ライフサイエンスコーパス: graphite

1 cle of a full electrochemical cell (LiCoO(2)/graphite).

2 a highly defective turbostratic graphite (T-graphite).

3 for quantification of organic carbon detect graphite.

4 ies, including diamagnetic materials such as graphite.

5 glucose oxidase immobilized on Pt-decorated graphite.

6 substrates such as highly ordered pyrolytic graphite.

7 ilms prepared by liquid phase exfoliation of graphite.

8 cal exfoliation of highly oriented pyrolytic graphite.

9 d with hexagonal boron nitride and few-layer graphite.

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

11 000 degrees C on a nuclear-grade Gilsocarbon graphite.

12 4) (6) and trimethylphosphine with potassium graphite.

13 arbon nanostructures in between graphene and graphite.

14 ink can be stabilized by as little as 1 wt% graphite.

15 h is clearly distinguished from turbostratic graphite.

16 conditions that promote phase transition to graphite.

17 ds of graphene oxide straightforwardly as in graphite.

18 the 1-phenyloctane/highly oriented pyrolytic graphite (1-PO/HOPG) interface.

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

20 The increased potential compared to graphite(6,7) reduces the likelihood of lithium metal pl

21 2,4,6-Ph(3)C(6)H(2))dipyrrin) with potassium graphite afforded the novel Co(I) synthon ((Ar)L)Co(I).

22 This nanostructured graphite allows fast and reversible intercalation/deinte

23 Graphite, amorphous, and ZrC(1-x) carbon signatures are

24 ith a novel conductive ink, that consists of graphite and automotive varnish mixture, deposited over

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

26 Here, we exploit the diamagnetism of graphite and demonstrate contactless magnetic positionin

27 e temperature (T(NP)) for sets of individual graphite and graphene NPs.

28 on metals(5-11), insulating surfaces(12-16), graphite and graphene(17,18) and under strong confinemen

29 This gating effect is observed in both graphite and hexagonal boron nitride channels but exhibi

30 Moreover, the inherent stability of the graphite and NFC components contributes to the strong fu

31 Graphite and other lamellar materials are used as dry lu

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

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

34 ted method with inexpensive materials (i.e., graphite and thermoplastic binder).

35 re carbon composite electrodes consisting of graphite and thermoplastic polymer binder.

36 s were ~400 times faster than those for bulk graphite, and there were large NP-to-NP variations.

37 e we show the formation of the SEI between a graphite anode and a carbonate electrolyte through combi

38 1) in 4.57 V pouch full-cells matched with a graphite anode and an ultralean electrolyte (2 g Ah(-1)

39 compatible macroporous architecture for a Si-graphite anode to maximize the volumetric energy density

40 By coupling this cathode with a passivated graphite anode, we create a 4-volt-class aqueous Li-ion

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 Plating of metallic Li on graphite anodes is a critical reason for Li-ion battery

44 Direct comparisons of the SEI grown on graphite anodes suggest that LEMC, instead of LEDC, is l

45 ple high-voltage cathodes with low-potential graphite anodes(1-4).

46 r of which doubles that of the cell based on graphite anodes.

47 ergy density in comparison with conventional graphite anodes.

48 bulk electronic states in such rhombohedral graphite are gapped(8) and, at low temperatures, electro

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

50 These analyses thereby classify graphite as either dissolved or particulate organic carb

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

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

53 We directly observed second sound in graphite at temperatures above 100 kelvins by using time

54 urrent lithium-ion batteries, however, adopt graphite-based anodes with low tap density and gravimetr

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

56 Here we design a nacre-mimetic graphite-based nanofluidic structure in which the nanome

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

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

59 echargeable LMBs has been revived to replace graphite-based, Li-ion batteries because of the much hig

60 , we demonstrate the holistic design of dual-graphite batteries, which circumvent the sluggish ion-de

61 h the low-cost, high-voltage chemistry of Zn/graphite batteries.

62 c configuration in monolayer VSe(2) grown on graphite by molecular-beam epitaxy.

63 The employed L effectively formed graphite C-encapsulated metal NPs after heat treatment.

64 Graphite calorimetry, the UK primary standard, has been

65 Our results prove that micrometer-sized graphite can be magnetically manipulated in liquid media

66 dulating the charge distribution of numerous graphite carbon materials to impart new properties to ca

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

68 pha-MoO(3) anode with an anion-intercalation graphite cathode, operating well over a wide discharge r

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

70 The dual-graphite cells, when compared to industry-type graphite

71 this on LiNi(0.8)Mn(0.1)Co(0.1)O(2) (NMC811)/graphite cells, which are typical high-energy LIBs.

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

73 equency (lambda = 1,064 nm) to ablate Ag and graphite composite target submerged in ethylene glycol (

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

75 ity (sigma(e) <= 10(-9) S/cm), even when the graphite concentration is up to 50 wt %, well above the

76 At these graphite-conjugated catalysts (GCCs) bearing organic aci

77 ish that hydrogen evolution catalysis at the graphite-conjugated Rh molecule proceeds without first r

78 vering, a nonfilling porous structure, and a graphite core.

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

80 trodes composed of covalently functionalized graphite, decorated with various functional affinity and

81 eversible insertion of Mg-Cl superhalides in graphite delivers a record-high reversible capacity of 1

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

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

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

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

86 The insertion of Mg-Cl superhalides in graphite does not form staged graphite intercalation com

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

88 tes by 0.45 V and enable the operation of Zn/graphite dual-ion cells at 2.80 V with a long cycle life

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

90 e explained by catalyzed transformation from graphite during an impact shock event characterized by p

91 t of metallic Fe-Ni-C liquid coexisting with graphite during this shock event.

92 We find that SEI formation starts at graphite edge sites with dimerization of solvated Li(+)

93 onjugating organic acid functional groups to graphite edges though aromatic phenazine linkages.

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

95 /poly-L-methionine-gold nanoparticles/pencil graphite electrode (DNA/PMET-AuNPs/PGE).

96 ltammetric method using edge plane pyrolytic graphite electrode (EPPGE) as a novel sensor is presente

97 are a low-cost and binder free MoS(2)-pencil graphite electrode (i.e., MoS(2)-PGE) for the electroche

98 Cu) and poly xylenol orange modified pencil graphite electrode (p-XO/PGE) were used as working elect

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

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

101 sentative measurements were carried out on a graphite electrode cycled with LiI-incorporated sulfide-

102 droplets immobilized on paraffin impregnated graphite electrode in 0.1 mol dm(-3) HClO(4) and KNO(3)

103 al activation of a 2D-Co-MOF@Nafion-modified graphite electrode in aqueous solution improves the ioni

104 these (nonoxidized) cutting agents onto the graphite electrode surface.

105 Herein, the pencil graphite electrode was initially spin coated with D-Seri

106 of electrodes (carbon nanotube electrode and graphite electrode) was combined with chemometric method

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

108 n behaviour of choloraluminate anions in the graphite electrode.

109 (2) reduction when adsorbed onto a pyrolytic graphite electrode.

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

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

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

113 acetonitrile) solutions by employing common graphite electrodes and a simple controlled current prot

114 square wave voltammetry measurements at bare graphite electrodes at pH 7.0 and pH 12.0, in order to e

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

116 odified electrode with other modified pencil graphite electrodes like single layered acrylamide funct

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

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

119 The screen-printed carbon graphite electrodes were made reusable through an ethano

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

121 edox reactions of polysulfide/iodide ions on graphite electrodes, which has become the main obstacle

122 icate graphene and highly oriented pyrolytic graphite electrodes.

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

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

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

126 he quantum Hall effect, whereby rhombohedral graphite exhibits phase transitions between a gapless se

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

128 The afforded graphite features high crystallinity, a high degree of g

129 d, a modular electro-flow cell with a porous graphite felt anode was designed to ensure efficient tur

130 stribution, which are synthesized in situ on graphite felt by a one-step solvothermal process, can si

131 The use of graphite felt for both the cathode and the anode was key

132 allowed us to make high-quality rhombohedral graphite films up to 50 graphene layers thick and study

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

134 uidic structure in which the nanometer-thick graphite flakes are wrapped by negatively charged nanofi

135 exfoliated mica and highly ordered pyrolytic graphite flakes used as reference substrates.

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

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

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

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

140 ped method combining microwave digestion and graphite furnace AAS.

141 impurities in edible-oils were determined by graphite furnace atomic absorption spectrometer (GFAAS)

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

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

144 horesis (2D-PAGE) for protein fractionation, graphite furnace atomic absorption spectrometry (GFAAS)

145 trations in protein spots were determined by graphite furnace atomic absorption spectrometry (GFAAS).

146 samples by high-resolution continuum source graphite furnace atomic absorption spectrometry (HR-CS G

147 milk using high-resolution continuum source graphite furnace atomic absorption spectrometry (HR-CS G

148 mples using high-resolution continuum source Graphite Furnace Atomic Absorption Spectrometry (HR-CS-G

149 Spectrometry (HR-CS-GF-AAS) and line source Graphite Furnace Atomic Absorption Spectrometry (LS-GF-A

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

151 lakes using high-resolution continuum source graphite furnace atomic absorption spectrometry is prese

152 Graphite furnace atomic absorption spectrometry quantifi

153 isted acid digestion and transversely heated graphite furnace atomic absorption spectrometry to measu

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

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

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

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

158 Sample digest is introduced into the graphite furnace together with Pd/Mg(NO(3))(2) modifier.

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

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

161 rrent before anions can be inserted into the graphite gallery.

162 Graphite has become a critical material because of its h

163 e-step green synthesis of GQDs directly from graphite has been developed.

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

165 Of the two stable forms of graphite, hexagonal and rhombohedral, the former is more

166 In pouch cells paired with graphite, high-Ni NMA outperforms both NMC and NCA and o

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

168 en imaged at "aged" highly ordered pyrolytic graphite (HOPG), where apparently enhanced electrochemic

169 ovalently modified highly-oriented pyrolytic graphite (HOPG).

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

171 Oxidative anion insertion into graphite in an aqueous environment represents a signific

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

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

174 lly biocompatible transport for lipid-coated graphite in NaCl aqueous solution, paving the way for pr

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

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

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

178 x)Cu(2)(mu(2)-N(C(6)H(4)OMe)) with potassium graphite initiates an intramolecular, benzylic C-H amina

179 as used as a bulk-modifier of the conductive graphite ink constituting the working electrode, allowin

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

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

182 pecific capacity to a densely packed stage-I graphite intercalation compound, C(3.5)[Br(0.5)Cl(0.5)],

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

184 uperhalides in graphite does not form staged graphite intercalation compounds; instead, the insertion

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

186 Li plating is caused by the slow kinetics of graphite intercalation, but in this paper, we demonstrat

187 te potential retention of D by the boronized graphite interface and correlated back to the surface ch

188 stalline polymorphs (5 degrees ) at solution-graphite interfaces.

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

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

191 Graphite is an inexpensive material with useful electric

192 a mixture of the individual metal oxides and graphite is deoxidised in a melt of CaCl(2) at a tempera

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

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

195 Expanded graphite is gently exfoliated creating "defect-free" gra

196 However, submerged graphite is not known to be amenable to magnetic manipul

197 Moreover, Li metal deposition on graphite is observed at low temperature, which is an imp

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

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

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

201 ing texture pseudomorphing inferred original graphite laths.

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

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

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

205 tion of solvated Li(+) intercalation between graphite layers.

206 NTs) can be doped with potassium, similar to graphite, leading to intercalation compounds.

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

208 Here, a lithium-graphite (Li-C) composite anode is fabricated, which sho

209 battery has similar power characteristics of graphite-LIBs.

210 aphite cells, when compared to industry-type graphite LiCoO(2) full-cells demonstrated an 11 times in

211 raphitic carbon nitride (g-C(3)N(4)) made of graphite-like covalent link connects nitrogen, nitride,

212 ssy carbon to structural transformation from graphite-like sp(2)-bonded structure to diamond-like sp(

213 ly indicate that the glassy carbon maintains graphite-like structure up to 49.0 GPa.

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

215 eoretical model for magnetic manipulation of graphite microflakes and demonstrate experimentally magn

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

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

218 is demonstrated to afford highly crystalline graphite nanosheets at ambient temperature.

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

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

221 By tuning the hydration degree of graphite-NFC composites, the surface-charge-governed ion

222 At the same time, the graphite-NFC structure exhibits an ultralow electrical c

223 On graphite, nucleation occurs above approximately 35 degre

224 qualitatively valid for weakly hydrophilic (graphite) ones.

225 agnetism in single layers of VSe(2) grown on graphite or MoS(2) substrate has opened new opportunitie

226 probes, it is possible to select a specific graphite or polymer type for the analyte of interest.

227 onventional solid lubricants such as MoS(2), graphite, or diamond-like carbon films demonstrate excel

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

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

230 In graphite oxide, however, pi electrons develop ferromagne

231 construction of a biosensor device based on graphite oxide, platinum nanoparticles and biomaterials

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

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

234 he insertion of Mg-Cl superhalides makes the graphite partially turbostratic.

235 try; the coating of the covalently bonded BP-graphite particles with electrolyte-swollen polyaniline

236 ent field are a source for (sub)micron-sized graphite particles.

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

238 Among these devices, pencil-drawn graphite patterns (or combined with other compounds) ser

239 drawn on an electroluminescent panel using a graphite pencil.

240 difying the surface of the disposable pencil graphite (PGE) with physical adsorption to perform a sim

241 l modeling predicts a direct liquid to solid graphite phase transition for DNTF products ~200 ns post

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

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

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

245 -C(5) (i) Pr(5) )(2) UI] (1) with potassium graphite produces the "second-generation" uranocene [(et

246 s study could be a promising alternative for graphite production.

247 MD) simulations suggest that the defective T-graphite provide numerous nucleation sites for the nanop

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

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

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

251 Graphite's capacity of intercalating lithium in recharge

252 tu to elucidate surface evolution of a cored graphite sample with an intrinsic concentration of boron

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

254 0.5 for the volatiles and solute contents of graphite-saturated fluids in the systems COH, SiO2-COH (

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

256 adsorption experiments were performed on the graphite screen printed electrodes both with and without

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

258 The edge plane pyrolytic graphite sensing platform is recommended as a potential

259 We use a commercial thermal graphite sheet and a mesoporous carbon scaffold to encap

260 he electrolyte-facing surface of the sealing graphite sheet, which cathodically shifts the onset pote

261 stalline layer (denoted as RZx) on pyrolytic graphite sheets (PGS), which was then utilized as the se

262 e this mechanism, the catalyst was coated to graphite sheets and a galvanic oxidation process (GOP) w

263 vior in transition metal dichalcogenides and graphite/SiO(x) heterostructures beyond the widely accep

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

265 d by an interfacial trapping method in which graphite spontaneously exfoliates to graphene.

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

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

268 This interaction between nanoparticles and T-graphite substrate strengthens the anchoring and provide

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

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

271 trodeposited copper nanostructures on pencil graphite substrate.

272 grow high-quality monolayer boron nitride on graphite substrates.

273 competitive reactions between the lithiated graphite surface and the Li(2)O formation caused by the

274 f cyclic porphyrin polymers, nanorings, on a graphite surface, that flexible molecules can exhibit a

275 alization of the phosphate near the nonpolar graphite surface.

276 tinuous conjugation between the acid and the graphite surface.

277 nonbiological macrocycles, in this case, at graphite surfaces.

278 us carbon to a highly defective turbostratic graphite (T-graphite).

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

280 alogen conversion-intercalation chemistry in graphite that produces composite electrodes with a capac

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

282 Moreover, in rhombohedral graphite thinner than four nanometres, a gap is present

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

284 c coupling between the GCC acid site and the graphite to enable interfacial field-driven PCET at the

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

286 Although chemical oxidation of graphite to graphene oxide promotes exfoliation, it requ

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

288 n Staudenmaier's method for the oxidation of graphite, to produce both epoxy and hydroxy groups on th

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

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

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

292 hich is a layered bulk material analogous to graphite, was derived from its 3D phase, Ti3AlC2 MAX.

293 The ink formulation contains only pristine graphite, water, and non-toxic alkanes formed by an inte

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

295 This method is demonstrated in graphite, where we investigate the dynamics of photoinje

296 produced by a top-down approach, exfoliating graphite, which often requires large amounts of solvent

297 electrodes of carbon-nanotube@silicon@carbon-graphite with a practical loading (3 mAh cm(-2)) deliver

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

299 trochemical cell (SPC) based on iron-sparked graphite working electrode modified with glucose oxidase

300 ical reduction of ((Tr)L)CoCl with potassium graphite yielded the high-spin (S = 1) Co(I) synthon ((T