ライフサイエンスコーパス: photocatalyst

1 nsfer could be initiated in the absence of a photocatalyst.

2 aryl radical with no need for an additional photocatalyst.

3 MoSe(2) works as cocatalyst of the Z-scheme photocatalyst.

4 f alkenes and alkynes is achieved using a Cu photocatalyst.

5 s, using the [Ir(ppy)(2)(dtb-bpy)](+) (1(+)) photocatalyst.

6 D) irradiation at room temperature without a photocatalyst.

7 , and direct speciation by the assistance of photocatalyst.

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

9 on-rich aromatic disulfides were employed as photocatalyst.

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

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

12 They served as non-toxic and low cost photocatalyst.

13 using feedstock substrates and a commercial photocatalyst.

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

15 el catalytic cycle is saturated with excited photocatalyst.

16 isible light and a readily available organic photocatalyst.

17 PO(4) )(8) }, reminiscent of the Ag(3) PO(4) photocatalyst.

18 es as the sulfonyl source and eosin Y as the photocatalyst.

19 atalysis but without the use of an expensive photocatalyst.

20 actions using this class of transition metal photocatalysts.

21 es an accessible pathway for next-generation photocatalysts.

22 action in enabling efficient water splitting photocatalysts.

23 fully applied to probe the photostability of photocatalysts.

24 ration dynamics and activity of carbon-based photocatalysts.

25 at the subsurface regions of inorganic solid photocatalysts.

26 rrier lifetime, which are also desirable for photocatalysts.

27 r the construction of other plasmon-mediated photocatalysts.

28 ion of redox-active esters without auxiliary photocatalysts.

29 limit ground-state mobilities in metal oxide photocatalysts.

30 rials available for optimized performance as photocatalysts.

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

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

33 engineering high-performance heptazine-based photocatalysts.

34 s a useful strategy for developing efficient photocatalysts.

35 processes induced by visible light absorbing photocatalysts.

36 lytic role of such metal clusters in polymer photocatalysts.

37 and/or employment of costly transition-metal photocatalysts.

38 xygen tolerance and wide range of compatible photocatalysts.

39 cesses in semiconductor and (supra)molecular photocatalysts.

40 ir growing potential as light sensitizers or photocatalysts.

41 n reported using precious-metal- or Cd-based photocatalysts.

42 ical rebonding actualized by 2D single-layer photocatalysts.

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

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

45 eaction has been developed using the organic photocatalyst 4CzIPN, visible light, and N-(acyloxy)phth

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

47 rradiation and without the requirement for a photocatalyst, a radical initiator, or tin or silicon hy

48 rom a hydridic C-H bond using a benzophenone photocatalyst, a trithiocarbonate-derived disulfide, and

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

50 rocyclic carbenes with an oxidizing pyrylium photocatalyst affords excellent temporal and spatial res

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

52 alyzed by the combination of an iridium(III) photocatalyst and a dialkyl phosphate base.

53 alent complex formed between an iridium(III) photocatalyst and a monobasic phosphate base.

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

55 ansfer from a commercially available iridium photocatalyst and allows for [2+2] cycloaddition with a

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

57 ht irradiation in the presence of an iridium photocatalyst and an aryl thiol hydrogen atom donor.

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

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

60 tantially misinterpret the emissivity of the photocatalyst and assume a linear intensity-dependent te

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

62 was the utilization of a highly reducing Ir-photocatalyst and orchestration of the intrinsic reactiv

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

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

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

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

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

68 An iridium photocatalyst and visible light facilitate a room temper

69 tive, and rapid screening platform for novel photocatalysts and flow chemistry in general.

70 ses occurring at the interface of perovskite photocatalysts and photoelectrodes with different electr

71 es for the characterization of semiconductor photocatalysts and potentially other relevant materials.

72 um dots serve as visible-light chromophores, photocatalysts and reusable scaffolds for homo- and hete

73 ers, we have assimilated redox potentials of photocatalysts and substrates for a better sense of spon

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

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

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

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

78 ses inexpensive reagents, does not require a photocatalyst, and displays broad functional group toler

79 Visible light activates the photocatalyst, and it acts as an electron-transfer reage

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

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

82 are organized as "dark" cathodes, colloidal photocatalysts, and photocathodes, and their figures of

83 By using a photocatalyst-antibody conjugate to spatially localize c

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

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

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

87 ystems, in dye-sensitized solar cells and as photocatalysts are presented.

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

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

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

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

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

93 transfer using inexpensive decatungstate as photocatalyst at room temperature.

94 tic studies point to the crucial role of the photocatalyst-base interaction.

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

96 Hybrid photocatalysts based on inorganic semiconductors (ISs) a

97 ed as an example of emerging carbon nitrides photocatalysts because of its excellent charge storage a

98 n also determines the stability of Pd-TiO(2) photocatalysts, because nonuniformly distributed nanopar

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

100 using Fe(II)-based polypyridyl complexes as photocatalysts, but there is limited mechanistic informa

101 d in the Z-scheme In(2) O(3) -ZISe nanosheet photocatalyst by forming the Mo Se bond, confirmed by X-

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

103 to enhance the performance of this class of photocatalysts by conformally coating Cu atoms onto the

104 s(-1) , which exceeds the rates of available photocatalysts by two orders of magnitude.

105 roach was designed to remove the role of the photocatalyst, by which only the intrinsic behaviors of

106 is demonstrated that an interesting Z-scheme photocatalyst can be constructed by coupling In(2) O(3)

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

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

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

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

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

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

113 However, the influence of the photocatalyst counteranion has received little attention

114 ited-state evolution of the employed iridium photocatalyst, determine the resting states of both irid

115 test progress in hydrogen evolution on these photocatalysts, discussion has been extended to the pote

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

117 bacterial organelles, these SPs can serve as photocatalysts, enantioselectively converting L- or D-ty

118 al results, we propose a mechanism where the photocatalyst engages in concurrent tandem catalysis by

119 ive olefins, tris(trimethylsilyl)silane, and photocatalyst Eosin Y.

120 n the synthesis of nano-metallic electro and photocatalysts, especially silver nanoparticles, is a si

121 o drive photoinduced H(2) generation in many photocatalysts, excessive electron accumulation may resu

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

123 t attenuation in water/wastewater results in photocatalysts exhibiting a low quantum efficiency.

124 The optimum Ag@U-g-C(3) N(4) -NS photocatalyst exhibits enhanced electrochemical properti

125 led triplet energy levels of the quantum dot photocatalysts facilitate efficient and selective hetero

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

127 Novel semiconductor und molecular photocatalysts focusing on one-step excitation processes

128 amental materials aspects of high efficiency photocatalysts followed by six open questions that may n

129 ork, we present the first example of a novel photocatalyst for both full broadband- and NIR-mediated

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

131 e MOF structure was employed as an efficient photocatalyst for carbon dioxide conversion to formate u

132 Here, we report a photocatalyst for CO(2) reduction that consists of a pol

133 ks as an efficient wide-visible-light-driven photocatalyst for converting CO(2) into CO and CH(4) , a

134 This work provides a novel design of a photocatalyst for hydrogen evolution using non-noble Cu(

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

136 c scaffold that acts as a single-chromophore photocatalyst for hydrogen-gas generation and operates w

137 s on TiO(2) (PC-50) and use of the resulting photocatalyst for OCM in a flow reactor operated at room

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

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

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

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

142 f polyheptazine imide (K-PHI) is a promising photocatalyst for various chemical reactions.

143 Semiconductor nanocrystals are promising photocatalysts for a wide range of applications, ranging

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

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

146 s nanocrystals are exceptional candidates as photocatalysts for fundamental organic reactions, for ex

147 ) O(3) -ZISe) spontaneous Z-scheme nanosheet photocatalysts for greatly enhancing photocatalytic H(2)

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

149 we use a mobile robot to search for improved photocatalysts for hydrogen production from water(15).

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

151 Conjugated polymers are an emerging class of photocatalysts for hydrogen production where the large b

152 remaining challenges in selected metal-free photocatalysts for hydrogen production.

153 advances in the development of hybrid IS-CP photocatalysts for pollutant degradation and energy conv

154 The design of efficient and stable photocatalysts for robust CO(2) reduction without sacrif

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

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

157 rgy conversion and have gained popularity as photocatalysts for sunlight-driven hydrogen production.

158 Moreover, reactants can compete with photocatalysts for the absorption of incident light, lim

159 Single-chromophore single-molecule photocatalysts for the conversion and storage of solar e

160 The development of efficient photocatalysts for the degradation of organic pollutants

161 Highly effective photocatalysts for the hydrogen-evolution reaction were

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

163 e use of CuInS(2) /ZnS quantum dots (QDs) as photocatalysts for the reductive deprotection of aryl su

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

165 Photocatalysts for this transformation are typically bas

166 erovskite QDs and quasi-2D nanoplatelets, as photocatalysts for triplet excited state chemistry.

167 s (QDs) address the limitations of molecular photocatalysts for TT EnT-driven organic transformations

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

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

170 The reaction was performed under photocatalyst-free and solvent-free conditions without b

171 A metal- and photocatalyst-free photoinduced radical cascade hydroalk

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

173 d that may facilitate the scalability of the photocatalyst from microscale to macroscale production i

174 Ir(ppy)(3)) with a competitive heterogeneous photocatalyst (graphitic carbon nitride).

175 Of note, the C(1)-symmetric organo/photocatalyst has shown a better catalytic activity than

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

177 recious metal/organic dyes based homogeneous photocatalysts have been developed, their toxic and nonr

178 Riboflavin-derived photocatalysts have been extensively studied in the cont

179 These photocatalysts have been used in the synthesis of medici

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

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

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

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

184 eview is limited to the metal-free elemental photocatalysts (i.e. B, C, P, S, Si, Se etc.), binary ph

185 lysts (i.e. B, C, P, S, Si, Se etc.), binary photocatalysts (i.e. BC(3), B(4)C, C(x)N(y), h-BN etc.)

186 h-BN etc.) and their heterojunction, ternary photocatalysts (i.e. BCN) and their heterojunction, and

187 terojunction, and different types of organic photocatalysts (i.e. linear, covalent organic frameworks

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

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

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

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

192 Our strategy, which uses an organic photocatalyst in combination with azide ion as a hydroge

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

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

195 ctures were in situ generated on Ag(3) PO(4) photocatalysts in a reversible addition-fragmentation ch

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

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

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

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

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

201 e most important properties of semiconductor photocatalysts, including their chemical composition (el

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

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

204 on, comparing a state-of-the-art homogeneous photocatalyst (Ir(ppy)(3)) with a competitive heterogene

205 We have designed a highly oxidative Ir(III) photocatalyst, [Ir(ttpy)(pq)Cl]PF(6) ([1]PF(6), where 't

206 mance of the Bi(24) O(31) Br(10) (OH)(delta) photocatalyst is associated with basic surface sites and

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

208 ly efficient and bandedge-tunable perovskite photocatalyst is expected to bring new insights in chemi

209 echanistic hypothesis, which states that the photocatalyst is only involved to trigger reductive elim

210 rbon nitride/nickel phosphide (CN(x)|Ni(2)P) photocatalyst is utilized to successfully reform poly(et

211 how that the Bi(24) O(31) Br(10) (OH)(delta) photocatalyst is very efficient in the selective oxidati

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

213 uinoline-platinum(II) complexes as efficient photocatalysts is presented.

214 for rapid adoption of these nanoparticles as photocatalysts is their ability to act as photoinitiator

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

216 out the requirement of organic cosolvents or photocatalysts, is enhanced by glutathione, and operates

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

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

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

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

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

222 This autonomous search identified photocatalyst mixtures that were six times more active t

223 e development of even more efficient polymer photocatalysts must target materials that combine both r

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

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

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

227 Most photocatalysts only function under illumination, while m

228 ep excitation processes via single component photocatalysts or via two-step excitation processes mimi

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

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

231 mportant for water decontamination on single photocatalyst particles.

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

233 methodologies utilizing a Ni(II) salt with a photocatalyst (PC) have emerged as promising methodologi

234 Development of photocatalysts (PCs) with diverse properties has been es

235 nality of a photoactive semiconductor (i.e., photocatalysts, photoelectrodes, etc.) is largely dictat

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

237 ows convincingly that the Nd(1-x)Sr(x)MnO(3) photocatalysts possess great promise for visible light d

238 Consequently, this unique photocatalyst possesses the extended absorption region,

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

240 visible light by electrochemically priming a photocatalyst prior to excitation.

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

242 Photocatalysts provide a sustainable way to remove pollu

243 study further enabled the discovery of a new photocatalyst providing a >30-fold rate increase.

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

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

246 , the direct synthesis of efficient Z-scheme photocatalysts remains a grand challenge.

247 Notably, the photocatalyst retains 60 % CO evolution activity under v

248 e introduce the research area of nanocrystal photocatalysts, review their studies as Quantum PIs for

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

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

251 oach was applied to continuously recover the photocatalyst [Ru(bpy)(3)](2+) from a homogeneous, aceto

252 The photocatalyst sheet design enables efficient and scalabl

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

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

255 The NPs as photocatalysts show a good activity for CO(2) reduction.

256 t device technologies that include displays, photocatalysts, solar energy conversion devices, photovo

257 Especially, molecular photocatalysts still suffer from limited long-term stabi

258 utility of using heterogeneous semiconductor photocatalysts such as TiO(2) for promoting challenging

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

260 ion phase), using unmodified Ru(bpy)(3)Cl(2) photocatalyst, sun energy, atmospheric O(2), and at ambi

261 bled monolayers (SAMs) of organic molecules, photocatalyst surfaces, small molecules within biologica

262 nsity dependence of charge accumulation in a photocatalyst suspension, and its impact on both charge

263 A precious-metal- and Cd-free photocatalyst system for efficient H(2) evolution from a

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

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

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

267 er counterparts and most of analogous hybrid photocatalyst system.

268 r(1) /CN-NT is a highly efficient and robust photocatalyst that exhibits outstanding CO(2) RR perform

269 xamples of linear conjugated organic polymer photocatalysts that produce oxygen from water after load

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

271 that the annihilator itself can be used as a photocatalyst, thus simplifying the reaction.

272 d for low and high NaCl concentrations, at a photocatalyst (TiO(2)) concentration of 0.5 g.L(-1), and

273 pectroscopy, energy transfer from an iridium photocatalyst to a catalytically relevant Ni(II)(aryl) a

274 s reductants and uses an inexpensive organic photocatalyst to access medicinally valuable beta-phenet

275 Herein, we describe the utilization of a photocatalyst to oxidize an organopalladium(II) intermed

276 ence for the energy transfer from an iridium photocatalyst to the allylic chloride substrate followed

277 te that the use of a visible light activated photocatalyst to transform substrates in combination wit

278 or photoreduction of CO(2) via Bi-based PeNC photocatalysts to form CO, CH(4), and other possible sid

279 itride gave higher selectivity, even at high photocatalyst-to-nickel ratios.

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

281 phthoquinone using Ru(bpy)(3)(PF(6))(2) as a photocatalyst under blue LED light irradiation to yield

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

283 n of N-hydroxyphthalimide esters using an Ir photocatalyst under visible light irradiation.

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

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

286 nanoparticles could be used as a switchable photocatalyst which has good catalytic activity to absor

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

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

289 ed in the creation of numerous semiconductor photocatalysts, which stimulated the development of vari

290 f benzamides has been developed by merging a photocatalyst with a cobalt catalyst for the synthesis o

291 catalyzed by phenothiazine, a simple organic photocatalyst with MW < 200 that mediates the previously

292 -C(3)N(4)) is a robust organic semiconductor photocatalyst with proven H(2) evolution ability.

293 Red phosphorus is a promising photocatalyst with wide visible-light absorption up to 7

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

295 between ISs and CPs leads to more efficient photocatalysts with enhanced light absorption in the ove

296 Nanoparticles offer unique properties as photocatalysts with large surface areas.

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

298 Most notably, photocatalysts with more noncoordinating counteranions y

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

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