Cited Article:    Holt JK. Fast mass transport through sub-2-nanometer carbon nanotubes
 Alert Expires:    09 NOV 2010
 Number of Citing Articles:    3 new records this week (3 in this e-mail)
 Organization ID:  3b97d1bbc1878baed0ab183d8b03130b
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*Record 1 of 3. 
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AU Khan, SH
   Matei, G
   Patil, S
   Hoffmann, PM
AF Khan, Shah H.
   Matei, George
   Patil, Shivprasad
   Hoffmann, Peter M.
TI Dynamic Solidification in Nanoconfined Water Films
SO PHYSICAL REVIEW LETTERS
LA English
DT Article
ID INTERFACIAL WATER; VISCOSITY
AB Mechanical properties of nanoconfined water layers are still poorly
   understood and continue to create controversy, despite their importance
   for biology and nanotechnology. We report on dynamic nano-mechanical
   measurements of water films compressed to a few single molecular
   layers. We show that the mechanical properties of nanoconfined water
   layers change significantly with their dynamic state. In particular, we
   observed a sharp transition from viscous to elastic response even at
   extremely slow compression rates, indicating that mechanical relaxation
   times increase dramatically once water is compressed to less than 3-4
   molecular layers.
C1 [Khan, Shah H.; Matei, George; Hoffmann, Peter M.] Wayne State Univ, Dept Phys & Astron, Detroit, MI 48201 USA.
   [Patil, Shivprasad] Indian Inst Sci Educ & Res, Pune 411021, Maharashtra, India.
RP Khan, SH, Wayne State Univ, Dept Phys & Astron, Detroit, MI 48201 USA.
EM hoffmann@wayne.edu
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   10.1088/0957-4484/16/3/009
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   ZHU Y, 2003, LANGMUIR, V19, P8148, DOI 10.1021/la035155+
   ZHU YX, 2001, PHYS REV LETT, V87, ARTN 096104
NR 23
TC 0
PU AMER PHYSICAL SOC; ONE PHYSICS ELLIPSE, COLLEGE PK, MD 20740-3844 USA
SN 0031-9007
DI 10.1103/PhysRevLett.105.106101
PD AUG 30
VL 105
IS 10
AR 106101
SC Physics, Multidisciplinary
GA 644LH
UT ISI:000281378400007
ER
PT J
*Record 2 of 3. 
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AU Garaj, S
   Hubbard, W
   Reina, A
   Kong, J
   Branton, D
   Golovchenko, JA
AF Garaj, S.
   Hubbard, W.
   Reina, A.
   Kong, J.
   Branton, D.
   Golovchenko, J. A.
TI Graphene as a subnanometre trans-electrode membrane
SO NATURE
LA English
DT Article
ID CARBON NANOTUBES; LARGE-AREA; DNA; NANOPORES; MOLECULES; WATER
AB Isolated, atomically thin conducting membranes of graphite, called
   graphene, have recently been the subject of intense research with the
   hope that practical applications in fields ranging from electronics to
   energy science will emerge(1). The atomic thinness, stability and
   electrical sensitivity of graphene motivated us to investigate the
   potential use of graphene membranes and graphene nanopores to
   characterize single molecules of DNA in ionic solution. Here we show
   that when immersed in an ionic solution, a layer of graphene becomes a
   new electrochemical structure that we call a transelectrode. The
   trans-electrode's unique properties are the consequence of the
   atomic-scale proximity of its two opposing liquid-solid interfaces
   together with graphene's well known inplane conductivity. We show that
   several trans-electrode properties are revealed by ionic conductance
   measurements on a graphene membrane that separates two aqueous ionic
   solutions. Although our membranes are only one to two atomic
   layers(2,3) thick, we find they are remarkable ionic insulators with a
   very small stable conductance that depends on the ion species in
   solution. Electrical measurements on graphene membranes in which a
   single nanopore has been drilled show that the membrane's effective
   insulating thickness is less than one nanometre. This small effective
   thickness makes graphene an ideal substrate for very high resolution,
   high throughput nanopore-based single-molecule detectors. The
   sensitivity of graphene's in-plane electronic conductivity to its
   immediate surface environment and trans-membrane solution potentials
   will offer new insights into atomic surface processes and sensor
   development opportunities.
C1 [Garaj, S.; Golovchenko, J. A.] Harvard Univ, Dept Phys, Cambridge, MA 02138 USA.
   [Hubbard, W.; Golovchenko, J. A.] Harvard Univ, Sch Engn & Appl Sci, Cambridge, MA 02138 USA.
   [Reina, A.] MIT, Dept Mat Sci & Engn, Cambridge, MA 02139 USA.
   [Kong, J.] MIT, Dept Elect Engn & Comp Sci, Cambridge, MA 02139 USA.
   [Branton, D.] Harvard Univ, Dept Mol & Cellular Biol, Cambridge, MA 02138 USA.
RP Golovchenko, JA, Harvard Univ, Dept Phys, Cambridge, MA 02138 USA.
EM sgaraj@fas.harvard.edu
   golovchenko@physics.harvard.edu
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   REINA A, 2009, NANO LETT, V9, P30, DOI 10.1021/nl801827v
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NR 21
TC 1
PU NATURE PUBLISHING GROUP; MACMILLAN BUILDING, 4 CRINAN ST, LONDON N1
   9XW, ENGLAND
SN 0028-0836
DI 10.1038/nature09379
PD SEP 9
VL 467
IS 7312
BP 190
EP U73
SC Multidisciplinary Sciences
GA 647KB
UT ISI:000281616300030
ER
PT J
*Record 3 of 3. 
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AU Schoen, DT
   Schoen, AP
   Hu, LB
   Kim, HS
   Heilshorn, SC
   Cui, Y
AF Schoen, David T.
   Schoen, Alia P.
   Hu, Liangbing
   Kim, Han Sun
   Heilshorn, Sarah C.
   Cui, Yi
TI High Speed Water Sterilization Using One-Dimensional Nanostructures
SO NANO LETTERS
LA English
DT Article
DE Nanowires; nanotubes; environmental applications; multiscale; textile
ID SILICON NANOWIRES; CARBON NANOTUBES; SOLAR-CELLS; MEMBRANES;
   PERFORMANCE; PARTICLES
AB The removal of bacteria and other organisms from water is an extremely
   important process, not only for drinking and sanitation but also
   industrially as biofouling is a commonplace and serious problem. We
   here present a textile based multiscale device for the high speed
   electrical sterilization of water using silver nanowires, carbon
   nanotubes, and cotton. This approach, which combines several materials
   spanning three very different length scales with simple dying based
   fabrication, makes a gravity fed device operating at 100000 L/(h m(2))
   which can inactivate >98% of bacteria with only several seconds of
   total incubation time. This excellent performance is enabled by the use
   of an electrical mechanism rather than size exclusion, while the very
   high surface area of the device coupled with large electric field
   concentrations near the silver nanowire tips allows for effective
   bacterial inactivation.
C1 [Schoen, David T.; Schoen, Alia P.; Hu, Liangbing; Kim, Han Sun; Heilshorn, Sarah C.; Cui, Yi] Stanford Univ, Dept Mat Sci & Engn, Stanford, CA 94305 USA.
RP Cui, Y, Stanford Univ, Dept Mat Sci & Engn, Stanford, CA 94305 USA.
EM yicui@stanford.edu
CR AKHAVAN O, 2009, SCI TECHNOL ADV MAT, V10, ARTN 015003
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   10.1088/0957-4484/16/10/059
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   10.1289/ehp.7339
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   10.1016/j.synthmet.2007.04.010
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NR 32
TC 0
PU AMER CHEMICAL SOC; 1155 16TH ST, NW, WASHINGTON, DC 20036 USA
SN 1530-6984
DI 10.1021/nl101944e
PD SEP
VL 10
IS 9
BP 3628
EP 3632
SC Chemistry, Multidisciplinary; Nanoscience & Nanotechnology; Materials
   Science, Multidisciplinary
GA 645WZ
UT ISI:000281498200068
ER
EF
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