ライフサイエンスコーパス: electrocatalytic

1 complex shows selective and highly efficient electrocatalytic 4e(-)/4H(+) O2-reduction to H2O with a

2 The modified electrode exhibited excellent electrocatalytic ability to the reduction of FA at 0.3 V

3 With this excellent electrocatalytic ability, comparable to that of the stat

4 arbon composites have demonstrated excellent electrocatalytic activities and durability towards oxyge

5 ickel demonstrated oxygen evolution reaction electrocatalytic activities commensurate with films of t

6 ult, this discovery of the structure-related electrocatalytic activities could provide guidance in th

7 It exhibits excellent bifunctional electrocatalytic activities for oxygen reduction and oxy

8 and F tri-doped graphene exhibited excellent electrocatalytic activities for the oxygen reduction rea

9 oporous gold exhibits significantly enhanced electrocatalytic activities in comparison with conventio

10 ation between the defective atomic sites and electrocatalytic activities of 2D TaS2 .

11 The multifunctional electrocatalytic activities originate from a synergistic

12 nanoparticles show significantly more robust electrocatalytic activities than the enzymatic peroxidas

13 d N-HPCNPs hybrid materials exhibit superior electrocatalytic activities towards ORR, besides excelle

14 s are shown to be very stable with excellent electrocatalytic activities.

15 All four phases were tested for their electrocatalytic activity (linear sweep voltammetry) and

16 ace of the electrode, and SWCNT improves the electrocatalytic activity along with conductivity of gla

17 hat these nanocomposite exhibited attractive electrocatalytic activity and also yielded large surface

18 -Ni2 P-NS array cathode exhibits outstanding electrocatalytic activity and long-term durability towar

19 tions reveal that the significantly enhanced electrocatalytic activity and selectivity at lowered ove

20 ctrodes that provide insights on controlling electrocatalytic activity and selectivity for this react

21 dy demonstrates a promising approach to tune electrocatalytic activity and selectivity of metal catal

22 eutral catalytic system exhibited ultra-high electrocatalytic activity and stability for CO electroox

23 -platinum electrocatalysts for enhancing the electrocatalytic activity and stability for the oxygen-r

24 eat opportunities for a systematic tuning of electrocatalytic activity and stability.

25 Although the initial aim was to improve electrocatalytic activity by greatly boosting the active

26 ots in nanocomposite practically induced the electrocatalytic activity by lowering the oxidation over

27 ein we present an understanding of trends in electrocatalytic activity for carbon dioxide reduction o

28 ombined use of CoPc and MWCNTf results in an electrocatalytic activity for GSH oxidation and GSSG red

29 (MoS(2)) nanoparticles with high-performance electrocatalytic activity for hydrogen evolution reactio

30 The as-prepared MoS2 QDs exhibit excellent electrocatalytic activity for hydrogen evolution reactio

31 ies significantly contribute to the enhanced electrocatalytic activity for OER.

32 a result, HQDC-X catalysts exhibit excellent electrocatalytic activity for ORR via a dominant four-el

33 e N-graphene/CNT hybrids exhibit outstanding electrocatalytic activity for several important electroc

34 lized redox nanomaterial exhibits reversible electrocatalytic activity for the H2 /2 H(+) interconver

35 prisingly, the as-prepared BP shows advanced electrocatalytic activity for the oxygen evolution react

36 Co3O4/NiCo2O4 DSNCs also exhibit much better electrocatalytic activity for the oxygen evolution react

37 We investigated the dependence of the electrocatalytic activity for the oxygen evolution react

38 Moreover, the modified film exhibited high electrocatalytic activity for the reduction of hydrogen

39 ess resulted in a tunable enhancement in the electrocatalytic activity for water oxidation, demonstra

40 The enhanced mechanism of electrocatalytic activity has been investigated in detai

41 The role of Co-salophen, IL and ERGO in the electrocatalytic activity has been systematically invest

42 The sensor showed electrocatalytic activity in both aqueous and micellar m

43 M-ITS-cg3s exhibit electrocatalytic activity in proton reduction that arise

44 le size, geometry, and surface attachment on electrocatalytic activity in real-world application envi

45 ted modified electrode exhibited outstanding electrocatalytic activity in terms of nitrite oxidation

46 Electrocatalytic activity of a water-soluble nickel comp

47 Due to the excellent electrocatalytic activity of Ag@Pt-GRs towards the oxida

48 We report a synthetic method to enhance the electrocatalytic activity of birnessite for the oxygen e

49 ng are further demonstrated by the increased electrocatalytic activity of CoS2 nanowire electrodes ov

50 The electrocatalytic activity of Fe3O4 nanodots toward the e

51 culations were used to uncover the origin of electrocatalytic activity of graphene-based electrocatal

52 scale SECM, which can be utilized to map the electrocatalytic activity of individual nanoparticles in

53 hasis of this review is on the origin of the electrocatalytic activity of nanostructured catalysts to

54 e effects are essential for the bifunctional electrocatalytic activity of our material.

55 ctrochemical detection of adenosine based on electrocatalytic activity of Pt-NPs toward H2O2 reductio

56 The electrocatalytic activity of SOD1 towards NO2(-) oxidati

57 The excellent electrocatalytic activity of SWCNT-Polytyr towards NADH

58 Enhancement of electrocatalytic activity of the composite-modified elec

59 Electrocatalytic activity of the electrode toward glucos

60 the CYP3A4, clearly observed as a diminished electrocatalytic activity of the enzyme.

61 rove protein stabilization and to ensure the electrocatalytic activity of the immobilized enzyme, did

62 bined with fast hole transport leads to high electrocatalytic activity of the NP films.

63 ly attractive electrochemical properties and electrocatalytic activity of these elite nanomaterials h

64 The electrocatalytic activity of this sensor was good as a r

65 Furthermore, the electrocatalytic activity of triangular NiONPs compared

66 unced effect of the crystal structure on the electrocatalytic activity tested under different conditi

67 ve, 4-acetamido-TEMPO (ACT), exhibits higher electrocatalytic activity than AZADO and ABNO for the ox

68 re open access to the cobalt site has higher electrocatalytic activity than CTGU-6 with the lattice w

69 between EY and MWNTs-OH that enabled a high electrocatalytic activity to 2,4-DCP.

70 ar configuration, which possesses comparable electrocatalytic activity to that of precious metal benc

71 The proposed biosensor showed excellent electrocatalytic activity to the H2O2 reduction in the w

72 he proposed modified electrode exhibits high electrocatalytic activity toward electrooxidation of AP,

73 resulting hybrid material exhibits efficient electrocatalytic activity toward HER under acidic condit

74 er, the PEY/MWNTs-OH/GCE exhibited excellent electrocatalytic activity toward intracellular electroac

75 fastest electrochemical response and highest electrocatalytic activity toward methanol oxidation.

76 , and Ni-Fe mixed phosphate lead to superior electrocatalytic activity toward OER and HER.

77 mmetry and amperometry demonstrate excellent electrocatalytic activity toward oxygen reduction in add

78 Prepared MoSe2 nanoparticles (NPs) exhibit electrocatalytic activity toward the hydrogen evolution

79 als exhibit highly efficient and ultrastable electrocatalytic activity toward the hydrogen evolution

80 heteroatom doped carbons exhibited superior electrocatalytic activity toward the oxygen reduction re

81 cceptable stability, fast response, and high electrocatalytic activity toward the reduction of paraox

82 ical sensing using BiO-SPEs exhibited strong electrocatalytic activity toward the sensing of APAP and

83 The origin of the superior electrocatalytic activity toward water oxidation appears

84 en-IL/ERGO/SPE biosensor exhibited excellent electrocatalytic activity towards glucose oxidation in 0

85 The developed electrode presented high electrocatalytic activity towards glucose through synerg

86 nergistic effect and exhibited an unexpected electrocatalytic activity towards GSH oxidation, compare

87 such hybrid materials possess an outstanding electrocatalytic activity towards ORR comparable to the

88 rbon paste electrode (SNMCPE) displayed high electrocatalytic activity towards oxidation of 1.0mM MOX

89 the optimized Co@C-800 also showed enhanced electrocatalytic activity towards oxygen evolution react

90 ered electrochemical impedance and excellent electrocatalytic activity towards the oxidation of dopam

91 the modified electrode on PADs had excellent electrocatalytic activity towards the oxidation of gluco

92 s modified electrode also exhibits excellent electrocatalytic activity towards the oxidation of hydro

93 that the biosensor can significantly enhance electrocatalytic activity towards the oxidation of RIF,

94 The GC/N-CDs electrode shows higher electrocatalytic activity towards UA, Tyr and AP by not

95 Optimized electrocatalytic activity was reached for the architectu

96 t challenge is to deliver high, long-lasting electrocatalytic activity while ensuring cost- and time-

97 noble metal nanoparticles (NPs) exhibit high electrocatalytic activity, and could be employed for the

98 can provide a large surface area, excellent electrocatalytic activity, and high stability, which wou

99 e CNNB biosensor electrodes showed efficient electrocatalytic activity, enhanced kinetics for electro

100 ic glucose sensor presents one of the record electrocatalytic activity, stability and response toward

101 art solubility, film-forming capability, and electrocatalytic activity, while largely retaining the p

102 to the role of elastic strain in controlling electrocatalytic activity.

103 l oxidation potentials of a compound and its electrocatalytic activity.

104 ining step to achieve excellent bifunctional electrocatalytic activity.

105 heme for detection of microRNA (miRNA) using electrocatalytic amplification (ECA).

106 The Pt-ceria nanoparticles provided electrocatalytic amplification for the detection of the

107 ons to platinum metal species followed by an electrocatalytic amplification of proton reduction on an

108 tramicroelectrode (UME) (5 mum radius) using electrocatalytic amplification provided by 15 mM hydrazi

109 The method employed is based on electrocatalytic amplification, where small quantities o

110 Improving energy efficiency of electrocatalytic and photocatalytic CO2 conversion to us

111 electrocatalysts is of great importance for electrocatalytic and photoelectrochemical hydrogen produ

112 cles, including those employed in catalytic, electrocatalytic, and photocatalytic conversions, have s

113 etal-free carbocatalysts for a wide range of electrocatalytic applications.

114 n electrode, hydrogenases display reversible electrocatalytic behavior close to the 2H(+)/H2 potentia

115 rocatalyst on NiO shows that in the dark the electrocatalytic behavior is rectified toward CO oxidati

116 The electrocatalytic behavior of the modified electrode towa

117 old nanoparticles (AuNPs) exhibit attractive electrocatalytic behavior stimulating in the last years,

118 ectrodes can provide new insights into their electrocatalytic behavior, mass transport, and interacti

119 es (NPs) can provide new insights into their electrocatalytic behavior.

120 the trinuclear Au-Ni-Au complex facilitates electrocatalytic C-X bond activation of alkyl halides in

121 The electrocatalytic capabilities of the new sensor were tes

122 etal-organic surface to generate very active electrocatalytic cathode materials for hydrogen generati

123 Such modification induced electrocatalytic characteristics by decreasing analyte o

124 We report the electrodeposition of electrocatalytic clusters of platinum from femtomolar pl

125 ce of the [(MeO)2Ph]2bpy ligand framework on electrocatalytic CO2 reduction and its dependence upon t

126 The greatly improved onset potential for electrocatalytic CO2 reduction at gold electrodes is due

127 quantifying formate production we show that electrocatalytic CO2 reduction is specific.

128 ng matrix domain of the ion gel and displays electrocatalytic CO2 reduction to CO in the gel.

129 Electrocatalytic CO2 reduction to CO was achieved with a

130 high selectivity for ethylene formation from electrocatalytic CO2 reduction.

131 y, minimizing the required overpotential for electrocatalytic CO2 to CO conversion by Mn(I) polypyrid

132 ust route that can prepare this magnetic and electrocatalytic compound on various conductive substrat

133 Herein, we report trends in the electrocatalytic conversion of CO2 on a broad group of s

134 HPG surface was confirmed by monitoring the electrocatalytic conversion of testosterone to 6beta-hyd

135 AuNC causes significant enhancements in the electrocatalytic current densities at the electrode.

136 reversible hydrogen electrode (RHE) for the electrocatalytic current density of j = -10 mA cm(-2) ,

137 e/rGO composites offered a ~2.3 times higher electrocatalytic current density with a negative shift o

138 This change results in an enhancement in the electrocatalytic current when the sensors are interrogat

139 ing reagents produces higher and more stable electrocatalytic currents than those obtained with eithe

140 An electrocatalytic cycle is also feasible.

141 We report the electrocatalytic dehalogenation of trichloroethylene (TC

142 ide-FePt/CNTs carbon paste electrode for the electrocatalytic determination of glutathione (GSH) in t

143 Furthermore, a simple proof-of-concept electrocatalytic DNA biosensor is demonstrated for disti

144 The observed electrocatalytic effect at 2D-hBN has not previously bee

145 particle (AuNP) tags monitored through their electrocatalytic effect towards hydrogen evolution react

146 ecause the CNTs enhance sensitivity and have electrocatalytic effects.

147 hed lights onto the development of effective electrocatalytic electrodes due to their open structure

148 role of the proton donor in the kinetics of electrocatalytic energy conversion reactions.

149 l, making them paradigms for efficiency: the electrocatalytic "exchange" rate (measured around zero d

150 osensor has been developed by exploiting the electrocatalytic functionality of nitrogen (N) doped zin

151 Herein, we show that electrocatalytic generation of H2 by a redox-active liga

152 A new pathway for homogeneous electrocatalytic H2 evolution and H2 oxidation has been

153 Both the Co(III) 4 and Co(II) 5 show electrocatalytic H2 generation in weakly acidic media as

154 nsient Co(III)H and Co(II)H intermediates of electrocatalytic H2 production by [Co(II)(P(tBu)2N(Ph)2)

155 rcumvent the need for precious metal ions in electrocatalytic H2 production.

156 , but the complex becomes active for aqueous electrocatalytic H2O oxidation.

157 ing a strong dependence of NiO NW photo- and electrocatalytic HER performance on the density of expos

158 dge, there is no report about a catalyst for electrocatalytic hydrogen evolution beyond metals.

159 The electrocatalytic hydrogen evolution reaction (HER) activ

160 ced by either rapid electron transfer or the electrocatalytic hydrogen evolution reaction at a single

161 because it provides a large-surface area for electrocatalytic hydrogen evolution, and improves the ma

162 ntity and capability of active sites towards electrocatalytic hydrogen evolution, which may also be e

163 pment for important energy applications like electrocatalytic hydrogen production, where there is a g

164 are leaders as earth abundant materials for electrocatalytic hydrogen production.

165 ctrocatalyst at single-particle level during electrocatalytic hydrogen-oxidation reaction.

166 ic Cu electrodes in acidic electrolytes: (i) electrocatalytic hydrogenation (ECH) and (ii) direct ele

167 Here we show a tridimensional electrocatalytic interface, featuring a hierarchical, co

168 gher quantity of analyte and consequently of electrocatalytic label, when compared with commercially

169 f broad interest for amorphous Mo-S (a-MoSx) electrocatalytic materials and anion-redox chalcogel bat

170 electrochemical and topographical imaging of electrocatalytic materials at the nanoscale.

171 the development of earth-abundant photo- or electrocatalytic materials with high activity and long-t

172 matched imprinted cavities on the excellent electrocatalytic matrix of MWCNTs and the electronic bar

173 ction of CO2 to CO, and thereby altering the electrocatalytic mechanism at the nanoparticle surface.

174 d sticky rice to probe the underlying oxygen electrocatalytic mechanism.

175 Electrocatalytic mediator demonstrated a significant imp

176 Electrocatalytic methods for organic synthesis could off

177 mmetry and amperometry studies confirmed the electrocatalytic nature of V2O5 nanoplates modified Au e

178 amperometry, correspond to the formation of electrocatalytic nuclei on the electrode surface, capabl

179 The electrocatalytic oxidation of A and G on the electrode w

180 therefore be monitored and amplified by the electrocatalytic oxidation of AA.

181 e of different experimental variables on the electrocatalytic oxidation of ACTZ by the bio-inspired s

182 trated in both carbon monoxide oxidation and electrocatalytic oxidation of alcohol.

183 The assay employs the electrocatalytic oxidation of ascorbic acid (AA) by a th

184 The total faradaic efficiencies of electrocatalytic oxidation of both alcohols exceed 94%.

185 antigen was based on its obstruction to the electrocatalytic oxidation of catechol by Ag@Pt-GRs afte

186 Highly efficient electrocatalytic oxidation of ethanol and methanol has b

187 These results demonstrate that electrocatalytic oxidation of ethanol and methanol occur

188 nt stability and high catalytic activity for electrocatalytic oxidation of glucose in alkaline soluti

189 Taking the electrocatalytic oxidation of H2O2 at ruthenium oxide (R

190 In particular, the electrocatalytic oxidation of HMF to the value-added 2,5

191 change in the potential, which is due to the electrocatalytic oxidation of hydrazine exactly at the t

192 er mild oxidizing conditions, inhibiting the electrocatalytic oxidation of hydrogen as recorded by pr

193 rGO composites demonstrated excellent direct electrocatalytic oxidation toward NADH, providing a larg

194 determination of salicylic acid based on its electrocatalytic oxidation.

195 ed as model catalyst/support systems for the electrocatalytic oxygen evolution reaction (OER).

196 Electrocatalytic oxygen reduction at carbon electrodes f

197 down native CcO (bovine 500 s(-1)), allowing electrocatalytic oxygen reduction rates of 5,000 s(-1) f

198 Bifunctional catalysts for the electrocatalytic oxygen reduction reaction (ORR) and the

199 ransfer (ET) and lowers the overpotential of electrocatalytic oxygen reduction reaction (ORR) by appr

200 CoO hybrid nanocatalysts are fabricated for electrocatalytic oxygen reduction reaction.

201 )2(2+) (1) is capable of traversing multiple electrocatalytic pathways.

202 ch in turn affects the crystal structure and electrocatalytic performance for hydrogen evolution reac

203 roxides (Co0.54Fe0.46OOH) show the excellent electrocatalytic performance for OER with an onset poten

204 esoporous carbon particles manifest enhanced electrocatalytic performance for oxygen reduction reacti

205 The electrocatalytic performance is further considered at an

206 We critically evaluate the potential electrocatalytic performance of 2D-hBN modified electrod

207 e beneficial role of sulfur vacancies in the electrocatalytic performance of pentlandite and give ins

208 d active sites contributed to the remarkable electrocatalytic performance of the Ag-CoSe2 nanobelts.

209 morphous phases with distinctively different electrocatalytic performance reveals that high activity

210 trathin nanowire networks exhibits excellent electrocatalytic performance toward ethanol oxidation, h

211 nomeshes lead to a remarkable improvement in electrocatalytic performance, where CoO0.87 S0.13 /GN ex

212 ore-shell nanowires, which leads to improved electrocatalytic performance.

213 ture, which results in marked improvement in electrocatalytic performance.

214 d inner structural control to strengthen the electrocatalytic performance.

215 d with p-block elements has shown impressive electrocatalytic performances in processes which have be

216 The electrocatalytic performances of the SB were investigate

217 sitive electrochemical immunosensor based on electrocatalytic platinum nanoparticles conjugated to a

218 e to the profound knowledge of the nature of electrocatalytic processes accumulated over the past sev

219 he oxygen reduction reaction (ORR) and other electrocatalytic processes requires detailed knowledge o

220 tron-transfer reactions and for more complex electrocatalytic processes.

221 ative to noble metal catalysts for efficient electrocatalytic production of hydrogen in both alkaline

222 convoluted relations between composition and electrocatalytic properties are established.

223 en incorporated into the flow cell and their electrocatalytic properties evaluated.

224 a of approximately 1,663 m(2) g(-1) and good electrocatalytic properties for both ORR and OER.

225 57:H7 in meat and water samples based on the electrocatalytic properties of gold nanoparticles (AuNPs

226 results revealed that f-MWCNTs increased the electrocatalytic properties of Ni nanoparticles regardin

227 great improvement in the electrochemical and electrocatalytic properties of the CAT/PLL/f-MWCNT biose

228 Notable electrocatalytic properties of the developed electrode t

229 ing the synthetic conditions, can affect the electrocatalytic properties of the materials.

230 The remarkably improved electrocatalytic properties of the present peroxidase bi

231 In other words, the electrocatalytic properties of the PtNPs are reactivated

232 rticles and to obtain evidence for different electrocatalytic properties of the two enzymes.

233 theory calculations reveal that its unusual electrocatalytic properties originate from an intrinsic

234 Additionally, we investigate the anomalous electrocatalytic properties that allow 4-amino-TEMPO to

235 nced diffusion kinetics, exhibiting superior electrocatalytic properties to Pt and RuO2 as a bifuncti

236 structured metallopolymer exhibits efficient electrocatalytic properties toward oxidation of NADH.

237 R = H (1), Me (2), and allyl (3)), and their electrocatalytic properties were explored.

238 ratios, which lead to unique mechanical and electrocatalytic properties, but directly measuring this

239 -hydroxyphenalenone) displaying an excellent electrocatalytic property as cathode material for one co

240 process was monitored as the decrease in the electrocatalytic protein signal, peak H, observed at hig

241 vity of the immunoassay, these scFV labelled electrocatalytic PtNPs were then used for covalent hybri

242 Herein, we developed a protein-facilitated electrocatalytic quadroprobe sensor (Sens(PEQ)) for dete

243 e appears to be aided by propulsion from the electrocatalytic reaction at the NP.

244 echanism relies on the previously unexplored electrocatalytic reaction between Cr(VI) and surface-imm

245 The detection strategy is based on the electrocatalytic reaction between the Pt(IV) center of S

246 ime, detection of the current produced in an electrocatalytic reaction by a single redox enzyme molec

247 Identifying the intermediate species in an electrocatalytic reaction can provide a great opportunit

248 ique way for a real-time investigation of an electrocatalytic reaction pathway at various well-define

249 rived for two-electron, two-step homogeneous electrocatalytic reactions in the total catalysis regime

250 examples, including voltammetric mapping of electrocatalytic reactions on electrodes and high-speed

251 nd activity of individual NPs, by either (i) electrocatalytic reactions or (ii) volumetric (dissoluti

252 Extended applications to various electrocatalytic reactions with different types of elect

253 This not only enhances electrocatalytic reactions, but also provides excellent

254 surface of the AuNP is still accessible for electrocatalytic reactions.

255 ization to analyze the mechanisms of various electrocatalytic reactions.

256 phthalene diimide (PIND) functionalized with electrocatalytic redox Os(bpy)2Cl(+) moieties (PIND-Os))

257 Electrocatalytic reduction of carbon monoxide on copper

258 The complexity of the electrocatalytic reduction of CO to CH4 and C2H4 on copp

259 The electrocatalytic reduction of CO2 has been studied exten

260 Electrocatalytic reduction of CO2 to CO is reported for

261 y demonstrates a predominant shape-dependent electrocatalytic reduction of CO2 to CO on triangular si

262 as shifting the rate-determining step in the electrocatalytic reduction of CO2 to CO, and thereby alt

263 -performance gas diffusion electrode for the electrocatalytic reduction of CO2 to formate.

264 ctive, durable, gas permeable electrodes for electrocatalytic reduction of CO2 to formate.

265 The electrocatalytic reduction of CO2 to industrial chemical

266 obilization of the molecular catalyst allows electrocatalytic reduction of CO2 under fully aqueous co

267 zed graphene nanoribbon (GNR) matrix for the electrocatalytic reduction of CO2.

268 u2-bpy)(CO)3, which is a precatalyst for the electrocatalytic reduction of CO2.

269 ow-generation dendrimers rapidly grow during electrocatalytic reduction of CO2.

270 trochemical label in the sandwich format and electrocatalytic reduction of H2O2 in the presence of en

271 or displayed an excellent performance to the electrocatalytic reduction of H2O2 with a detection limi

272 Mb rebinding was detected by direct electrocatalytic reduction of Mb by square wave voltamme

273 Here we report the electrocatalytic reduction of protons to hydrogen by a n

274 rode were examined for their efficacy toward electrocatalytic reduction of UO2(2+) ions and observed

275 Electrocatalytic reduction of water to molecular hydroge

276 The glucose biosensor shows a good electrocatalytic response in the presence of (hydroxymet

277 G-Au modified GCE exhibited an enhanced electrocatalytic response towards the oxidation of NO as

278 The FSG- modified sensor showed an excellent electrocatalytic response towards the sensing of COD wit

279 obes, the DNAzyme-linked LCR products induce electrocatalytic responses that are proportional to the

280 Importantly, this accessibility-based electrocatalytic sensing strategy is versatile and can p

281 lete new battery of devices with fascinating electrocatalytic, sensitivity, and selectivity propertie

282 he Anti-IgY-HRP is detected by recording the electrocatalytic signal caused by addition of H2O2 and m

283 ical catalytic activity and offers long-term electrocatalytic stability for the hydrogen evolution re

284 the optimized porous NiO NWs offer long-term electrocatalytic stability of over one day and 45 times

285 Electrocatalytic studies showed that nickel (7.7 atomic

286 stem comprising nanoparticulate Au, a common electrocatalytic support, and nanoparticulate MnO(x), a

287 r future studies in spatial heterogeneity of electrocatalytic surfaces.

288 emonstrate a tangible path for the design of electrocatalytic systems for C-H bond activation that af

289 The development of high-performance electrocatalytic systems for the controlled reduction of

290 ced catalytic activity of the captured AuNPs electrocatalytic tags are exploited for the first time.

291 We utilize black phosphorus nanoparticles as electrocatalytic tags in a competitive immunoassay for r

292 in a Li-S battery can be stabilized by using electrocatalytic transition metal dichalcogenides (TMDs)

293 trial solvent chlorobenzene, signifying that electrocatalytic treatment has tremendous potential as a

294 Electrocatalytic water oxidation activity increased with

295 r process at 1.25 V, associated with a large electrocatalytic water oxidation wave (overpotential of

296 nmentally friendly approach to generate H2 , electrocatalytic water splitting has attracted worldwide

297 Commercial hydrogen production by electrocatalytic water splitting will benefit from the r

298 Hydrogen production by electrocatalytic water splitting will play a key role in

299 lications may include batteries, fuel cells, electrocatalytic water splitting, corrosion protection,

300 ent use of this composition in heterogeneous electrocatalytic WO.