ライフサイエンスコーパス: graphite

1 glucose oxidase immobilized on Pt-decorated graphite.

2 000 degrees C on a nuclear-grade Gilsocarbon graphite.

3 4) (6) and trimethylphosphine with potassium graphite.

4 arbon nanostructures in between graphene and graphite.

5 s to look for alternative anode materials to graphite.

6 bon layers is the unique crystalline form of graphite.

7 +/- 0.1 eV with no chemical intermixing with graphite.

8 ct angle of a macroscopic mercury droplet on graphite.

9 noparticles into the interspaces of expanded graphite.

10 previously assumed for gold nanocrystals and graphite.

11 or to graphene via the chemical oxidation of graphite.

12 c diamonds in remnants of explosively driven graphite.

13 and rate capability much superior to that of graphite.

14 ers) by epitaxial growth on a rigid support, graphite.

15 d based on the self-retraction phenomenon in graphite.

16 ilms prepared by liquid phase exfoliation of graphite.

17 cal exfoliation of highly oriented pyrolytic graphite.

18 f magnitude to beyond that of single-crystal graphite.

19 substrates such as highly ordered pyrolytic graphite.

20 htly higher than the theoretical capacity of graphite (372 mAh/g) in Li-ion half-cell configurations.

21 ure, a 150% improvement compared to expanded graphite (4.6 W.m(-1).K(-1)) owing to the existence of A

22 of 46 wt % of dual-shell SiNPs@C, 46 wt % of graphite, 5 wt % of acetylene black, and 3 wt % of carbo

23 s research has suggested that black carbons (graphite, activated carbon, and biochar) mediate the deg

24 e macroscopic deformations, to determine the graphite adhesion energy of 0.221+/-0.011 J m(-2).

25 This nanostructured graphite allows fast and reversible intercalation/deinte

26 rable to those of the benchmark 2D materials graphite and Bi2Sr2CaCu2O(6+delta).

27 Hydrophobic solid substances like graphite and carbon nanotubes are smoothly dispersed in

28 of printed anode and cathode layers based on graphite and lithium cobalt oxide, respectively, on thin

29 Graphite and other lamellar materials are used as dry lu

30 Solution processing of graphite and other layered materials provides low-cost i

31 nitrobenzene was observed in the presence of graphite and sulfite, thiosulfate, or polysulfides.

32 chemical method, simultaneous exfoliation of graphite and the reduction of gold chloride occurs to pr

33 onic coupling between tobacco peroxidase and graphite and to the formation of intra- and intermolecul

34 roscopy (AFM) at a highly oriented pyrolytic graphite and voltammetry at a glassy carbon electrode.

35 in oxide, aluminum, highly ordered pyrolytic graphite, and glassy carbon, was achieved using a very f

36 higher friction than multilayer graphene and graphite, and that this friction increases with continue

37 g(-1) ), three times higher than that of the graphite anode (372 mAh g(-1) ).

38 he degradation of LCO cathode is larger than graphite anode at elevated temperature.

39 pecies, and the replacement of Li metal with graphite anode can circumvent potential safety issues.

40 t lithium Li-ion batteries is to replace the graphite anode with a Li metal anode.

41 ment of more than 100 % compared to the pure graphite anode.

42 Se) were tested as cathode materials against graphite anodes (single cells); They perform outstanding

43 performs conventionally used slurry-prepared graphite anodes by over two times on an active material

44 the strength and fracture toughness of this graphite are improved at elevated temperature.

45 ral sizes >10 mum, using chemically expanded graphite as the starting material.

46 This spreading, or exfoliation, of graphite at an oil/water interface stabilizes water-in-o

47 enhanced lubricity) of gold nanocrystals on graphite at high surface speeds, we use the quartz micro

48 rode (AuSPE) and gold nanoparticles modified graphite (AuNPs/gr) was examined in mixed water-alcohol

49 d to swell (volumetrically expand) more than graphite based LIB (graphite-LIB) and beyond practical l

50 The graphite-based amperometric sensor gave a selective and

51 Pencil lead was used to fabricate a graphite-based electrode for sensing applications.

52 In this study, we describe a graphite-based nanocomposite electrode (Au-rGO/MWCNT/gra

53 gel/BChE films were built up on a surface of graphite-based screen-printed electrodes (SPEs) premodif

54 ent MnO2-mediated thiocholine oxidation at a graphite-based SPE.

55 re we study the unoccupied band structure of graphite, boron nitride and their heterostructures using

56 directly onto polished basal plane pyrolytic graphite (BPG), edge plane pyrolytic graphite (EPG), gla

57 key process steps such as powder compaction, graphite burnout during partial sintering, machining in

58 However, since graphite can be hypothetically derived from diamond by s

59 ke 2D materials, such as boron nitride (BN), graphite-carbon nitride (g-C3N4), transition metal dicha

60 ng the ssDNA probe on the surface of an AuNP/graphite cathode.

61 uminium ion batteries with aluminium anodes, graphite cathodes and ionic liquid electrolytes has incr

62 ing stability and capacity retention of LNMO/graphite cells can be considerably improved by a simple

63 erando gas analysis of LiNi0.5Mn1.5O4 (LNMO)/graphite cells with reasonably high loading, containing

64 sets composed of various chemicals sorbed to graphite, charcoal, and activated carbon.

65 on the "graphite" factor were in the order: graphite coating < without coating (p < 0.05).

66 ures of about 1100 K, which generates porous graphite comprising petaloid nanoflakes.

67 at edge planes of graphitic carbon generates graphite-conjugated pyrazines (GCPs) that are active for

68 fects on graphitic carbon surfaces generates graphite-conjugated rhenium (GCC-Re) catalysts that are

69 This work establishes graphite-conjugation as a powerful strategy for generati

70 se of a highly concentrated pomegranate dye, graphite counter electrode and TiCl4 treatment of the ph

71 e grown in printed microwells on a pyrolytic graphite detection chip and decorated with capture antib

72 ntal materials, including tungsten, silicon, graphite, diamond and graphene, for point defects such a

73 of a film made of alumina fibers between the graphite die and the graphite punches, which are protect

74 l system including an electrically insulated graphite die for Spark Plasma Sintering (SPS) is describ

75 erials, controlling sample shape by an added graphite die, and an energy efficient mass production of

76 ngsten cathode and a liquid drop placed on a graphite disk anode.

77 The arrangement of the graphite disk placed on a PTFE chip platform as well as

78 Surface-coating with graphite does not improve bonding of the laser-treated l

79 that is opposite to the case of graphene and graphite due to the absence of reflection symmetry in pu

80 e electrode and an Au nanoparticles modified graphite electrode (AuNP/graphite electrode) were used a

81 electrochemical setup with a minium-modified graphite electrode (C|Pb3O4) was used.

82 a DNA-based Au-nanoparticle modified pencil graphite electrode (PGE) biosensor for detection of Baci

83 edure was used which includes coating pencil graphite electrode (PGE) by means of electro-polymerizat

84 old nanorods (nano Au) deposited onto pencil graphite electrode (PGE) has been utilized for covalent

85 V) in combination with the disposable pencil graphite electrode (PGE) was progressed for sensitive an

86 of caffeic acid (CA) on a disposable pencil graphite electrode (PGE).

87 /Chi hybrid bionanocomposite modified pencil graphite electrode (PGE).

88 A graphite electrode and an Au nanoparticles modified grap

89 mediated by Os-PVP complex on the surface of graphite electrode at applied potential of 0.31 V vs. Ag

90 photoelectrochemical process (PEC) based on graphite electrode modified with electroactive polyvinyl

91 currents produced at an edge-plane pyrolytic graphite electrode was diagnosed analytically at concent

92 Graphite electrode was modified using multi-walled carbo

93 anotubes (SWCNT) mixture on the surface of a graphite electrode with a Nafion film.

94 tion of tobacco peroxidase and the pyrolytic graphite electrode with the cross-coupling reagents prod

95 oparticles modified graphite electrode (AuNP/graphite electrode) were used as anode and cathode in th

96 te an electrocatalytically active Ni/Ni(OH)2/graphite electrode.

97 mically fabricated on C-dots modified pencil graphite electrode.

98 zation on the surface of the modified pencil graphite electrode.

99 the surface of vinyl silane modified pencil graphite electrode.

100 n behaviour of choloraluminate anions in the graphite electrode.

101 yric acid frameworks on edge plane pyrolytic graphite electrodes (PGE/MWNT/Py) to which an anti-insul

102 peptide nanoparticles (PNPs) modified pencil graphite electrodes (PGEs) for construction of electroch

103 phene oxide (rGO) modified disposable pencil graphite electrodes (PGEs) were developed herein for ele

104 olymerized polypyrrole (PPy) modified pencil graphite electrodes (PPy/PGE).

105 d is presented for making low-cost composite graphite electrodes containing a thermoplastic binder.

106 ng long-term DEMS measurements was tested on graphite electrodes in Ethylene Carbonate/Dimethyl Carbo

107 ide electrochemistry is totally inhibited on graphite electrodes modified with an insulating nitrocel

108 on nanotube conductive scaffolds in films on graphite electrodes provides enzyme electrodes for gluco

109 systems such as carbon nanotube electrodes, graphite electrodes, polymer electrodes and metals).

110 icate graphene and highly oriented pyrolytic graphite electrodes.

111 ic electrochemical exfoliation of iso-molded graphite electrodes.

112 fate dehydrogenase, TsdA, family adsorbed on graphite electrodes.

113 e, we present the development of an expanded graphite embedded with Al metal nanoparticles (EG-MNPs-A

114 rolytic graphite (BPG), edge plane pyrolytic graphite (EPG), glassy carbon (GC), or high-purity graph

115 timal proportion of the transducer material (graphite-epoxy ratio) was chosen using constant amount o

116 t the construction of immunosensors based on graphite-epoxy which incorporate RIgG to the composite m

117 drofluoric acid-etching), Er:YAG laser + HF, Graphite + Er:YAG laser + HF, Nd:YAG laser + HF, and Gra

118 Kinetically controlled AA' graphite exhibits unique nano- and single-crystalline fe

119 der: Er:YAG > Nd:YAG (p < 0.05), and on the "graphite" factor were in the order: graphite coating < w

120 i3N4 nanobelts from quartz and graphite on a graphite-felt substrate was successfully achieved by cat

121 ion battery cell made using pristine natural graphite flakes achieves a specific capacity of approxim

122 ials) as in DRS and EDS, or through the thin graphite foil (non-conductive materials) as in IRS, and

123 e protected from the alumina fiber film by a graphite foil.

124 rough chloroaluminate anion intercalation of graphite followed by thermal expansion and electrochemic

125 onolithic integration of InAs nanowires with graphite for flexible and functional hybrid devices.

126 ive devices based on platinum (Pt)-decorated graphite for glucose determination in physiological flui

127 tegy to generate the Ni/Ni(OH)2 interface on graphite from Ni deposits is promising for electrochemic

128 ion of metal-oxide sub-micron powders with a graphite fugitive phase that is burned out to create int

129 ped method combining microwave digestion and graphite furnace AAS.

130 ch was generated at high temperatures in the graphite furnace after the addition of Ca.

131 irectly introduced into the ruthenium coated graphite furnace as 0.05 to 0.50mg.

132 l emission spectrometry (ICP OES), and Se by graphite furnace atomic absorption spectrometry (GF AAS)

133 ein fractions were collected and analyzed by graphite furnace atomic absorption spectrometry (GFAAS)

134 f vanadium in real water and food samples by graphite furnace atomic absorption spectrometry (GFAAS).

135 nitric acid for direct analysis of Pb using graphite furnace atomic absorption spectrometry - GF AAS

136 Graphite furnace atomic absorption spectrometry quantifi

137 and total selenium in food samples by using graphite furnace atomic absorption spectrometry.

138 by comparing with those results obtained by graphite furnace atomic absorption spectrometry.

139 Applying a fast graphite furnace heating program without any chemical mo

140 Graphite furnace heating programs, effects/amounts of th

141 ation using high-resolution continuum source graphite furnace molecular absorption spectrometry (HR-C

142 ption of calcium monofluoride generated in a graphite furnace of high-resolution continuum source ato

143 A complete optimization of the graphite furnace temperature program was developed for a

144 eviously reported ((Ar)L)FeCl with potassium graphite furnished a low-spin (S = 1/2) iron complex ((A

145 )FeCl((*)N(C6H4-p-(t)Bu)) (2) with potassium graphite furnished the corresponding high-spin (S = (5)/

146 erstanding many of the unusual properties of graphite, graphene and carbon nanotubes.

147 as graphene (graphynes and graphdiynes) and graphite ("graphitynes") have long been addressed at the

148 It is well known that graphite has a low capacity for Na but a high capacity f

149 We have also demonstrated InAs-NWs/graphite heterojunction devices exhibiting rectifying be

150 xane solution onto highly oriented pyrolytic graphite (HOPG) and carbon-coated Si(100) spontaneously

151 e contamination of highly oriented pyrolytic graphite (HOPG) causes the nonideal asymmetry of paired

152 Highly oriented pyrolytic graphite (HOPG) is an important electrode material as a

153 nium (FcTMA(+)) at highly oriented pyrolytic graphite (HOPG) is used as a model system to demonstrate

154 f interest and of a highly ordered pyrolytic graphite (HOPG) reference sample, was reviewed and criti

155 erminal alkynes on highly oriented pyrolitic graphite (HOPG).

156 te (EPG), glassy carbon (GC), or high-purity graphite (HPG) electrodes.

157 eport electrochemical potassium insertion in graphite in a nonaqueous electrolyte, which can exhibit

158 easily prepared by oxidation-exfoliation of graphite in agitated solutions, the size of these sheets

159 one (H2BQ) aqueous solution as catholyte and graphite in aprotic electrolyte as anode.

160 he controlled electrochemical exfoliation of graphite in aqueous ammonium sulfate electrolyte to prod

161 the intercalation of single microcrystals of graphite in concentrated sulfuric acid.

162 dispersion and exfoliation of functionalized graphite in ethylene glycol.

163 rocess to allow the use of highly functional graphite in high-aspect-ratio nanoscale components.

164 ere deposited onto highly oriented pyrolitic graphite in order to study their hierarchy in assembly b

165 Efficient exfoliation of graphite in solutions to obtain high-quality graphene fl

166 ropic friction observed on graphene and bulk graphite in terms of adsorbates.

167 ure growth and results in single-crystal AA' graphite in the form of nanoribbons (1D) or microplates

168 CG and HCNDG were prepared by exfoliation of graphite in the presence of liquid-phase, microwave-assi

169 transition metal dichalcogenides (TMDs) and graphite in water by using protein, bovine serum albumin

170 alization of carbon materials (CNTs/graphene/graphite) in a polyphosphoric acid (PPA)/phosphorous pen

171 o PAHs differs from that into fullerenes and graphite, in which the cation sites are pre-defined by t

172 ied one >3.8-Ga zircon that contains primary graphite inclusions.

173 s of grams) comprising (1) forming a stage 1 graphite intercalation compound (GIC) in concentrated su

174 ion of what is referred to as a Hyperstage-1 graphite intercalation compound (GIC), which has a very

175 hesized via benchmark reductive routes using graphite intercalation compounds (GICs), in particular K

176 acity and to understand details of the anion-graphite intercalation mechanism.

177 The conversion of doped graphite into a C80 cage is shown to occur through botto

178 Nuclear-grade graphite is a critically important high-temperature stru

179 The basal plane cleavage energy (CE) of graphite is a key material parameter for understanding m

180 udies of C3B have suggested that boron-doped graphite is a promising H2- and Li-storage material, wit

181 bon allotropes, even amorphous carbons, into graphite is extremely hard.

182 phene sheets is driven thermodynamically, as graphite is found to act as a 2D surfactant and is sprea

183 The non-Bernal AA' allotrope of graphite is synthesized by the thermal- and plasma-treat

184 In LiBs, graphite is the most common anode material, although hig

185 Although, in the carbon family, graphite is the most thermodynamically stable allotrope,

186 bonding on the surface, or edges of natural graphite, is found using X-ray absorption spectroscopy.

187 rcalation of layered materials, particularly graphite, is fundamental to the operation of rechargeabl

188 2) for the incommensurate state of bicrystal graphite, is nearly invariant with respect to temperatur

189 , two-electron reduction of 3 with potassium graphite (KC8) afforded 1, making a fully reversible 1 <

190 bstitution of the N-atoms for C atoms in the graphite layer.

191 y influence our current understanding of how graphite, layered silicates, the MAX phases, and many ot

192 c cobalt nanoparticles encased in protective graphite layers are the dominant forms of cobalt species

193 -ions can electrochemically intercalate into graphite layers, exhibiting a high reversible discharge

194 , while micromechanical pencils (mounting 4B graphite leads, 0.5 mm in diameter) were adopted for aut

195 ically expand) more than graphite based LIB (graphite-LIB) and beyond practical limits.

196 battery has similar power characteristics of graphite-LIBs.

197 SCC-LIBs) and the potential improvement over graphite-LIBs.

198 ness occur due to the formation of different graphite-lithium intercalation compounds during cycling.

199 ofiles during galvanostatic experiments with graphite-lithium metal cells containing the electrolyte

200 dology for practical batteries with data for graphite-LMO cells after high-temperature cycling or sta

201 these requirements, were from 16% to 17% of graphite loading.

202 ene dispersion-stabilizing agents during the graphite LPE process.

203 method based on liquid-phase exfoliation of graphite (LPE) holds potential for applications in opto-

204 phorus in water samples using screen-printed graphite macroelectrodes for the first time.

205 e most promising alternatives to traditional graphite materials in lithium-ion batteries.

206 predicted with a root-mean square error for graphite (n = 13), charcoal (n = 11), Darco GAC (n = 14)

207 rein, we describe the development of a novel graphite nanocomposite-based electrochemical sensor for

208 ay, for the measurement of fructose, using a graphite-nanoparticle modified screen-printed electrode

209 + Er:YAG laser + HF, Nd:YAG laser + HF, and Graphite + Nd:YAG laser + HF.

210 electrolyte interphase surface layer at the graphite negative electrode.

211 s with lithium manganate spinel positive and graphite negative electrodes chemistry.

212 On graphite, nucleation occurs above approximately 35 degre

213 st method for electrochemical exfoliation of graphite offers great promise for the preparation of gra

214 synthesis of Si3N4 nanobelts from quartz and graphite on a graphite-felt substrate was successfully a

215 lished negative electrode references such as graphite or hard carbon.

216 e powders are prepared by the exfoliation of graphite or the reduction of graphene oxide, while graph

217 studies suggesting that the chosen method of graphite oxidation can influence the physical properties

218 electrolysis control, the microbial assisted graphite oxidation produced high rate of graphite oxide

219 ted graphite oxidation produced high rate of graphite oxide and graphene oxide (BEGO) sheets, CO2, an

220 The spin-glass behavior of graphite oxide is corroborated by the frequency dependen

221 ll results indicate that magnetic moments in graphite oxide slowly interact and develop magnetic frus

222 Graphite oxide with large lateral dimensions has an exfo

223 In graphite oxide, however, pi electrons develop ferromagne

224 are only mobile in the graphitic regions of graphite oxide, which are dispersed and surrounded by sp

225 a Pseudomonas aeruginosa biofilm on a Papyex graphite (PA) and a carbon aerogel (CA) in the presence

226 es (PDQCM) were used for the modification of graphite paste electrode (GPE) for simultaneous voltamme

227 drawn on an electroluminescent panel using a graphite pencil.

228 A graphite-potassium intercalation compound (KC8) was disp

229 egraded by sulfide (5 mM) in the presence of graphite powder (21 g/L) after 28 days at pH 7.

230 udy, laser desorption ionization (LDI) using graphite powder as the support material has been used in

231 ation of graphite rods packed with Sc2O3 and graphite powder under a helium atmosphere.

232 reactor experiments with sulfide-pretreated graphite powder were used to differentiate the involveme

233 hearii FREI-39 esterase on halloysite, using graphite powder, multi-walled carbon nanotubes and miner

234 of a Joule-heated tantalum tube filled with graphite powder.

235 mina fibers between the graphite die and the graphite punches, which are protected from the alumina f

236 ort that platinum nanoparticles supported on graphite-rich boron carbide show a 50-100% increase in a

237 In graphite, ripplocations are attracted to other ripplocat

238 In addition, P(EDOT-PdBPI-co-HKCN) modified graphite rod electrode was improved for amperometric glu

239 oot obtained by electric arc vaporization of graphite rods packed with Sc2O3 and graphite powder unde

240 Graphite's capacity of intercalating lithium in recharge

241 y of 654.3 mAh g(-1) - nearly 2x higher than graphite's theoretical value (372 mAh g(-1)).

242 Here, the authors show that experimental graphite-saturated COH fluids interacting with silicates

243 0.5 for the volatiles and solute contents of graphite-saturated fluids in the systems COH, SiO2-COH (

244 r-NH2) and Au nanoparticles (AuNPs) modified graphite screen printed electrode (GSPE) surface for the

245 BiO nanorods were cast onto mass disposable graphite screen-printed electrodes (BiO-SPEs), allowing

246 sensor based upon disposable and economical graphite screen-printed electrodes (GSPEs) is demonstrat

247 Four fullerenes- or nanotubes-modified graphite sensor-biosensor systems (SBs), coupled with a

248 Graphite shows moderate rate capability and relatively f

249 (sanding, polishing, plasma treatment), and graphite source were found to significantly impact fabri

250 e a superporous, superhydrophobic ultra-thin graphite sponge.

251 howed that for both the factors "laser" and "graphite", statistically significant differences were ob

252 The universal graphite structure is synthesized at 2,600~3,000 degrees

253 for hypothetical polybenzene (pbz) or "cubic graphite" structure, described 70 years ago.

254 slands, and the enhanced surface area of the graphite substrate facilitating HO-H cleavage followed b

255 from solid SiO2 are electrodeposited onto a graphite substrate to form a dense film of crystalline S

256 trodeposited copper nanostructures on pencil graphite substrate.

257 ith the alignment of the hBN lattice and the graphite substrate.

258 f potassium created by epitaxial growth on a graphite substrate.

259 ll nanostructures on a cost-effective pencil graphite substrate.

260 ut 0.25 eV smaller than those on graphene or graphite substrates.

261 e, TiS3 possesses lower cleavage energy than graphite, suggesting easy exfoliation for TiS3 .

262 be generated on a highly oriented pyrolitic graphite surface by combinations of a suitably designed

263 /Li and can result in lithium plating on the graphite surface, raising safety concerns.

264 alization of the phosphate near the nonpolar graphite surface.

265 nation is initiated by anodic oxidation at a graphite surface.

266 t levels of residual tensile stresses in the graphite that are 'frozen-in' following processing.

267 ing pH as the amines became ionized, even on graphite that had no significant fixed or variable charg

268 -based nanocomposite electrode (Au-rGO/MWCNT/graphite) that uses a simple electro-co-deposition appro

269 In the transition from graphene to graphite, the addition of each individual graphene layer

270 Graphite, the dominant anode in rechargeable lithium bat

271 the top-down electrochemical exfoliation of graphite, the electrochemical reduction of graphene oxid

272 ighly pristine graphene was synthesised from graphite through liquid phase sonication and then mixed

273 otassiation, whereas depotassiation recovers graphite through phase transformations in an opposite se

274 ocesses of the shock-induced transition from graphite to diamond and uniquely resolves the dynamics t

275 The shock-induced transition from graphite to diamond has been of great scientific and tec

276 ort the high-magnetic field phase diagram of graphite to exhibit just such a crossover.

277 Herein, we leverage atomistic simulations of graphite to extend the ripplocation idea to bulk layered

278 sion of pyrolytic as well as polycrystalline graphite to pressures from 19 GPa up to 228 GPa.

279 heir initial stacked morphology, as found in graphite, to a percolating network of exfoliated sheets,

280 anotubes (MWCN) increased the sensitivity of graphite toward AA and phenols 1.2, 1.5, 5.1 and 5.1 tim

281 determined at CaF wavelength, 606.440nm in a graphite tube applying a pyrolysis temperature of 1000 d

282 were directly introduced into the pyrolytic graphite tube without use of a chemical modifier, which

283 irectly grow on a continuous basis ultrathin graphite (uG) on uneven nanoscale surfaces.

284 bioelectrochemical method to produce GO from graphite under ambient conditions without chemical amend

285 hydrogen/deuterium source, the nature of the graphite (used as starting material), the potassium conc

286 curate experimental measurement of the CE of graphite using a novel method based on the self-retracti

287 lity hexagonal boron nitride (hBN) layers on graphite using high-temperature plasma-assisted molecula

288 tercalation of chloroaluminate anions in the graphite, using a non-flammable ionic liquid electrolyte

289 on of graphene atop highly ordered pyrolytic graphite, utilizing atomic-scale 'blisters' created in t

290 mplex assembled in microwells on a pyrolytic graphite wafer are housed in dual microfluidic chambers.

291 orption on a biochar and reference adsorbent graphite was conducted of triazine herbicides, substitut

292 In different sets of experiments graphite was substituted with delithiated LiFePO4 (LFP)

293 0 GPa for both pyrolytic and polycrystalline graphite, we also record the direct formation of lonsdal

294 formed carboxyl groups on the surface of the graphite were cross-linked to amino groups in the enzyme

295 Silicon, tin, and graphite were successfully prelithiated with these NPs t

296 are comparable to the experimental values of graphite, which indicates that the exfoliation of BiI3 i

297 we provide evidence for a metastable form of graphite with an AA' structure.

298 The hydrogenation and deuteration of graphite with potassium intercalation compounds as start

299 he efficiency of liquid-phase exfoliation of graphite, with the photochromic molecules acting as disp

300 tammetric cell with a bismuth citrate-loaded graphite working electrode.