陈光明.一种采用曲率补偿技术的高精度带隙基准电压源的设计[J].微计算机信息,2004,20(12):104-105. 被引量:8
  • 2吴金,刘桂芝,张麟.CMOS亚阈型带隙电压基准的分析与设计[J].固体电子学研究与进展,2005,25(3):375-378. 被引量:11
  • 3Siezen RJ, Thomson JA, Kaplan ED, et al. Human lens gamma-crystallins: isolation, identification, and characterization of the expressed gene products. Proc Nat Acad Sci U S A, 1987,84∶6088-6092.
  • 4Litt M, Kramer P, LaMorticella DM, et al. Autosomal dominant congenital cataract associated with a missense mutation in the human alpha crystalline gene CRYAA. Hum Mol Genet, 1998, 7∶471-474.
  • 5Berry V, Francis P, Reddy MA, et al. Alpha-B crystalline gene (CRYAB) mutation causes dominant congenital posterior polar cataract in humans. Am J Hum Genet, 2001,69∶1141-1145.
  • 6Kannabiran C, Rogan PK, Olmos L, et al. Autosomal dominant zonular cataract with sutural opacities is associated with a splice mutation in the beta A3/A1-crystallin gene. Mol Vis, 1998,4∶21.
  • 7Litt M, Carrero-Valenzuela R, LaMorticella DM, et al. Autosomal dominant cerulean cataract is associated with a chain termination mutation in the human beta-crystallin gene CRYBB2. Hum Mol Genet, 1997,6∶665-668.
  • 8Heon E, Priston M, Schorderet DF, et al. The gamma-crystallins and human cataracts: a puzzle made clearer. Am J Hum Genet, 1999,65∶1261-1267.
  • 9Kmoch S, Brynda J, Asfaw B, et al. Link between a novel human γ D-crystallin allele and a unique cataract phenotype explained by protein crystallography. Hum Mol Genet, 2000,9∶1779-1786.
  • 10Semina EV, Ferrell RE, Mintz-Hittner HA, et al. A novel homeobox gene PITX3 is mutated in families with autosomal-dominant cataracts and ASMD. Nat Genet, 1998,19∶167-170.

共引文献23

同被引文献10

引证文献2

二级引证文献2

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部