Photothermal Temperature Research Articles

Lignin-carbohydrate complex-based polyurethane elastomer with outstanding mechanical strength, photothermal efficiency, and enhanced recyclability

Addressing plastic pollution and reducing reliance on petroleum reserves necessitates the development of bio-based materials from renewable resources. Lignin-carbohydrate complexes (LCC) extracted from lignocellulose, abundant in aromatic rings and hydroxyl groups, offer a promising alternative to conventional polyols in polyurethane synthesis. Historically, the limited solubility of LCC in polyols has posed significant challenges in fabricating high-performance biomass-based polyurethanes. This study presents an innovative LCC-based polyurethane elastomer, synthesized from LCC, polyols, and isocyanate building blocks. By replacing traditional polyols with hydroxyl-rich LCC, the resulting polyurethane elastomer (PUC) exhibits exceptional mechanical properties and photothermal conversion efficiency. The material boasts a maximum tensile strength of 20.94 MPa, a fracture strain of 1167.39 %, an elastic recovery rate of 91.4 %, and a peak photothermal conversion temperature of 125 °C. These outstanding attributes are ascribed to a robust network of dynamic covalent and hydrogen bonds. Moreover, the incorporation of LCC notably enhances the recyclability of the polyurethane elastomer and provides effective UV-blocking properties. This research not only broadens the spectrum of raw materials available for polyurethane production but also introduces innovative methodologies for the practical utilization of LCC, representing a notable advancement in sustainable materials science.

Generation of oxygen vacancies in CuO/TiO2 heterojunction induced by diatomite for highly efficient UV–Vis-IR driven photothermal catalytic oxidation of HCHO

Photothermal catalytic oxidation is a promising and sustainable method for the degradation of indoor formaldehyde (HCHO). However, the excessively high surface temperature of existing photothermal catalysts during catalysis hinders the effective adsorption and degradation of formaldehyde under static conditions. Catalyst loading and oxygen vacancies (OVs) modulation are commonly employed strategies to reduce the photothermal catalytic temperature and enhance the efficiency of photothermal catalytic oxidation. In this work, a p-n type CuO/TiO2 heterojunction is successfully loaded onto diatomite using a wet precipitation method. Under the irradiation of a 300W xenon lamp, the prepared composite material achieved a 100% removal rate of HCHO within 2 h, with a 98% conversion rate to CO2, surpassing the performance of both individual photocatalysts and thermocatalysts. Additionally, by adjusting conditions such as light irradiation and temperature, we have demonstrated that this material exhibits synergistic photothermal catalytic properties. Based on HRTEM, XPS, Raman, and EPR analyses, the introduction of diatomite as a catalyst support was shown to effectively increase the number of OVs. Experimental results, along with O2-TPD, photoelectrochemical characterization, and radical detection, demonstrate that the presence of OVs enhances the oxidative efficiency of both photocatalysis and thermocatalysis, as well as the UV–Vis-IR photothermal catalytic performance. The ternary composite material generates weak hydroxyl (•OH) and superoxide (•O2−) radical under high-temperature with dark conditions, indicating its catalytic oxidation activity under this condition. The increase in temperature and the expansion of the spectral range both enhance the generation of these radicals. In summary, this work demonstrates that the use of diatomite as a support increases the material's specific surface area and OVs content, thereby enhancing adsorption and photothermal catalysis. It elucidates the enhanced catalytic degradation mechanism of this mineral-based photothermal catalyst.

Photothermal Temperature-Modulated Cancer Metastasis Harnessed Using Proteinase-Triggered Assembly of Near-Infrared II Photoacoustic/Photothermal Nanotheranostics.

Here we demonstrate that cancer metastasis could be modulated by the judicious tuning of physical parameters such as photothermal temperature in nanoparticle-mediated photothermal therapy (PTT). This is supported by theranostic nanosystem design and characterization, in vitro and in vivo analyses, and transcriptome-based gene profiling. In this work, the highly efficient near-infrared II (NIR-II) photoacoustic image (PA)-guided PTT are selectively activated using our developed matrix metalloproteinase (MMP)-triggered in situ assembly of gold nanodandelions (GNDs@gelatin). Unlike other "always-on" NIR PTT agents lacking specific bioactivation and suffering from the intrinsic nonspecific pseudosignals and treatment-related side effects such as metastasis, our GNDs@gelatin possesses important advantages while deployed in cancer PTT that include the following: (1) The theranostic effects could be "turned on" only after specific MMP-2/-9 activity and with acidity in the tumor microenvironment. (2) The quantitative PA diagnosis allows for precise PTT planning for better cancer treatment. (3) GNDs@gelatin could noninvasively quantify MMP activity and efficiently harness NIR-I (808 nm) and NIR-II (1064 nm) energies for tumor ablation. (4) The multibranched nanostructures reabsorb scattered laser photons, thus enhancing the surface plasmons for the pronounced photothermal conversion of aggregated GNDs@gelatin in situ. (5) It is noteworthy that in situ tumor eradication at higher PTT temperature (>55 °C) mediated by GNDs@gelatin could induce subsequent metastasis, which could be otherwise abolished at lower PTT temperatures (50 °C > T > 43 °C). (6) Furthermore, the gene profiling using transcriptome-based microarray including GO and KEGG analyses revealed that 315 differentially expressed genes were identified in higher PTT temperature treated tumors compared with lower PTT temperature ones. These were enriched into some well-known cancer-related pathways, such as cell migration pathway, signal transductions, cell proliferation, wound healing, PPAR signaling, and metabolic pathways. These observations suggest a new perspective of "moderate-is-better" in nanoparticle-mediated PTT for maximizing its therapeutic/prognosis benefits and translational potential with metastasis inhibition.

Multi-modal triggered-release sonodynamic/chemo/phototherapy synergistic nanocarriers for the treatment of colon cancer.

Most colon cancer patients are diagnosed at an advanced stage, with a grim prognosis. In clinical, various combination therapies have been employed to enhance the efficacy of colon cancer treatment. The essence of combined treatment is the judicious selection and combination of various treatment units. Phototherapy (PT), sonodynamic therapy (SDT), and chemotherapy are treatment modalities that rely on the active molecules to treat tumors, and have been demonstrated to synergistically enhance tumor treatment efficacy. However, the differences in the metabolism of active molecules and hypoxic microenvironment of tumors have limited the synergistic effects of the aforementioned methods. To address this significant issue, in this study, we utilized polydopamine (PDA) as the encapsulated material to form a rigid shell that contains the therapeutic molecules IR-780 and methotrexate (MTX) on the surface of perfluorohexane (PFH) microdroplets through self-assembling method to develop an SDT/chemotherapy/PT combined nanoparticles (SCP NPs). Transmission electron microscopy (TEM) revealed that the nanoparticles exhibited a hollow shell structure, with an average size of approximately 100nm. SCP NPs have excellent stability and biocompatibility in both in vitro and in vivo. The absorption and emission spectrum of the loaded IR-780 did not exhibit any significant shift, and the photothermal temperature rose to 92°C. Their ultrasonic cavitation effect was good and their cell inhibitory effect of MTX was maintained. SCP NPs can achieve multi-modal triggered release through ultrasound, laser irradiation, and pH, ensuring a simultaneous accumulation of therapeutic molecules in the tumor area and effectively alleviating tumor hypoxia. Additionally, both the near-infrared fluorescence (NIF) signal and the ultrasonic cavitation signal of the nanoparticles can be utilized for tracking and monitoring treatment efficacy. Most notably, SCP NPs exhibited outstanding synergistic treatment effects at low intervention levels, resulting in a 67% cure rate of tumors. These results provide an experimental basis for developing the new clinical treatments for colon cancer.

Fe/LiNO3/TiN co–modified MgO for enhanced thermochemical energy storage performance in MgO/Mg(OH)2 cycles

MgO/Mg(OH)2 thermochemical energy storage can convert solar energy and industrial waste heat into forms that are easier to store and transport by cyclic hydration/dehydration reactions. To achieve excellent energy storage performance, cyclic stability and optical absorption capability of MgO/Mg(OH)2, Fe/LiNO3/TiN co–modified MgO were synthesized for energy storage cycles by wet-mixing method. The energy storage performance, cyclic stability and dehydration kinetics of Fe/LiNO3/TiN co–modified MgO were studied in dual fixed–bed system and simultaneous thermal analyzer. The experimental results show that the Fe and LiNO3 in the composite not only increase the hydration conversion of MgO by 6.3 times at 30 min, but also reduce the dehydration temperature and dehydration activation energy of Mg(OH)2 by 99.4 °C and 64 %, respectively. TiN overcomes aggregation of MgO and sustains the excellent porous structure, which results in only a 9 % decrease in energy storage performance of Fe/LiNO3/TiN co–modified MgO after 15 energy storage cycles. Subsequently, TiN significantly strengthens the optical absorption performance of Mg(OH)2 and photothermal temperature under xenon-lamp simulated sunlight radiation. Furthermore, density functional theory calculation reveals that Fe and Li enhance the adsorption of H2O on MgO model and reduce energy barrier for hydration reactions by 62.76 %, while TiN effectively inhibits MgO clusters migration within the material and enhances the optical absorption coefficient. Hence, Fe/LiNO3/TiN co–modified MgO shows significant research value in MgO/Mg(OH)2 energy storage process.

Flexible multifunctional magnetic-conductive Janus nanocomposite films towards highly-efficient electromagnetic interference shielding and thermal management

The rapid development of aerospace, intelligent wearable electronics and 5G communications puts forward higher demands for electromagnetic interference (EMI) shielding materials. Herein, the flexible multifunctional magnetic-conductive Janus nanocomposite films with magnetic cobalt carbide nanowires/bacterial cellulose (Co@C NW/BC) blends as the upper side, and conductive Ti3C2Tx MXene as the bottom side are obtained via the layer-by-layer (LBL) vacuum assisted filtration-hot pressing method. The two magnetic and conductive sides endow the Janus nanocomposite films with distinctly different performances in EMI shielding and thermal management. When the electromagnetic waves are incident from Co@C NW/BC side, the films exhibit a high EMI shielding effectiveness (EMI SE) of 49.8 dB with an enhanced microwave absorption (SEA) of 33.9 dB at the ultralow thickness of 43 μm. Meanwhile, the Ti3C2Tx side exhibits improved electrical heating performances with a surface temperature of 120 °C at 6 V voltage, increased photothermal conversion temperature of 77.8 °C upon 2.0 kW/m2 light intensity, as well as excellent thermal stealth properties with a low radiation temperature of 88.4 °C on the 240 °C hot stage. Moreover, the Janus nanocomposite films show a high tensile strength of 80.0 MPa. The resultant Janus nanocomposite films possess great application prospects in highly-efficient EMI shielding and thermal management.

Solar collector inspired by the polar bear: Fluorescent‐reinforcing photothermal conversion efficiency

AbstractThe crucial point of solar thermal utilization makes solar heat collector gathering much attention. In this study, imitating polar bears' fur structure, fluorescent materials are modified into a solar heat collector, and the photothermal conversion is evaluated to examine the influence of polyvinyl alcohol concentration, fluorescent luminescence type and fluorescence concentration. The test results indicate that fluorescent materials that has a greater Stokes shift show the greater photothermal effect. Moreover, when composed of a PVA concentration being 5.0% and a fluorescent concentration being 0.50%, the composites exhibit the maximal photothermal conversion temperature (99.4°C) that is 17.9% higher than that of the solar heat collectors without fluorescent materials. This study proposes creating solar heat collector with modified fluorescent materials, and the new perspective of which demonstrates that the composites have a great potential and application prospect in the solar photothermal field.

Copper peroxide loaded gelatin/oxide dextran hydrogel with temperature and pH responsiveness for antibacterial and wound healing activity

Bacterial infection and tissue hypoxia always prevent wound healing, so multifunctional platforms with antimicrobial and oxygen-supplying functions were developed. However, they face many difficulties such as complex preparation and low oxygen release. To address this challenge, a copper peroxide loaded gelatin/oxide dextran hydrogel (CGO) was prepared. Surprisingly, CGO hydrogel as a wound dressing not only had good biocompatibility, injectivity, and mechanical properties, but also exhibited mild photothermal properties, temperature responsiveness, and pH responsiveness. After being applied to wounds infected with bacteria, CGO hydrogel released copper peroxide under near-infrared laser irradiation, which produced copper ions and hydrogen peroxide, combined with PTT to kill bacteria. After the bacteria were cleared from the wound and the pH of the wound was changed to be acidic, CGO hydrogel released copper peroxide via pH response. Copper ions and oxygen produced from copper peroxide accelerated wound healing by promoting angiogenesis. The multi-responsive and multi-mode treatment platform provided a potential strategy for treating bacteria-infected wounds.

A Processible and Ultrahigh‐temperature Organic Photothermal Material through Spontaneous and Quantitative [2+2] Cycloaddition–Cycloreversion

AbstractEnergy conversion, particularly light to heat conversion, has garnered significant attention owing to its prospect in renewable energy exploitation and utilization. Most previous efforts have focused on developing organic photothermal materials for low‐temperature applications, whereas the importance of simplifying the preparation methods of photothermal materials and enhancing their maximum photothermal temperature have been less taken. Herein, we prepare an organic near‐infrared (NIR) photothermal material namely ATT by a spontaneous [2+2] cycloaddition‐cycloreversion reaction. In addition to the solution‐based method, ATT could also be readily preapred by ball milling in a high yield of 90 % in just 15 min. ATT powder exhibits a broad absorption extending beyond 2000 nm, excellent processability, and thermal stability. Remarkably, ATT powder can reach an unprecedently temperature as high as 450 °C while maintaining excellent photostability upon photoirradiation. Leveraging its extraordinary photothermal and processable properties, ATT was used in the high‐temperature applications, such as photo‐ignition, photo‐controlled metal processing and high‐temperature shape memory, all of which offer spatiotemporal control capabilities. This work provides a new approach to prepare organic photothermal materials with high temperatures, and pave the way for their applications in extreme environments.

A Processible and Ultrahigh-temperature Organic Photothermal Material through Spontaneous and Quantitative [2+2] Cycloaddition-Cycloreversion.

Energy conversion, particularly light to heat conversion, has garnered significant attention owing to its prospect in renewable energy exploitation and utilization. Most previous efforts have focused on developing organic photothermal materials for low-temperature applications, whereas the importance of simplifying the preparation methods of photothermal materials and enhancing their maximum photothermal temperature have been less taken. Herein, we prepare an organic near-infrared (NIR) photothermal material namely ATT by a spontaneous [2+2] cycloaddition-cycloreversion reaction. In addition to the solution-based method, ATT could also be readily preapred by ball milling in a high yield of 90 % in just 15 min. ATT powder exhibits a broad absorption extending beyond 2000 nm, excellent processability, and thermal stability. Remarkably, ATT powder can reach an unprecedently temperature as high as 450 °C while maintaining excellent photostability upon photoirradiation. Leveraging its extraordinary photothermal and processable properties, ATT was used in the high-temperature applications, such as photo-ignition, photo-controlled metal processing and high-temperature shape memory, all of which offer spatiotemporal control capabilities. This work provides a new approach to prepare organic photothermal materials with high temperatures, and pave the way for their applications in extreme environments.

Direct deposition of Ti/MgF2 photoabsorber on PTFE membrane with enhanced robustness via plasma pretreatment for photothermal membrane distillation

Deposition of metal-dielectric hybrid composite on the polymer based membrane is important for the electrochemical, photochemical and photothermal reactions on the membrane surface. The hydrophilic reactants such as catalysts and photothermal materials are not easy to be deposited directly on the hydrophobic membrane surface, so in most cases, binder material has been adapted to stably combine them. In this study, commercial PTFE membrane and Ti/MgF2 photothermal layers were combined without any binder. Ar plasma pretreatment was applied to a membrane surface before depositing optimized Ti/MgF2 stacks to fabricate a mechanically robust photothermal membrane. The successful fabrication of Ar plasma pretreated Ti/MgF2 photothermal membrane was demonstrated by scanning electron microscopy (SEM), energy dispersive X-ray spectroscopy (EDS), atomic force microscope (AFM) characterization. Through Ar plasma pretreatment, an increase in Ti/MgF2 photothermal membrane heating temperature of 40.5 % was achieved under 1 sun condition compared with unpretreated membrane. This membrane showed improved performance and reduced energy loss in solar desalination. Utilizing these membranes in a membrane distillation system, water flux increased by up to 26.9 %, performance ratio (PR) increased by 18.9 % and thermal efficiency improved by 21.9 %. After 24-h stress test, the Ar plasma pretreated Ti/MgF2 photothermal membranes demonstrated durability and maintained thermal efficiency.

Enhanced ultraviolet aging resistance of epoxy resins through surface enrichment achieved by fluorinated graphene oxide@CeO2

Fluorinated graphene oxide@CeO2 (FGO@CeO2) was synthesized using an in-situ growth method and incorporated as a filler into epoxy resins to improve their UV aging resistance. On UV irradiation, it facilitated the surface enrichment of the modified epoxy resin (MEP), forming a UV-blocking layer. Incorporating FGO@CeO2 induced n→π* electronic transitions within the MEP and lowered the electronic excitation threshold, expanding the UV spectral absorption band and enhancing the UV absorption intensity. A 785% increase in the UV absorption capacity was achieved in the MEP compared with that in the pristine epoxy resin. After 300 h of UV exposure, the photothermal temperature rise in the MEP was 13.67 ± 2 °C higher than that in pure epoxy resin.

New Na5Y(MoO4)4: Yb3+, Er3+ phosphors: Up-conversion luminescence and temperature sensing characteristics

Currently, the development of new up-converting fluorescent materials for manufacturing optical temperature sensing device with high accuracy and precision has always been significant pursuits of many researchers. In this work, we have synthesized new Na5Y(MoO4)4: Yb3+/Er3+ phosphors via solid-state reaction route, and the influences of dopant concentration on UCL performance were discussed. The results revealed that the introduction of Yb3+ enhanced the luminescence intensity, and the optimal concentration combination was 0.20Yb3+/0.04Er3+. Doping Yb3+ and Er3+ did not affect the phase structure of the phosphor. Several emission peaks at 529, 552 and 668 nm of Er3+ were found to be temperature-dependent within the scope of 298–573 K. Through the utilization of fluorescence intensity ratio technique (FIR, I529/I552 and I529/I668), dual-mode temperature measurement was realized. The maximum relative sensitivity (Sr-max) of 1.77 % K−1 (@298 K) utilizing thermally coupled energy levels (TCELs) and the maximum absolute sensitivity (Sa-max) of 12.0 % K−1 (@573 K) based on the non-TCELs were achieved. Furthermore, Yb3+/Er3+ co-doped Na5Y(MoO4)4 phosphors exhibited excellent photothermal repeatability and temperature resolution. The results indicated that the novel Na5Y(MoO4)4 phosphor provided the possibility for the development of temperature sensing materials with high sensitivity.

Strong absorption of (Mn2O3)3CuSiO3 with Jahn–Teller elongation and direct photothermal storage of (Mn2O3)3CuSiO3–Mg(OH)2

To improve photon harvesting, we demonstrated that Jahn–Teller defects can efficiently reduce the band gap and increase the carrier density, which significantly intensify light harvesting and widen the absorption band. This may be an effective method for designing solar materials. The substitution of Mn2+ with Jahn–Teller active Cu2+ leads to quasi-metallic (Mn2O3)3CuSiO3 nanoparticles with a high concentration of charge carriers, displaying intense absorption in entire solar spectrum. Silicates may represent a new type of photon harvesting material. Mg(OH)2 powder coated by Cu-braunite shows a 150 % increase in photothermal temperature, a tenfold improvement in photothermal-dehydration conversion and a 15.8-fold increase in the reversibility of 30 cycles of heat storage and release. This material may be practicable for directly harvesting solar energy and storing thermoenergy. Jahn–Teller effects are effective for tuning photon harvesting.

Graphene oxide modified sodium alginate/polyethylene glycol phase change material hydrogel scaffold composite with photothermal temperature control for potential bone tissue regeneration

The challenge of precisely regulating temperature during the photo-thermal bone promotion remains unresolved. Phase change material (PCM), capable of undergoing a phase transition at a specific temperature, offers a solution by photothermal temperature regulation through the storage and release of heat. This study incorporated biocompatible polyethylene glycol (PEG) with specific phase transition points as PCM. A phase change hydrogel scaffold was then synthesized through semi-crosslinking PEG with calcium-ion-chelated sodium alginate (SA) acting as the structural framework. Additionally, the newly developed graphene oxide (GO) modified composite scaffolds (GO-PHSC), featuring 0.5 wt% GO, not only demonstrated outstanding photothermal conversion efficiency and an optimal phase change temperature (42.2 °C) but also exhibited desirable values for latent enthalpy (100 J/g) and latent heat recovered (LHR) (93.3%). Moreover, the form-stability test demonstrated the PCM scaffolds' exceptional resistance to leakage and maintenance of shape stability even at elevated temperatures (70 °C). Beyond achieving passive temperature control in photothermal therapy, experimental findings highlighted that the phase change hydrogel, incorporating calcium ions and GO, met various requirements such as physicochemical properties, microstructure, mechanics, mineralization, biocompatibility, and cell affinity. These collective attributes suggest that GO-PHSC emerges as a promising scaffold composite candidate for temperature-controlled photothermal therapy in bone regeneration.

Thermal-Responsive Gel-Based Overheat Limiter Enabled Intelligent Photothermal Therapy.

Uncontrolled and excessive photothermal heating in photothermal therapy (PTT) inevitably causes thermal damage to surrounding normal tissues, severely limiting the universality and safety of PTT. To address this issue, an intelligent cooling thermal-responsive (ICTR) gel containing poly(N-isopropylacrylamide-co-acrylamide) (P(NIPAM-AM))microgel is applied onto the skin to realize intelligent PTT, which can avoid excessive heating and accidental injury. The high near-infrared (NIR) light transmittance (>95%) of the ICTR gel ensures effective light delivery at low temperatures, while the refractive index of the P(NIPAM-AM) microgel increases remarkably when the temperature exceeds a predetermined threshold, resulting in progressively enhanced light scattering and weakened photothermal conversion. In animal studies, the negative feedback regulation of ICTR gel on light transmittance and photothermal heating allows the photothermal temperature in the lesion site to be stabilized within the effective therapeutic range (45°C) while ensuring that the skin surface temperature does not exceed 35°C. Compared with the severe skin thermal damage found in the histological staining of mice skin receiving conventional PTT, the mice skin receiving the ICTR gel-enabled intelligent PTT remains in good condition. This study establishes an intelligent and universal paradigm for PTT thermal regulation, which is of great significance for achieving safe and effective PTT.

Nonlinear dynamic analysis of opto-electro-thermo-elastic perovskite plates

AbstractPhotostrictive materials have attracted tremendous interest as the new generation of smart materials that can achieve a direct conversion from optical energy to mechanical energy. Understanding their nonlinear mechanical properties under light illumination is of paramount significance for their realistic optomechanical applications. This article proposes a novel opto-electro-thermo-elastic constitutive model that can consider the effects of photostriction, photothermal temperature, and electrostriction for metal halide perovskite crystals and investigates the nonlinear static and dynamic responses of the perovskite plates. The nonlinear governing equations are established based on the first-order shear deformation theory and von Kármán nonlinearity and are numerically solved by the differential quadrature method. A detailed parametric investigation is performed to analyze the effects of light and electricity on the nonlinear mechanical behaviors of perovskite plates. It is concluded that light illumination leads to the presence of optical stress and thermal stress in the perovskite plates, giving rise to increased static and dynamic deformations and stresses, as well as reduced postbuckling and free vibration characteristics. The research findings pave the way for the optomechanical applications of perovskite-based smart materials and structures.

Portable hydrogel kit driven by bimetallic carbon dots nanozyme for H2O2-self-supplying dual-modal monitoring of atmospheric CH3SH

Due to the typical volatility of gaseous pollutant methyl mercaptan (CH3SH), the development of a facile, reliable, and accurate onsite environmental surveillance of highly toxic CH3SH faces many challenges, but it is critical to environmental atmosphere assessment and safeguarding public health. Here, we prepared a novel bimetallic carbon dots (Fe&Cu@CDs) nanozyme with high peroxidase-mimicking activity to design a portable hydrogel kit for onsite visual H2O2-self-supplying enzymatic cascade catalytic colorimetric and photothermal signal synergistic amplification dual-modal monitoring of CH3SH in atmospheric environment. Assisted by alcohol oxidase (AOX), CH3SH could be specifically converted into H2O2 for oxidizing chromogenic substrate 3,3′,5,5′-tetramethylbenzidine (TMB) catalyzed by Fe&Cu@CDs to produce dark blue ox-TMB with absorption at 652 nm and photothermal characters. Consequently, a CH3SH concentration-dependent change both in naked-eye color and photothermal effect-triggered temperature were observed. By hybridizing AOX-assisted Fe&Cu@CDs + TMB with agarose, a H2O2-self-supplying colorimetric and photothermal signal synergistic amplification sensory hydrogel kit integrated with Color Picker APP-installed smartphone and 660 nm laser-equipped handheld thermal imager for CH3SH was proposed with acceptable results in atmospheric environment around wastepile (e.g., solid waste and food waste piles), which exhibited great potentials to further develop commercial onsite monitoring platforms in warning-early abnormal atmospheric CH3SH for safeguarding environmental health.

Rapid quantitative PCR equipment using photothermal conversion of Au nanoshell

The emergence of infectious diseases worldwide necessitates rapid and precise diagnostics. Using gold nanoshells in the PCR mix, we harnessed their unique photothermal properties in the near-infrared regime to attain efficient heating, reaching ideal photothermal PCR cycle temperature profile. Our photothermal PCR method expedited DNA amplification while retaining its detection sensitivity. Combining photothermal quantitative PCR with real-time fluorometry and non-invasive temperature measurement, we could amplify the target DNA within just 25 min, with a minimum detectable DNA amount of 50 picograms. This innovation in photothermal qPCR, leveraging the photothermal properties of gold nanoshells, will pave the way for immediate point-of-care diagnostics of nucleic acid biomarkers.

Efficient Thermal Management with Selective Metamaterial Absorber for Boosting Photothermal CO2 Hydrogenation under Sunlight.

Photothermal catalytic CO2 hydrogenation is a prospective strategy to simultaneously reduce CO2 emission and generate value-added fuels. However, the demand of extremely intense light hinders its development in practical applications. Herein, this work reports the novel design of Ni-based selective metamaterial absorber and employs it as the photothermal catalyst for CO2 hydrogenation. The selective absorption property reduces the heat loss caused by radiation while possessing effectively solar absorption, thus substantially increasing local photothermal temperature. Notably, the enhancement of local electric field by plasmon resonance promotes the adsorption and activation of reactants. Moreover, benefiting from the ingenious morphology that Ni nanoparticles (NPs)are encapsulated by SiO2 matrix through co-sputtering, the greatly improved dispersion of Ni NPs enables enhancing the contact with reaction gas and preventing the agglomeration. Consequently, the catalyst exhibits an unprecedented CO2 conversion rate of 516.9mmol gcat -1 h-1 under 0.8W cm-2 irradiation, with near 90% CO selectivity and high stability. Significantly, this designed photothermal catalyst demonstrates the great potential in practical applications under sunlight. This work provides new sights for designing high-performance photothermal catalysts by thermal management.