Light-emitting Diode Irradiation Research Articles

Interdental Plaque Microbial Community Changes under In Vitro Violet LED Irradiation.

Oral microbiome dysbiosis has important links to human health and disease. Although photodynamic therapy influences microbiome diversity, the specific effect of violet light irradiation remains largely unknown. In this study, we analyzed the effect of violet light-emitting diode (LED) irradiation on interdental plaque microbiota. Interdental plaque was collected from 12 human subjects, exposed to violet LED irradiation, and cultured in a specialized growth medium. Next-generation sequencing of the 16S ribosomal RNA genes revealed that α-diversity decreased, whereas β-diversity exhibited a continuous change with violet LED irradiation doses. In addition, we identified several operational taxonomic units that exhibited significant shifts during violet LED irradiation. Specifically, violet LED irradiation led to a significant reduction in the relative abundance of Fusobacterium species, but a significant increase in several species of oral bacteria, such as Veillonella and Campylobacter. Our study provides an overview of oral plaque microbiota changes under violet LED irradiation, and highlights the potential of this method for adjusting the balance of the oral microbiome without inducing antibiotic resistance.

Rapid inactivation of SARS-CoV-2 with LED irradiation of visible spectrum wavelengths

Difficulty in controlling SARS-CoV-2 transmission made the ability to inactivate viruses in aerosols and fomites to be an important and attractive risk reduction measure. Evidence that light frequencies have the ability to inhibit microorganisms has already been reported by many studies which, however, focused on ultraviolet (UV) wavelengths, which are known to induce potential injury in humans. In the present study, the effect on suspensions of SARS-CoV-2 of a Light Emitting Diode (LED) device capable of radiating frequencies in the non-hazardous visible light spectrum (VIS) was investigated. In order to evaluate the efficiency of viral inactivation, plaque assay and western blot of viral proteins were performed. The observed results showed a significant reduction in infectious particles that had been exposed to the LED irradiation of visible light. Furthermore, the analysis of the intracellular expression of viral proteins confirmed the inactivating effect of this irradiation technology. This in vitro study revealed for the first time the inactivation of SARS-CoV-2 through LED irradiation with multiple wavelengths of the visible spectrum. However additional and more in-depth studies can aim to demonstrate the data obtained during these experiments in different matrices, in mutable environmental conditions and on other respiratory viruses such as the influenza virus. The type of LED technology can decisively contribute on reducing virus transmission through the continuous sanitation of common environments without risks for humans and animals.

Induced pluripotent stem cells can improve thrombolytic effect of low-dose rt-PA after acute carotid thrombosis in rat

BackgroundIntravenous thrombolysis using recombinant tissue plasminogen activator (rt-PA) is the standard treatment for acute ischemic stroke. Standard-dose rt-PA (0.9 mg/kg) is known to achieve good recanalization but carries a high bleeding risk. Lower dose of rt-PA has less bleeding risk but carries a high re-occlusion rate. We investigate if induced pluripotent stem cells (iPSCs) can improve the thrombolytic effect of low-dose rt-PA (0.45 mg/kg).MethodsSingle irradiation with 6 mW/cm2 light-emitting diode (LED) for 4 h at rat common carotid artery was used as thrombosis model according to our previous report. Endothelin-1 (ET-1), intercellular adhesion molecule-1 (ICAM-1), and interleukin 1 beta (IL-1 beta) were used as the inflammatory markers for artery endothelial injury. Angiopoietin-2 (AP-2), brain-derived neurotrophic factor (BDNF) and vascular endothelial growth factor (VEGF) were examined in artery wall and iPSCs culture. Animal ultrasound was used to evaluate the stenosis degree of common carotid artery before and at 2 h, 24 h, 4 days and 7 days after LED irradiation.ResultsAfter LED irradiation alone, there was a persistent occlusion from 2 h to 7 days. Standard-dose rt-PA alone could recanalize the occluded artery from 24 h to 7 days to stenotic degree ≤ 50%. Low-dose rt-PA or 1 × 106 mouse iPSCs alone could not recanalize the occluded arteries from 2 h to 7 days. Combination use of low-dose rt-PA plus 1 × 106 mouse iPSCs caused better recanalization from 24 h to 7 days. ET-1, ICAM-1 and IL-1 beta were strongly expressed after LED irradiation but reduced after iPSCs treatment. AP-2, BDNF and VEGF were rarely induced after LED irradiation but strongly expressed after iPSCs treatment. In vitro study showed iPSCs could express AP-2, BDNF and VEGF.ConclusionThe adjuvant use of iPSCs may help improving the thrombolytic effect of low-dose rt-PA by suppressing inflammatory factors and inducing angiogenic trophic factors. Stem cells could be a potential regimen in acute thrombolytic therapy to improve recanalization and reduce complications.

635nm LED irradiation may prevent endoplasmic reticulum stress in MC3T3-E1 cells.

Although endoplasmic reticulum (ER) stress is thought to be involved in various diseases such as cancer, metabolic, and inflammatory disorders, the relationship between ER stress and bone diseases, are remains unclear. Tunicamycin-treated MC3T3-E1 osteoblasts were used as the ER stress model in this study. 635nm light-emitting diode irradiation (635nm-IR) was carried out for 1h before and after inducing ER stress. To investigate the effects of 635nm-IR on ER stress-induced MC3T3-E1 osteoblasts and the underlying mechanism, western blot, reverse transcription polymerase chain reaction, alkaline phosphatase and Alizarin red staining, 2',7'-dichlorodyhydrofluorescein diacetate assay, Fluo-3AM and immunocytochemistry were performed. Pretreatment with 635nm-IR effectively prevented intracellular reactive oxygen species production and alleviated ER stress through the pancreatic ER kinase (PERK)-eukaryotic initiation factor 2 (eIF2)-activating transcription factor 4 (ATF4)-nuclear factor-like 2 (Nrf2) signaling pathway. Hence, 635nm-IR may serve a protective role in the treatment of ER stress-related bone diseases.

Impact on Porphyromonas gingivalis of antimicrobial photodynamic therapy with blue light and Rose Bengal in plaque-disclosing solution

ObjectivesAntimicrobial photodynamic therapy (aPDT) in periodontal pockets using lasers is difficult to perform in some cases because of the high cost of irradiation equipment and the narrow irradiation field. The purpose of the present study was to examine the effects of aPDT in combination with a plaque-disclosing solution and blue light-emitting diode (LED), which are used for composite resin polymerization. MethodsThe reactive oxygen species generated by irradiating 0.001% RB or MB with blue light were analyzed using electron spin resonance spectroscopy. Blue-light exposure was performed at 6.92, 20.76 and 124.6 J. The microorganism to be sterilized was Porphyromonas gingivalis. After aPDT, colony-forming units (CFUs) were measured to estimate cell survival. Carbonylated protein (PC) levels were used to evaluate oxidative stress. All statistical analyses were performed with Tukey's multiple comparisons test or the unpaired t-test. ResultsSinglet oxygen (1O2) generation was confirmed by RB+blue LED. 1O2 production was significantly greater with the blue LED irradiation of RB than that of MB (p < 0.0001). CFUs were significantly lower in the blue LED-irradiated group than in the non-LED-irradiated group (p < 0.01). The bactericidal effect increased in a time-dependent manner. aPDT increased PC levels. No morphological changes were observed in P. gingivalis. ConclusionsThe present results suggest that aPDT exerts bactericidal effects against P. gingivalis by increasing oxidative stress through the generation of 1O2 in cells. Periodontal disease may be treated by aPDT using the equipment available in dental offices.

Effect of 850 nm near-infrared light emitting diode irradiation on the production of 5-aminolevulinic acid in Rhodobacter sphaeroides

Effect of 850 nm near-infrared light emitting diode irradiation on the production of 5-aminolevulinic acid in <i>Rhodobacter sphaeroides</i>

Antibiofilm and cytotoxic effect of 3,3′-dihydroxycurcumin (DHC) as photosensitizer agent in antimicrobial photodynamic therapy for endodontic purposes

BackgroundCurcuminoids have been designed not only to improve chemical and metabolic stability of curcumin (CUR), but also to increase its antimicrobial activity, without effecting its ability as photosensitizer agent in antimicrobial photodynamic therapy (aPDT) with light emitting diode (LED). This study evaluated the antimicrobial and antibiofilm action of curcumin analog DHC (or 3,3′-dihydroxycurcumin), submitted or not to LED irradiation, on microorganisms of endodontic importance and its influence on fibroblasts viability. MethodsDHC was synthetized by modified Pablon's methodology and the experiments were conducted under irradiation or not with indium gallium nitride-based LED (440-480nm, 100 mW/cm2, 0.78 cm2,60 s). The antimicrobial activity of CUR and DHC were determined by the Minimum Inhibitory and Bactericidal Concentration assays against Gram-positive and Gram-negative bacteria and the effect of both compounds on fibroblast viability was tested using colorimetric assays. They were also evaluated on 72h and 7days single-species biofilms and on 14 days multispecies biofilms formed inside dentin tubules by bacterial colonies counts and confocal microscopy, respectively. Data were analyzed statistically considering p<0.05. ResultsDHC had bactericidal effect against all bacteria tested higher than CUR, in planktonic conditions. CUR and DHC (at 39 and 19 μg/mL, respectively) were cytocompatible and LED irradiation reduced fibroblast viability, regardless of compound. CUR and DHC reduced the growth of single-species biofilms and the effect of aPDT was bacteria dependent. DHC reduced more than 70% of microorganisms from multispecies biofilms, superior to CUR effect. ConclusionsDHC showed low cytotoxicity and antibiofilm effect similar to curcumin, when submitted or not to aPDT, and could be further explored as a bioactive compound for endodontic purposes.

Photo-Promoted Decarboxylative Alkylation of α,β-Unsaturated Carboxylic Acids with ICH2CN for the Synthesis of β,γ-Unsaturated Nitriles.

An efficient, catalyst/photocatalyst-free, and cost-effective methodology for the decarboxylative alkylation of α,β-unsaturated carboxylic acids to synthesize β,γ-unsaturated nitriles has been developed. The reaction proceeded in an environmentally benign atmosphere of blue light-emitting diode irradiation with K2CO3 and water at room temperature. The methodology worked for a wide range of substrates (22 examples) with up to 83% yield. The protocol is also compatible for gram-scale synthesis.

Energy efficient photocatalytic activation of peroxymonosulfate by g-C3N4 under 400 nm LED irradiation for degradation of Acid Orange 7

Photocatalytic activation of peroxymonosulfate (PMS) by graphitic carbon nitride (g-C3N4) is emerging as a sulfate radical anion based advanced oxidation process (S-AOP) for degradation of organic pollutants. Importantly, photocatalytic activation of PMS by g-C3N4 is energy intensive as light irradiation requires high electrical energy. Here, we studied activation of PMS by g-C3N4 under 400 nm light emitting diode (LED) irradiation (g-C3N4/PMS/400-LED system) for degradation of Acid Orange 7 (AO7). LED array having optical emission maximum around 400 nm (FWHM = 16 nm), with electrical input power of 1.54 W (14 V and 110 mA) was used for irradiation. Pseudo-first order rate constant (kobs) value for degradation of AO7 by g-C3N4/PMS/400-LED system was determined to be 0.094 min−1. O2·-, SO4·- were revealed by radical scavenging and ESR investigations. kobs value in simulated ground and real tap water were determined to be 0.068 min−1 and 0.063 min−1, respectively. g-C3N4 was stable, and reused four times without any significant loss in its photocatalytic activity. Importantly, electrical energy per order (EEO) for degradation of AO7 by g-C3N4/PMS/400-LED system was determined to be 24.51 kWh m−3 order−1. In contrast, the EEO value for the degradation of AO7 by g-C3N4 activated PMS under visible light irradiation (>400 nm), using conventional xenon lamp, (g-C3N4/PMS/Vis-Xe system) was found to be very high as 2702 kWh m−3 order−1. Thus, the study highlights, LED irradiation source is promising for the development of energy efficient g-C3N4 photocatalytic activation of PMS for removal of organic pollutants.

Synergistic effect of photobiomodulation and phthalocyanine photosensitizer on fibroblast signaling responses in an in vitro three-dimensional microenvironment.

Photobiomodulation (PBM) is a promising medical treatment modality in the area of photodynamic therapy (PDT). In this study, we investigated the effect of combined therapy in a 3D microenvironment using aluminum chloride phthalocyanines (AlClPc) as the photosensitizing agent. Normal human fibroblast-containing collagen biomatrix was prepared and treated with an oil-in-water (o/a) AlClPc-loaded nanoemulsion (from 0.5 to 3.0μM) and irradiated at a range of fluences (from 0.1 to 3.0J/cm2) using a continuous-wave light-emitting diode (LED) irradiation system (660nm). PBM at 1.2J/cm2 and AlClPc/NE at 0.5μM modified the fibroblast signaling response under 3D conditions, promoting collagen synthesis, ROS production, MMP-9 secretion, proliferation of the actin network, and facile myofibroblastic differentiation. PBM alone (at 1.2J/cm2 and 0.3J/cm2) had no significant effect on any of these parameters. The combined therapy affected myofibroblastic differentiation, inflammatory response, and extracellular matrix pliability, and should thus be examined further in subsequent studies considering that no side effects of PBM have been reported. Even though significant progress has been made in the field of phototherapy in recent years, it is necessary to further elucidate the detailed mechanisms underlying its effects already shown in 2D conditions to increase the acceptance of this beneficial and non-invasive therapeutic approach.

Effects of Combined Aerosolization with Ultraviolet C Light-Emitting Diode on Enterohemorrhagic Escherichia coli and Staphylococcus aureus Attached to Soft Fresh Produce.

Washing soft fresh produce such as strawberries, baby leaves, and sliced onions with sanitizing agents is challenging due to their fragile texture. Thus, treatments like aerosolization using slightly acidic electrolyzed water (SAEW) and ultraviolet C light-emitting diode (UVC LED) irradiation may be good alternatives. In the present study, the reduction effects of a combined treatment of aerosolization using SAEW and UVC LED irradiation on enterohemorrhagic Escherichia coli (EHEC) and Staphylococcus aureus attached to strawberries, baby leaves, and sliced onions were investigated. The behaviours of EHEC and S. aureus, moisture loss, colour measurement, and visual appearance were also analyzed at 10 and 15 °C for 7 days. The reduction effect of the combined treatment with 100 SAEW and UVC LED was higher (0.53–0.92 log CFU g−1) than a single aerosolization treatment (0.11–0.41 log CFU g−1), regardless of samples or pathogens. A greater effect on EHEC and S. aureus reduction was observed in strawberries (0.74 and 0.92 log CFU g−1) than in baby leaves (0.62 and 0.53 log CFU g−1) and sliced onions (0.55 and 0.62 log CFU g−1). The combined treatment further reduced the EHEC and S. aureus populations in strawberries during 7 days of storage at 10 and 15 °C. However, the EHEC and S. aureus populations were maintained in baby leaves and sliced onions at 10 °C for 7 days. Additionally, the greatest effect on the maintenance of colour and appearance was obtained in the combined treatment. Since the combined treatment reduces EHEC and S. aureus populations and preserves visual quality, it could be expected to extend the shelf life of soft fresh produce at the retailer stage of the supply chain.

Preventative treatment of red light-emitting diode protected osteoarthritis-like chondrocytes from oxidative stress-induced inflammation and promoted matrix gene expression

BackgroundOsteoarthritis (OA) has become the most common type of arthritis, and the cellular and molecular mechanisms involved in OA is complex and not fully understood. Inflammation and matrix degradation have been indicated to play vital roles in pathogenesis of OA. Apart from biochemical molecules such as anti-oxidants which have been suggested to reduce inflammatory responses, photobiomodulation has become interesting targets for developing therapeutic strategies of cartilage repair and regeneration. MethodsTo investigate the effect of photobiomodulation on OA, red light-emitting diode (LED) was preventatively applied to hydrogen peroxide induced OA-like chondrocytes. Lumen density was measured for the level of free radicals and gene expression of IL-1β, TNF-α, MMP-1, MMP-13, and COL-2 was analyzed. Significant FindingsOur results showed that pre-treatment of 635-nm LED for 2 h significantly reduced free radical formation (from 100% to 8.25%) and inflammatory gene IL-1β, TNF-α expression in OA-like cells while matrix gene COL-2 was enhanced. Furthermore, combination of preventative LED treatment with anti-oxidant(s) (vitamin E or/and resveratrol) exerted synergistic effects of anti-inflammation and MMP-13 reduction. In conclusion, preventative LED irradiation combined with anti-oxidants provides a novel therapeutic strategy for treating early OA prior to the progression of the disease.

In Vitro Evaluation of the Effectiveness of Dental Bleaching with Carbamide Peroxide and Violet Light.

Objective: The aim of the current study was to use the CIELab system to evaluate the performance of the whitening treatment involving violet light-emitting diode (LED) combined with a home 10% and 22% carbamide peroxide dental bleaching technique on dental enamel. Methods: Fifty blocks of bovine dental enamel were divided into five groups: control group (control), receiving only LED irradiation; Whitening 10%, receiving 10% carbamide peroxide treatment; Whitening 10%+VL, receiving 10% carbamide peroxide treatment combined with LED irradiation; Whitening 22%, receiving 22% carbamide peroxide treatment; and Whitening 22%+VL, receiving 22% carbamide peroxide treatment combined with violet LED irradiation. Color tests were performed before the protocols, after 1 week and after 2 weeks of treatment by using a spectrophotometer and the CIELab parameters: L*, (a*) and (b*). The Whitening 10%, Whitening 10%+VL, Whitening 22% and Whitening 22%+VL groups were submitted to 10% and 22% carbamide peroxide 8 h per day for 14 days, whereas the Control was only stored in artificial saliva. For irradiation in the Control, Whitening 10%+VL, and Whitening 22%+VL groups, we used violet LED at a wavelength of 405-410 nm activated for 60 permanent seconds and 30 sec of pause once per week. As all data exhibited normal distribution, the comparisons were performed by using two-way repeated-measures analysis of variance. A post hoc t-test was employed, followed by the Ryan-Holm stepdown Bonferroni procedure. Results: After 1 week, the Whitening 22%+VL group differed significantly from all other groups in relation to hue, while no difference was found between the remaining groups (p < 0.05). Analyzing lightness, the Whitening 22%+VL and Whiteness10%+VL groups differed from the other groups (p > 0.05). In the 2nd week, the Whitening 22%+VL groups differed significantly from all other groups (p < 0.05) in hue, chroma, and lightness. The comparative analysis of bleaching times within the same group revealed significant differences in the Whitening 22%+VL group between baseline and week 1, baseline and week 2, as well as weeks 1 and 2 in terms of hue (p > 0.05). In the Whitening 22%+VL group, significant differences (p < 0.05) were found between baseline and week 2 as well as between weeks 1 and 2 in chroma (p > 0.05). In the Whitening 22%+VL group, statistically significant differences (p < 0.05) were found between baseline and week 1, baseline and week 2, as well as between weeks 1 and 2 in lightness. In the Whitening 10%+VL group, statistically significant differences (p < 0.05) were found between baseline and week 1, between baseline and week 2, as well as between weeks 1 and 2 in lightness. Conclusions: Tooth whitening treatment involving 10% and 22% carbamide peroxide combined with violet light promoted changes in the three axes of color (ΔH, ΔC, and ΔL) of the specimens evaluated. The use of the gel bleach alone was more efficient when the higher concentration was used. When violet light was combined with the gel, the lower concentration was more efficient.

Blue Light Monochromatic Irradiation for 12 Hours in Lighting Pattern with Combinations of Blue and Red Light Elongates Young Cos Lettuce Leaves and Promotes Growth under High Daily Light Integral

Cos lettuce was grown under different spectral photon flux density distribution (SPFD) change patterns with blue- and/or red light-emitting diode (LED) irradiation with a 24-hour cycle. Twelve treatments were designed with a combination of four relative SPFD (RSPFD) change patterns and three photosynthetic photon flux density (PPFD) levels. The RSPFD change patterns were as follows: BR/BR, simultaneous blue- and red-light irradiation (BR) for 24 h; R/BR, red-light monochromatic irradiation (R) for 12 h followed by 12 hours of BR; B/BR, blue-light monochromatic irradiation (B) for 12 hours followed by 12 hours of BR; and B/R, 12 hours of B followed by 12 hours of R. Each RSPFD change pattern was conducted at three daily average photosynthetic photon flux densities (PPFDave) of 50, 100, and 200 µmol·m−2·s−1. The RSPFD change patterns that included B (B/BR and B/R) resulted in elongated leaves. A low ratio of active phytochrome to total phytochrome under B was considered the reason for leaf elongation. Shoot dry weight was significantly greater under the RSPFD change patterns that included B when the PPFDave was 200 µmol·m−2·s−1. The leaf elongation caused by B would have increased the amount of light received and thereby promoted growth. However, excessive leaf elongation caused the plants to fall, and growth was not promoted under the RSPFD change patterns that included B when the PPFDave was 50 µmol·m−2·s−1. Thus, 12-hour B promoted growth under conditions in which leaf elongation leads to increases in the amount of light received.

Editorial overview: Strategies for obtaining healthy meat products

Ice refrigeration is one of the most widely used methods for food preservation with the use of a low temperature to delay the growth of any microbial contaminants. The production of safe edible ice with antimicrobial properties is of importance to food safety and human health, and has attracted increasing interest in recent years. This manuscript summarizes the advancements of the recent technologies to produce activated ice containing bactericidal agents, which can be potentially applied for the microbial decontamination and freshness retention of raw foods, such as fresh vegetables, seafood and fisheries. Cold atmospheric plasma and acidic electrolysis of water are two technologies that have been recently proposed for the treatment of water that is intended for the production of safe ice. Additionally, the application of ultraviolet light-emitting diode (UVC-LED) irradiation for the efficient disinfection of the edible ice is also discussed.

Application of light-emittingdiodes (LEDs) in the extensionof the cultivation period of Spirulina in Northern Vietnam

Spirulina (Arthrospira platensis) is cultured in Vietnam mainly as a functional food for humans and supplementary food for aquatic species. In the North, the most suitable time to cultivate Spirulina is from early May to late September. Other times, due to the decrease in light intensity and temperature, the growth of Spirulina significantly reduced and gave low yield, especially in the period from December to the end of February. This study investigated the influence of LEDs light on the growth of Spirulina during the periods from early March to late April (T3-T4), from early October to late November (T10-T11), and from early December to late February (T12-T2) in Hanoi. The results showed that the continuous irradiation of red LEDs increased the yield of Spirulina and pigments, phycocyanin, and chlorophyll in the two stages (T3-T4) and (T10-T11). The irradiation of both red and blue LEDs did not show a significant effect in the period T12-T2. Green LEDs did not significantly affect the growth of Spirulina. The research results provided an initial basis for the application of red LEDs to the extent of the cultivation time of Spirulina in the North of Vietnam

Comparing the cytotoxic effect of light-emitting and organic light-emitting diodes based light therapy on human adipose-derived stem cells

Light has attracted significant attention as a promising tool in the biomedical and cosmetic industries. However, little is known about the cytotoxic effects of conventional light sources based on their physical effects such as temperature and luminance. Here, the cytotoxic effects of representative light sources, a light-emitting diode (LED) and an organic light-emitting diode (OLED), were studied with human adipose-derived stem cells (hADSCs). Regardless of the identical light energy conditions, LED group induced a higher apoptotic activity in hADSCs than the OLED group due to its significant heat generation compared to OLED as further demonstrated with heat shock protein family gene expression. Additionally, we further confirmed the effect of luminance by irradiating light from LED and OLED under the same temperature and energy conditions. Increased cell proliferation was confirmed in the OLED group, and a significant expression of intracellular reactive oxygen species was observed in the LED group without showing heat shock protein upregulation. Taken together, the differences in cytotoxicity and cellular response after LED irradiation compared with OLED irradiation can be varied with temperature and luminance control. This study suggests that OLED based device could be an alternative and promising light source for future biomedical and cosmetic applications.

Near‐infrared light for polymer re‐shaping and re‐processing applications

AbstractThe re‐shaping and reprocessing of polymers are usually associated with strong energetic costs, strongly limiting their practical usage. In this article, a new approach is proposed based on a near‐infrared (NIR) activation of the material in presence of a NIR heater for a highly efficient process upon ecofriendly NIR light emitting diodes irradiation. Markedly, due to this light‐triggered process, a spatial control of the shaping/reprocessing behavior can be obtained, that is, only the needed parts are irradiated preventing a heating of all the sample. In this work, different thermoplastics are reshaped or reprocessed due to NIR activation in presence of an organic NIR dye used as heater. As other examples of photothermal treatment upon NIR light, the on‐demand dehydration of polyethylene glycol (PEG‐based) hydrogels are also provided. All the processes are followed in real time by thermal imaging camera.

Thermal coupled photocatalysis over Pt/g-C3N4 for selectively reducing CO2 to CH4via cooperation of the electronic metal–support interaction effect and the oxidation state of Pt

Pt nanoparticle-loaded g-C3N4 (Pt/CN) that consisted of integrating Pt0 and Pt2+ species was prepared for selectively reducing CO2 to CH4 with H2O by thermal coupled photocatalysis. A strong electronic metal-support interaction was constructed between Pt nanoparticles and the g-C3N4 substrate, which limited the activity for CO evolution and improved the charge transfer from g-C3N4 to Pt for selective CH4 production. The formed Pt2+ species in the Pt nanoparticles completely suppress the side reaction of H2 production from reducing H2O. Moreover, a moderate heat input in the photocatalytic reaction facilitated the transfer of the photogenerated electrons from Pt nanoparticles to CO2, which further increased the photocatalytic activity for CH4 evolution. As a result, a significant enhancement of CO2 methanation performance (∼100 % selectivity, 14.8 μmol g−1 h−1) was realized on a 2 % Pt-loaded g-C3N4 photocatalyst under low intensity light-emitting diode (420 nm, on the order of solar intensity) irradiation at 125 °C.

Enhancing Singlet Oxygen Photocatalysis with Plasmonic Nanoparticles

Photocatalysts able to trigger the production of singlet oxygen species are the topic of intense research efforts in organic synthesis. Yet, challenges still exist in improving their activity and optimizing their use. Herein, we exploited the benefits of plasmonic nanoparticles to boost the activity of such photocatalysts via an antenna effect in the visible range. We synthesized silica-coated silver nanoparticles (Ag@SiO2 NPs), with silica shells which thicknesses ranged from 7 to 45 nm. We showed that they served as plasmonically active supports for tris(bipyridine)ruthenium(II), [Ru(bpy)3]2+, and demonstrated an enhanced catalytic activity under white light-emitting diode (LED) irradiation for citronellol oxidation, a key step in the commercial production of rose oxide fragrance. A maximum enhancement of the plasmon-mediated reactivity of approximately 3-fold was observed with a 28 nm silica layer along with a 4-fold enhancement in the emission intensity of the photocatalyst. Using electron energy loss spectroscopy (EELS) and boundary element method simulations, we mapped the decay of the plasmonic signal around the Ag core and provided a rationale for the observed catalytic enhancement. This work provides a systematic analysis of the promising properties of plasmonic NPs used as catalysis-enhancing supports for common homogeneous photocatalysts and a framework for the successful design of such systems in the context of organic transformations.