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      KCI등재 SCOPUS SCIE

      Superparamagnetic NiO-doped mesoporous silica flower-like microspheres with high nickel content

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      https://www.riss.kr/link?id=A106829396

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      다국어 초록 (Multilingual Abstract)

      Morphology oriented synthesis of metal oxide doped silica structures have fascinating properties whichneeded to be explored extensively. In this work, NiO doped silica microsphere with beautifulflower-likemorphology has been achieved by adopting a facile surfactant-assisted synthetic route using CTAB-ammonia in H2O–ethanol mixed solvent media. The sol–gel synthesis with effective variations of Ni/Si ratiosup to 7.0, followed by a simple hydrothermal treatment and subsequent calcination leads to the formation ofNiO–silica mesostructures with high nickel content. Detailed structural and elemental characterizations byusing powder X-ray analysis (XRD), scanning electron (SEM) and transmission electron microscopy (TEM),N2 adsorption–desorption, X-ray photoelectron spectroscopy (XPS) revealed that single cubic phase NiOdoped mesoporous silica microspheres (for Ni/Si = 5:1 and 7:1) with good surface area (169 and 205 m2 g 1for sample with Ni/Si = 7:1 and 5:1, respectively) and pore width 3–5 nm, have been formed with 3Dflower-like shape and 500–600 nm particle size. These NiO–silica microspheres containing high Ni content up to 76wt% have shown excellent paramagnetic properties at room temperature.
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      Morphology oriented synthesis of metal oxide doped silica structures have fascinating properties whichneeded to be explored extensively. In this work, NiO doped silica microsphere with beautifulflower-likemorphology has been achieved by adopting a fac...

      Morphology oriented synthesis of metal oxide doped silica structures have fascinating properties whichneeded to be explored extensively. In this work, NiO doped silica microsphere with beautifulflower-likemorphology has been achieved by adopting a facile surfactant-assisted synthetic route using CTAB-ammonia in H2O–ethanol mixed solvent media. The sol–gel synthesis with effective variations of Ni/Si ratiosup to 7.0, followed by a simple hydrothermal treatment and subsequent calcination leads to the formation ofNiO–silica mesostructures with high nickel content. Detailed structural and elemental characterizations byusing powder X-ray analysis (XRD), scanning electron (SEM) and transmission electron microscopy (TEM),N2 adsorption–desorption, X-ray photoelectron spectroscopy (XPS) revealed that single cubic phase NiOdoped mesoporous silica microspheres (for Ni/Si = 5:1 and 7:1) with good surface area (169 and 205 m2 g 1for sample with Ni/Si = 7:1 and 5:1, respectively) and pore width 3–5 nm, have been formed with 3Dflower-like shape and 500–600 nm particle size. These NiO–silica microspheres containing high Ni content up to 76wt% have shown excellent paramagnetic properties at room temperature.

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      참고문헌 (Reference)

      1 S. K. Maji, 6 (6): 13648-, 2014

      2 F. Motahari, 4 : 27654-, 2014

      3 N. Pal, 8 : 35294-, 2018

      4 R. Barik, 7 : 49083-, 2017

      5 J. Kim, 120 : 8566-, 2008

      6 N. Pal, 8 : 285-, 2016

      7 B. Li, 10 (10): 29435-, 2018

      8 X. Chen, 513 : 788-, 2018

      9 W. Cai, 7 : 2340-, 2014

      10 J. Lee, 1 : 610-, 2013

      1 S. K. Maji, 6 (6): 13648-, 2014

      2 F. Motahari, 4 : 27654-, 2014

      3 N. Pal, 8 : 35294-, 2018

      4 R. Barik, 7 : 49083-, 2017

      5 J. Kim, 120 : 8566-, 2008

      6 N. Pal, 8 : 285-, 2016

      7 B. Li, 10 (10): 29435-, 2018

      8 X. Chen, 513 : 788-, 2018

      9 W. Cai, 7 : 2340-, 2014

      10 J. Lee, 1 : 610-, 2013

      11 M. Yang, 6 : 81237-, 2016

      12 Y. Wang, 180 : 35-, 2016

      13 Z. Guo, 2911-, 2008

      14 N. Pal, 3 : 6029-, 2018

      15 Y. Yang, 93 : 5-, 2013

      16 J. C. Park, 7345-, 2009

      17 Q. Rong, 153 : 63-, 2015

      18 Y. Cui, 13 : 4930-, 2011

      19 F. Qu, 132 : 167-, 2014

      20 Q. Xie, 5 : 8351-, 2015

      21 M. Salavati-Niasari, 24 : 365-, 2013

      22 J. H. Pan, 5 (5): 6292-, 2013

      23 E. -B. Cho, 1 : 12595-, 2013

      24 T. Ahmad, 8 : 425-, 2006

      25 T. Ahmad, 28 : 1245-, 2013

      26 T. Ahmad, 99 : 1207-, 2016

      27 M. Jaroniec, 22 : 6757-, 2006

      28 A. E. Danks, 3 : 91-, 2016

      29 N. Pal, 516 : 121-, 2018

      30 S. J. Wang, 80 : 2541-, 2002

      31 M.J. Guittet, 63 (63): 125117-, 2001

      32 N. Weidler, 121 : 6455-, 2017

      33 N. Pal, 118 : 15892-, 2014

      34 P. Bindu, 8 : 123-, 2014

      35 J. Park, 3 : 891-, 2004

      36 M. Y. Ge, 21 : 425702-, 2010

      37 E. Winkler, 19 : 185702-, 2008

      38 S. Rakshit, 3 : 19348-, 2013

      39 N. Pal, 262 : 1116-, 2015

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      학술지 이력

      학술지 이력
      연월일 이력구분 이력상세 등재구분
      2023 평가예정 해외DB학술지평가 신청대상 (해외등재 학술지 평가)
      2020-01-01 평가 등재학술지 유지 (해외등재 학술지 평가) KCI등재
      2011-01-01 평가 등재학술지 유지 (등재유지) KCI등재
      2009-01-01 평가 등재학술지 유지 (등재유지) KCI등재
      2007-01-01 평가 등재학술지 유지 (등재유지) KCI등재
      2004-01-01 평가 등재학술지 선정 (등재후보2차) KCI등재
      2003-01-01 평가 등재후보 1차 PASS (등재후보1차) KCI등재후보
      2001-07-01 평가 등재후보학술지 선정 (신규평가) KCI등재후보
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      학술지 인용정보

      학술지 인용정보
      기준연도 WOS-KCI 통합IF(2년) KCIF(2년) KCIF(3년)
      2016 3.4 0.75 2.84
      KCIF(4년) KCIF(5년) 중심성지수(3년) 즉시성지수
      2.39 2.24 0.397 0.56
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