ライフサイエンスコーパス: electrocatalytic

1 First, the current knowledge about electrocatalytic active sites is briefly summarized.

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

3 g N and Ni codoped np-graphene has excellent electrocatalytic activities for both the ORR and the OER

4 olvothermal process, can significantly boost electrocatalytic activities of I(-)/I(3)(-) and S(2-)/S(

5 articles (Iso-AgNPs), and photocatalytic and electrocatalytic activities of Iso-AgNPs are evaluated.

6 The multifunctional electrocatalytic activities originate from a synergistic

7 n materials, their general properties, their electrocatalytic activities toward the HzOR, and their d

8 tive conditions, and attributed the improved electrocatalytic activities toward various analytes to t

9 tive information on the surface property and electrocatalytic activities.

10 for evaluating and comparing their intrinsic electrocatalytic activities.

11 molybdenum disulfide (MoS(2)), where higher electrocatalytic activity (i.e., lower overpotential at

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

13 EPPGE exhibited strong electrocatalytic activity and enhanced reduction signal

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

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

16 gives rise to the observed high ORR and OER electrocatalytic activity and small discharge/charge ove

17 c electron coupling, which endow exceptional electrocatalytic activity and stability simultaneously.

18 The electrocatalytic activity can be mapped from the same SE

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

20 r O(2) reduction and Ni-NC SAC exhibits high electrocatalytic activity for CO(2) reduction.

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

22 e a metallic nature exhibited by an enhanced electrocatalytic activity for hydrogen evolution reactio

23 Here we report the remarkable electrocatalytic activity for hydrogen evolution reactio

24 The electrocatalyst exhibits promising electrocatalytic activity for ORR with a half-wave poten

25 e heterophase gold nanorods possess superior electrocatalytic activity for the carbon dioxide reducti

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

27 a Pt-like hydrogen evolution reaction (HER) electrocatalytic activity in acidic solution with a smal

28 sorbed into the palladium decreased, and HER electrocatalytic activity increased.

29 The excellent electrocatalytic activity is attributed to the considera

30 his further confirms that the enhancement in electrocatalytic activity is due to the electrochemical

31 systems, and this was correlated to the high electrocatalytic activity observed.

32 Comparing the electrocatalytic activity of 2D core-shell systems with

33 tric that reasonably evaluates the intrinsic electrocatalytic activity of a particular catalyst.

34 The electrocatalytic activity of bismuth considered as a low

35 The electrocatalytic activity of Ir-PEDOT/CFP electrode towa

36 The electrocatalytic activity of M-N-C materials toward four

37 and reported the significant enhancement in electrocatalytic activity of MoSe(2) due to the Co dopin

38 Identifying the intrinsic electrocatalytic activity of nanomaterials is challengin

39 The demonstration of an enhancement in the electrocatalytic activity of new oxides by preadjusting

40 Tensile strain is known to improve the electrocatalytic activity of palladium electrodes for re

41 on of a carbon support allows to enhance the electrocatalytic activity of Pd to hydrogenate benzaldeh

42 to be the main reason for the enhancement in electrocatalytic activity of the activated GCE (AGCE).

43 The electrocatalytic activity of the nanograin film is compr

44 ified orange juice, this shows the selective electrocatalytic activity of the ZrO(2)-Cu(I) nanosphere

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

46 (4) catalyst, which illustrates the improved electrocatalytic activity previously reported on this mi

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

48 l and how these can influence the subsequent electrocatalytic activity that is displayed.

49 flexible cotton electrode with an excellent electrocatalytic activity to oxidize glucose.

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

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

52 he as-prepared Iso-AgNPs exhibited excellent electrocatalytic activity toward hydrogen peroxide (H(2)

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

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

55 ized Nano-Fe(3)C@PGC exhibits an outstanding electrocatalytic activity toward the charge transfer bet

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

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

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

59 assy carbon electrode exhibited an excellent electrocatalytic activity toward the sensing of Metol (L

60 , fundamental and practical aspects of their electrocatalytic activity toward two-electron ORR to H(2

61 used for the evaluation of the Au@Pt/Au NPs electrocatalytic activity toward WOR.

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

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

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

65 The HAP- ZnO-Pd NPs/CPE exhibited excellent electrocatalytic activity towards the oxidations of AT a

66 fiber counter electrode exhibits significant electrocatalytic activity towards the reduction of triio

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

68 n outstanding durability, maintaining decent electrocatalytic activity with no degradation for more t

69 ests were performed in order to evaluate the electrocatalytic activity ZrO(2)-Cu(I) modified electrod

70 n the M synergistic effects in improving the electrocatalytic activity, as exemplified by the oxygen

71 greatly enhanced cell performance with high electrocatalytic activity, stability, and selectivity.

72 Applying SECCM to map electrocatalytic activity-specifically the electro-oxida

73 ta) (BSCF) exhibits exceptional sigma(o) and electrocatalytic activity.

74 ee of ordering in intermetallics to optimize electrocatalytic activity.

75 itate the higher electronic conductivity and electrocatalytic activity.

76 ining step to achieve excellent bifunctional electrocatalytic activity.

77 al within a series of M-N-C catalysts on the electrocatalytic activity/selectivity for ORR (H(2)O(2)

78 at is the real cause for this improvement in electrocatalytic activity?

79 ., ethanol or ethylene glycol in the case of electrocatalytic alcohol oxidation) is decreased by a sp

80 pplied to elucidate the intermediates during electrocatalytic alcohol oxidation.

81 his is a well-defined system for homogeneous electrocatalytic ammonia oxidation.

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

83 f hydroxide oxidation in accordance with the electrocatalytic amplification model.

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

85 ram on the single Pt deposits is observed by electrocatalytic amplification of the HER, with a neglig

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

87 nt types of experiments: single nanoparticle electrocatalytic amplification, photocatalytic amplifica

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

89 ocomposite on an electrode for the following electrocatalytic amplification.

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

91 ymer-supported [2Fe-2S] catalyst systems for electrocatalytic and photocatalytic hydrogen evolution r

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

93 Photocatalytic, electrocatalytic and physicochemical properties of the a

94 ent of next-generation molecular-electronic, electrocatalytic, and energy-storage systems depends on

95 omaterials, and demonstrates their promising electrocatalytic application.

96 fullerene-based LD nanomaterials for (photo)electrocatalytic applications are emphasized.

97 encapsulation of electroactive catalysts and electrocatalytic applications of such supramolecular ass

98 solutions that provide insight into distinct electrocatalytic applications.

99 Electrocatalytic approaches to the activation of unsatur

100 d in detail, presenting that this sensor had electrocatalytic behavior for oxidizing sudan I due to t

101 thod allows one to study electrochemical and electrocatalytic behavior of metal NPs in a chemical env

102 The electrocatalytic behavior of the modified electrode towa

103 f heterostructures with unprecedented (photo)electrocatalytic behavior, involving the combination of

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

105 e projected costs and CO(2) emissions across electrocatalytic, biocatalytic, and fossil fuel-derived

106 covalent organic framework was developed for electrocatalytic carbon dioxide reduction to carbon mono

107 hallenging and requires a rational design of electrocatalytic centers.

108 ciency and selectivity in photocatalytic and electrocatalytic CO(2) hydrogenation.

109 Electrocatalytic CO(2) reduction (ECR) is a promising te

110 A comprehensive mechanistic study of electrocatalytic CO(2) reduction by ruthenium 2,2':6',2"

111 The stability of metal nanocatalysts for electrocatalytic CO(2) reduction is of key importance fo

112 rials but also improves the understanding of electrocatalytic CO(2) reduction on carbon defects.

113 porous carbon materials possess an enhanced electrocatalytic CO(2) reduction performance, yielding a

114 g array structure gives rise to an excellent electrocatalytic CO(2) reduction performance.

115 When employed in electrocatalytic CO(2) reduction, Ni(1) -N-C exhibited a

116 ative yield, demonstrating its potential for electrocatalytic CO(2) reduction.

117 ucture sensitivity of Au single crystals for electrocatalytic CO(2) reduction.

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

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

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

121 Under the optimized electrocatalytic conditions, the nickel complex immobili

122 ight irradiation has a positive impact under electrocatalytic conditions.

123 Electrocatalytic conversion of biomass-derived feedstock

124 for the thermocatalytic, photocatalytic, and electrocatalytic conversion of CO(2) into synthesis gas

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

126 The electrocatalytic current was established to be a linear

127 al, computational studies suggested that the electrocatalytic cycle involves striking metal carbonyls

128 validated by fitting a kinetic model to the electrocatalytic data, but also acts to alleviate RGO ag

129 mances of LSGE were observed in terms of the electrocatalytic detection of paracetamol (PCM).

130 , to our knowledge, and demonstrate its high electrocatalytic efficiency for formate (HCOO(-)) format

131 riority of plasmonic excitation on improving electrocatalytic efficiency of MOFs and provides a novel

132 tional bio-anode concurrently exhibiting bio-electrocatalytic energy harvesting and charge storing.

133 Electrocatalytic experiments are described that revealed

134 0 years that focuses on carefully controlled electrocatalytic experiments which, in combination with

135 dye sensitized solar cell (DSSC), and better electrocatalytic features are introduced in the electrod

136 oxide in the ventral tegmental area with the electrocatalytic fibres evoked neuronal excitation in th

137 With these structural features, the electrocatalytic framework exhibits a faradaic efficienc

138 e chemical modularity in order to tailor the electrocatalytic function of MOF-anchored active sites a

139 The electrocatalytic functions of the NiCu nanoalloys were e

140 e first time that VB and V(3) B(4) have high electrocatalytic HER activity.

141 ineering offers a novel route to promote the electrocatalytic HER/OER performances for efficient wate

142 rface misorientation identified as potential electrocatalytic "hot spots".

143 Au nanorods (NRs) dramatically improves the electrocatalytic hydrogen evolution activity of CoFe-met

144 nced activity and excellent stability toward electrocatalytic hydrogen evolution in acidic solution.

145 and investigation of their role in alkaline electrocatalytic hydrogen evolution reaction (HER) is pr

146 up VI TMDs displayed leading performance for electrocatalytic hydrogen evolution, high volumetric cap

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

148 present here detailed mechanistic studies of electrocatalytic hydrogenation (ECH) in aqueous solution

149 t operate at low temperatures are needed for electrocatalytic hydrogenation (ECH) to upgrade the feed

150 t organic functionalities are accessible for electrocatalytic hydrogenation under a set of reaction c

151 This novel Au@Pt/Au NPs-based electrocatalytic immunoassay has the advantage, over com

152 rofoundly affected by the liquid side of the electrocatalytic interface.

153 ic techniques led us to identify elusive key electrocatalytic intermediates derived from complex [L(N

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

155 ch opens up new opportunities to develop new electrocatalytic materials and innovative sensing approa

156 paving the way for the design of even better electrocatalytic materials through structure-activity re

157 stimulated intense investigation of various electrocatalytic materials.

158 theory now frequently leading the design of electrocatalytic materials.

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

160 Then, the electrocatalytic mechanisms of the five above-mentioned

161 Herein, we present a Janus electrocatalytic membrane realizing ultra-efficient (1)O

162 onds, and it was previously shown that rapid electrocatalytic methane monofunctionalization could be

163 The optimized electrocatalytic method was applied to the quantificatio

164 similar approach is used to assess molecular electrocatalytic methods for electrochemical oxidation o

165 Electrocatalytic methods for organic synthesis could off

166 t, we investigate the dynamic behavior of an electrocatalytic Mn-porphyrin-containing MOF system (Mn-

167 Being one of the very few hydrogen evolving electrocatalytic MOFs based on a redox-active metallo-li

168 future efforts to enhance the efficiency of electrocatalytic MOFs should also consider other importa

169 isomerism of the -NO(2) substituents for the electrocatalytic multi electron oxidation of As(III), a

170 The ambient electrocatalytic N(2) reduction reaction (NRR) enabled b

171 NH(3) synthesis by the electrocatalytic N(2) reduction reaction (NRR) under amb

172 Electrocatalytic N(2) reduction to ammonia is an attract

173 Integrating these electrocatalytic nanoclusters with multimaterial fibres

174 is feature in a generalized approach with an electrocatalytic nanoparticle for the carbon dioxide red

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

176 O(2) nanoreactor enhances the performance of electrocatalytic nitrogen fixation.

177 ficient catalysts impedes the development of electrocatalytic nitrogen reduction reaction (eNRR) for

178 al energy-related CO2 emissions, the ambient electrocatalytic nitrogen reduction reaction has attract

179 tatus and challenges in the study of ambient electrocatalytic nitrogen reduction, followed by a thoro

180 i(3+) formation, which markedly improves the electrocatalytic NRR performance.

181 le-atom non-precious-metal catalysts for the electrocatalytic NRR.

182 rogen adsorption energy, and facilitates the electrocatalytic NRR.

183 ith consideration of practical factors under electrocatalytic operating conditions.

184 xed with carbon nanotubes exhibits excellent electrocatalytic ORR activity (E(1/2) =0.83 V vs. RHE, n

185 pK(a), on the H(2)O(2)/H(2)O selectivity in electrocatalytic ORR by iron(tetramesitylporphyrin) (Fe(

186 ive facets, is shown to improve activity for electrocatalytic oxidation of 5-hydroxymethylfurfural (H

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

188 effective electrochemical mediators for the electrocatalytic oxidation of alcohols by an iridium ami

189 adsorbent), and during release, synergistic electrocatalytic oxidation of As(III) to As(V) with >90%

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

191 Unravelling the intrinsic mechanism of electrocatalytic oxygen evolution reaction (OER) by use

192 roxide-mediated chain reaction, initiated by electrocatalytic oxygen reduction on the cathodic membra

193 of both redox-based MOF conductivity and the electrocatalytic oxygen reduction reaction (ORR).

194 viously shown exceptional performance in the electrocatalytic oxygen reduction reaction (ORR).

195 gen evolution reaction (OER) can enhance the electrocatalytic performance and help elucidate underlyi

196 metal phosphates, have demonstrated superior electrocatalytic performance compared with their crystal

197 ction, the ultrathin PtNiM NWs show enhanced electrocatalytic performance for both methanol oxidation

198 articles (NPs) is crucial to obtain superior electrocatalytic performance for fuel cell reactions, bu

199 ation, high-loading Fe-NC SAC shows superior electrocatalytic performance for O(2) reduction and Ni-N

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

201 single-atom Rh-Fe catalyst renders excellent electrocatalytic performance for the hydrogen evolution

202 MOF@Nafion composite exhibits an outstanding electrocatalytic performance for the OER at neutral pH,

203 The electrocatalytic performance is further considered at an

204 fects have a profound positive impact on the electrocatalytic performance of bismuth.

205 vacancy (3Co(Mo)-V(S)) renders the distinct electrocatalytic performance of MoS(2) with much reduced

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

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

208 Moreover, we demonstrate impressive electrocatalytic performance of these aerogels for the e

209 nus material exhibits excellent bifunctional electrocatalytic performance, in which the outer Fe-N(4)

210 d inner structural control to strengthen the electrocatalytic performance.

211 ingle-atom catalysts can display outstanding electrocatalytic performance; however, given their singl

212 to studying fundamental electrochemical and electrocatalytic phenomena, whereby nanoscale-resolved i

213 Overall, this liquid metal enabled electrocatalytic process at room temperature may result

214 n, considering the simplest and most typical electrocatalytic process, the hydrogen evolution reactio

215 ment control the selectivity of this complex electrocatalytic process.

216 ite catalysts and those active in photo- and electrocatalytic processes are critically reviewed.

217 Electrocatalytic processes hold great potential for high

218 version of chemicals and electricity through electrocatalytic processes is central to many renewable-

219 he product selectivity of many heterogeneous electrocatalytic processes is profoundly affected by the

220 s provide a mechanistic understanding of the electrocatalytic processes of trimetallic oxides under r

221 version encompasses redox chain reactions in electrocatalytic processes, photoredox cascades, design

222 Despite progress in small scale electrocatalytic production of hydrogen peroxide (H(2)O(

223 ace enhanced RR (SERR) spectroscopy, and the electrocatalytic properties are analyzed by electrochemi

224 metals, and surface Bi modification to their electrocatalytic properties are experimentally explored,

225 nd discover that SA-Rh/CN exhibits promising electrocatalytic properties for formic acid oxidation.

226 zOR, and their dopant- and structure-related electrocatalytic properties for the HzOR are summarized.

227 ith dense heterointerfaces exhibits superior electrocatalytic properties in an alkaline electrolyte,

228 Herein, we report on the synthesis and electrocatalytic properties of an iron-porphyrin aerogel

229 an effective tool for dynamically tuning the electrocatalytic properties of HER and OER electrocataly

230 Notable electrocatalytic properties of the developed electrode t

231 tive Co(Fe)OOH phase, which enhances the OER electrocatalytic properties of the underlying conductive

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

233 nd C(60)-C(60) interactions as well as their electrocatalytic properties were finely controlled by va

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

235 fundamental relevance for its catalytic and electrocatalytic properties.

236 s a grand challenge to unveil their pristine electrocatalytic properties.

237 states and reaction intermediates as well as electrocatalytic properties.

238 metallic nanostructures with multifunctional electrocatalytic properties.

239 not the only factor that limits the overall electrocatalytic rate.

240 t have been limited by their reliance on the electrocatalytic reaction between NH(4)(+) and a metal/n

241 y balancing the mass transport processes and electrocatalytic reaction rates at the electrode diffusi

242 xpected to have high activity for other core electrocatalytic reactions and open the way for advances

243 ains how particle shape impacts the relevant electrocatalytic reactions and the resulting electrokine

244 variety of energy storage devices, including electrocatalytic reactions at electrode/membrane interfa

245 chnique for the operando characterization of electrocatalytic reactions at the molecular scale.

246 es in activating various elementary steps of electrocatalytic reactions can help rational design of b

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

248 ue material structures of MGNs on individual electrocatalytic reactions is made, including the hydrog

249 influence of structural surface features on electrocatalytic reactions is vital for the development

250 electrochemical device and for accelerating electrocatalytic reactions that consume protons in neutr

251 s studied via a series of photocatalytic and electrocatalytic reactions varying the atmospheric compo

252 s strategy might also be applicable to other electrocatalytic reactions where gas consumption is invo

253 Only a few electrocatalytic reactions within cages have been report

254 s to identify the activity of step sites for electrocatalytic reactions, as demonstrated for the bulk

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

256 at show promise for the development of novel electrocatalytic reactions.

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

258 ctivity in other multi-proton/multi-electron electrocatalytic reactions.

259 rformance in a large number of catalytic and electrocatalytic reactions.

260 lecular catalysts to drive energy-conversion electrocatalytic reactions.

261 pproach that can be easily extended to other electrocatalytic reactions.

262 The enhancement of electrocatalytic reduction is realized by the participat

263 The electrocatalytic reduction of carbon dioxide (CO(2)) cou

264 The electrocatalytic reduction of carbon dioxide, powered by

265 The electrocatalytic reduction of CO to hydrocarbons on Cu e

266 results serve as a proof of concept for the electrocatalytic reduction of CO(2) by sustainable, recy

267 The electrocatalytic reduction of CO(2) provides a sustainab

268 Electrocatalytic reduction of CO2 to CO is reported for

269 Examples include efficient and selective electrocatalytic reduction of CO2 to CO or formate - rea

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

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

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

273 The selective electrocatalytic reduction of dioxygen (O(2)) to hydroge

274 = [(tbu)dhbpy](2-), which is active for the electrocatalytic reduction of O(2) to H(2)O(2) (ca. 80%

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

276 ve elimination pathway on rhodium(III) in an electrocatalytic regime.

277 e-specific organic materials, owing to their electrocatalytic response to the oxidation of glucose.

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

279 oses a conundrum regarding the properties of electrocatalytic reversibility and associated bidirectio

280 otential, clearly signaling a departure from electrocatalytic reversibility as electron and proton tr

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

282 We believe that such an IrO(2) NPs-based electrocatalytic sensing system can lead to a rapid, sen

283 What is the identity of the true electrocatalytic species?

284 r future studies in spatial heterogeneity of electrocatalytic surfaces.

285 Such an electrocatalytic synergy is pivotal to the high-rate oxy

286 The resulting electrocatalytic system is practical, scalable, and broa

287 M has been employed to benchmark a promising electrocatalytic system, the hydrogen evolution reaction

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

289 lication of MOFs as dynamic, enzyme-inspired electrocatalytic systems.

290 Electrocatalytic transformation of carbon dioxide (CO(2)

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

292 here can be generalized to other photo- and electrocatalytic transition metal oxide systems.

293 d, we report a catalyst that maintained high electrocatalytic turnover frequency at pH values as low

294 Cu-catalyzed selective electrocatalytic upgrading of carbon dioxide/monoxide to

295 Electrocatalytic voltammograms, which show the rate of e

296 The active site for electrocatalytic water oxidation on the highly active ir

297 Efficient hydrogen evolution via electrocatalytic water splitting holds great promise in

298 NPs to energy conversion is highlighted with electrocatalytic water splitting on CoFeLaNiPt HEMG-NPs.

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

300 nuclease (DSN)-assisted target recycling and electrocatalytic water-splitting is demonstrated for the