ライフサイエンスコーパス: photocatalyst

1 ing, relative to a purely fluorine-doped VLA photocatalyst.

2 using feedstock substrates and a commercial photocatalyst.

3 O2 as solvent and a dual-function solid acid/photocatalyst.

4 f-cleaning ability of this schottky junction photocatalyst.

5 photo corrosion, although it is an efficient photocatalyst.

6 r regeneration of the organic methylene blue photocatalyst.

7 ability study confirmed the stability of the photocatalyst.

8 ature of the ketyl radical precursor and the photocatalyst.

9 and commercially available Ru(bpy)3Cl2 as a photocatalyst.

10 etallic oxide, Sr(1-x)NbO(3) as an effective photocatalyst.

11 anocavities' (<2 nm in diameter) on a TiO(2) photocatalyst.

12 ocess and coupled with another semiconductor photocatalyst.

13 e is the prototypical transition metal oxide photocatalyst.

14 radiation in the presence of a ruthenium(II) photocatalyst.

15 evailing back reaction on the bare Pt/SrTiO3 photocatalyst.

16 on-rich aromatic disulfides were employed as photocatalyst.

17 using a Ru(II)-Re(I) dinuclear complex as a photocatalyst.

18 processes induced by visible light absorbing photocatalysts.

19 et highly efficient and stable semiconductor photocatalysts.

20 ration dynamics and activity of carbon-based photocatalysts.

21 that observed for any other existing g-C3N4 photocatalysts.

22 , nonmetallic clusters as novel atomic-level photocatalysts.

23 tic efficiency as compared with conventional photocatalysts.

24 the presence of transition metal polypyridyl photocatalysts.

25 mainly by the lack of low-cost and efficient photocatalysts.

26 two phases and highlight a route to improved photocatalysts.

27 o overcome the drawbacks of single component photocatalysts.

28 -oxo clusters, are proposed as visible light photocatalysts.

29 ing visible-light-absorbing transition metal photocatalysts.

30 ions of transition metal oxide semiconductor photocatalysts.

31 f photoluminescence from single nanoparticle photocatalysts.

32 oxidation state are potential visible light photocatalysts.

33 lic nanostructures represent a new family of photocatalysts.

34 lications such as low-cost photovoltaics and photocatalysts.

35 egradation properties as magnetic recyclable photocatalysts.

36 almost exclusively focused on semiconductor photocatalysts.

37 routes toward the design of highly selective photocatalysts.

38 litting limits the efficiency of metal-oxide photocatalysts.

39 l design and development of high-performance photocatalysts.

40 at the subsurface regions of inorganic solid photocatalysts.

41 rrier lifetime, which are also desirable for photocatalysts.

42 r the construction of other plasmon-mediated photocatalysts.

43 limit ground-state mobilities in metal oxide photocatalysts.

44 rials available for optimized performance as photocatalysts.

45 icient UV, visible, and NIR light responsive photocatalysts.

46 fully applied to probe the photostability of photocatalysts.

47 for the synthesis of high-efficiency g-C3 N4 photocatalysts.

48 engineering high-performance heptazine-based photocatalysts.

49 s a useful strategy for developing efficient photocatalysts.

50 of methane production above 2000 mumol (g of photocatalyst)(-1) h(-1).

51 approximately 8.1 g), and the iridium-based photocatalyst 1a can be prepared in a 56% overall yield

52 ocedures described here, the ruthenium-based photocatalyst 2a can be synthesized in a 78% overall yie

53 ld conditions: a combination of a metal-free photocatalyst, a chain-transfer agent, and light irradia

54 chemical reaction system uses an 8-oxo-G-Ru photocatalyst, a derivative of [tris(2,2'-bipyridine)-Ru

55 ce of evaluating hydrocarbon conversion over photocatalysts active in converting CO2 to hydrocarbons

56 t example of a RP process is with respect to photocatalyst activity indicator inks. paiis, which prov

57 The use of the photocatalyst-adsorbent hybrid material enhanced the pho

58 ditionally, changes in the ratios of the two photocatalysts afford complementary chemical control ove

59 The work found a new application of the photocatalyst, Ag3PO4/g-C3N4, in simultaneous environmen

60 Utilizing an Ir photocatalyst, alpha-hydroxyalkyl radicals are generated

61 complished using a readily available iridium photocatalyst and a chiral imidazolidinone catalyst.

62 f a visible light-absorbing transition-metal photocatalyst and a stereocontrolling Lewis acid cocatal

63 In this protocol, an excited-state iridium photocatalyst and a weak phosphate base cooperatively se

64 acement by iodoanilines, generating a better photocatalyst and accelerating the reaction.

65 on transfer between an excited-state iridium photocatalyst and an amine substrate.

66 nteraction between an electronically excited photocatalyst and an organic molecule can result in the

67 Everything else-solvents, photocatalyst and aqueous acid-can be recycled.

68 oduct and regenerate the active forms of the photocatalyst and base.

69 The fuel cell uses polyoxometalates as the photocatalyst and charge carrier to generate electricity

70 r cysteine conjugation using Ru(bpy)3(2+) as photocatalyst and inexpensive RFI as coupling partner.

71 bination of a thiol catalyst with an iridium photocatalyst and subsequent radical-radical coupling wi

72 strength of ion pairing between the oxidized photocatalyst and the bromide anion and thus the ability

73 ibit a dual role, i.e., the oxidation of the photocatalyst and the formation of the initiating radica

74 te processes and guided the selection of the photocatalyst and the optimization of experimental condi

75 abundant transition metal acting as both the photocatalyst and the source of asymmetric induction.

76 the importance of the size and shape of the photocatalyst and the substrate in controlling the elect

77 ntly enhanced by employing the nanocomposite photocatalyst and using prereduction and signal-enhancem

78 An iridium photocatalyst and visible light facilitate a room temper

79 dual catalyst system comprised of an iridium photocatalyst and weak phosphate base that is capable of

80 radical-mediated mechanism using commercial photocatalysts and a household light bulb.

81 ison is made against PSII-inspired synthetic photocatalysts and materials for artificial photosynthes

82 -shifted light absorption of these potential photocatalysts and simultaneously suggests a lowered pot

83 ween the reactive excited state of molecular photocatalysts and surrounding solvent dictate reaction

84 xidative and reductive quenching pathways of photocatalysts and the ability to predictably direct rea

85 sign of the photomicroreactor, the choice of photocatalysts and the techniques for assembling the cat

86 The silver particles serve as photocatalysts and, under plasmon excitation, facilitate

87 or-acceptor complex (EDA) between eosin (the photocatalyst) and the pyridinium salt (the oxidation ag

88 Blue light irradiation, a [Ru] or [Ir] photocatalyst, and ascorbic acid in a water-acetonitrile

89 experienced a renaissance as a highly active photocatalyst, and the metal-free polymer was shown to b

90 hotocatalysis encompassing a wide variety of photocatalysts, and modifications thereof, as well as th

91 Many hydrogen-evolving photocatalysts are active in the ultraviolet range, but

92 Although heterogeneous photocatalysts are almost exclusively semiconductors, it

93 The photocatalysts are also active for amine dehydrogenation

94 ure directions in the area of heterojunction photocatalysts are also provided.

95 CO(2) conversion, the nanoscale carbon-based photocatalysts are also useful for the photogeneration o

96 The photocatalysts are efficient and readily recyclable.

97 Visible-light photocatalysts are not required for activation, and alky

98 preparation methods of AuNP-based plasmonic photocatalysts are reviewed.

99 icularly, properly engineered heterojunction photocatalysts are shown to be able to possess higher ph

100 Titanium dioxide (TiO2)-based photocatalysts are studied most frequently because they

101 e basic principles of various heterojunction photocatalysts are systematically discussed.

102 e-dependent structural changes in this model photocatalyst, as well as the changes in the solvation s

103 al quality to fabricate a microfluidic-based photocatalyst-assisted reduction device (microfluidic-ba

104 ed a nanocomposite-coated microfluidic-based photocatalyst-assisted reduction device (PCARD) as a vap

105 A hybrid photocatalyst based on anatase TiO2 was designed by dopi

106 III) oxides could be promising visible light photocatalysts because of their small band gap enabling

107 primary factor in the design of nanocrystal photocatalysts, because the reduction of particle size i

108 emical-thermochemical process, fitted with a photocatalyst better matched to the solar spectrum, coul

109 dioxide (TiO(2)) is one of the most studied photocatalysts, but the shape dependence of its activity

110 contingent upon the oxidation of the reduced photocatalyst by the dithiocarbamate radical concomitant

111 ostructures, have been explored for improved photocatalysts by increasing the light absorption, promo

112 This novel organic photocatalyst can also be explored for water splitting.

113 We show that the synthesized Cu2S photocatalyst can be efficiently used for the reduction

114 The hydrogen generation activity of PCP photocatalyst can be further enhanced to 164 mumol/h wit

115 The corn-like gamma-Fe2O3@SiO2@TiO2 photocatalyst can be recycled and reused by magnet extra

116 le in air or water under irradiation and the photocatalyst can be repeatedly used without degradation

117 The Re(I) catalyst unit in the photocatalyst can efficiently capture CO2, which proceed

118 The alloy photocatalysts can absorb incident light, and the light-

119 Recovery of the (Cu-Fe2O3/Fe)@C photocatalysts can be attained by applying external magn

120 on of hydrogen from water with semiconductor photocatalysts can be promoted by adding small amounts o

121 The (Cu-Fe2O3/Fe)@C photocatalysts can effectively oxidize dye molecules, pr

122 active radicals, and visible light excitable photocatalysts can provide the required oxidation potent

123 ations, which use Ru(bpy)(3)(2+) and related photocatalysts, can be conducted using almost any source

124 Photocatalysts capable of promoting this reaction are of

125 The importance of oxides as thermal and photocatalysts, chemical sensors, and substrates for epi

126 provide the UV light to activate the titania photocatalyst coating on the inside of the NMR tube.

127 authors report polymer heterojunction (PHJ) photocatalysts consisting of polyfluorene family polymer

128 lasmon-enhanced water splitting on composite photocatalysts containing semiconductor and plasmonic-me

129 ns indicated that the oxidative quenching of photocatalysts could effectively be utilized for ATRA, a

130 nostructures suggest that this new family of photocatalysts could prove useful for many heterogeneous

131 Moreover, to reduce the consumption of photocatalysts during analytical procedures, a microflui

132 e performance of traditional nanoparticulate photocatalysts (e.g., Aeroxide P25) with the greatest re

133 We present a novel high throughput photocatalyst efficiency assessment method based on 96-w

134 PSS has a profound impact on the photocatalyst efficiency, increasing H2 production over

135 A method for rapid screening of photocatalysts employing a form of scanning electrochemi

136 The complete, as-designed photocatalysts exhibit excellent activity in CO2 reducti

137 We demonstrate that these photocatalysts exhibit fundamentally different behaviour

138 Evidence suggests that the iridium photocatalyst facilitates nickel excitation and bromine

139 Ru(II) polypyridyl complex that served as a photocatalyst for bromide oxidation.

140 hitic carbon nitride, g-C3N4) is a promising photocatalyst for hydrogen evolution.

141 The use of an organic photocatalyst for hydrogen production has been demonstra

142 roups, and the resulting MOF is an efficient photocatalyst for overall water splitting.

143 rk (MOF) made from 2-aminoterephthalate is a photocatalyst for oxygen evolution.

144 an earth-abundant and environmentally benign photocatalyst for solar hydrogen generation.

145 how that Ru(bpy)(3)(2+) is also an effective photocatalyst for the [2+2] cycloaddition of electron-ri

146 strates the exciting potential of this novel photocatalyst for the degradation of organic contaminant

147 H(2)(PPh(2))(2)) is shown to be an effective photocatalyst for the H(2) evolution reaction (HER).

148 isible region, wisely, PQ has been used as a photocatalyst for the hydrogen production under solar li

149 lex 1 is also shown to function as an active photocatalyst for the oxidation of PPh(3) to OPPh(3).

150 shown to function as an effective gas-phase photocatalyst for the reduction of CO2 to CO via the rev

151 silica-alumina is an efficient and reusable photocatalyst for the reduction of CO2 to methane by H2,

152 PM-120-ZnGeS could also function as a robust photocatalyst for water reduction to generate H2.

153 -C3N4 and Pt/g-C3N4, respectively, acting as photocatalysts for CO2 reduction were investigated by de

154 neration of hydrogen from water and as redox photocatalysts for decarboxylative fluorination of sever

155 l be useful for the design of nanostructured photocatalysts for energy applications.

156 ne-semiconductor nanocomposites as efficient photocatalysts for extensive applications.

157 f inorganic nanostructures have been used as photocatalysts for generating H2.

158 sulting Pt@MOF assemblies serve as effective photocatalysts for hydrogen evolution by synergistic pho

159 nitrides (g-C3N4) have emerged as promising photocatalysts for hydrogen evolution using visible ligh

160 ar poly(p-phenylene)s are modestly active UV photocatalysts for hydrogen production in the presence o

161 heterostructures are promising visible light photocatalysts for many chemical reactions.

162 toward the development of delicate composite photocatalysts for photocatalytic water purification and

163 ticular, CTF-HUSTs are found to be promising photocatalysts for sacrificial photocatalytic hydrogen e

164 talytic CO2 reduction could lead to improved photocatalysts for solar fuel production.

165 t on the development of better visible light photocatalysts for solar-to-chemical energy conversion.

166 facilitate the design of suitable plasmonic photocatalysts for solar-to-fuel energy conversion.

167 ioxide (TiO2) is one of the most widely used photocatalysts for the degradation of organic contaminan

168 give polymers that are robust and effective photocatalysts for the evolution of hydrogen from water

169 fide quantum dots (CdS QDs) as visible-light photocatalysts for the reduction of nitrobenzene to anil

170 ver, many still rely on the use of UV-active photocatalysts for the requisite high-energy hydrogen at

171 ch on nanoscale-enhanced photoelectrodes and photocatalysts for the water splitting reaction.

172 itania (TiO(2)) is one of the most promising photocatalysts for this purpose, and nanostructured TiO(

173 Photocatalysts for this transformation are typically bas

174 rts toward the development of heterojunction photocatalysts for various photocatalytic applications a

175 structured nanotubes as efficient and stable photocatalysts for visible light CO2 reduction.

176 using photo electrochemical cells (PECs) and photocatalysts for water purification.

177 These materials can be used as photocatalysts for water splitting reaction for hydrogen

178 ones for the oxygen reduction reaction) and photocatalysts (for solar energy conversion to fuels) ba

179 The metal- and photocatalyst-free synthesis of substituted allylarenes

180 athways for the preparation of new efficient photocatalysts from readily available nanostructured tem

181 conversion of solar to chemical energy using photocatalysts has received significant attention.

182 the brookite polymorph of TiO2, a promising photocatalyst, has been difficult in both powder and thi

183 hly efficient semiconductor nanocrystal (NC) photocatalysts have been synthesized by growing wurtzite

184 These photocatalysts have been used in the synthesis of medici

185 Solid-state crystalline photocatalysts have light absorption profiles that are a

186 ated by studying afresh a popular and viable photocatalyst, hematite, alpha-Fe2O3 that exhibits most

187 step photoexcitation of a hydrogen evolution photocatalyst (HEP) and an oxygen evolution photocatalys

188 G-ZnO-Au NC photocatalyst holds great potential in removal of organi

189 rst example of a molecular and semiconductor photocatalyst hybrid-constructed photoelectrochemical ce

190 Here we report a high efficiency photocatalyst, i.e., Mn(2+)-doped and N-decorated ZnO na

191 a Ru(II)-Re(I) supramolecular metal complex photocatalyst immobilized on a NiO electrode (NiO-RuRe)

192 he dye is reduced irreversibly, but when the photocatalyst in an ink is used to reversibly photoreduc

193 of capping ligands, suspensions of the same photocatalyst in aqueous sodium formate generate up to 1

194 ronic properties and redox potentials of the photocatalyst in both the excited and the ground states

195 as a metal-free and visible-light-responsive photocatalyst in the arena of solar energy conversion an

196 The reaction is mediated by a ruthenium photocatalyst in the presence of a substoichiometric amo

197 Past studies of using fullerene as a photocatalyst in water have exclusively focused on using

198 zines as well as previously reported organic photocatalysts in organocatalyzed atom transfer radical

199 iridium and ruthenium have served as popular photocatalysts in recent years due to their long excited

200 to increase the efficiency of supramolecular photocatalysts in solar H2 production schemes under aque

201 t approaches to the use of metal polypyridyl photocatalysts in synthetic organic transformations.

202 be a promising method for the other unstable photocatalysts in the degradation of environmental pollu

203 d by Zr(IV)-based MOFs bearing visible-light photocatalysts in the form of Ir(III) polypyridyl comple

204 hat ultrathin layered-double-hydroxide (LDH) photocatalysts, in particular CuCr-LDH nanosheets, posse

205 article-decorated CZTS (Au/CZTS and Pt/CZTS) photocatalysts, indicating the MoS2-rGO hybrid is a bett

206 The efficient distribution of the opaque photocatalyst inside the tubular reactor was achieved by

207 ical cation acts as an oxidant to return the photocatalyst into the original state.

208 to olefins is efficiently performed with the photocatalyst Ir[(dF(CF(3))ppy)(2)(dtbbpy)]PF(6).

209 ic reductive C-O bond cleavage utilizing the photocatalyst [Ir(ppy)2(dtbbpy)]PF6 is described.

210 rbon nitride (g-C3N4) as a benchmark polymer photocatalyst is attracting significant research interes

211 st that a reductive quenching pathway of the photocatalyst is operable.

212 Herein, a new group of visible light photocatalysts is described.

213 ls as well as the requirements for efficient photocatalysts is first provided.

214 hat BiOI, previously considered to be a poor photocatalyst, is promising for photovoltaics.

215 NaInS(2) , a H(2) -evolving photocatalyst, is synthesized as single-crystalline hexa

216 avin (vitamin B2) as an inexpensive, organic photocatalyst (J.

217 A stable visible-light-driven photocatalyst (lambda>/=450 nm) for water oxidation is r

218 oncentration, and mass ratio between the two photocatalysts, leading to a stable and reproducible H2

219 in yields of 41-95 % without the need for a photocatalyst, light, or a strong oxidant.

220 adicals from carboxylic acid derivatives, no photocatalyst, light, or arylmetal reagent is needed, on

221 xides such as TiO2, Nb2O5 and ZnO; plasmonic photocatalysts like nanostructured Au, Ag or Cu supporte

222 is present in the ink, and the semiconductor photocatalyst-loaded ink film coats an easily reduced su

223 This was partly attributed to a lower photocatalyst loading as the rate of mediated electron e

224 Ideal solar-to-fuel photocatalysts must effectively harvest sunlight to gene

225 photocatalyst (HEP) and an oxygen evolution photocatalyst (OEP) are suited to harvesting of sunlight

226 Here a novel composite photocatalyst of SnO2 nanoparticle-decorated Cu2O nanocu

227 ive organic dye eosin Y could be used as the photocatalyst of the organocatalytic hydroimination reac

228 The new methodology uses heterogenerous photocatalysts of gold-palladium alloy nanoparticles on

229 Supramolecular photocatalysts of the architecture [{(TL)2 Ru(BL)}2 RhX2

230 hosphate-bearing flavin mononucleotide (FMN) photocatalyst on high surface area metal-oxide films.

231 Most photocatalysts only function under illumination, while m

232 uring semiconductor (such as TiO(2)) or to a photocatalyst, or induced by energy transfer in a neighb

233 Conventional TiO(2)-based photocatalysts oxidize NO(x) to nitrate species, which d

234 those achieved by the commercially available photocatalyst (P-25 TiO2).

235 Also, these TM photocatalysts participate in the bond-forming/breaking

236 on metal (TM = Co, Fe, Cu, Pd, Pt, Au)-based photocatalyst (PC) has led to the dramatic acceleration

237 ate that, in sharp contrast to semiconductor photocatalysts, photocatalytic quantum efficiencies on p

238 nism that can be used to guide the design of photocatalysts, photovoltaics, and other optoelectronic

239 using BiOBr/methyl orange (MO) as the model photocatalyst/pollutant system.

240 generation from water using noble metal-free photocatalysts presents a promising platform for renewab

241 This first example of a heptametallic Ru,Rh photocatalyst produces over 300 turnovers of H2 upon pho

242 s present in mineral dust act as atmospheric photocatalysts promoting the formation of gaseous OH rad

243 of polyfluoroarenes (FA) using pyrene-based photocatalysts (Py).

244 lysis, the potential of copper to serve as a photocatalyst remains underexplored.

245 des with visible light in the presence of Ru photocatalysts results in the formation of reactive nitr

246 eveloped in the presence of the nonhazardous photocatalyst Rose Bengal under irradiation of visible l

247 2-arylallyl bromides in the presence of the photocatalyst Ru(bpy)3(PF6)2, a Hantzsch ester, and i-Pr

248 active CPA radical cation 1(+*), the reduced photocatalyst Ru(I)(bpz)3(+), and the [3 + 2] annulation

249 The photocatalyst sheet design enables efficient and scalabl

250 Here, we present photocatalyst sheets based on La- and Rh-codoped SrTiO3

251 A practical photocatalyst should be able to integrate together vario

252 Thus, novel photocatalysts should be developed, which could store pa

253 Photocatalysts show great potential in environmental rem

254 The optimal Ag3PO4/g-C3N4 photocatalyst showed a CO2 conversion rate of 57.5 mumol

255 ys composed of approximately 300-microm-size photocatalyst spots with different compositions onto con

256 ng the scope of the reaction in terms of the photocatalysts, substrates, and solvents.

257 ification of reaction conditions under which photocatalysts such as fac-Ir(ppy)3 can be utilized to f

258 e past decade, semiconductor water-splitting photocatalysts (such as (Ga1-xZnx)(N1-xOx)) do not exhib

259 In addition, nonsemiconductor type photocatalysts, such as Ti-Si molecular sieves and carbo

260 l analysis have allowed one to detect on the photocatalyst surface the presence of CO2(*-), Cu-CO, an

261 directly visualized in the case of the model photocatalyst surface TiO(2)(110) in reactions with wate

262 These results suggest that modifying photocatalyst surface to increase contaminant adsorption

263 Herein, a near-ideal plasmon-mediated photocatalyst system is developed.

264 ven CO2 reduction in water using a synthetic photocatalyst system that is entirely free of precious m

265 owed a CQD-molecular nickel bis(diphosphine) photocatalyst system to reach a benchmark lifetime of mo

266 rogen donor molecules, and a ruthenium-based photocatalyst that employs a linked nucleobase (8-oxo-gu

267 epared in aims of creating a fullerene-based photocatalyst that is capable of producing (1)O2 in the

268 ly shown that Ru(bpy)(3)(2+) is an efficient photocatalyst that promotes the [2+2] cycloadditions of

269 To address this, organo-photocatalysts that are based on atropisomeric thioureas

270 sult opens a door in the quest for efficient photocatalysts that could further increase the apparent

271 uel source, but it is challenging to produce photocatalysts that use the solar spectrum effectively.

272 aching the surface of microsized rutile TiO2 photocatalyst, thus significantly enhancing its photocat

273 The prototypical photocatalyst TiO2 exists in different polymorphs, the m

274 When used as a photocatalyst, titanium dioxide (TiO(2)) absorbs only ul

275 been investigated previously, but the use of photocatalysts to split water into stoichiometric amount

276 inated by radical chain processes and not by photocatalyst turnover.

277 ussion comprises three sections based on the photocatalyst type: metal oxides such as TiO2, Nb2O5 and

278 he reaction mechanism using Ru(bpy)3Cl2 as a photocatalyst under aerobic and anaerobic conditions.

279 g a C70 modified TiO2 (C70-TiO2) hybrid as a photocatalyst under visible light (lambda > 420 nm) irra

280 In 1 N HBr (aq), the photocatalyst undergoes excited-state electron injection

281 ntly at room temperature, utilize an organic photocatalyst, use simple and readily available material

282 atalytic properties of Pt/n-Si/Ag photodiode photocatalysts using Au/Ag core/shell nanorods.

283 a full availability of a new multifunctional photocatalyst, via integrating the much enhanced ferroma

284 activity of the resulted Bi7Fe(3-x)CoxTi3O21 photocatalyst were extended to the long wavelength as fa

285 These photocatalysts were found to be efficient in promoting t

286 The photocatalysts were synthesized from non-active CoO micr

287 this report, a multifunctional single-phase photocatalyst which possesses a high photoactivity exten

288 g-C3N4 can serve as a multifunctional robust photocatalyst, which could also be used in other systems

289 del for the charge carrier dynamics in these photocatalysts, which includes carrier relaxation into a

290 ficant efforts to date, a practically viable photocatalyst with sufficient efficiency, stability and

291 d significantly by combining a semiconductor photocatalyst with tailored plasmonic-metal nanostructur

292 ew gives a concise overview of heterogeneous photocatalysts with a focus on the relationship between

293 cilitate the next generation of g-C3N4-based photocatalysts with ameliorated performances by harnessi

294 Photocatalysts with electron withdrawing groups exhibit

295 provides the structural basis for designing photocatalysts with long-lived photo-induced states.

296 The heterogeneous photocatalysts with multiple integrated functional compo

297 e focus upon the cooperative interactions of photocatalysts with redox mediators, Lewis and Bronsted

298 A new method of modifying TiO2 photocatalysts with SiO2 is developed in which SiO2 nano

299 t the selection of decoration components for photocatalysts with the post-illumination photocatalytic

300 us-phase photosensitization of semiconductor photocatalysts (WO(3) loaded with Pt) through triplet-tr