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1 arbon black particles, carbon nanotubes, and graphene sheets).
2  extending up to 30 A from both sides of the graphene sheet.
3 amical screening of charge in a freestanding graphene sheet.
4 confined space between a metal surface and a graphene sheet.
5 ng wire has been embedded in another perfect graphene sheet.
6 ybridized carbon rings embedded in a perfect graphene sheet.
7 , experimental phonon dispersion of a single graphene sheet.
8 ed by nitrogen atoms embedded in an extended graphene sheet.
9  via the resistance of an adjacently stacked graphene sheet.
10 ol the crumpling and unfolding of large-area graphene sheets.
11 shrinkage of giant fullerenes generated from graphene sheets.
12 l % of the solute is present as single-layer graphene sheets.
13 films corroborated the presence of monolayer graphene sheets.
14 nsional capillaries formed by closely spaced graphene sheets.
15 eties sufficient to enable the separation of graphene sheets.
16 ded graphite basal planes to give functional graphene sheets.
17 nd directly produce large, highly conductive graphene sheets.
18 3 J m(-2) for samples containing two to five graphene sheets.
19 rticles and nanowires, carbon nanotubes, and graphene sheets.
20 not ideal for the manufacture of processable graphene sheets.
21 the thermodynamic stability of free-standing graphene sheets.
22 ortions and flexible bending at the edges of graphene sheets.
23 es not readily exfoliate to yield individual graphene sheets.
24  magnified by their structure, intercalating graphene sheets.
25  via AFs complexation and a huge porosity of graphene sheets.
26 n nanotubes (MWCNTs) positioned over stacked graphene sheets.
27 , or Al) nanoparticles encapsulated by large graphene sheets.
28 ied with twist angle in bilayer and trilayer graphene sheets.
29 iform and open-networked array of aggregated graphene sheets.
30 place on the surface of exfoliated few-layer graphene sheets.
31 rier by "locking in" favourable stackings of graphene sheets.
32 high-mobility semiconductor quantum wells or graphene sheets.
33 ut to study the morphology of functionalized graphene sheets.
34 ensions of crystalline single- and few-layer graphene sheets.
35  spaces through folding and rearrangement of graphene sheets.
36 ovide evidence for the presence of monolayer graphene sheets.
37 lvated in a water monolayer confined between graphene sheets.
38 ng adsorption saturation of NaC molecules on graphene sheets.
39 i nanoparticles due to the highly conductive graphene sheets.
40 ween the guest molecules and the polarizable graphene sheets.
41 n, reduction or covalent modification of the graphene sheets.
42 hment of monodisperse Fe3O4 nanoparticles to graphene sheets.
43 e the nature of catalytic sites on ultrathin graphene sheets.
44  TEMPO-assisted exfoliation results in large graphene sheets (5-10 mum on average), which exhibit out
45  Hall insulator, inherently protected by the graphene sheet above and the H-passivated substrate belo
46 rammable photoactuation enabled by graphene: Graphene sheets aligned in liquid crystalline elastomers
47 , we report graphene structures with tunable graphene sheet alignment and orientation, obtained via m
48 lline Ni(OH)(2) nanoplates directly grown on graphene sheets also significantly outperform small Ni(O
49 croscopy imaging of water locked between two graphene sheets, an archetypal example of hydrophobic co
50 n of a nanohybrid by a combination of the 2D graphene sheet and 0D graphene quantum dots (GQDs).
51 e semiconducting channel between a monolayer graphene sheet and a metal thin film.
52 When the particles were sandwiched between a graphene sheet and a proton exchange membrane that is we
53 self-assembly over planar sp(2) carbons of a graphene sheet and furnishes the basis for fabrication o
54 nd AD molecules reduces the voids within the graphene sheet and improves the alignment of graphene pl
55 ond to correlations between electrons in the graphene sheet and ions in the electrolyte.
56 etween the strain energy of curvature of the graphene sheet and the dangling-bond energy of the open
57 from changes in commensurability between the graphene sheet and the substrate when the sheet deforms
58          Ripples are an intrinsic feature of graphene sheets and are expected to strongly influence e
59 ing the preparation and functionalization of graphene sheets and carbon nanotubes to impart oxygen co
60 posing surface morphologies originating from graphene sheets and COF nanofibers or nanospheres, prese
61 ve development of large-scale semiconducting graphene sheets and devices.
62 re effective reduction of chemically derived graphene sheets and graphite oxide than low-temperature
63                       Carbon nanotube films, graphene sheets and metal-nanowire meshes can be both st
64 atures below 0 degrees C, due to its aligned graphene sheets and pores.
65               The findings on exfoliation of graphene sheets and related adsorption properties highli
66 of the dual signal amplification strategy of graphene sheets and the multienzyme labeling, the develo
67 formed by depositing alternating wafer-scale graphene sheets and thin insulating layers, then pattern
68 illared graphene (PG) membranes, composed of graphene sheets and vertically aligned carbon nanotubes
69 nar units (unbounded or bounded fragments of graphene sheets), and variable ratios of in-plane to edg
70  poly(acrylonitrile) at 1 wt% functionalized graphene sheet, and with only 0.05 wt% functionalized gr
71               Large fullerenes, fullertubes, graphene sheets, and double- and multiwalled CNTs togeth
72 e recently developed approaches to preparing graphene sheets, and then focus on the methods to assemb
73 erties arising from the nature of individual graphene sheets, and which assemble into monolithic thre
74                                    Monolayer graphene sheets are employed to preserve and template mo
75                       The large voids in the graphene sheets are occupied by chloride ions with an eq
76                                          The graphene sheets are self-assembled and deeply crumpled i
77              Nanographenes, finite models of graphene sheets, are endowed with intriguing optical, el
78 g, we fabricated Ti(3)C(2)T(x) MXene-bridged graphene sheets at room temperature with isotropic in-pl
79 most of the observed transport properties of graphene sheets at zero magnetic field can be explained
80 constructed by slightly rotating a monolayer graphene sheet atop a thin bulk graphite crystal.
81 ng of such composites requires not only that graphene sheets be produced on a sufficient scale but th
82 band that is primarily localized to a single graphene sheet below the moire interface.
83 rit some of the key properties of individual graphene sheets, but also develop additional functions t
84 ate the solublization/suspension of pristine graphene sheets by an equimolar mixture of benzene and h
85 n selectively remove monolayers in few-layer graphene sheets by means of electron-beam-induced sputte
86  were fabricated from single- and multilayer graphene sheets by mechanically exfoliating thin sheets
87 od for the scalable synthesis of few-layered graphene sheets by the microwave-assisted functionalizat
88 ith horizontally and perpendicularly aligned graphene sheets by tuning the elongational and extension
89 idized sp(3) carbon atoms and vacancies in a graphene sheet can degrade its mechanical strength, they
90                  Amyloid protein fibrils and graphene sheets can be combined to make a material that
91 ns of graphene with clean and well-separated graphene sheets can be obtained in both aqueous and orga
92 pproaches, unfunctionalized and non-oxidized graphene sheets can be produced; among them an inexpensi
93                            Single-atom-thick graphene sheets can now be produced by chemical vapour d
94 (2)/g, the maximum surface area for infinite graphene sheets, carried mainly by edge sites; we call t
95 raphite flakes to single-layer and few-layer graphene sheets combined with functionalization of the g
96  to ripples in the membrane that stiffen the graphene sheets considerably, to the extent that gamma i
97                                          The graphene sheets contain extremely small amounts of irons
98           The readily available, super-clean graphene sheets contribute to an enhancement in the opti
99                                Moreover, the graphene sheets dampen capillary waves such that rotatio
100 associated with the moire corrugation of the graphene sheet due to local variations in the graphene-s
101 tion sites might be realized across a single graphene sheet, facilitating the development of graphene
102                           Interestingly, the graphene sheets favor the Janus-type assembly of COF nan
103 d dispersing small amounts of functionalized graphene sheets (FGSs) in liquid NM.
104 ed arrangement intercalated with small-sized graphene sheets filling the space and microvoids.
105  4.2 A [(12,12) to (3,3)] as well as a C(2)F graphene sheet fluorinated on one side only.
106    Additionally, the impact of the number of graphene sheets for the optimum efficiency of the propos
107                                  Whereas the graphene sheets formed from the unzipped part of the out
108 nner fiber structure consists of large-sized graphene sheets forming a highly ordered arrangement int
109 ITO) nanocrystals directly on functionalized graphene sheets, forming an ITO-graphene hybrid.
110  of the exfoliated accompanying carboxylated graphene sheet from pristine is achieved via Friedel-Cra
111  the spontaneous twisting and peeling off of graphene sheets from the polymer substrate.
112  synthesized by the controlled reassembly of graphene sheets; from their initial stacked morphology,
113 The existence of layered structures based on graphene sheets gives rise to an electronic structure re
114                   Electrical measurements on graphene sheets, graphene nanoribbons, and large graphen
115 ing is opened and attaches covalently to the graphene sheet (Gs) to form exfoliated graphene with gra
116 wth behaviors were observed on low-oxidation graphene sheets (GS) and highly oxidized graphite oxide
117 on lightly oxidized, electrically conducting graphene sheets (GS) exhibit a high specific capacitance
118 eriodic perforation and heteroatom doping of graphene sheets have been developed, patterning closely
119                                      Bilayer graphene sheets have been found to be superconductive wh
120 nd recent studies have shown that individual graphene sheets have extraordinary electronic transport
121                       In-situ TEM shows that graphene sheets help maintain the capacity even in the c
122 supported on N-doped carbon black or N-doped graphene sheets, highlighting the importance of the 3D m
123 on lattice are detected, indicating that the graphene sheets host the ideal charge density wave.
124 oes beyond the traditional model of parallel graphene sheets hosting layers of physisorbed hydrogen i
125 mical functionalization by doping a pristine graphene sheet in a certain pattern with hydrogen atoms
126 sheet, and with only 0.05 wt% functionalized graphene sheet in poly(methyl methacrylate) there is an
127 ies for applications would be to incorporate graphene sheets in a composite material.
128  of the chemical composition of the edges of graphene sheets in both flat and curved sp(2)-hybridized
129 ates, and also holds together the individual graphene sheets in multilayer samples.
130  of stabilization of liquid-phase-exfoliated graphene sheets in N-methylpyrrolidone (NMP), N,N'-dimet
131 orphology that reflects the structure of the graphene sheets in solution.
132 loid aggregation to model the aggregation of graphene sheets in the liquid phase in order to predict
133 enhanced through the excellent dispersion of graphene sheets in the matrix material and the strong gr
134                           The highly ordered graphene sheets in the plane of the membrane make organi
135                                 However, the graphene sheets in these devices have irregular shapes a
136 r since the first isolation of free-standing graphene sheets in year 2004.
137 al reduction removed oxygen and defects from graphene sheets, increased the size of sp(2) domains, an
138 n nitride (hBN)(7,8) used to encapsulate the graphene sheets indicates the importance of the microsco
139                          The rolling up of a graphene sheet into a tube is a standard visualization t
140  scalable self-assembly of randomly oriented graphene sheets into additive-free, essentially homogeno
141 port a prompt electrochemical exfoliation of graphene sheets into aqueous solutions of different inor
142  However, the actual processes of rolling up graphene sheets into CNTs in laboratory syntheses have n
143                                   Processing graphene sheets into nanoribbons with widths of less tha
144 zable approach for fashioning one-atom-thick graphene sheets into resilient and movable parts with mi
145      Here we develop a method to incorporate graphene sheets into vanadium pentoxide nanoribbons via
146 ergy gaps that are sometimes observed when a graphene sheet is placed on a hexagonal boron nitride su
147                         The self-assembly of graphene sheets is driven thermodynamically, as graphite
148              Mass production of high-quality graphene sheets is essential for their practical applica
149                 The bonding between adjacent graphene sheets is investigated by molecular dynamics si
150 on between two model hydrophobic plates, and graphene sheets, is reduced when urea is added to the so
151 rowth enlarged, over one hour, the nuclei to graphene sheets larger than one hundred nm(2) in area.
152 anus-binding were periodically weaved on the graphene sheet, leading to four different types of zones
153 transfer from the electron beam to few-layer graphene sheets leads to unique structural transformatio
154 d identification of the fluence at which the graphene sheet loses long-range order.
155 ectrical behaviour of both doped and undoped graphene sheets maintain excellent properties, with low
156 graphene surface, the carrier equilibrium in graphene sheet might be altered, and manifested by the c
157 Formula: see text]0.08 can be obtained for a graphene sheet modified with kirigami-inspired cuts when
158 ional (3D) hybrid material of nitrogen-doped graphene sheets (N-RGO) supporting molybdenum disulfide
159      Surfactant-wrapped chemically converted graphene sheets obtained from reduction of graphene oxid
160 lore the non-local correlation dynamics in a Graphene sheet of disordered electrons in a two-dimensio
161 the role of surface mediators on the buckled graphene sheets of acid-microwaved CNTs.
162                     Synthesis of large-scale graphene sheets of high quality and at low cost has been
163  and scalable approach produces high-quality graphene sheets of low oxygen content, enabling a broad
164 ousands of tonnes per year, while continuous graphene sheets of tens of metres in length have become
165 o various industries, producing high-quality graphene sheets on a large scale becomes crucial.
166                                              Graphene sheets--one-atom-thick two-dimensional layers o
167 nd porphyrinic and is located at the edge of graphene sheets or pores.
168 arge MoO(2) film is created/deposited on the graphene sheet, originating and expanding from the origi
169 ctrical-circuit model is established and the graphene-sheet pattern is designed optimally for maximiz
170 R selectivity, we treated partially oxidized graphene sheets (po-Gr) with NR to obtain po-Gr-NR dispe
171 imilar trend, with values for functionalized graphene sheet- poly(methyl methacrylate) rivaling those
172 he molecular migration on a wrinkled/rippled graphene sheet preferentially happens from the valley (p
173 ur bottom-up chemical approach of tuning the graphene sheet properties provides a path to a broad new
174 anchorage, pi-stacking interactions with the graphene sheets provide further pi-delocalization that i
175 ased on our super-tough MXene-functionalized graphene sheets provides a combination of energy and pow
176 cts of graphene-metal contact resistance and graphene sheet resistance, enabling pronounced NDR effec
177 we characterize the hydrophobicity of curved graphene sheets, self-assembled monolayers (SAMs) with c
178 a-fetoprotein (AFP) is described that uses a graphene sheet sensor platform and functionalized carbon
179                              Atomically thin graphene sheets serve as folding hinges during a process
180 perating at room temperature, where a single graphene sheet serves simultaneously as the plasmonic me
181  of pre-synthesized Ni(OH)(2) nanoplates and graphene sheets shows lower specific capacitance, highli
182 been observed on all suspended and supported graphene sheets studied so far.
183         However, the finite curvature of the graphene sheet that forms the nanotubes and the broken s
184                    At the positively charged graphene sheet, the electrowetting response is amplified
185                       With the protection of graphene sheets, the large and freestanding LixM/graphen
186 ain metal atoms are intercalated between its graphene sheets, the same has not been achieved in a sin
187 on-neighboring carbon atoms across an entire graphene sheet, thereby producing only a minimum concent
188                           In contrast to the graphene sheet, they are chemically versatile.
189 e may therefore apply ideas from kirigami to graphene sheets to build mechanical metamaterials such a
190 pathways used so far for modification of 2-D graphene sheets to make is three-dimensional.
191 ical concentration of defects, free-standing graphene sheets undergo a dynamic transition from freely
192                       Second, functionalized graphene sheets used for the biosensor platform increase
193  discrete electronic domains within a single graphene sheet using scanning transmission X-ray microsc
194 potential of mean force between two solvated graphene sheets using molecular dynamics (MD) simulation
195 wo-dimensional periodic ripples in suspended graphene sheets, using both spontaneously and thermally
196 on of 1,1'-ferrocenedicarboxylic acid on the graphene sheet via the pai-pai stacking.
197            Decorating Fe3O4 nanoparticles on graphene sheets was performed via a facile one-step chem
198 ring descending local curvatures) and a flat graphene sheet, we confirm that adsorption capacity is i
199 y electrically tuning the Fermi level of the graphene sheet, we demonstrate modulation of the guided
200 s and nanotubes tunneling multiple layers of graphene sheets were also observed.
201 m fluorescence property from nanohybrid, the graphene sheets were chemically doped with cadmium sulph
202                                          The graphene sheets were deposited on 1.00mm thick copper sh
203       With the aid of sonication, multilayer graphene sheets were exfoliated by NaC, leading to bette
204 lectronic properties of molecularly pillared graphene sheets were explored by performing Density Func
205                                              Graphene sheets were found in the TEM images of the carb
206       Herein, single-layered and few-layered graphene sheets were produced by dispersion and exfoliat
207 id of Ag nanoparticles anchored onto the 2-D graphene sheets were synthesized using a two-step laser
208                      Herein, two-dimensional graphene sheets were utilized as the suitable grafter du
209 ext]) at MoO(2) nanowire decorated monolayer graphene sheets, when edge plane like- sites/defects hav
210 on the edge plane like- sites/defects of the graphene sheets, where the basal plane sites remain unal
211 inate from periodic nanoscale ripples in the graphene sheet, which enhance puckering around a sliding
212                              Thus, separated graphene sheets, which are referred to as microwave-enab
213 n be obtained by fragmentation/truncation of graphene sheets, which creates surface areas exceeding o
214 f polymer nanocomposites with functionalized graphene sheets, which overcome these obstacles and prov
215 er of confined solvent molecules between the graphene sheets, which results from the strong affinity
216 rbed atoms flipping to the other side of the graphene sheet with a relatively low activation energy o
217 t to directly measure the adhesion energy of graphene sheets with a silicon oxide substrate.
218  (tDBG) comprises two Bernal-stacked bilayer graphene sheets with a twist between them.
219 we find that, counter to standard reasoning, graphene sheets with large-angle tilt boundaries that ha
220 y attaching chemical moieties at the edge of graphene sheets with minimal damage of the carbon basal
221 t an interconnected macroporous framework of graphene sheets with uniform dispersion of Fe(3)O(4) nan
222              Ni(OH)(2) nanocrystals grown on graphene sheets with various degrees of oxidation are in
223 nanoclusters of platinum were supported on a graphene sheet within a catalytic condenser device that
224 ispersion of individual, chemically modified graphene sheets within polymer hosts.
225  nitrogen atoms can be incorporated into the graphene sheet without destroying it.
226 oscopic flattening and in-plane shrinkage of graphene sheets without a complete loss of crystallinity

 
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