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1 rated exceptional optoelectronic properties, photocatalytic ability in superoxide anion radical-media
2                            To understand the photocatalytic act of dust particles, both GDD and ATD w
3 o understanding degradation processes of the photocatalytic active material.
4 ch techniques are highly suited for studying photocatalytic active material.
5 s exhibit excellent visible light responsive photocatalytic activities for efficiently degrading orga
6                                          The photocatalytic activities of the Al-TiO2 samples were in
7            The homogeneous and heterogeneous photocatalytic activities of the TBPCExBox(4+) , for the
8 lsion direction, by exploiting the different photocatalytic activities on both sides.
9 n in the visible region and greatly enhanced photocatalytic activities on H2 generation comparing wit
10  prepared from Al(NO3)39H2O exhibit the best photocatalytic activity among the four kinds of samples,
11 anocatalyst exhibits excellent visible-light photocatalytic activity and an apparent quantum efficien
12 A linear correlation was established between photocatalytic activity and the reciprocal of inter acti
13 lysts are shown to be able to possess higher photocatalytic activity because of spatial separation of
14                                  Despite the photocatalytic activity decreased with each cycle, it ca
15 BiVO(4) content in the network overcomes the photocatalytic activity due to the decrease in the reduc
16            The demonstration of an efficient photocatalytic activity for a composite based on lead-fr
17 ZTS/MoS2-rGO system also demonstrated stable photocatalytic activity for a continuous 20 h reaction.
18 s and exhibit superior UV- and visible-light photocatalytic activity for ammonia synthesis at ambient
19  among the highest in Zr-MOFs) but also high photocatalytic activity for reduction of CO2 into CO ( a
20 ular CuCr-LDH nanosheets, possess remarkable photocatalytic activity for the photoreduction of N2 to
21          PeNC of Cs(3)Bi(2)I(9) had the best photocatalytic activity for the reduction of CO(2) at th
22 cade that correlates with a near-doubling in photocatalytic activity from 2050 to 3810 mumol h(-1) g(
23 OFs, changes in the photoelectrochemical and photocatalytic activity have been rationalized with comp
24 arbon nitride (C(3) N(4) ) for enhancing its photocatalytic activity is still a challenging issue.
25                          Here, we assess the photocatalytic activity of MIL-125, a TiO2/1,4-benzenedi
26                    This superior behavior in photocatalytic activity of Nd(0.3)Sr(0.7)MnO(3) nanocomp
27                                          The photocatalytic activity of the (PW(12),Cp*Rh)@UiO-67 com
28 itching can also be achieved by coupling the photocatalytic activity of the SnO2-x NCs with the color
29                                          The photocatalytic activity of these bpy-containing PCPs can
30 mers, and that the key challenge to optimize photocatalytic activity of these materials is to prevent
31 re of the frontier orbitals, relevant to the photocatalytic activity of these solids.
32 1} facets could provide a way to enhance the photocatalytic activity of this material.
33 eration from the Cerenkov radiation-assisted photocatalytic activity of TiO(2) The model predictions
34 is correlation between electron transfer and photocatalytic activity provides new insight into struct
35 /MoS2-rGO heterostructure showed much higher photocatalytic activity than both Au and Pt nanoparticle
36 zo[b,d]thiophene sulfone co-polymer has a UV photocatalytic activity that rivals TiO2, but is much mo
37 ngle-crystalline nanosheets with outstanding photocatalytic activity toward CO2 reduction is prepared
38 ed, and the TiO2-S/rGO hybrid exhibited high photocatalytic activity under simulated sunlight.
39              We propose that the increase in photocatalytic activity upon heterogenization of the cat
40 42 backbone that show improved and prolonged photocatalytic activity with respect to equivalent physi
41 hibits the superior luminescent property and photocatalytic activity, which may find potential applic
42 350 degrees C, the crystalized TiO2 enhanced photocatalytic activity, while Fe3O4 was converted to ga
43 HP hybrid exhibited a significantly enhanced photocatalytic activity, with HER rates reaching 33.2 an
44 sheets of g-C(3) N(4) attain much intriguing photocatalytic activity.
45 separation efficiency and subsequently boost photocatalytic activity.
46 rder to reduce the band gap and maximize the photocatalytic activity.
47 e in carrier lifetime, and strongly enhanced photocatalytic activity.
48 e reduces its electron transport ability and photocatalytic activity.
49 he complexes have helped to understand their photocatalytic activity.
50 he MOF is not required to obtain the maximum photocatalytic activity.
51 e to a high photoconductive gain and reduced photocatalytic activity.
52 relates well with the observed trends in the photocatalytic activity.
53                                          The photocatalytic air pretreatment transforms NO gas into N
54                                              Photocatalytic alpha-functionalization of amines provide
55   This review aims to introduce the field of photocatalytic amino acid modification and discusses the
56 nanoparticle electrocatalytic amplification, photocatalytic amplification, and nanoimpacts of single
57                                              Photocatalytic and (photo) electrochemical responses of
58  strategies to incorporate microorganisms in photocatalytic and (photo)electrochemical systems to pro
59  upon photoexcitation is necessary to expand photocatalytic and biological imaging applications.
60                                  We report a photocatalytic and diastereoselective isomerization of a
61 diated silver nanoparticles (Iso-AgNPs), and photocatalytic and electrocatalytic activities of Iso-Ag
62 ation, and low efficiency and selectivity in photocatalytic and electrocatalytic CO(2) hydrogenation.
63 cyclic framework was studied via a series of photocatalytic and electrocatalytic reactions varying th
64                         We report a combined photocatalytic and hydrogen atom transfer (HAT) approach
65 nSe as a state-of-the-art light absorber for photocatalytic and photoelectrochemical H(2) generation.
66          They have also gained a foothold in photocatalytic and photoelectrochemical processes recent
67  of efficient light-harvesting systems, like photocatalytic and photovoltaic ones.
68  of these materials for the thermocatalytic, photocatalytic, and electrocatalytic conversion of CO(2)
69 OS generation have been further exploited in photocatalytic antibacterial activity against methicilli
70 of heterojunction photocatalysts for various photocatalytic applications are also presented and appra
71 ojunction for solar-cell, photodetector, and photocatalytic applications are discussed.
72 ctivated O2s-Ti bond that may be relevant in photocatalytic applications in an aqueous medium.
73 amics important for photoelectrochemical and photocatalytic applications remains contentious and poor
74 eparation dynamics, properties essential for photocatalytic applications, using optical (OTA) and X-r
75 eworks (MOFs) for photovoltaic, sensing, and photocatalytic applications.
76 orks are regarded as promising materials for photocatalytic applications.
77 O-66(Hf) are among the most studied MOFs for photocatalytic applications.
78 eveloping new materials for photovoltaic and photocatalytic applications.
79 al design of 2D MOFs for photoelectronic and photocatalytic applications.
80 onstrated potential in photo-electronics and photocatalytic applications.
81 y diverse boronates, but a broadly efficient photocatalytic borylation method that can effect borylat
82  a general, metal-free visible light-induced photocatalytic borylation platform that enables borylati
83                                          The photocatalytic C-F functionalization of highly fluorinat
84                         A mild and selective photocatalytic C-H (18)F-fluorination reaction has been
85           By evaluating the performance of a photocatalytic C-N cross-coupling reaction across multip
86 dation of the mechanistic underpinnings to a photocatalytic C-N cross-coupling reaction.
87  mechanistic insights into an iridium/nickel photocatalytic C-O cross-coupling reaction from time-res
88  photoinduced charge carriers to enhance the photocatalytic capability.
89 roenvironment-mapping platform that exploits photocatalytic carbene generation to selectively identif
90 this review, the development in the field of photocatalytic carbonylation is described by compiling t
91 sfer to exfoliated carbon nitride containing photocatalytic chain terminations.
92 mputationally, followed by the synthesis and photocatalytic characterization of a sub-library of more
93 rate the utility of these nanostructures for photocatalytic chemical reactions in the preferential ox
94 of catalyst loading and is key for achieving photocatalytic CO(2) conversion.
95  A mechanistic understanding of electro- and photocatalytic CO(2) reduction is crucial to develop str
96 pure-water system, hinder the development of photocatalytic CO(2) RR owing to the lack of effective c
97 crucial role of single Er atoms in promoting photocatalytic CO(2) RR.
98 ng energy efficiency of electrocatalytic and photocatalytic CO2 conversion to useful chemicals poses
99 reservoir would represent a role for TiO2 in photocatalytic CO2 reduction that has previously not bee
100 technique is reported for the synthesis of a photocatalytic composite material consisting of orthorho
101             The stability of Co4O4-dpk under photocatalytic conditions ([Ru(bpy)3](2+)/S2O8(2-)) was
102              In situ XANES experiments under photocatalytic conditions show that the {Co(II)4O4} core
103 pate in chlorine atom abstraction under mild photocatalytic conditions.
104                        Herein, we report the photocatalytic construction of 2,7-diazabicyclo[3.2.1]oc
105 mbination rate has been the big challenge to photocatalytic conversion efficiency.
106                                              Photocatalytic conversion of CO(2) to reduced carbon sta
107                                              Photocatalytic conversion of CO2 into carbonaceous feeds
108                                          The photocatalytic conversion of the greenhouse gas CO(2) to
109 employed in catalytic, electrocatalytic, and photocatalytic conversions, have surfaces that are typic
110 e, we describe a high-performance recyclable photocatalytic core-shell nanofibre system that integrat
111                 Reductive termination of the photocatalytic cycle generates an anion that undergoes a
112                         Turnover of this new photocatalytic cycle occurs along with the reformation o
113           Herein, we report conditions for a photocatalytic decarboxylative C-O bond formation reacti
114 luated electrochemical degradation (ECD) and photocatalytic degradation (PCD) technologies for saline
115  hydrocarbons were formed in solution, while photocatalytic degradation did not show the formation of
116 findings lay a foundation for predicting the photocatalytic degradation efficiency for the myriad of
117 f free chlorine and chlorinated compounds in photocatalytic degradation is discussed based on photoel
118  NS served dual role of detection as well as photocatalytic degradation of food colorant.
119              The potential of MXenes for the photocatalytic degradation of organic pollutants in wate
120 3 is a well known catalyst, the simultaneous photocatalytic degradation of organic pollutants present
121                         Here, we examine the photocatalytic degradation of rhodamine B by visible lig
122 results in a record-high and stable sunlight photocatalytic degradation rate of 0.24 s(-1) , which ex
123 nd demonstrates the online monitoring of the photocatalytic degradations of methylene blue and methyl
124 approach gives a detailed description of the photocatalytic desulfurization process on TiO(2), in whi
125  devices, such as perovskite solar cells and photocatalytic devices, it is important to tailor its ba
126                           An intermolecular, photocatalytic dicarbofunctionalization (DCF) of olefins
127                                    Efficient photocatalytic disinfection of Escherichia coli O157:H7
128 rid and bacteria is not indispensable in the photocatalytic disinfection process.
129                                          The photocatalytic effect endows the adsorbent with high ant
130 hotoinduced photothermal, photoelectric, and photocatalytic effects of black phosphorus (BP) nanoshee
131                             Plasmon-assisted photocatalytic efficiencies can improve when intermediat
132 03<x<0.20) were reported to show competitive photocatalytic efficiencies under visible light, which w
133 flexible spectral tunability, stability, and photocatalytic efficiencies.
134 ts with surface defects is proposed to boost photocatalytic efficiency by simultaneously promoting bu
135 ith a mass ratio of (1:10) shows the highest photocatalytic efficiency compared to the other composit
136 as an interesting alternative to improve the photocatalytic efficiency due to the possibility of cont
137                                          The photocatalytic efficiency of Nd(0.3)Sr(0.7)MnO(3) nanoco
138 cted considerable attention in enhancing the photocatalytic efficiency of TiO2 under visible light ir
139 allographic positions of MOFs promoted their photocatalytic efficiency.
140 fer of charge carriers and in turn boost the photocatalytic efficiency.
141                                              Photocatalytic, electrocatalytic and physicochemical pro
142 y the amidyl radical, which was generated by photocatalytic fragmentation of a pre-functionalized ami
143 s tutorial review, the integration of CDs in photocatalytic fuel generation systems with metallic, mo
144  are promising emerging light-harvesters for photocatalytic fuel production systems.
145               In terms of energy conversion, photocatalytic fuel production, such as hydrogen evoluti
146                         Herein we report the photocatalytic generation of a mononuclear non-haem [(13
147 makes it exhibit 21.7 and 232.6 times higher photocatalytic H(2) evolution activity than those of In(
148 a simple, efficient, and low-cost all-in-one photocatalytic H(2) evolution system composed of a thiaz
149  In(2) O(3) -ZISe-Mo is also very stable for photocatalytic H(2) production by showing almost no acti
150 nosheet photocatalysts for greatly enhancing photocatalytic H(2) production is made.
151 nic dyes, carbon nitride, and COF-sensitized photocatalytic H(2)O reduction systems.
152 acilitate electron-hole transfer for raising photocatalytic H2 evolution activity.
153  stability and activity in both electro- and photocatalytic HER in neutral water.
154 separation and transfer, which benefited the photocatalytic HER performance.
155 ore active 1T' phase as true active sites in photocatalytic HERs, resulting in a "catalytic site self
156 unactivated internal alkenes(5-7), including photocatalytic hydroamination(8,9), and no asymmetric in
157 O(4) Br displays 4.9 and 30.9 times enhanced photocatalytic hydrogen evolution and nitrogen fixation
158 but the fast charge recombination limits its photocatalytic hydrogen evolution reaction (HER) activit
159 S] catalyst systems for electrocatalytic and photocatalytic hydrogen evolution reactions.
160                               We demonstrate photocatalytic hydrogen evolution using COF photosensiti
161  be promising photocatalysts for sacrificial photocatalytic hydrogen evolution with a maximum rate of
162  MoS2-rGO hybrid is a better co-catalyst for photocatalytic hydrogen generation than the precious met
163                                           In photocatalytic hydrogen generation under visible light i
164  Semiconductor compounds are widely used for photocatalytic hydrogen production applications, where p
165 e catalyst exhibits a superior visible-light photocatalytic hydrogen production rate (~212 umol h(-1)
166 ecoupling of the light and dark reactions of photocatalytic hydrogen production through the radical's
167 harge conversion efficiencies, (ii) gains in photocatalytic longevity, and (iii) insights into the ET
168 vel composition named carbon-based composite photocatalytic material of zinc oxide and zinc sulphide
169 ominantly used for semiconducting and hybrid photocatalytic materials will be reviewed as surface are
170 -organic frameworks (MOFs) as highly tunable photocatalytic materials, systematic studies that interr
171 stereoselective C-C oxidative coupling via a photocatalytic means using specially designed perovskite
172 lectron trapping recombination and plausible photocatalytic mechanism are also explored, and the repo
173 abrication of STAO and its unique quasi-atom photocatalytic mechanism lays new ground for achieving n
174 Quantum PIs, and provided insights for their photocatalytic mechanism of action.
175      The radical species involved within the photocatalytic mechanisms were also explored through use
176 or photocatalysts with the post-illumination photocatalytic "memory" could be largely expanded to sem
177  h(-1) ), it might also be the highest among photocatalytic methane conversions reported so far under
178 ndence on light intensity cause the unheated photocatalytic methane production rate to exceed the the
179                                            A photocatalytic method for the aerobic oxidative cleavage
180                             We report here a photocatalytic method for the intermolecular anti-Markov
181                                 An efficient photocatalytic method was developed for the remote C5-H
182                  With the development of new photocatalytic methods over recent decades, the translat
183 -assembly to vesicles; and (iii) the role of photocatalytic minerals in harvesting light energy to dr
184 des low-potential photoexcited electrons for photocatalytic N(2) reduction.
185 ane (Fe4S4) biomimetic clusters demonstrates photocatalytic N2 fixation and conversion to NH3 in ambi
186                         Reported herein is a photocatalytic non-chain-radical aroyl chlorination of a
187                                          The photocatalytic O-H dissociation of water absorbed on a r
188                                            A photocatalytic olefin hydroaminoalkylation brings togeth
189 olution rate and TON, coupled with long-term photocatalytic operation of this hybrid system in water,
190                       Visible light-mediated photocatalytic organic transformation has drawn signific
191 y reactions at the interface that may govern photocatalytic organic transformations in natural and en
192                                              Photocatalytic overall water splitting proceeded using M
193 tive sites and fine-tuned the selectivity in photocatalytic oxidation of tetrahydrofuran (THF) to exc
194               This system is a model for the photocatalytic oxidation of water by TiO2 in an aqueous
195         The method was shown to provide fast photocatalytic oxidation reactions and analysis with thr
196 latform for studying titanium dioxide (TiO2) photocatalytic oxidation reactions by performing reactio
197 d CH3OH may also be an active species in the photocatalytic oxidation to CH2O.
198 ant binary metal catalyst displays excellent photocatalytic oxygen evolution activity with almost 100
199                 We report the enhancement of photocatalytic performance by introduction of hydrogen-b
200 search interest because of its visible light photocatalytic performance combined with good stability
201 -x , monolayer BiO2-x has exhibited enhanced photocatalytic performance for rhodamine B and phenol re
202                                          The photocatalytic performance is evaluated by quantifying t
203                                 The improved photocatalytic performance is primarily attributed to th
204 c systems is very promising for boosting the photocatalytic performance of H(2) production and CO(2)
205 edance spectroscopy reveal that the enhanced photocatalytic performance of In(2) O(3) -ZISe-Mo is mai
206                                          The photocatalytic performance of the Nd(1-x)Sr(x)MnO(3) nan
207 ovide key mechanistic understanding on their photocatalytic performance, including the photo-reductio
208 thesize TiO2-S/rGO hybrid, and its excellent photocatalytic performance, such TiO2-S/rGO hybrids are
209 rons into g-C(3) N(4) with markedly improved photocatalytic performance.
210 rge recombination impede the sunlight-driven photocatalytic performance.
211 bination, is responsible for the outstanding photocatalytic performance.
212 O2 was evaluated to demonstrate its improved photocatalytic performance.
213             However, the manner in which the photocatalytic performances are impacted by the amount o
214 and output modules to implement a UV-induced photocatalytic/peroxidation nanoparticle/DNAzyme reactio
215 eration is missing from both the thermo- and photocatalytic perspectives.
216                                          The photocatalytic polymerization clearly depends on the con
217 e can serve as electron acceptors during the photocatalytic polymerization reaction.
218                                              Photocatalytic polymers offer an alternative to prevaili
219                    The complexity-generating photocatalytic process also provides direct access to no
220          We report a visible-light-activated photocatalytic process that introduces a covalent modifi
221 pping active oxygen species generated in the photocatalytic process, polymerization could be implemen
222  This competition can be exploited to design photocatalytic processes to favor specific chemical tran
223 dition to the well-known behaviour of ISs in photocatalytic processes, CPs have emerged as an interes
224 o energy-rich molecules (solar fuel) through photocatalytic processes, invariably starts with photoin
225 the excited populations that have utility in photocatalytic processes.
226 mized conditions, the nanofibres promote the photocatalytic production of hydrogen from water with an
227                          Due to the superior photocatalytic properties of poly(heptazine imide) (PHI)
228 rphologies, thermal stability of anatase and photocatalytic properties of the as-prepared Al-TiO2 nan
229 sses of optoelectronic devices and excellent photocatalytic properties.
230 g the plasmon decay) are responsible for the photocatalytic property of this material under visible l
231                       This mild and reliable photocatalytic protocol enables C-S coupling at the most
232                  A new visible light-induced photocatalytic protocol enabling the formation of second
233                           Reported here is a photocatalytic protocol for the functionalization of ben
234                              We report a new photocatalytic protocol for the redox-neutral isomerizat
235                     In the last few decades, photocatalytic radical carbonylation strategies have rec
236 matic impact on the rate of a representative photocatalytic radical cation Diels-Alder reaction.
237                             Methods: Using a photocatalytic radical fluorination, we prepared a serie
238 phonyl-arylations of vinyl ureas by way of a photocatalytic radical-polar crossover mechanism.
239 creased amounts of bdc-NH2 yielded increased photocatalytic rates, followed by a plateau up to 100% b
240  physics, light interaction with matter, and photocatalytic reaction engineering.
241 lations indicate that the chiral bias of the photocatalytic reaction is associated with the chiral en
242                                   Their main photocatalytic reaction products were mostly similar to
243 miconductor-based electrodes to achieve high photocatalytic reaction rates.
244 on processes that are key components of many photocatalytic reaction schemes.
245                                          The photocatalytic reaction was successfully performed on a
246 sing inorganic compounds and for single site photocatalytic reactions in confined space.
247 an empirically derived parameter for scaling photocatalytic reactions in flow.
248                   However, the efficiency of photocatalytic reactions remains low due to the fast ele
249                          The products of the photocatalytic reactions were analyzed using a gas chrom
250 their superior optoelectronic properties for photocatalytic reactions, including high absorption coef
251  the transfer of electrons to participate in photocatalytic reactions.
252 s trapping reduces the efficiency of surface photocatalytic reactions.
253                                          Its photocatalytic reactivity was evaluated by the degradati
254                    Mass-, surface area-, and photocatalytic reactivity-based functional units are sel
255                                         This photocatalytic redox imbalance strategy offers a new app
256 f free radicals from thiazolinium salts upon photocatalytic reduction is described.
257 e nanocrystals (PeNCs) with applications for photocatalytic reduction of carbon dioxide to methane an
258                             The solar-driven photocatalytic reduction of CO(2) (CO(2) RR) into chemic
259                   The possible mechanism for photocatalytic reduction of CO2 -to-CO over ZrPP-1-Co is
260                                              Photocatalytic reduction of molecular oxygen is a promis
261 n of a pyridinium linker that immolates upon photocatalytic reduction with a ruthenium complex to yie
262 e conversion efficiency of the nanocomposite photocatalytic reduction.
263 CTF-HUST-HC1 has superior performance in the photocatalytic removal of nitric oxide (NO) than its les
264    This mechanistic insight provided a novel photocatalytic route based on N-substituted auxiliaries
265 al reactivity in solar energy conversion and photocatalytic schemes.
266  fission will pave the way for improving the photocatalytic selectivity and turnover.
267                                           In photocatalytic solar fuel production, these electron pro
268 lable photocatalytic system allows efficient photocatalytic solar transformations.
269                               Semiconducting photocatalytic solar-hydrogen conversion (SHC) from wate
270                                       Recent photocatalytic strategies for the formation of O-CF(3) ,
271        Herein we report the development of a photocatalytic strategy for the divergent preparation of
272                       The conventional batch photocatalytic studies on lignin, often using dissolved
273 expand possibilities for developing designer photocatalytic substrates.
274 with paragraphs discussing the visible-light photocatalytic synthetic protocols so far available for
275 Overall, the use of a metal-free, recyclable photocatalytic system allows efficient photocatalytic so
276                         The development of a photocatalytic system for lignin depolymerization in a c
277                                            A photocatalytic system for the dearomative hydroarylation
278                                         This photocatalytic system operates in pure and untreated sea
279 by boosting the activity of a titania (TiO2) photocatalytic system.
280 riphenylphosphine in the presence of various photocatalytic systems (dicyanoanthracene/biphenyl, N-me
281 ver commonly used heterogeneous catalysts in photocatalytic systems by increasing the efficiency of r
282 lopment of inorganic catalysts, electro- and photocatalytic systems for fuel generation have evolved
283                             Plasmon-mediated photocatalytic systems generally suffer from poor effici
284                                However, most photocatalytic systems involve rare and expensive platin
285 al electron transfer processes present in CD photocatalytic systems is outlined and various avenues f
286 l photosynthesis, the design of new Z-scheme photocatalytic systems is very promising for boosting th
287                                              Photocatalytic systems that combine light-harvesting mat
288 )-catalyzed systems or visible-light-induced photocatalytic systems that would be capable of mediatin
289 ide perovskite solar cells, and finally some photocatalytic systems.
290 ucted to characterize surface changes in the photocatalytic TiO2 powder using near-ambient-pressure X
291 onments, where they play a prominent role in photocatalytic transformations of bound organics.
292                                    Selective photocatalytic transformations of chemicals derived from
293 f visible light, it has been applied for the photocatalytic uphill conversion of trans-stilbene to ci
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                                              Photocatalytic water splitting is attracting enormous in
297 d reviews focussing on various materials for photocatalytic water splitting, to date only few reviews
298 any of its practical applications, including photocatalytic water splitting.
299 ergy technologies, including solar cells and photocatalytic water splitting.
300 lkylated amines, we herein rationally design photocatalytic water-splitting to furnish [H] or [D] and

 
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