ライフサイエンスコーパス: Au

1 Au protuberances growth on the surface of Au@Pt NPs allo

2 Au(191) has an anisotropic, singly twinned structure wit

3 Au@Rh-ICG-CM shows good biocompatibility, high tumor acc

4 the two-coordinate cation, [(C(6)H(11)NC)(2)Au](+).

5 6)H(11)NC)(2)Au](PF(6)) and [(C(6)H(11)NC)(2)Au](AsF(6)) contain single chains of cations and are vap

6 6))(0.50)(SbF(6))(0.50) and [(C(6)H(11)NC)(2)Au](AsF(6))(0.50)(SbF(6))(0.50) are not.

7 6)H(11)NC)(2)Au](PF(6)) and [(C(6)H(11)NC)(2)Au](AsF(6)).

8 as the yellow polymorphs of [(C(6)H(11)NC)(2)Au](PF(6)) and [(C(6)H(11)NC)(2)Au](AsF(6)) contain sing

9 aining equimolar amounts of [(C(6)H(11)NC)(2)Au](PF(6)) and [(C(6)H(11)NC)(2)Au](AsF(6)).

10 hereas neither polymorph of [(C(6)H(11)NC)(2)Au](PF(6)) nor [(C(6)H(11)NC)(2)Au](SbF(6)) is thermochr

11 ))(0.50)(AsF(6))(0.50), and [(C(6)H(11)NC)(2)Au](PF(6))(0.25)(AsF(6))(0.75) are vapochromic, whereas

12 Mixed crystals such as [(C(6)H(11)NC)(2)Au](PF(6))(0.50)(AsF(6))(0.50) have been prepared by add

13 PF(6))(0.75)(AsF(6))(0.25), [(C(6)H(11)NC)(2)Au](PF(6))(0.50)(AsF(6))(0.50), and [(C(6)H(11)NC)(2)Au]

14 reas the yellow crystals of [(C(6)H(11)NC)(2)Au](PF(6))(0.50)(SbF(6))(0.50) and [(C(6)H(11)NC)(2)Au](

15 the colorless mixed crystal [(C(6)H(11)NC)(2)Au](PF(6))(0.50)(SbF(6))(0.50) is thermochromic and conv

16 The yellow crystals of [(C(6)H(11)NC)(2)Au](PF(6))(0.75)(AsF(6))(0.25), [(C(6)H(11)NC)(2)Au](PF(

17 sform a crystal of the type [(C(6)H(11)NC)(2)Au](PF(6))(n)(AsF(6))(1-n) from colorless (blue-emitting

18 and are vapochromic, yellow [(C(6)H(11)NC)(2)Au](SbF(6)) does not form the same polymorph and is not

19 6)H(11)NC)(2)Au](PF(6)) nor [(C(6)H(11)NC)(2)Au](SbF(6)) is thermochromic, the colorless mixed crysta

20 g the effects of the concentrations of H(2), Au-Pd NPs, and resazurin on the color change response ti

21 nduced H(2) dissociation using a simple H(2)@Au(6) model.

22 66 surface atoms, arranged as [Au(3)@Au(23)@Au(63)]@Au(66) concentric shells of atoms.

23 We show that annealing 2DC/Au films on SiO(2) results in a reverse epitaxial proces

24 ick reactions between Au(I) acetylides PPh(3)Au-C=CR, where R = nitrophenyl (PhNO(2)), phenyl (Ph), t

25 ore and 66 surface atoms, arranged as [Au(3)@Au(23)@Au(63)]@Au(66) concentric shells of atoms.

26 doamine) (PAMAM) dendrimer nanocomposite (3D-Au-PAMAM) covalently immobilized onto electrografted p-a

27 raldehyde (GA) on the amino groups of the 3D-Au-PAMAM-p-ABA-SPCE, where tau protein was sandwiched wi

28 ace atoms, arranged as [Au(3)@Au(23)@Au(63)]@Au(66) concentric shells of atoms.

29 l crater (0.6 mum x 130 nm ) morphology in a Au-coated glass target and carbon-coated silica wafer wa

30 es to Me-DalphosAu(+) for the formation of a Au(III) -Ar intermediate.

31 to obtain Au L-edge subtraction imaging of a Au-Ni grid test sample.

32 The networks are formed on a Au(111) surface through coadsorption of cyclic dialanine

33 ity of the achiral molecule to assemble on a Au(111) surface to a highly ordered layer composed of en

34 tures of 2D bilayer hexagonal ice grown on a Au(111) surface.

35 we report a rationally designed redox-active Au(I) bis-N-heterocyclic carbene that induces ICD both i

36 acile preparation of asymmetric redox-active Au(I) bis-N-heterocyclic carbenes.

37 The adsorbed Au produced a SP-ICP-MS signal allowing the counting of

38 Metal-catalyzed (Cu, Ag, Au) reactions of alkynylphosphonates with 1-(2-aminophen

39 ns that the AMX (A = Ca, Sr, Ba; M = Cu, Ag, Au; X = P, As, Sb) compounds consisting of MX honeycomb

40 -induced emission gold clustoluminogens (AIE-Au) to achieve efficient low-dose X-ray-induced photodyn

41 Under low-dose X-ray irradiation, AIE-Au strongly absorbed X-rays and efficiently generated hy

42 nd in vivo experiments demonstrated that AIE-Au effectively triggered the generation of reactive oxyg

43 sibly and stereospecifically to give alkenyl-Au(III) complexes.

44 Here, an Au metal patch electrode capacitive sensor is introduced

45 ctively controlling oxidative addition on an Au surface using an applied bias.

46 ubstantial deformation upon deposition on an Au(111) surface, as demonstrated by its pristine form in

47 nisotropic, singly twinned structure with an Au(155) core protected by a ligand shell made of 24 mono

48 (biTh), and dimethyl aniline (PhNMe(2)), and Au(I)-azide PPh(3)AuN(3) provide digold complexes of the

49 stoichiometry between alpha-cyclodextrin and Au(CN)(2)(-) is favored in the presence of ethanol.

50 i), Cu(i), Ni(ii), Fe(0), Zn(ii), Ag(i), and Au(i/iii) metal based precursors.

51 2) as sensing material over SiO(2) layer and Au as a metal electrode.

52 yer was formed between them through Au-N and Au-S bond which reduced IFE of AuNPs.

53 om Au alone exhibit low-index facets, Pt and Au form PtAu heterostructured nanoparticles with high-in

54 olayers (SAMs) of the wires in Au-SAM-Pt and Au-SAM-graphene junctions, from which the conductance pe

55 arying the relative amounts of resazurin and Au-Pd NPs in solution.

56 rostructured, multimetallic (Pt, Pd, Rh, and Au) tetrahexahedral nanoparticles was synthesized throug

57 arcodes and as ligand-free nano-segments and Au segments for ligand coating while maintaining both na

58 ttky) junctions formed between n-type Si and Au nanoparticles as light-addressable electrochemical se

59 and injectable DNA-mediated upconversion and Au nanoparticle hybrid (DNA-UCNP-Au) hydrogel is develop

60 o gold/lead clusters, [Au(8)Pb(33)](6-) and [Au(12)Pb(44)](8-), both of which contain nido [Au@Pb(11)

61 y large, nonreactive building blocks such as Au colloids.

62 it for metal-coordination complexes, such as Au(CN)(2)(-) and Ag(CN)(2)(-) with linear geometries, wh

63 nner core and 66 surface atoms, arranged as [Au(3)@Au(23)@Au(63)]@Au(66) concentric shells of atoms.

64 When compared to bare self-assembled Au chip which was shown to exhibit a limit of detection

65 electrode is 4.3 times greater than the bare Au electrode.

66 s barcoding system, including ligand-bearing Au and ligand-free Fe nano-segments, is developed to ind

67 iClick reactions between Au(I) acetylides PPh(3)Au-C=CR, where R = nitrophenyl (P

68 Moreover, the synergy between Au and Pt metals on the NP surface also lead to an incre

69 We show that biicosahedral [Au(13)Ag(12)(PPh(3))(10)Cl(8)]SbF(6) nanoclusters compos

70 d morphology modification of the SnSe NSs by Au deposition.

71 de of SAMs of n-alkanethiolates supported by Au were characterized with both dc and ac techniques, re

72 ed inner core structure of the ligand capped Au(191) nanomolecule provides the critical missing link,

73 A series of (carbene)Au((I))(aryl) complexes are reported.

74 s creates a bimetal single cluster catalyst (Au(4)Pt(2)/G) with exceptional activity for electrochemi

75 amolecular relationship between the cationic Au(I) center and the phosphate counterion.

76 te an efficient deposition of singly charged Au(144) (SC(4) H(9) )(60) ions (33.7 kDa), which opens u

77 rt the synthesis of two gold/lead clusters, [Au(8)Pb(33)](6-) and [Au(12)Pb(44)](8-), both of which c

78 edral Au(7)Ag(6) units by sharing one common Au vertex can produce two temperature-responsive conform

79 In contrast, Au accumulated on/in the macrophytes where it oxidized a

80 duced the first examples of a low-coordinate Au(III) center with two cis accessible coordination site

81 Employing Pt(111) supported 2D Pt-core Au-shell model catalysts, we demonstrate that 2D core-sh

82 ous reports of both dative Au-I and covalent Au-C contacts.

83 ct has a lower conductance than the covalent Au-C interaction, which we propose occurs via an in situ

84 hange barriers separate Cu adatoms from a Cu-Au mixture, leaving behind a fluid phase enriched with A

85 point, with ambiguous reports of both dative Au-I and covalent Au-C contacts.

86 odine and thiomethyl to show that the dative Au-I contact has a lower conductance than the covalent A

87 me WSe(2) flake using conventional deposited Au contacts with pronounced n-type characteristics.

88 on ASV is 17.8 +/- 0.6% for 4.1 nm diameter Au NPs, 87.2 +/- 2.9% for 1.6 nm Au NPs, and an unpreced

89 ing replacement with 4.1 and 1.6 nm diameter Au NPs, respectively, consistent with qualitative change

90 precedented full 100% Ag for 0.9 nm diameter Au NPs.

91 fferences in surface reactivity of different Au sites in the DFT model.

92 eling revealed that nonuniformly distributed Au nanoparticles suffer from local depletion of surface

93 )), giving rise to a two-shelled M(54) (i.e. Au(52)Cu(2)) full decahedron.

94 s coated successfully on the gold electrode (Au).

95 yst consisting of partially ligand-enveloped Au(4)Pt(2) clusters supported on defective graphene.

96 e shift in the standard potential (E(0)) for Au oxidation with decreasing NP size.

97 It is discovered that at the defect-free Au/TiO(2) interface electrons transfer from Ti(3+) speci

98 Although nanoparticles formed from Au alone exhibit low-index facets, Pt and Au form PtAu h

99 ecutive and pH-dependent transformation from Au(22) to both well-defined clusters and small Au(I)SR s

100 atom triggers the structural transition from Au(22) with a 10-atom bioctahedral kernel to Au(22)Cd(1)

101 noparticles of different compositions (e.g., Au and quantum dots) and shapes (e.g., spheres and rods)

102 Homogeneous gold (Au) complexes have demonstrated tremendous utility in mo

103 obase adenine (ADN) in the presence of gold (Au) and iron (Fe) nanoparticles (NPs).

104 e salt-induced aggregation kinetics of gold (Au) and silver (Ag) nanoparticles (NPs) at the prism int

105 phobic quasi-spherical and star-shaped gold (Au)NPs are synthesized to explore the antibacterial mech

106 n be utilized to form both heterobimetallic (Au(I)(-)/Ag(I)(+); Au(I)(-)/Ir(I)(+)) and organometallic

107 0 nm length and ~15 nm wall thickness hollow Au-Ag nanoboxes with smooth and rough surfaces.

108 M(54) decahedron with the truncated homogold Au(49) kernel in similar-sized gold nanoparticles provid

109 then enclosed by a second shell of homogold (Au(47)), giving rise to a two-shelled M(54) (i.e. Au(52)

110 rm both heterobimetallic (Au(I)(-)/Ag(I)(+); Au(I)(-)/Ir(I)(+)) and organometallic/main group ion pai

111 f the F(n)ArH, followed by selective Au((I))/Au((III))-catalyzed coupling with electron-poor or -rich

112 (6) nanoclusters composed of two icosahedral Au(7)Ag(6) units by sharing one common Au vertex can pro

113 The approach involves the Fe(II)/Au(I)-catalyzed rearrangement of key 4-propargylisoxazol

114 ly consistent cyclic voltammetric signals in Au surface cleaning experiments and detecting benchmark

115 -assembled monolayers (SAMs) of the wires in Au-SAM-Pt and Au-SAM-graphene junctions, from which the

116 odegradation compared to the other indicator/Au-Pd NP systems tested, (2) the observed redox chemistr

117 The individual Au microelectrodes are further selectively functionalize

118 electrons transfer from Ti(3+) species into Au nanoparticles (NPs) and further migrate into adsorbed

119 vesicles were disassembled into small Janus Au-MnO nanoparticles (NPs) with promoted penetration abi

120 es))-based immunoassay coupled to thin layer Au-based electrochemical microfluidics operating at -0.2

121 nohydride protected by diphosphine ligands, [Au(22) H(4) (dppo)(6) ](2+) [dppo=1,8-bis(diphenylphosph

122 he inner 7-atom decahedral kernel (M(7), M = Au/Cu).

123 ed glassy carbon electrode (MNP/CNT/GCE, M = Au or Cu) and poly xylenol orange modified pencil graphi

124 onjunction with different capping materials (Au, Pt, and SiO(2)) and fuels (H(2)O(2) and alcohols).

125 ting nanoplastics with functionalized metal (Au)-containing nanoparticles (NPs), thus making them det

126 ranging from 1 to 50 nM, the AuNPs modified Au chip was proven to clearly be a better analytical too

127 ngle-component MOF superlattices, binary MOF-Au single crystals, and two-dimensional MOF nanorod asse

128 The released MTX accelerated destroying MUA-Au NCs through inducing the generation of hROS.

129 ffibody sealed methotrexate (MTX)-loaded MUA-Au NCs through charge effect, as well as leaving the res

130 ecanoic acid-modified gold nanoclusters (MUA-Au NCs) for tumor-targeted drug delivery.

131 hout a partnering gold ion only a distinct N-Au-P bending occurs, revealing a potential mechanism for

132 , from a pre-existing amorphous nanocluster (Au) or by coalescence of two separate amorphous sub-nano

133 violet (CV) and thiolated gold nanocluster ([Au(25)(Cys)(18)]) activated at a low flux levels of whit

134 xial process where initially nanocrystalline Au films gain texture, crystallographically orient with

135 eport the discovery of a Janus nanomolecule, Au(191)(SPh-tBu)(66) having both molecular and metallic

136 (Au NRs), and gold spherical nanoparticles (Au SNPs).

137 nanostructures, gold triangular nanoprisms (Au TNPs), gold nanorods (Au NRs), and gold spherical nan

138 angular nanoprisms (Au TNPs), gold nanorods (Au NRs), and gold spherical nanoparticles (Au SNPs).

139 Gold "Janus" nanorods (Au JNRs), partially coated with silica to enhance their

140 ttering enhancement on chiral nanostructured Au films (CNAFs) equipped in the normal Raman scattering

141 and biphasic Rh-based core-shell nanosystem (Au@Rh-ICG-CM) is developed to address tumor hypoxia whil

142 hotothermal effect into a single nanosystem, Au@Rh-ICG-CM can readily serve as a promising nanoplatfo

143 hly-oriented [Formula: see text] nanotwinned Au films could be an ideal material in many gold product

144 The resilience of the NHC-Au bond allows for multi-step post-synthetic modificatio

145 (12)Pb(44)](8-), both of which contain nido [Au@Pb(11)](3-) icosahedra surrounding a core of Au atoms

146 As a model system, 10.9 +/- 1.0 nm Au NPs were analyzed to demonstrate the effects of incre

147 tion of microscopic arrays composed of 50 nm Au nanoparticles situated underneath a graphene interfac

148 nm diameter Au NPs, 87.2 +/- 2.9% for 1.6 nm Au NPs, and an unprecedented full 100% Ag for 0.9 nm dia

149 the hue (color) value of thousands of 67 nm Au nanoparticles immobilized on a glass coverslip surfac

150 The proposed method is applied to obtain Au L-edge subtraction imaging of a Au-Ni grid test sampl

151 linewidths as narrow as 4 nm from arrays of Au, Ag, Al, and Cu NPs.

152 ssfully loaded and retained in the cavity of Au@Rh-CM.

153 A comparison of Au-thiolate NCs with Au-phosphine ones further reveals t

154 ) to create organometallic -ate complexes of Au(I) that serve both as WCAs and functional catalysts.

155 rated that a plasmonic thin film composed of Au nanoparticles embedded in a CuO matrix can be used to

156 ng an optical cavity substrate consisting of Au/Al(2) O(3) to enhance its absorption near the bandgap

157 Pb(11)](3-) icosahedra surrounding a core of Au atoms.

158 fically, we demonstrate thermal dewetting of Au ultrathin metal films and growth of MoS(2) on NaCl at

159 ansformation upon a 10 dpa radiation dose of Au(4+) ions.

160 As noted, the mild photothermal effect of Au@Rh-ICG-CM also improves PDT efficacy.

161 red-shifting of the fluorescence emission of Au nanoclusters (AuNCs) into NIR-II region with improved

162 able the site-selective oxidative etching of Au(0), which leads to nonuniform growths along different

163 ontributed to the morphological evolution of Au-Ag nanocrystals synthesized with different DNA sequen

164 rimeter O(2) molecules (i.e., in the form of Au-O-O-Ti), facilitating O(2) activation and leading to

165 method based on core-satellite formation of Au nanoparticles was introduced for the detection of int

166 ying low-energy van der Waals integration of Au electrodes, we observed robust and optimized p-type t

167 including domains that are primarily made of Au.

168 better understand the molecular mechanism of Au-carbene binding to G-quadruplexes, we employed molecu

169 e support on directing the nanostructures of Au-based monometallic and bimetallic nanoparticles.

170 of each system with H(2) in the presence of Au-Pd NPs caused visual and irreversible color changes t

171 d in relation to the catalytic properties of Au-based monometallic and bimetallic nanoparticles using

172 tical signal, allowing the quantification of Au@Pt/Au NPs at 10(13) NPs/mL levels.

173 edge-selective to layer-by-layer removal of Au atoms as the reaction progresses.

174 triguingly, we show that the ligand shell of Au(25) nanoclusters becomes more fragile and rigid after

175 te nanoparticles, the Cu-thiolate surface of Au(52)Cu(72) forms an extended cage.

176 Au protuberances growth on the surface of Au@Pt NPs allowed their easy bioconjugation with antibod

177 se results highlight the untapped utility of Au catalysis in providing access to new macromolecular c

178 namics simulations to study the behavior of [Au(CH(3))(2))](-) in bulk and interfacial aqueous enviro

179 es of key hydrogen-bonded configurations of [Au(CH(3))(2))](-), combined distribution functions, and

180 However, encapsulation of [Au(25)(Cys)(18)] and CV into the polymer activates poten

181 nism shows that additional encapsulation of [Au(25)(Cys)(18)] into the CV treated polymer promotes re

182 reaction can be reversed by CO reduction of [Au(25)SR(19)](0), leading back to [Au(25)SR(18)](-) and

183 e in a prototypical system: CO adsorption on Au(111).

184 onolayer (SAM) and the influence of AuNPs on Au chip for Aflatoxin B(1) (AFB(1)) detection using SPRi

185 ingle-step aptasensor was developed based on Au nanocap-supported UCNPs (Au/UCNPs), which were partia

186 0'-(2,6-dimethylphenyl)-9,9'-bianthracene on Au(111) have been investigated by scanning tunneling mic

187 ion of a well-defined graphene-like t-COF on Au(111).

188 picture of photoinduced H(2) dissociation on Au clusters, which has important implications in plasmon

189 input from UV photoemission measurements on Au-protein systems, these striking differences in conduc

190 a brominated polycyclic aromatic molecule on Au(111) and demonstrate that standard STM measurements c

191 covalent C-N bonds in tetraazateranthene on Au(111) and Ag(111) surfaces.

192 y more stable than the traditional thiols on Au system.

193 cated [Formula: see text] preferred-oriented Au thin films by DC plating at 5 mA/cm(2).

194 coordination sphere is closest to the other Au electrode, with which only physical contact is made.

195 Our Au TNPs, NRs, and SNPs display refractive index unit (RI

196 Arrhenius studies during H(2) oxidation over Au/TiO(2) catalysts, we found different apparent activat

197 +)) and organometallic/main group ion pairs (Au(I)(-)/(CPh(3)(+) or SiEt(3)(+)).

198 onductor NWs capped with metallic particles (Au, Ag, Co, Ni).

199 In this work, we designed and fabricated Pd/Au bimetallic thin film electrodes with isolated Pd nano

200 faces affect the nature and reactivity of Pd/Au surface electrochemistry including the adsorbed/absor

201 The Pd/Au electrode was characterized by AFM and XPS as well as

202 2)O(2) and 3-nitrotyrosine (3-NT)) at the Pd/Au thin film surfaces affect the nature and reactivity o

203 ct on the electrode probe-functionalized PDA-Au@SPCE.

204 The electrode modifier, PDA-Au, provided a functionalizable interface for the sensit

205 The PDA-Au composite was synthesized in a alkaline condition whe

206 erent lateral directions to form six-pointed Au nanostars.

207 Such porous Au@Rh core-shell nanostructures are expected to exhibit

208 o demonstrated the robustness of the present Au/SnSe NHS.

209 tween electrodes in a solid-state Au-protein-Au junction, have an orientation opposite that of WT Az

210 and rare-Earth metal ions (e.g. Ru, Ir, Pt, Au, Eu) in these applications by abundant ions are outli

211 signal, allowing the quantification of Au@Pt/Au NPs at 10(13) NPs/mL levels.

212 ry were used for the evaluation of the Au@Pt/Au NPs electrocatalytic activity toward WOR.

213 e platinum/gold core-shell nanoparticles (Pt@Au NPs) as a signal probe, and a smartphone was develope

214 For the first time, bis(pyridine)Au(I) complexes are shown to be catalytically active, wi

215 n-nitrogen distance, bidentate bis(pyridine)-Au(III) complexes convert into dimers.

216 HI) to interrogate single, high aspect ratio Au nanowires (NWs).

217 ed vdW interaction between the reconstructed Au(4)S(4) interfacial phase and TMD monolayers results i

218 or change response time within the resazurin/Au-Pd NP system revealed that the H(2)-sensing elements

219 The resazurin/Au-Pd NP system was deemed best-suited for our research

220 Here we report an atomically resolved [Au(52)Cu(72)(p-MBT)(55)](+)Cl(-) nanoalloy (p-MBT = SPh-

221 The Fe/RGD-Au nanobarcode implants exhibit high stability and no lo

222 than that on the oxygen vacancy (V(o))-rich Au/TiO(2) interface, at which electrons from Ti(3+) spec

223 monomeric [-S-Au-S-] and 6 dimeric [-S-Au-S-Au-S-] staples.

224 of 24 monomeric [-S-Au-S-] and 6 dimeric [-S-Au-S-Au-S-] staples.

225 d by a ligand shell made of 24 monomeric [-S-Au-S-] and 6 dimeric [-S-Au-S-Au-S-] staples.

226 ionalized lipoic acid AuNPs deposited on SAM Au chips followed by in situ activation of functional gr

227 The SAM Au chip was sequentially modified by EDC-NHS crosslinker

228 polung of the F(n)ArH, followed by selective Au((I))/Au((III))-catalyzed coupling with electron-poor

229 o demonstrate this concept, we prepared n-Si/Au nanoparticle Schottky junctions by electrodeposition

230 ntational mobility was observed for a single Au-carbene binding at the second G-quadruplex surface.

231 In hydrazine oxidation by single Au nanoparticles, digital filtering does not complicate

232 lity of this method by producing single-site Au, Pd, Ru and Pt catalysts supported on carbon in a fac

233 Single-site Au/C catalysts have previously been validated commercial

234 (22) to both well-defined clusters and small Au(I)SR species was identified by ESI-MS and UV-vis spec

235 degradation simultaneously released smaller Au NPs as numerous cavitation nucleation sites and Mn(2+

236 sitioned between electrodes in a solid-state Au-protein-Au junction, have an orientation opposite tha

237 Organothiol monolayers on metal substrates (Au, Ag, Cu) and their use in a wide variety of applicati

238 into allylic alcohols catalyzed by supported Au nanoparticles proceeds via an unsymmetrical concerted

239 Widely investigated systems (Au-TiO(2) for CO oxidation thermocatalysis and Pd-TiO(2)

240 ied on the 1H-1,2,4-triazole-3-thiol-Au (T3T-Au) electrode.

241 ic peak current of VAN obtained with the T3T-Au electrode is 4.3 times greater than the bare Au elect

242 etermination of VAN was performed on the T3T-Au electrode using a differential pulse voltammetry (DPV

243 rformed on electroplated [Formula: see text] Au films show a hardness 47% greater than random and unt

244 s, one to two orders of magnitude lower than Au-, C-, and Si-based nanomaterials.

245 n vitro and in vivo results demonstrate that Au@Rh-ICG-CM is able to effectively convert endogenous h

246 The Au and Ag nanoparticles were synthesized using tyrosine,

247 The Au L-edge subtraction is particularly relevant for the i

248 The Au nanocaps allowed the UCNPs to emit upconverted light

249 The Au NP excited by the laser at the surface plasmon resona

250 The Au(155) core is composed of an 89-atom inner core and 66

251 The Au(I)-catalyzed reaction between terminal alkynes and ar

252 The extent of the reaction increases as the Au NP size decreases.

253 n in situ oxidative addition reaction at the Au surface.

254 the manipulation of atomic structures at the Au/TiO(2) interface significantly alters the interfacial

255 Within the digold triazolate complexes the Au(I) atoms are held in close proximity but beyond the d

256 ulations predict lower work function for the Au/SnSe NHS compared to the SnSe NSs as the primary orig

257 xperimentally intriguing observations in the Au(I)-catalyzed cyclization of cyclic and acyclic acetal

258 the urease-bound aggregation kinetics of the Au and Ag NPs which has not been explored earlier by thi

259 hization-crystallization oscillations of the Au clusters.

260 Dissolution of the Au shell slows down when both metals are exposed, which

261 ely coupled plasma mass spectrometry) of the Au signal intensities.

262 ere determined from the kinetic study of the Au(22) transformation.

263 n of the size transformation products of the Au(22)(SG)(18) nanocluster under representative working

264 y, we demonstrate selective promotion of the Au-C bond formation by controlling the bias applied acro

265 erometry were used for the evaluation of the Au@Pt/Au NPs electrocatalytic activity toward WOR.

266 be explained by the observation that, on the Au electrode, water reduction improves with more alkalin

267 mpetition between these two reactions on the Au surface in 0.1 M bicarbonate electrolyte.

268 By introducing a perturbation onto the Au(22) surface, significant changes in the activation pa

269 The results showed that the Au:CuO thin film system is a RI sensitive platform able

270 , despite limited electronic coupling to the Au electrode, demonstrating the potential of this approa

271 Compared to the Au-thiolate NCs, the Ag/Cu/Cd-thiolate systems exhibit d

272 The [Au(22) H(4) (dppo)(6) ](2+) nanohydride is found to lose

273 secondary pai-type interactions between the [Au@Pb(11)](3-) ligands and the gold core play a signific

274 H-related transformations suggests that the [Au(22) H(4) (dppo)(6) ](2+) nanohydride is a versatile m

275 The simulation results suggest that the [Au(CH(3))(2))](-) complex forms one and two gold-ion-ind

276 was studied on the 1H-1,2,4-triazole-3-thiol-Au (T3T-Au) electrode.

277 alated layer was formed between them through Au-N and Au-S bond which reduced IFE of AuNPs.

278 rs results in the transition from n-type TMD-Au Schottky contact to p-type one with reduced energy ba

279 d the extinction rates on the surface due to Au and Ag NPs aggregation and examined the variations du

280 at the sensors behaved almost identically to Au disk electrodes for the oxidation of an outer-sphere

281 ion regarding the bonding of aryl iodides to Au electrodes is a case in point, with ambiguous reports

282 e addition of alkenyl and alkynyl iodides to Au(I) are reported.

283 Au(22) with a 10-atom bioctahedral kernel to Au(22)Cd(1) with a 13-atom cuboctahedral kernel, and cor

284 idene, binds even more strongly than NHCs to Au surfaces without altering the surface structure.

285 ction of [Au(25)SR(19)](0), leading back to [Au(25)SR(18)](-) and eliminating precisely one surface l

286 -triphenylphosphinegold(I) 1,2,3-triazolate (Au(2)-R).

287 We then achieved direct bonding between two Au [Formula: see text] surfaces operating at 200 degrees

288 Whereas very restricted mobility of two Au-carbene ligands was found upon binding as a doublet t

289 version and Au nanoparticle hybrid (DNA-UCNP-Au) hydrogel is developed.

290 veloped based on Au nanocap-supported UCNPs (Au/UCNPs), which were partially embedded in a solid subs

291 while also maintaining a partially uncoated Au surface to facilitate photocatalysis, were synthesize

292 are found to bridge the eight uncoordinated Au atoms at the interface.

293 rdness 47% greater than random and untwinned Au.

294 Using Au as a model catalyst where CO is the only product, we

295 u monitoring of cell-secreted dopamine using Au-coated arrays of micropyramid structures integrated d

296 , leaving behind a fluid phase enriched with Au adatoms that subsequently aggregate into supported cl

297 reen-printed carbon electrodes modified with Au nanoparticles decorated reduced graphene oxide flakes

298 ough an electrochemical sensor modified with Au nanostructures, LiClO(4) -doped conductive polymer, a

299 A comparison of Au-thiolate NCs with Au-phosphine ones further reveals the important roles of

300 By decorating the SnSe NSs with Au nanoparticles, significant improvement in field emiss