ライフサイエンスコーパス: Pt

1 Pt was plated from solutions of femtomolar PtCl6(2-), wh

2 Pt-DA showed photocytotoxicity against cisplatin-resista

3 Pt@UiO-66-NH2 also outperforms Pt nanoparticles supporte

4 distortion in the premartensite phase of 10% Pt-substituted Ni2MnGa.

5 ,in isomer, trans- Cl2(P((CH2)14)3 P) (M = 2/Pt, 3/Pd, 4/Ni), then form.

6 A Pt nanoparticle is deposited on the orifice of a solid-s

7 A Pt-catalyzed hydrosilylation helped stymie unwanted rear

8 sfer torque is strongly enhanced by adding a Pt capping layer.

9 ected electrons induce proton reduction at a Pt electrode.

10 Evolved oxygen is detected by reduction at a Pt UME, allowing for the determination of onset potentia

11 The nanoscale cell is formed by bringing a Pt/TiO2-coated atomic force microscope tip into contact

12 hemical microscopy-(SECM) like approach of a Pt microelectrode (ME), which was leveled with the WE to

13 tional control through judicious design of a Pt(II)-acetylide charge-transfer donor-bridge-acceptor-b

14 ty with platinum triggers the formation of a Pt-CO film that prevents the reaction process.

15 that a monolayer of PtSe2 can be grown on a Pt substrate in the form of a triangular pattern of alte

16 and does not cross-react with satraplatin, a Pt(IV) prodrug.

17 d a stable current, which is comparable to a Pt wire auxiliary electrode.

18 ssive sigma-bond metathesis steps, whereby a Pt(II) -H intermediate engages in C(sp(3) )-H bond activ

19 75 V, were the same as those obtained with a Pt cathode at a loading of 0.1 milligram of Pt per centi

20 the combination of an enzymatic anode with a Pt cathode.

21 miniaturize the sensor and couple it with a Pt electrode (25 mum diameter each) for use as a dual sc

22 rgistic activity of the catalytically active Pt nanoparticles on a high surface area multiwalled carb

23 gas permeation, impeding contact with active Pt.

24 nd (110) surfaces of Al, Cu, Ru, Rh, Pd, Ag, Pt, and Au.

25 The edgeless Ag-Pt bimetallic nanocages with hollow interior performed n

26 rimental and theoretical investigation of Ag-Pt sub-nanometer clusters as heterogeneous catalysts in

27 ugh plasmonic effects, in which plasmonic Ag-Pt bimetallic nanocages were synthesized with an edgeles

28 es, while Ag binds and activates O2 , and Ag/Pt surface proximity disfavors poisoning by CO or oxidiz

29 /C (95 % vs. 81 % retained OER activity) and Pt/C (92 % vs. 78 % retained ORR activity after 10 h run

30 ty are ascribed to a synergic role of Ag and Pt in ultranano-aggregates, in which Pt anchors the clus

31 her photocatalytic activity than both Au and Pt nanoparticle-decorated CZTS (Au/CZTS and Pt/CZTS) pho

32 Pt nanoparticle-decorated CZTS (Au/CZTS and Pt/CZTS) photocatalysts, indicating the MoS2-rGO hybrid

33 Most notably, Pt-DA and Pt-G4K(+)B hydrogels show selective phototoxicity for ca

34 surements over PEDOT(PSS)-coated Au, GC, and Pt electrode surfaces.

35 g and for the activation of Pt-hunchback and Pt-twist expression.

36 sed on the established capacity of Au(I) and Pt(0) complexes to act as Lewis acidic and basic fragmen

37 The ORR rates of Ag, Au, Cu, Ni, Pd, Rh and Pt measured at 600 degrees C form a volcano plot versus

38 tin (Sn) is added to CeO2 , the single-atom Pt catalyst undergoes an activation phase where it trans

39 The reactivity and stability of single-atom Pt species was explored for the industrially important l

40 The single-atom Pt/CeO2 catalysts are stable during propane dehydrogenat

41 e truncated octahedron shape adopted by bare Pt nanoparticles undergoes a reversible, facet selective

42 is the prevailing back reaction on the bare Pt/SrTiO3 photocatalyst.

43 tic activities approaching that of benchmark Pt/C in an acidic medium have been obtained on the catal

44 Compared to the benchmark Pt/C catalyst, the optimized Co@C-800 (carbonized at 800

45 icate that strong interaction exists between Pt and the vacancies.

46 an be tuned by controlling the ratio between Pt and Ni precursors such that either a completely hollo

47 t, in the absence of coherent strain between Pt and Pd, finite size effects introduce local compressi

48 lic nanoparticles (NPs) employing bimetallic Pt-based NPs (PtM, where M = Pd, Rh, and Ni) via a prote

49 rimental studies using different cis-blocked Pt(II) complexes and metalloligands with four divergent

50 These accomplishments have brought Pt complexes to the forefront of academic research.

51 anoframe that minimizes the number of buried Pt sites.

52 C-H bond activation and functionalization by Pt complexes are surveyed.

53 d the performance surpasses that of the Ir/C-Pt/C couple for sufficiently high overpotentials.

54 firm oxidase-like activity of citrate-capped Pt NPs, their activity toward oxygen reduction reaction

55 adsorption on the surface of citrate-capped Pt NPs.

56 and selectivity, in comparison to Pt/carbon, Pt@UiO-66, and Pd@UiO-66-NH2 .

57 rmance to the state-of-the-art ORR catalyst (Pt/C) and OER catalyst (Ir/C).

58 ance than the state of the art ORR catalyst (Pt/C) and the oxygen evolution reaction catalyst (Ir/C).

59 dyl [Pd3(L)4](6+) cages that bind cisplatin [Pt(NH3)2Cl2] within their internal cavities and interact

60 al spin Seebeck effect (LSSE) in the classic Pt/yttrium iron garnet (YIG) system and its association

61 Co/Pt double stack is a modification proposed for the high

62 ong and against current flow direction in Co/Pt double stack wires with Ta capping.

63 tic/ferroelectric structure with Pt/Co/Ni/Co/Pt layers on PMN-PT substrate.

64 iving maximum values of 20 fNm for the CoFeB/Pt and 75 fNm for the Py vortex particles.

65 med from a repeated motif of ultrathin CoFeB/Pt layers.

66 imes higher ORR activity than for commercial Pt/C (2.7 A mgPt(-1) at 0.9 VRHE) was reproducibly obser

67 is 9.7 times higher than that of commercial Pt/C.

68 -conjugated platinum(IV) anticancer complex (Pt-DA) has been incorporated into G-quadruplex G4K(+) bo

69 platinum (boryl)iminomethane (BIM) complex [Pt(kappa(2) -N,B-(Cy2) BIM)(CNAr(Dipp2) )] can effect th

70 ry promising alternative to the conventional Pt/C and Ir/C catalyst for an air cathode in alkaline el

71 Here we assess the current Pt drug landscape and challenges for future Pt developme

72 sed emitters and tetradentate cyclometalated Pt and Pd complexes have significantly improved the emis

73 A tetradentate cyclometalated Pt(II) complex (PtN3N) is developed as an efficient, sta

74 Here, we show that the three-dimensional Pt anisotropy of Pt-Ni rhombic dodecahedra can be tuned

75 We document discovery of a distinct Pt anomaly spread widely across North America and dating

76 s can form various types of DNA lesions (DNA-Pt) and trigger pleiotropic DNA damage responses.

77 -extraction protocol and the labeling of DNA-Pt by means of click chemistry in cells.

78 bitor SAHA led to detectable clusters of DNA-Pt that colocalized with the ubiquitin ligase RAD18 and

79 Here, we report a strategy to visualize DNA-Pt with high resolution, taking advantage of a novel azi

80 imized utilization of the expensive element, Pt.

81 ting from the major advancements in emissive Pt and Pd square planar complexes are discussed.

82 cies up to 5.9%, out-performing all existing Pt-containing materials.

83 work, we found that the transcription factor Pt-Ets4 is needed for cumulus integrity, dorsoventral pa

84 ction (ORR)-active ordered intermetallic Fe3 Pt NPs.

85 ron nitride (Ni3 FeN) supporting ordered Fe3 Pt intermetallic nanoalloy.

86 h activity for the OER while the ordered Fe3 Pt nanoalloy contributes to the excellent activity for t

87 Robust Ni3 FeN-supported Fe3 Pt catalysts show superior catalytic performance to the

88 The Fe3 Pt/Ni3 FeN bifunctional catalyst enables Zn-air batterie

89 extraordinarily high performance of the Fe3 Pt/Ni3 FeN bifunctional catalyst makes it a very promisi

90 ensity functional theory calculations on FeO/Pt(111) reveals that benzyl alcohol enriches preferentia

91 preferentially at the oxygen-terminated FeO/Pt(111) interface and undergoes readily O-H and C-H diss

92 ored spaces may reveal new opportunities for Pt drug development.

93 yst holds great promise as a replacement for Pt in future PEMFCs.

94 y revealed significant core-level shifts for Pt shells supported on TiWN cores, corresponding to incr

95 rve as a Lewis acid to accept electrons from Pt, and on the contrary, when Pt sits on N-vacancies, th

96 Different UME probe dimensions ranging from Pt diameters of 20 mum down to 0.6 mum were used.

97 2) , only six-times-less as compared to full-Pt conventional PEMFC.

98 Furthermore, Pt-Sn iNPs are shown to be a robust catalytic platform f

99 Pt drug landscape and challenges for future Pt development and discuss opportunities for improving o

100 ctive thermopower 350 +/- 50 microV/K at GST-Pt interfaces.

101 CO2 was reduced at a hemisphere-shaped Hg/Pt ultramicroelectrode (UME) or a Hg/Au film UME, which

102 metallic Lewis adducts and confers the Au(I)/Pt(0) pair a remarkable capacity to activate dihydrogen

103 consequence, unusual heterobimetallic Au(I)/Pt(II) complexes containing hydride (-H), acetylide (-C

104 picked up by the inverse spin-Hall effect in Pt.

105 e velocity obtained reduces with increase in Pt spacer thickness due to reduction in DMI and enhances

106 as a function of Au and Ir spacer layers in Pt/Co/Au,Ir/Pt.

107 Here IDMI and PIM are reported in Pt determined as a function of Au and Ir spacer layers i

108 perimental collision frequency of individual Pt nanoparticles (NPs) undergoing collisions at a Au ult

109 cumvent the use of expensive and inefficient Pt catalysts, multicopper oxidases (MCOs) have been envi

110 ive catalytic sites are cationic interfacial Pt atoms bonded to TiO2 and that Ptiso exhibits optimal

111 an activation phase where it transforms into Pt-Sn clusters under reaction conditions.

112 Thus, intracellular Pt concentration could be considered as a biomarker of c

113 gh-coverage sensor, formation of intrastrand Pt(II)-AG adducts rigidifies the oligo-AG probe, resulti

114 on of Au and Ir spacer layers in Pt/Co/Au,Ir/Pt.

115 A particular example is Pt clusters deposited on alumina, which have been shown

116 In these structures, isolated Pt atoms, Ptiso, remain stable through various condition

117 te hydrogels by using borate ester linkages (Pt-G4K(+)B hydrogel).

118 queous solution of K2MCl4 (charging arm; M = Pt, Pd), and an aqueous solution of excess KCl (receivin

119 Such an interfacial electronic effect makes Pt favour the adsorption of O2, alleviating CO poisoning

120 ion of a parent core-shell carbide material (Pt/TiWC).

121 extensively developed to replace noble metal Pt and RuO2 catalysts for the oxygen reduction reaction

122 1mWm(-2)), which is slightly higher than MFC-Pt/C (20%) (704mWm(-2)).

123 inently represented by the cinchona-modified Pt and Pd catalysts for the asymmetric hydrogenation of

124 heparin, we prepared the protamine-modified Pt NPs through direct adsorption on the surface of citra

125 ted on the external surface of the same MOF (Pt/UiO-66-NH2 ).

126 ethod for the synthesis of size-monodisperse Pt, Pt3 Sn, and PtSn intermetallic nanoparticles (iNPs)

127 se selectivity, relative to the monometallic Pt, was observed using the PtSn@mSiO2 catalyst.

128 verall water splitting proceeded using MoOx /Pt/SrTiO3 with inhibited water formation from H2 and O2

129 Ceramic-based multisite Pt microelectrode arrays (MEAs) were characterized for t

130 l transformations involving a (kappa(2) -P,N)Pt(eta(3) -benzyl) complex, and either pinacolborane or

131 vation of twin nucleation in nanocrystalline Pt.

132 (II)-crosslinked single-chain nanoparticles (Pt(II) -SCNPs) to demonstrate their application as a rec

133 itanium tungsten nitride core nanoparticles (Pt/TiWN) by high temperature ammonia nitridation of a pa

134 hography techniques, platinum nanoparticles (Pt NPs) were deposited in a bridge-like arrangement, in

135 fibrous web and then platinum nanoparticles (Pt-NP) decoration was performed by ALD onto TiO2 coated

136 The nanoporous Pt surface formed during the ORR was visualized by AFM a

137 ficant window of time has passed since a new Pt drug has been approved for clinical use.

138 r metal-organic framework (MOF), UiO-66-NH2 (Pt@UiO-66-NH2 ) as a multifunctional catalyst in the one

139 city/nanoconfinement endowed by UiO-66-NH2 , Pt@UiO-66-NH2 exhibits remarkable activity and selectivi

140 Most notably, Pt-DA and Pt-G4K(+)B hydrogels show selective phototoxic

141 and detailed comparison of a series of novel Pt-bisacetylide containing conjugated small molecules po

142 Shape-controlled octahedral Pt-Ni alloy nanoparticles exhibit remarkably high activi

143 was evaluated in the presence and absence of Pt-Al2O3 support interactions.

144 ventral patterning and for the activation of Pt-hunchback and Pt-twist expression.

145 ation develops in which the high affinity of Pt for CO helps to decrease the overpotential for the re

146 Because the aggregation of Pt NPs can inhibit their oxidase-like activity and prota

147 that the three-dimensional Pt anisotropy of Pt-Ni rhombic dodecahedra can be tuned by controlling th

148 ional stability for isolated single atoms of Pt.

149 effective route to enhance the attachment of Pt-NP and to improve the structure stability of polymeri

150 umina) are limited to adatoms and cations of Pt, Pd, and Ru.

151 o achieve high selectivity, a combination of Pt/Al2O3 and ZnO have been found to slowly dehydrogenate

152 echnical barrier to the commercialization of Pt complexes for many applications.

153 es between the classical alkyne complexes of Pt(II) and their drastically more reactive Au(III) conge

154 verpotentials similar to the counterparts of Pt/C ORR electrode and IrO2 OER electrode.

155 ced annealing generates an optimal degree of Pt surface enrichment, while the others exhibited mostly

156 Further development of Pt alloy electrocatalysts relies on the design of archit

157 ch observations that led to the discovery of Pt complexes as DNA-binding agents that elicit cell arre

158 group previously observed the dissolution of Pt nanoelectrodes at moderately negative potentials duri

159 example of electrochemiluminescence (ECL) of Pt(II) complexes in aqueous solution having higher effic

160 cs also describe the structural evolution of Pt in the electrochemical environment.

161 Furthermore, ectopic expression of Pt-Ets4 is sufficient to induce cell delamination and mi

162 ect demonstrates an electron-rich feature of Pt after assembling on hexagonal boron nitride nanosheet

163 into discrete flakes after incorporation of Pt-DA.

164 oxide can also form on the square lattice of Pt(100).

165 The loss of Pt during the oxygen reduction reaction (ORR) affects th

166 Pt cathode at a loading of 0.1 milligram of Pt per centimeter squared.

167 nces in the formation and chemical nature of Pt-rich and Ni-rich surface domains in the octahedral (1

168 athin layer of ALD Al2O3 and an overlayer of Pt dendrimer-encapsulated nanoparticles (DENs) have been

169 R) of Au nanoparticles, low overpotential of Pt nanoparticles, and more importantly, the one-dimensio

170 in oxidation catalysis, the active phase of Pt remains uncertain, even for the Pt(111) single-crysta

171 ith the flexible nature with the presence of Pt and TiO2 on its surface.

172 The surface restructuring of Pt(111) electrodes upon electrochemical oxidation/reduct

173 strongly resembles that found in studies of Pt(111) homoepitaxial growth and ion erosion in ultrahig

174 resistive switching (RS) mechanism study of Pt/TiO2/Pt cell, one of the most widely studied RS syste

175 selective electrodes (ISEs), the surfaces of Pt, Au, and GC electrodes were coated with 0.1, 1.0, 2.0

176 Herein, we demonstrate the synthesis of Pt shell on titanium tungsten nitride core nanoparticles

177 reduction reaction (ORR) activity to that of Pt/C as well as a better stability than that of Ru/C (95

178 rtunities for improving our understanding of Pt drugs that utilize contemporary translational science

179 ped methodology to the comparative uptake of Pt-species in cisplatin resistant and sensitive cell lin

180 Here we show the use of Pt nanoparticle-decorated nanotubes as highly active cat

181 e site is created on CeO2 in the vicinity of Pt(2+), which provides the improved reactivity.

182 inking of single chains via the addition of [Pt(1,5-cyclooctadiene)Cl2 ] in dilute solution.

183 , such as carboplatin a metallodrug based on Pt coordination chemistry, these species may help to ove

184 embrace an interfacial electronic effect on Pt induced by the nanosheets with N-vacancies and B-vaca

185 Taming interfacial electronic effects on Pt nanoparticles modulated by their concomitants has eme

186 ate the system using Ag electrodeposition on Pt electrodes of gradually increasing R; the latter is a

187 ishing the electro-oxidation of hydrazine on Pt NPs.

188 g/AgCl) using glucose oxidase immobilized on Pt-decorated graphite.

189 of the potential of the step-related peak on Pt(553).

190 artial pressure of 10(-3) and 10(-5) torr on Pt (200 nm)/Ti (45 nm)/Si (001) substrates using pulsed

191 merged as an intriguing approach to optimize Pt catalytic performance.

192 r constructs encompasses two twisted [organo-Pt(II)<--pyridine] coordination based irregular hexagons

193 cificity for cisplatin and potentially other Pt(II) drugs and does not cross-react with satraplatin,

194 Pt@UiO-66-NH2 also outperforms Pt nanoparticles supported on the external surface of th

195 with different electrode materials (Au, Pd, Pt, and Ag) to assess the effect of the electrode materi

196 imple transition metal (TM = Co, Fe, Cu, Pd, Pt, Au)-based photocatalyst (PC) has led to the dramatic

197 upported in SBA-15 (MNPs/SBA-15 with M = Pd, Pt, Rh) were efficiently used as catalysts in the accept

198 Nanoparticles (Pd, Pt, Rh) stabilized by G4OH PAMAM dendrimers and supporte

199 hemiluminescence properties of square-planar Pt(II) complexes that result from the formation of supra

200 mising alternative to their costly platinum (Pt)-based counterparts in polymer electrolyte fuel cells

201 This is demonstrated for platinum (Pt) nanoparticle surface reconstruction induced by CO ad

202 ate how atomically dispersed ionic platinum (Pt(2+)) on ceria (CeO2), which is already thermally stab

203 que in their ability to trap ionic platinum (Pt), providing exceptional stability for isolated single

204 Previously, a large platinum (Pt) anomaly was reported in the Greenland ice sheet at t

205 , and inexpensive devices based on platinum (Pt)-decorated graphite for glucose determination in phys

206 Here we report that platinum (Pt) atomically dispersed on alpha-molybdenum carbide (al

207 al device employing an unselective platinum (Pt) cathode.

208 orticography (mu-ECoG) arrays with platinum (Pt) or glassy carbon (GC) electrodes were manufactured.

209 mainly composed of thin-film polycrystalline Pt, with some apparent nanoscale roughness that was not

210 preoxidized (Ptox) and prereduced (Ptmetal) Pt clusters on TiO2, we identify unique spectroscopic si

211 e OH* intermediate by Zn atoms, while a pure Pt system forms highly stable COH* and CO* intermediates

212 y absorption spectroscopy identified reduced Pt covered with an amorphous molybdenum oxyhydroxide hyd

213 ext-generation supported catalyst to replace Pt/C.

214 Here, we report Pt nanoparticles assembled on vacancy-abundant hexagonal

215 The resulting Pt NP microwires were chemically functionalized to allow

216 magnetic anisotropy field (H KS) in the same Pt/YIG system.

217 the electrodeposition of an isolated single Pt atom or small cluster, up to 9 atoms, on a bismuth ul

218 activator motor to the activated Janus SiO2 /Pt nanomotor.

219 The nanoparticles are obtained by in situ Pt(2+) reduction of a chalcogel network formed by the me

220 , which also showed approximately 5 nm sized Pt particles on the glass surface surrounding the electr

221 Formation of small Pt-Sn clusters allows the catalyst to achieve high selec

222 idation of cyclohexene, and that solubilized Pt clusters are also capable of generating initiators fo

223 ion between heparin and protamine-stabilized Pt NPs induced nanoparticle aggregation, inhibiting thei

224 on ultrasonic spray deposition of a standard Pt/carbon electrocatalyst directly onto a perfluorosulfo

225 med via highly efficient and stereoselective Pt(IV)-catalyzed cycloaddition reactions of the correspo

226 to the transformation mechanisms in strained Pt nanoparticles.

227 he entire transformation process of strained Pt icosahedral nanoparticles (ICNPs) into larger FCC cry

228 osed for the high spin-orbit torque strength Pt/Co/Ta stack, to improve its thermal stability and per

229 catalytic ability of the chalcogel-supported Pt nanoparticles is demonstrated in a recyclable manner

230 ibe a method to fabricate nanopore-supported Pt nanoparticle electrodes and their use in bipolar elec

231 viously, we have found that single supported Pt atoms are remarkable NO oxidation catalysts.

232 These catalysts exhibit higher activity than Pt/C and Ir/C catalysts and are also quite stable.

233 % higher CTC (charge transfer capacity) than Pt microelectrodes of similar geometry.

234 ficantly more active and less expensive than Pt/C and Ir/C, and are thus promising new anode catalyst

235 -PSS adhered significantly better to GC than Pt, and allowed drastic reduction of electrode size whil

236 ivity for the oxygen reduction reaction than Pt/C, and twice the mass activity of the hollow nanofram

237 The results obtained showed that Pt NP NPs can catalyze the oxidation of organic substrat

238 in cell density and tissue thickness and the Pt/P ratios together with the high resolution adopted in

239 cating considerable spin transparency at the Pt/MI interface.

240 The atomic coupling between the Pt and the CoO endows precise control of the atomic inte

241 control of the atomic interface between the Pt and the CoO, which directly results in electron donat

242 We expect the Pt anomaly to serve as a widely-distributed time marker

243 phase of Pt remains uncertain, even for the Pt(111) single-crystal surface.

244 equently, the dendrimer was removed from the Pt DENs using a UV/O3 treatment, and this provided direc

245 Thus by studying transformation in the Pt ICNPs at high time and spatial resolution, we obtain

246 0.1-2.0 THz with the driving current in the Pt layer from 10(8) A/cm(2) to 10(9) A/cm(2).

247 citation of energetic charge carriers in the Pt shell.

248 in the temperature dependence of LSSE in the Pt/YIG system.

249 and provided insights into the effect of the Pt dopants on the optical properties and stability of th

250 The surface morphology of the Pt substrates prior to and after Ag electrodeposition is

251 The structural evolution of the Pt surface morphology strongly resembles that found in s

252 responding to increased stabilization of the Pt valence d-states.

253 Finally, the activity of the Pt(II) -SCNPs as homogeneous, yet recyclable catalyst wa

254 le tuning of the electronic structure of the Pt.

255 that the reaction occurs exclusively on the Pt surface.

256 tropolymerizing o-phenylene diamine onto the Pt wire microtransducer, followed by the immobilization

257 ease in catalytic efficiency compared to the Pt loaded carbon sphere catalyst in aqueous hydrogenatio

258 (signal-to-noise ratio) when compared to the Pt ones.

259 lts in electron donation from the CoO to the Pt, and thus favorable tuning of the electronic structur

260 rial might be a promising alternative to the Pt-based electrocatalysts for water splitting.

261 One of the main limitations to the Pt-therapy in cancer is the development of associated dr

262 Even after multiple usage, the Pt-NP/TiO2-PAN nanofibrous webs were stable with the fle

263 h less than 7.5% impedance change, while the Pt microelectrodes delaminated after 1 million pulses.

264 rahydrogen-induced polarization NMR on these Pt-Sn catalysts.

265 Thus, these Pt MEAs provide an excellent microelectrode platform for

266 0.003, comparable to that of platinum, theta Pt = 0.076 +/- 0.007, and is much larger than that of bc

267 This Pt datum will facilitate the dating and correlating of a

268 increasing R; the latter is adjusted through Pt electrodeposition.

269 le of interfacial bonding at the active TiO2-Pt interface, as opposed to a physico-chemical change wi

270 ve switching (RS) mechanism study of Pt/TiO2/Pt cell, one of the most widely studied RS system, by fo

271 as a low overpotential that is comparable to Pt-based catalysts, as a result of both defects and oxyg

272 oxygen reduction reaction (ORR) compared to Pt/C catalyst in both alkaline and acidic media.

273 e activity and selectivity, in comparison to Pt/carbon, Pt@UiO-66, and Pd@UiO-66-NH2 .

274 ct as a Lewis base for donating electrons to Pt.

275 ting superior electrocatalytic properties to Pt and RuO2 as a bifunctional electrocatalyst for ORR an

276 For this aim, total Pt analysis in single cells has been implemented using a

277 t from the "dumbbell" designs in traditional Pt-bisacetylide containing conjugated polymers and small

278 structure revealed the self-assembly of two Pt-centered Ag icosahedra through vertex sharing.

279 ted in a hybrid microfluidic fuel cell using Pt/C as the cathode.

280 eral block in the 2D block co-micelles using Pt nanoparticles followed by dissolution of the interior

281 on exchange membrane fuel cell (PEMFC) using Pt/C at the cathode.

282 electrons from Pt, and on the contrary, when Pt sits on N-vacancies, the nanosheets act as a Lewis ba

283 ally important surface oxides form only when Pt is exposed to high pressure and temperature, highligh

284 ght) with a photocytotoxic index <2, whereas Pt-G4K(+)B hydrogels exhibited more potent photocytotoxi

285 Ag and Pt in ultranano-aggregates, in which Pt anchors the clusters to the support and binds and act

286 to contact with a flat substrate coated with Pt.

287 r C-H activation; reactions of dioxygen with Pt(II) complexes that may be relevant to substrate oxyge

288 5 V vs RHE and leaving only a 30 mV gap with Pt/C (60 mugPt/cm(2)).

289 midal microneedle structures integrated with Pt and Ag wires, each with a microcavity opening.

290 Complete blockage of the nanopore with Pt metal forms a closed bipolar nanoparticle electrode w

291 conductance of thiol-terminated silanes with Pt electrodes is lower than the ones formed with Au and

292 d ferromagnetic/ferroelectric structure with Pt/Co/Ni/Co/Pt layers on PMN-PT substrate.

293 er photosynthetic heterojunction system with Pt as an electron collector and WO3 as a hole collector.

294 Bader charge analysis shows that with Pt on B-vacancies, the nanosheets serve as a Lewis acid

295 ing from thermal gradient across an Y3Fe5O12/Pt interface.

296 apparent synchroneity of this widespread YDB Pt anomaly is consistent with Greenland Ice Sheet Projec

297 Ru, Os)-(porphinato)metal(II) (PM'; M' = Zn, Pt, Pd) molecular architecture (M-(PM')n-M), wherein hig

298 (PDNA) was immobilized on the surface of ZnO/Pt-Pd nanocomposites modified FTO electrode.

299 based on Zinc oxide/platinum-palladium (ZnO/Pt-Pd) modified fluorine doped tin oxide (FTO) glass pla

300 This PDNA modified electrode (PDNA/ZnO/Pt-Pd/FTO) served as a signal amplification platform for