ライフサイエンスコーパス: photocatalytic

1 nstance of employing [C(7)(0)] fullerene for photocatalytic (1)O(2) production in water, through cova

2 To understand the photocatalytic act of dust particles, both GDD and ATD w

3 Surprisingly, the photocatalytic activation of ethers by H-abstraction and

4 s exhibit excellent visible light responsive photocatalytic activities for efficiently degrading orga

5 Their photocatalytic activities for H2 production under visibl

6 The photocatalytic activities of Ce-TiO2 nanocrystals were i

7 The photocatalytic activities of the Al-TiO2 samples were in

8 n in the visible region and greatly enhanced photocatalytic activities on H2 generation comparing wit

9 nificantly enhanced photoelectrochemical and photocatalytic activities under visible light irradiatio

10 n successfully demonstrated to enhance their photocatalytic activities, especially in the report of b

11 metals obtained, and (iii) consequences for photocatalytic activities.

12 he nanosheets, responsible for the very high photocatalytic activities.

13 prepared from Al(NO3)39H2O exhibit the best photocatalytic activity among the four kinds of samples,

14 peak at 579 nm disappeared under the highest photocatalytic activity and 99.89% of RhB degraded under

15 anocatalyst exhibits excellent visible-light photocatalytic activity and an apparent quantum efficien

16 roperties, such as visible-light absorption, photocatalytic activity and high dielectric permittivity

17 es for perovskite catalysts to improve their photocatalytic activity and/or light adsorption capabili

18 films of the two polymorphs we evaluate the photocatalytic activity as a function of TiO2-film thick

19 lysts are shown to be able to possess higher photocatalytic activity because of spatial separation of

20 tocatalyst, thus significantly enhancing its photocatalytic activity by two orders of magnitude in te

21 Despite the photocatalytic activity decreased with each cycle, it ca

22 ZTS/MoS2-rGO system also demonstrated stable photocatalytic activity for a continuous 20 h reaction.

23 s and exhibit superior UV- and visible-light photocatalytic activity for ammonia synthesis at ambient

24 nd lambda > 455 nm and maintained their full photocatalytic activity for at least 1 day under full so

25 thesis, and the prepared ZnS samples exhibit photocatalytic activity for H2 production under visible-

26 On evaluating their photocatalytic activity for hydrogen evolution, the olig

27 among the highest in Zr-MOFs) but also high photocatalytic activity for reduction of CO2 into CO ( a

28 ular CuCr-LDH nanosheets, possess remarkable photocatalytic activity for the photoreduction of N2 to

29 Ps ( approximately 0.1 wt %) can enhance the photocatalytic activity for water splitting up to a fact

30 cade that correlates with a near-doubling in photocatalytic activity from 2050 to 3810 mumol h(-1) g(

31 w that hot electrons exhibiting the enhanced photocatalytic activity in H2 production reaction can be

32 , the a-TiO2 film-which is found to lack any photocatalytic activity in itself-is hypothesized to rea

33 bon nitride"), with the aim of improving its photocatalytic activity intrinsically.

34 Their photocatalytic activity is strongly correlated to the nu

35 were determined to be essential to the high photocatalytic activity observed with CD-NHMe2(+).

36 ple potential of intrinsically improving the photocatalytic activity of "carbon nitride", especially

37 Here, we assess the photocatalytic activity of MIL-125, a TiO2/1,4-benzenedi

38 About 26% of the photocatalytic activity of Ni/silica-alumina under solar

39 were exposed to visible light to induce the photocatalytic activity of the Au@GO nanoflakes towards

40 mpedance spectroscopy, we show that the high photocatalytic activity of the nanoparticles arises from

41 Light absorption and photocatalytic activity of the resulted Bi7Fe(3-x)CoxTi3

42 itching can also be achieved by coupling the photocatalytic activity of the SnO2-x NCs with the color

43 In addition, the reduced photocatalytic activity of the TiO2 layer leads to enhan

44 The photocatalytic activity of these bpy-containing PCPs can

45 mers, and that the key challenge to optimize photocatalytic activity of these materials is to prevent

46 1} facets could provide a way to enhance the photocatalytic activity of this material.

47 n the synthesis atmosphere; in this way, the photocatalytic activity of Ti(3+)-doped TiO2 under visib

48 This photocatalytic activity of ZnS increases steadily with i

49 is correlation between electron transfer and photocatalytic activity provides new insight into struct

50 ery provides a facile method of manipulating photocatalytic activity simply by varying the Au NP size

51 /MoS2-rGO heterostructure showed much higher photocatalytic activity than both Au and Pt nanoparticle

52 {001}-TiO(2) has 1.79 and 3.22 times higher photocatalytic activity than {010} and {101}-TiO(2), res

53 zo[b,d]thiophene sulfone co-polymer has a UV photocatalytic activity that rivals TiO2, but is much mo

54 ngle-crystalline nanosheets with outstanding photocatalytic activity toward CO2 reduction is prepared

55 significantly enhanced visible-light driven photocatalytic activity toward hydrogen evolution compar

56 le metal nanoparticles advance visible light photocatalytic activity toward new reactions not typical

57 e structures, the material exhibits superior photocatalytic activity toward the hydrogen evolution re

58 distinct mechanisms to clarify visible-light photocatalytic activity under different excitation condi

59 ed, and the TiO2-S/rGO hybrid exhibited high photocatalytic activity under simulated sunlight.

60 The films also showed good photocatalytic activity under UV-light illumination, wit

61 We propose that the increase in photocatalytic activity upon heterogenization of the cat

62 l charge-transfer excited state lifetime and photocatalytic activity was evidenced from the electron

63 the molecular catalyst, and intriguingly, no photocatalytic activity was observed using the CQDs and

64 hibits the superior luminescent property and photocatalytic activity, which may find potential applic

65 350 degrees C, the crystalized TiO2 enhanced photocatalytic activity, while Fe3O4 was converted to ga

66 relates well with the observed trends in the photocatalytic activity.

67 the solar energy absorption and enhances the photocatalytic activity.

68 bsorption, narrowing band gap, and improving photocatalytic activity.

69 he MOF is not required to obtain the maximum photocatalytic activity.

70 e to a high photoconductive gain and reduced photocatalytic activity.

71 The effect of photocatalytic air pretreatment on the growth and biomas

72 The photocatalytic air pretreatment transforms NO gas into N

73 upon photoexcitation is necessary to expand photocatalytic and biological imaging applications.

74 and anatase TiO2 is extremely important for photocatalytic and catalytic applications because of the

75 In addition, photocatalytic and photoelectrochemical mechanisms of th

76 his study provides fundamental insights into photocatalytic and photoelectrochemical performance of t

77 of efficient light-harvesting systems, like photocatalytic and photovoltaic ones.

78 ance of bulk charge diffusion for explaining photocatalytic anisotropies.

79 of heterojunction photocatalysts for various photocatalytic applications are also presented and appra

80 ctivated O2s-Ti bond that may be relevant in photocatalytic applications in an aqueous medium.

81 eparation dynamics, properties essential for photocatalytic applications, using optical (OTA) and X-r

82 O-66(Hf) are among the most studied MOFs for photocatalytic applications.

83 eveloping new materials for photovoltaic and photocatalytic applications.

84 xcitation, making this material suitable for photocatalytic applications.

85 the important family of 3d-4f complexes for photocatalytic applications.

86 This photocatalytic behavior is completely different from tha

87 The photocatalytic C-F functionalization of highly fluorinat

88 A mild and selective photocatalytic C-H (18)F-fluorination reaction has been

89 sfer to exfoliated carbon nitride containing photocatalytic chain terminations.

90 rate the utility of these nanostructures for photocatalytic chemical reactions in the preferential ox

91 ng energy efficiency of electrocatalytic and photocatalytic CO2 conversion to useful chemicals poses

92 s that pyridinium plays an important role in photocatalytic CO2 reduction on p-GaP photoelectrodes.

93 scheme mechanism and ultimately enhanced the photocatalytic CO2 reduction performance of the Ag3PO4/g

94 reservoir would represent a role for TiO2 in photocatalytic CO2 reduction that has previously not bee

95 onsidered to be very promising materials for photocatalytic CO2 reduction.

96 neration of reactive oxygen species from the photocatalytic coatings is the major factor that signifi

97 g, novel solar energy exploitation including photocatalytic coenzyme regeneration, templating, and ca

98 technique is reported for the synthesis of a photocatalytic composite material consisting of orthorho

99 first time to investigate the activities of photocatalytic composite, Ag3PO4/g-C3N4, in converting C

100 The stability of Co4O4-dpk under photocatalytic conditions ([Ru(bpy)3](2+)/S2O8(2-)) was

101 s of arylphosphine oxides with alkynes under photocatalytic conditions by using eosin Y as the cataly

102 Under photocatalytic conditions in CH3CN/TEOA, a common reacti

103 drogensulfate (EMIM), was investigated under photocatalytic conditions in the presence of irradiated

104 stability of the {Co(II)3Ln(OR)4} WOCs under photocatalytic conditions is demonstrated with a compreh

105 In situ XANES experiments under photocatalytic conditions show that the {Co(II)4O4} core

106 tivity, including interesting behavior under photocatalytic conditions.

107 mbination rate has been the big challenge to photocatalytic conversion efficiency.

108 key to extending their functionality to the photocatalytic conversion of absorbed gases.

109 Photocatalytic conversion of CO2 into carbonaceous feeds

110 ve system for the selective room-temperature photocatalytic conversion of formic acid into either hyd

111 employed in catalytic, electrocatalytic, and photocatalytic conversions, have surfaces that are typic

112 Herein we report conditions for the photocatalytic coupling via direct functionalization of

113 A critical determining factor of the photocatalytic cycle is the metal domain characteristics

114 cture and reactivity of intermediates in the photocatalytic cycle of a proton reduction catalyst, [Fe

115 The photocatalytic cycle proceeds by energy sharing via the

116 ing labile exchange at the QD surfaces and a photocatalytic cycle.

117 is therefore likely to be an intermediate in photocatalytic cycles.

118 surface also allows regeneration through the photocatalytic decomposition of adsorbates under UV irra

119 II nanojunctions that exhibit more efficient photocatalytic decomposition of aqueous organic molecule

120 es good stability and durability in repeated photocatalytic degradation experiments.

121 planation can be found in experiments on the photocatalytic degradation of a mixture of hydrocarbons

122 ionality is demonstrated through the in situ photocatalytic degradation of methyl orange (MO), as a m

123 ctivity than their bulk counterparts for the photocatalytic degradation of methylene blue dye under v

124 3 is a well known catalyst, the simultaneous photocatalytic degradation of organic pollutants present

125 nomically, more significantly, the following photocatalytic degradation of pesticide greatly benefit

126 nd demonstrates the online monitoring of the photocatalytic degradations of methylene blue and methyl

127 devices, such as perovskite solar cells and photocatalytic devices, it is important to tailor its ba

128 Efficient photocatalytic disinfection of Escherichia coli O157:H7

129 rid and bacteria is not indispensable in the photocatalytic disinfection process.

130 The confirmation of the photocatalytic effect was also confirmed using methylene

131 03<x<0.20) were reported to show competitive photocatalytic efficiencies under visible light, which w

132 ly effective, low-cost strategy for improved photocatalytic efficiency and stability of CdS is descri

133 ration, behavior that we attribute to higher photocatalytic efficiency from improved charge separatio

134 cted considerable attention in enhancing the photocatalytic efficiency of TiO2 under visible light ir

135 ent along with hydrogen, the selectivity for photocatalytic ethylene production relative to ethane is

136 Photocatalytic experiments and investigations on the ET

137 at the tips of Au nanorods, enabling various photocatalytic experiments, such as oxygen evolution fro

138 which provide a measure of the activity of a photocatalytic film under test via the rate of change of

139 The described photocatalytic formation process is highly efficient and

140 s tutorial review, the integration of CDs in photocatalytic fuel generation systems with metallic, mo

141 are promising emerging light-harvesters for photocatalytic fuel production systems.

142 investigated here assembly in water and the photocatalytic function of perylene monoimide chromophor

143 dress the effect of the gold tip size on the photocatalytic function, including the charge transfer d

144 eedstock for algae production by combining a photocatalytic gas pretreatment unit with a microalgal p

145 Herein we report the photocatalytic generation of a mononuclear non-haem [(13

146 ion of the complexes as photosensitizers for photocatalytic generation of hydrogen from water and as

147 current approaches for the photochemical and photocatalytic generation of reactive intermediates and

148 acilitate electron-hole transfer for raising photocatalytic H2 evolution activity.

149 CQDs) are new-generation light absorbers for photocatalytic H2 evolution in aqueous solution, but the

150 st [Fe2(bdt)(CO)6](-), a key intermediate in photocatalytic H2 formation, was generated by reaction w

151 es of such triadic nanorods, we examined the photocatalytic H2 generation quantum efficiency and the

152 0 +/- 60 h(-1) with a TON of 723 +/- 171 for photocatalytic H2 generation with a molecular Ni catalys

153 able platform for designing highly effective photocatalytic HER catalysts but also facilitate detaile

154 ore active 1T' phase as true active sites in photocatalytic HERs, resulting in a "catalytic site self

155 The photocatalytic hybrid system was limited by the lifetime

156 We describe a metal-free, photocatalytic hydrodefluorination (HDF) of polyfluoroar

157 This Communication describes a photocatalytic hydrodefluorination approach which begins

158 ns of the Meldrum's acid products as well as photocatalytic hydrodefluorination.

159 In Pd-decorated Al nanocrystals, photocatalytic hydrogen desorption closely follows the a

160 les and high surface areas, enable increased photocatalytic hydrogen evolution rate and extended work

161 nanostructured polymorphs into an efficient photocatalytic hydrogen evolution system to compare thei

162 We demonstrate photocatalytic hydrogen evolution using COF photosensiti

163 be promising photocatalysts for sacrificial photocatalytic hydrogen evolution with a maximum rate of

164 ) nanomaterials due to their applications in photocatalytic hydrogen generation and environmental pol

165 MoS2-rGO hybrid is a better co-catalyst for photocatalytic hydrogen generation than the precious met

166 In photocatalytic hydrogen generation under visible light i

167 d to be controlled to optimize complexes for photocatalytic hydrogen production and selective carbon-

168 Semiconductor compounds are widely used for photocatalytic hydrogen production applications, where p

169 tability of over one day and 45 times higher photocatalytic hydrogen production compared to commercia

170 Photocatalytic hydrogen production from water offers an

171 ecoupling of the light and dark reactions of photocatalytic hydrogen production through the radical's

172 Photocatalytic hydrogen production using a nickel-based

173 In this work, we demonstrate facile photocatalytic in situ synthesis of nAg particles by cru

174 harge conversion efficiencies, (ii) gains in photocatalytic longevity, and (iii) insights into the ET

175 d the rational development of more efficient photocatalytic materials for CO2 reduction.

176 se of graphene-based materials as sorbent or photocatalytic materials for environmental decontaminati

177 -organic frameworks (MOFs) as highly tunable photocatalytic materials, systematic studies that interr

178 ately be employed to obtain highly effective photocatalytic materials.

179 ic level is critical to developing efficient photocatalytic materials.

180 limited the efficiency of the most promising photocatalytic materials.

181 The radical species involved within the photocatalytic mechanisms were also explored through use

182 or photocatalysts with the post-illumination photocatalytic "memory" could be largely expanded to sem

183 ndence on light intensity cause the unheated photocatalytic methane production rate to exceed the the

184 A photocatalytic method for the aerobic oxidative cleavage

185 ion dynamics following excitation of a model photocatalytic molecular system [Ir2(dimen)4](2+), where

186 ane (Fe4S4) biomimetic clusters demonstrates photocatalytic N2 fixation and conversion to NH3 in ambi

187 organometallic rhodium complex designed for photocatalytic NAD(+)/NADH reduction.

188 ffect of weathering duration on a commercial photocatalytic nanocoating on the basis of its nanoparti

189 titania films show very high activity in the photocatalytic NO conversion and in the degradation of 4

190 The photocatalytic O-H dissociation of water absorbed on a r

191 cal reactions such as plasmonically-enhanced photocatalytic or photovoltaic processes.

192 Photocatalytic overall water splitting proceeded using M

193 re to light, which induces reprotonation via photocatalytic oxidation of adsorbed water.

194 th a hybrid functional (HSE06), we study the photocatalytic oxidation of CH3OH adsorbed at a coordina

195 tive sites and fine-tuned the selectivity in photocatalytic oxidation of tetrahydrofuran (THF) to exc

196 This system is a model for the photocatalytic oxidation of water by TiO2 in an aqueous

197 The method was shown to provide fast photocatalytic oxidation reactions and analysis with thr

198 latform for studying titanium dioxide (TiO2) photocatalytic oxidation reactions by performing reactio

199 d CH3OH may also be an active species in the photocatalytic oxidation to CH2O.

200 ven H2 evolution from water, heralding a new photocatalytic paradigm for solar energy conversion.

201 plement a bidirectional scattering model for photocatalytic particles and bubbles to calculate the lo

202 Photocatalytic pathways could prove crucial to the susta

203 The identification of new photocatalytic pathways expands our knowledge of chemica

204 search interest because of its visible light photocatalytic performance combined with good stability

205 -x , monolayer BiO2-x has exhibited enhanced photocatalytic performance for rhodamine B and phenol re

206 l role of morphology and surface area on the photocatalytic performance of carbon nitride materials.

207 We conclude that the improved photocatalytic performance of the hydrogels formed by su

208 xial-like construction can lead to excellent photocatalytic performance over conventional core-shell-

209 ovide key mechanistic understanding on their photocatalytic performance, including the photo-reductio

210 thesize TiO2-S/rGO hybrid, and its excellent photocatalytic performance, such TiO2-S/rGO hybrids are

211 O2 was evaluated to demonstrate its improved photocatalytic performance.

212 ts in short exciton lifetimes and diminishes photocatalytic performance.

213 o microscale morphologies that show improved photocatalytic performance.

214 bination, is responsible for the outstanding photocatalytic performance.

215 However, the manner in which the photocatalytic performances are impacted by the amount o

216 The photocatalytic polymerization clearly depends on the con

217 e can serve as electron acceptors during the photocatalytic polymerization reaction.

218 ade in optimizing the first two steps in the photocatalytic process, much less efforts have been put

219 To this end, photocatalytic processes represent new approaches for H2

220 o energy-rich molecules (solar fuel) through photocatalytic processes, invariably starts with photoin

221 r mechanism and rates as well as the overall photocatalytic processes.

222 erves as a precatalyst for the high-yielding photocatalytic production of COS from CO and S8 under ne

223 Photocatalytic production of hydrogen is observed in the

224 ensional crystals provide optoelectronic and photocatalytic properties complementing those of graphen

225 Hence, the significant enhanced visible photocatalytic properties for Mn-ZnO NFs are due to the

226 TS-cg3 system we can tailor the electro- and photocatalytic properties of chalcogels through the cont

227 stigations on photoelectrochemical (PEC) and photocatalytic properties of metal cluster-semiconductor

228 rphologies, thermal stability of anatase and photocatalytic properties of the as-prepared Al-TiO2 nan

229 y investigation was performed to explore the photocatalytic properties of the newly synthesized mesop

230 ed nanoparticles are shown to have excellent photocatalytic properties toward degradation of Rhodamin

231 synthesis of Ti(3+)-doped TiO2 with tunable photocatalytic properties using a hydrothermal method wi

232 both transparent conducting oxide (TCO) and photocatalytic properties were produced via aerosol-assi

233 g the plasmon decay) are responsible for the photocatalytic property of this material under visible l

234 We report a new photocatalytic protocol for the redox-neutral isomerizat

235 ogress in energy transfer, light-harvesting, photocatalytic proton and CO2 reduction, and water oxida

236 creased amounts of bdc-NH2 yielded increased photocatalytic rates, followed by a plateau up to 100% b

237 by exploiting the synergistic integration of photocatalytic reaction of Cu-EDTA and one-dimensional (

238 Their main photocatalytic reaction products were mostly similar to

239 Following the photocatalytic reaction, addition of the primary amine a

240 electrons produced in doped quantum dots in photocatalytic reaction.

241 iew on various aspects of reactor design for photocatalytic reactions and presents a scale-up study o

242 been exploited to design different types of photocatalytic reactions and to obtain NMR spectra of di

243 d anti-Stokes SERS, with kinetic analysis of photocatalytic reactions in an Ag nanocube-methylene blu

244 However, the efficiency of photocatalytic reactions remains low due to the fast ele

245 In general, the yields of these photocatalytic reactions were higher than the analogous

246 n transfer that plays a pivotal role in many photocatalytic reactions.

247 ymatic redox processes to meaningfully study photocatalytic reactions.

248 ial redox dyes using titanium oxide-assisted photocatalytic reactions.

249 s trapping reduces the efficiency of surface photocatalytic reactions.

250 Its photocatalytic reactivity was evaluated by the degradati

251 c reactions and presents a scale-up study of photocatalytic reactors.

252 halogens allowing for its application in the photocatalytic reduction of aryl chloride substrates.

253 The possible mechanism for photocatalytic reduction of CO2 -to-CO over ZrPP-1-Co is

254 In addition, the photocatalytic reduction of Cr(VI) in aqueous solution w

255 Photocatalytic reduction of nucleotide redox cofactors u

256 n of a pyridinium linker that immolates upon photocatalytic reduction with a ruthenium complex to yie

257 e conversion efficiency of the nanocomposite photocatalytic reduction.

258 hly sustainable light-absorbing material for photocatalytic schemes, which are not limited by cost, t

259 on and to capture intermediates of potential photocatalytic significance.

260 In photocatalytic solar fuel production, these electron pro

261 Semiconducting photocatalytic solar-hydrogen conversion (SHC) from wate

262 ly high H2 production rate and unprecedented photocatalytic stability.

263 The conventional batch photocatalytic studies on lignin, often using dissolved

264 expand possibilities for developing designer photocatalytic substrates.

265 This precious metal-free and nontoxic photocatalytic system displays better performance than a

266 The DPA-BP/NHPI/O2 photocatalytic system exhibits high efficiency toward th

267 The development of a photocatalytic system for lignin depolymerization in a c

268 ther hand, X-TAS experiments of the complete photocatalytic system in the presence of the electron do

269 The new photocatalytic system incorporates poly(4-styrenesulfona

270 nts under solar irradiation in a homogeneous photocatalytic system with a Ni-bis(diphosphine) catalys

271 A novel molecular photocatalytic system with not only high reduction abili

272 By using this photocatalytic system, CO2 of 10% concentration could be

273 by boosting the activity of a titania (TiO2) photocatalytic system.

274 architectures for an efficient bio-inspired photocatalytic system.

275 recorded for the noble- and toxic-metal free photocatalytic system.

276 ommonly used heterogeneous catalysts in this photocatalytic system.

277 nduced mechanism for H2 dissociation in this photocatalytic system.

278 riphenylphosphine in the presence of various photocatalytic systems (dicyanoanthracene/biphenyl, N-me

279 Recently, photocatalytic systems based on photosensitizing perylen

280 Plasmon-mediated photocatalytic systems generally suffer from poor effici

281 To increase activity, Z-scheme photocatalytic systems have been implemented that use mu

282 al electron transfer processes present in CD photocatalytic systems is outlined and various avenues f

283 Photocatalytic systems that combine light-harvesting mat

284 Most of the work on semiconductor photocatalytic systems uses oxygen as the electron accep

285 iciency is comparable to previously reported photocatalytic systems, performed under aerobic conditio

286 sonable activity in most semiconductor-based photocatalytic systems, which seriously restricts their

287 chemically stable nanoparticles for aqueous photocatalytic systems.

288 ide perovskite solar cells, and finally some photocatalytic systems.

289 ucted to characterize surface changes in the photocatalytic TiO2 powder using near-ambient-pressure X

290 inolines (THIQ) is one of the most exploited photocatalytic transformation and a test reaction for an

291 e synthesized by electrospinning to optimize photocatalytic treatment efficiency.

292 onal chemicals and subsequently reusable for photocatalytic treatment of other wastewater (glycerol)

293 esting plasmonic nanoantennas onto a typical photocatalytic unit with butterfly wings' 3D micro/nanoa

294 The initial step of photocatalytic water oxidation reaction at the metal oxi

295 to attach molecular units to photoanodes for photocatalytic water oxidation.

296 There are three crucial steps for the photocatalytic water splitting reaction: solar light har

297 Photocatalytic water splitting using particulate semicon

298 The major challenge of photocatalytic water splitting, the prototypical reactio

299 achieve cost-effective and highly efficient photocatalytic water splitting.

300 any of its practical applications, including photocatalytic water splitting.