Photothermal Efficiency Research Articles

Construction of sandwich-structured V2CTx@PDA@Ag nanosheet composite for enhanced near-infrared photothermocatalytic sterilization performance

The long-term use of antibiotics leads to drug resistance, it is insufficient to combat stubborn pathogens. Therefore, it urgently needs a material that can quickly and effectively eradicate bacteria, especially for resistant bacteria and their biofilm structures that are difficult to eliminate with conventional antibiotics. This article adopts a new 2D layered V2CTx MXene material, which utilizes in-situ coating method to stimulate dopamine self polymerization and fix nano silver onto V2CTx nanosheets. V2CTx@PDA@Ag showed very significant antibacterial effect under 808 nm laser illumination for 30 min. After analyzing the sterilization mechanism, the photothermal synergistic sterilization of composite mainly relies on physical contact, the generation of reactive oxygen species, and the photothermal synergistic effect. It is worth mentioning that after V2CTx is coated with PDA, the photothermal efficiency is improved, V2CTx and nano silver are also effectively connected. It proved that the composite has stable and efficient antibacterial properties.

Scalable absorber with tuneable water supply fabricated via centrifugal spinning for highly efficient and stable solar-driven interfacial desalination

Although realising tuneable water supply in photothermal evaporation is an effective way to boost solar-driven interfacial evaporation for water desalination, simultaneously achieving continuous water transport and appropriate water content in evaporators remains a significant challenge. To address this challenge, centrifugal spinning technology is proposed herein to fabricate a scalable, flexible and stable photothermal evaporator from a hydrophilic (polyacrylonitrile, (PAN)) and hydrophobic polymer medium (polyurethane, (PU)). Efficient water management can be realised by tuning the parameters of polymer materials to permit vapour escape and achieve salt resistance. In addition, the arched design of the evaporator allows for omnidirectional evaporation, which enhances the photothermal conversion efficiency. The scalable centrifugal spinning nonwoven membrane-based arched evaporator prepared at the optimal hydrophilic–hydrophobic polymer ratio (21 wt% PAN and 2 wt% PU) after polypyrrole modification (PPy/21PAN/2PU CSMAE) offers a highly efficient evaporation rate of 1.82 kg m−2 h−1 with photothermal efficiency of 97.33 % under 1-sun illumination and excellent salt resistance against high-salinity brine (10 wt%). Thus, the unique properties of centrifugal spinning technology enable the large-scale preparation application of multicomponent polymeric materials for realising tuneable water supply in solar-driven interfacial evaporation and desalination.

Bioinspired Multifunctional Self-Sensing Actuated Gradient Hydrogel for Soft-Hard Robot Remote Interaction

HighlightsThe bioinspired self-sensing actuated gradient hydrogel was developed by a wettability-based method via precipitation of MoO2 nanosheets.Self-sensing actuated gradient hydrogel combined ultrafast thermo-responsive actuation (21° s–1), exceptional photothermal efficiency (3.7 °C s–1) and high sensing properties (GF = 3.94).The first self-sensing remote interaction system based on gradient hydrogel actuators and robotic hands was constructed.

Synergistic Effect of Ti3C2Tx MXene Nanosheets and Tannic Acid-Fe3+ Network in Constructing High-Performance Hydrogel Composite Membrane for Photothermal Membrane Distillation.

Photothermal membrane distillation (PMD) has emerged as a promising and sustainable approach for seawater desalination and wastewater purification. However, the wide application of the technique is severely impeded by low freshwater production and membrane fouling/wetting issues. Herein, we developed an advanced hydrogel-engineered membrane with simultaneously enhanced photothermal conversion capacity and desired fouling and wetting resistance for PMD. By the synergies of photothermal Ti3C2Tx MXene nanosheets and the tannic acid-Fe3+ network in the hydrogel, the membrane was endowed with excellent surface self-heating ability, yielding the highest freshwater production rate (1.71 kg m-2 h-1) and photothermal efficiency among the fabricated hydrogel composite membranes under 1 sun irradiation. Meanwhile, the PMD membrane could robustly resist oil-induced fouling and surfactant-induced wetting, significantly extending the membrane lifespan in treating contaminated saline water. Furthermore, when desalinating real seawater, the membrane exhibited superior durability with a stable vapor flux and excellent ion rejection (e.g., 99.24% for boron) for 100 h.

Self-assembled hollow CuS@AuNRs/PDA nanohybrids with synergistically enhanced photothermal efficiency.

The design of multifunctional nanocarriers with enhanced photothermal efficiency is of great significance for the photothermal therapy of cancer. In this study, hollow CuS@gold nanorods/polydopamine (HCuS@AuNRs/PDA) nanohybrids with synergistically enhanced photothermal efficiency were prepared by electrostatic self-assembly method. The high photothermal conversion efficiency of HCuS@AuNRs (55.88%) is attributed to the interfacial electron transfer between CuS and AuNRs, as well as the increase in free charge carrier concentration. The excellent adhesion performance and strong negative charge of PDA ensure a high doxorubicin hydrochloride (DOX) loading efficiency of 96.08% for HCuS@AuNRs/PDA. In addition, HCuS@AuNRs/PDA reveals outstanding NIR/pH dual-responsive drug release properties owing to the weakened interaction between PDA and DOX in acidic media and the distinct NIR responsiveness of HCuS@AuNRs. In vitro cell viability results confirm that HCuS@AuNRs/PDA could efficiently kill tumor cells under the dual effect of acidic media and NIR laser. This study presents a novel nanocarrier with synergistically enhanced NIR photothermal responsiveness and high drug loading capacity, which provides a versatile platform in intelligent drug release and photothermal therapy.

Gold nanorods as biocompatible nano-agents for the enhanced photothermal therapy in skin disorders.

Rod-shaped gold nanomaterials, known as gold nanorods (GNRs), may undergo specific surface alterations, because of their straightforward surface chemistry. This feature makes them appropriate for use as functional and biocompatible nano-formulations. By optimizing the absorption of longitudinally localized surface plasmon resonance (LSPR) in the near-infrared (NIR) region, which corresponds to the NIR bio-tissue window, GNRs with appropriate modifications may improve the results of photothermal treatment (PTT). In dermatology, potential noninvasive uses of GNRs to enhance wound healing, manage infections, combat cutaneous malignancies, and remodel skin tissues via PTT have attracted research attention in recent years. In this review, the basic properties of GNRs, such as shape, size, optical performance, photothermal efficiency, and metabolism, are discussed firstly. Then, the disadvantages of using these particles in photodynamic therapy (PDT) are proposed. Next, biological applications of GNRs-based PTT are summarized in detail. Finally, the limitations and future perspectives of this research are summarized, providing a comprehensive outlook for prospective GNRs with PTT.

Injectable and NIR-responsive CDN-POM hydrogels for combined non-inflammatory photo-immunotherapy.

Similar to clinically applied thermal ablation techniques, the cellular necrosis that occurs during photothermal tumor therapy (PTT) can induce inflammatory response, severely compromising the therapeutic efficacy and clinical translation of the PTT. Inspired by the remarkable ROS-scavenging activity and high photothermal efficiency of molybdenum-based polyoxometalate (POM) and the immunostimulatory effect of cyclic dinucleotides (CDNs), a NIR-responsive and injectable DNA-mediated hybrid hydrogel (CDN-POM) has been developed. The hydrogels have superior photothermal efficiency (43.41%) to POM, impressive anti-inflammatory capability and prolonged intratumoral CDN-releasing behavior, thus enabling synergistic anti-tumor therapeutic outcomes. Meanwhile, local treatment induced by CDN-POM hydrogels displays minimal side effects on normal tissue. Taking advantage of the high phototherapeutic effect, ROS-scavenging activity and sustained CDN release of CDN-POM hydrogels, a novel combined approach that integrates photothermal therapy and immunotherapy of breast tumor is successfully pioneered.

Thermal control of photothermal implants inspired by polar bear skin for the treatment of infected bone defects.

Photothermal therapy (PTT) encounters challenges in addressing deep tissue infections, characterized by limited penetration or potential hyperthermal damage to surrounding tissues, initiating undesirable inflammatory cascades. Inspired by polar bear thermal regulation, we present a "bio-based endogenic thermal-adaptive booster" implant coating. This coating integrates a photothermal poly(tannic acid) (pTA) layer, mimicking the "polar bear dark skin", securely linked with anti-inflammatory dexamethasone (Dex), resembling the "secretion", and a red blood cell membrane (RBCM) layer, forming the insulating "transparent fur". The RBCM "fur" demonstrates unexpectedly superior local heat storage, amplifying the photothermal effect of the pTA "skin" by 1.30 times and boosting localized photothermal antibacterial efficiency by 1.30-fold (approximately 99%) compared to those without RBCM. Furthermore, RBCM sustains Dex release and offers additional protection against thermal inflammation, releasing Dex 1.90 times more under NIR irradiation than under non-photothermal conditions. In a rat infectious bone model, the photothermal-boosting implant coating provides a favorable biological interface and achieves a 99.97% photothermal antibacterial ratio, enhancing osseointegration without evident tissue harm, evidenced by a 2.47-fold increase in bone volume fraction and a 2.24-fold reduction in pro-inflammatory cytokines compared to those lacking a RBCM. Insights derived from cell membrane-based thermal-adaptive coatings herald a paradigm shift in efficient and safe PTT.

Three-dimensional Au-MnO2 nanostructure as an agent of synergistic cancer therapy: chemo-/photodynamic and photothermal approaches.

The design of multimodal cancer therapy was focused on reaching an efficient process and minimizing harmful effects on patients. In the present study, the Au-MnO2 nanostructures have been successfully constructed and produced as novel multipurpose photosensitive agents simultaneously for photodynamic therapy (PDT), photothermal therapy (PTT), and chemodynamic therapy (CDT). The prepared AuNPs were conjugated with MnO2 NPs by its participation in the thermal decomposition process of KMnO4 confirmed by X-ray diffraction (XRD), transmission electron microscopy (TEM), and Fourier transform infrared (FTIR) spectroscopy (FT-IR). The 16.5 nm Au-MnO2 nanostructure exhibited an absorbance at 438 nm, which is beneficial for application in light induction therapy due to the NIR band, as well as its properties of generating reactive oxygen species (ROS) associated with the 808 nm laser light for PDT. The photothermal transduction efficiency was calculated and compared with that of the non-irradiated nanostructure, in which it was found that the 808 nm laser induced a high efficiency of 83%, 41.5%, and 37.5% for PDT, PTT, and CDT, respectively. The results of DPBF and TMB assays showed that the efficiency of PDT and PTT was higher than that of CDT. The nanostructure also confirmed the time-dependent peroxidase properties at different H2O2, TMB, and H2TMB concentrations, promising good potency in applying nanomedicine in clinical cancer therapy.

Theranostic Phthalocyanine and Naphthalocyanine Nanoparticles for Photoacoustic Imaging and Photothermal Therapy of Tumors.

Background: Phthalocyanine (PC) and naphthalocyanine (NC) dyes have long garnered interest as theranostic agents for optical imaging and phototherapy due to their near-infrared absorbance, photostability, imaging contrast, and proven safety in clinical trials. Yet, only a small fraction of these dyes has been evaluated as photothermal therapy (PTT) agents for cancer treatment. Methods: Nearly 40 distinct NC and PC dyes were encapsulated within polymeric PEG-PCL micelles via oil-in-water emulsions. The optimal NC/PC-loaded micelle formulations for PTT and photoacoustic (PA) imaging were identified through in vivo and in vitro studies. Results: The most promising candidate, CuNC(Octa)-loaded micelles, demonstrated a strong PA signal with a peak absorbance at ~870 nm, high photothermal efficiency, and photostability. The CuNC(Octa)-loaded micelles exhibited heat generation as good or better than gold nanorods/nanoshells and >10-fold higher photoacoustic signals. Micelle preparation was reproducible/scalable, and the CuNC(Octa)-loaded micelles are highly stable under physiological conditions. The CuNC(Octa)-loaded micelles localize within tumors via enhanced permeability and retention and are readily detectable by PA imaging. In a syngeneic murine tumor model of triple-negative breast cancer, CuNC(Octa)-loaded micelles demonstrate efficient heat generation with PTT, leading to the complete eradication of tumors. Conclusions: CuNC(Octa)-loaded micelles represent a promising theranostic agent for PA imaging and PTT. The ability to utilize conventional ultrasound in combination with PA imaging enables the simultaneous acquisition of information about tumor morphology and micelle accumulation. PTT with CuNC(Octa)-loaded micelles can lead to the complete eradication of highly invasive tumors.

Finite element modeling of plasmonic resonances in photothermal gold nanoparticles embedded in cells.

The use of plasmonic nanoparticles in performing photothermal treatments in cancer cells requires a full knowledge about their optical properties. The surface plasmon resonance is easily foreseen and measurable in colloidal suspensions, however it can be strongly modified when located inside cells. Assessing the optical behavior of plasmonic nanoparticles in cells is essential for an efficient and controlled treatment. This requires the combination of experimental data and computational models to understand the mechanisms that cause the change in their optical response. In this work, we investigate the plasmonic response of Au nanospheres (AuNSs) internalized into cancer cells (MCF-7). Experimental data are compared to the simulations provided by a 3D model based on a finite element method. We demonstrate the impact of physical parameters such as the type of NS assembly, the surrounding medium and the interparticle gap, in the photothermal efficiency of AuNSs. Results open the avenue to predict, by numerical calculations, the optical properties of plasmonic nanoparticles inside cells to minimize treatment costs and times in photothermal therapies.

A bismuth-based double-network hydrogel-mediated synergistic photothermal-chemodynamic therapy for accelerated wound healing.

Multidrug-resistant bacterial infections present a significant challenge to wound healing. Non-antibiotic approaches such as photothermal therapy (PTT) and chemodynamic therapy (CDT) are promising but have suboptimal anti-bacterial efficacy. Herein, we developed a green bismuth-based double-network hydrogel (Bi@P-Cu) as a PTT/CDT synergistic platform for accelerated drug-resistant bacteria-infected wound healing. Bismuth (Bi) nanoparticles fabricated using a microwave method were used as a highly efficient and biocompatible PTT agent while the integration of a small amount of CDT agent Cu2+ endowed the hydrogel with excellent mechanical and self-healing properties, markedly increased photothermal efficiency, promoted cell migration ability, and negligible toxicity. Importantly, PTT enhanced the production of hydroxyl radicals in CDT and the destruction of bacterial cell membranes, which in turn enhanced the thermal sensitivity of bacteria. This synergistic anti-bacterial effect, together with the demonstrated capability to promote angiogenesis and anti-inflammation as well as enhanced fibroblast proliferation, led to accelerated wound healing in a full-thickness mouse model of resistant bacterial infection. This study provides an effective and safe strategy to eliminate drug-resistant bacteria and accelerate wound healing through green, non-antibiotic, double-network hydrogel-mediated synergistic PTT and CDT.

Novel rod‐like carbon nanomaterials as near infrared‐responsive drug delivery system for potential anticancer applications

AbstractThe combination of chemotherapy and photothermal therapy shows great potential in cancer treatment, and the carbon nanomaterials have been attracted great attention in biomedical technology. However, it is still a great challenge to design stimuli‐responsive nano‐carbon‐based drug release systems with integrated functions. In this paper, rod‐like carbon nanomaterials (RCNs) were prepared by the soft template hydrothermal method with glucose as raw materials, which were proved to have high photothermal efficiency (∼23.7%), as well as good biocompatibility and excellent drug‐loading capacity. After that, RCNs were used to load doxorubicin (DOX) as DOX@RCNs for integrated photothermal/chemotherapy towards cancer, which demonstrated 52.2% higher cancer cell killing efficiency than that of RCNs under near infrared (NIR) irradiation in vitro. The authors’ approach provided a novel NIR‐responsive nano platform for combined photothermal/chemotherapy towards cancer, which was considered to be of great potential in anticancer applications.

Structure/Composition/Phase Regulations of Dealloying-Derived Nanoporous Metals and Their Solar Steam Generation Performances.

Structural regulation is of primary importance in structure-property/application studies of dealloyed nanoporous metals. Three aspects are mainly considered to affect the microstructure of nanoporous metals: design of precursor alloy, choosing of dealloying parameter, and annealing treatment. Herein, through the combination of the above three strategies, the regulation of structure, composition and phase in nanoporous metals are simultaneously achieved. With a dilute Cu99Ag0.75Au0.25 as the precursor, three kinds of nanoporous films are fabricated, including bi-phase nanoporous Cu-Ag-Au (B-NP-CuAgAu), hierarchically nanoporous Au (H-NPG) and single-phase homogeneously nanoporous Au (S-NPG). In situ X-ray diffraction and ex situ characterizations are utilized to reveal the structure/composition/phase evolutions during dealloying of Cu99Ag0.75Au0.25, as well as the macroscopic changes of the dealloyed samples. Notably, the ultrafine ligaments/channels of B-NP-CuAgAu and the two-level nanoporous structure of H-NPG endow them with good broadband light absorption and excellent hydrophilicity, which contribute to their outstanding solar steam generation (SSG) performances. Specially, the B-NP-CuAgAu film shows a more efficient SSG performance with water evaporation rate of 1.49kgm-2h-1 and photothermal efficiency of 93.6% at 1kWm-2, and good seawater desalination ability.

The novel damage-reporting and self-healing coatings prepared by electrospinning technology based on AIE agents and photothermal shape memory polymer

The self-healing coatings for metals aroused researchers' interest due to their spontaneous repair of coating damage. In this study, intelligent damage-reporting and self-healing anti-corrosion coatings were developed using electrospun fiber as the core functional materials. The fibers exhibited core–shell structures, with the core materials being the solutions of the composite fluorescence probe RTPE. The shell materials consisted of the photothermal shape memory polymer, namely, phosphotungstic acid modified polyaniline-polyurethane composite polymer. Rhodamine Tetraphenylethylene (RTPE) demonstrated water-triggered aggregation-induced emission (AIE) effects and also exhibited fluorescence response to corrosive factors such as hydrogen ions and iron ions at the damaged area of the coatings. Under the trigger of the infrared laser, the modified polyaniline converted light energy into heat, causing the softening of epoxy and the shape memory effect of polyurethane. These processes facilitated the closure and repair of the damage, thus restoring their anti-corrosion functionality. Phosphotungstic acid played a role in enhancing the photothermal efficiency. The self-healing mechanism reinforced the corrosion resistance of the coatings. The self-indicating feature for damaged areas provided guidance for artificial repair in regions that did not self-heal satisfactorily. The synergistic and intelligent functionalities of the prepared coatings foreshadowed the significant potential applications in marine and aerospace corrosion protection fields.

CuS nanotube/chitin composite hydrogel with enhanced photothermal efficiency for near-infrared-activated bacteria-killing

The research on biocompatible materials which exhibit remarkable antibacterial capability has always attracted lots of interests. Among numerous antibacterial materials, CuS micro-/nanomaterial has gained attention as a promising option due to its low toxicity and efficiently photothermal effect. In this study, CuS nanotube/chitin composite hydrogel was prepared by crosslinking with chitin. Due to the prominent photothermal conversion efficiency of CuS nanotube which was up to 64.3 %, the as-prepared composite hydrogel showed enhanced photothermal effect under near-infrared (NIR) illumination. The composite hydrogel also showed a typical peroxidase-like activity which can convert H2O2 into an extremely oxidative and toxic hydroxyl radicals (•OH). The prominent photothermal effect and peroxidase-like activity made the composite hydrogel perform well in antibacterial against Escherichia coli with NIR activation. The possible mechanism of NIR-activated antibacterial from CuS nanotube/chitin composite hydrogel was discussed as well. The results of this work indicate that the CuS/chitin composite hydrogel with enhanced photothermal effect could be a new NIR-activated antibacterial agent used for sterilization.

Impact of Ligand Exchange on Gold Nanostars’ Reshaping, Stabilization, Photothermal Efficiency, and Cell Viability

Impact of Ligand Exchange on Gold Nanostars’ Reshaping, Stabilization, Photothermal Efficiency, and Cell Viability

Natural down fiber-reinforced and polypyrrole-modified silk fibroin composite aerogel for efficient solar steam generation toward seawater desalination and wastewater treatment

Poor mechanical properties and low photothermal efficiency of silk fibroin (SF)-based aerogels are current challenges that need to be addressed. Herein, SF composite aerogel was developed to enhance the mechanical properties through physical interpenetration of natural down fiber (Df) and hydrogen bonds formed among SF, Df, and polypyrrole (PPy) and to improve the evaporation performance via in-situ polymerization of PPy. The resultant Df/PPy@SF aerogel showed significant improvement of compressive stress (194.29 kPa), which was 6.96 times than that of SF aerogel (27.91 kPa), and also good compression resiliency. Furthermore, due to uniform distribution of PPy and high porosity of 95.27 %, Df/PPy@SF aerogel possessed high light absorbance of 99.87 % and low thermal conductivity (0.043 W·m−1·K−1). Thus, the Df/PPy@SF aerogel evaporator demonstrated high evaporation rates of 2.12 kg·m−2·h−1 for 3.5 wt% saline water, 2.04–2.15 kg·m−2·h−1 for various dye water, and 2.10 kg·m−2·h−1 for actual dye wastewater. Moreover, the developed aerogel exhibited evaporation stability and outstanding salt-resistance when treating seawater due to continuous water supply by superhydrophilic porous aerogel. Therefore, these findings demonstrate the excellent performance of Df/PPy@SF aerogel and will inspire further research on developing natural fiber-reinforced aerogels for use in the fields of solar water evaporation, energy, and other related applications.

One step hydrothermal preparation of leaf-like CuInS2 micro-nano structures on three-dimensional flexible substrate to enhance photothermal catalytic activity

One potential sustainable energy conversion technique is the photocatalytic reduction of CO2 by semiconductors. However, insufficient active sites and low utilization efficiency of solar energy lead to the unsatisfactory effect of photothermal catalytic reduction of CO2. Thus, in this study, leaf-like CuInS2 micro-nano structures are prepared on three-dimensional flexible substrate by one-step hydrothermal method to improve the photothermal CO2 reduction efficiency. Among them, the preparation process of hydrothermal method is simple, energy-saving and efficient. In addition, micro-nano structures can not only provide more active sites for photocatalysts due to their large specific surface area, but also form more pores that can promote electron transfer efficiency. Meanwhile, the introduction of sulfur vacancy can promote the separation of photogenerated carriers and improve the adsorption capacity of CO2. As a result, the yields of CO2 reduction to CO and CH4 by leaf-like CuInS2 micro-nano structures were 1285.2 μmol/m2/h and 231.4 μmol/m2/h, respectively, under the synergistic action of photothermal. At present, there are few reports about the preparation of CuInS2 micro-nano structures in flexible stainless steel mesh, which also provides a new idea for the design of efficient photothermal cocatalysts.

The Photothermal Conversion and UV Resistance of Silk Fabrics Being Achieved through Surface Modification with C@SiO2 Nanoparticles.

With the improvement in people's living standards, the development and application of smart textiles are receiving increasing attention. In this study, a carbon nanosurface was successfully coated with a SiO2 layer to form C@SiO2 nanomaterials, which improved the dispersion of carbon nanomaterials in an aqueous solution and enhanced the absorption of light by the carbon nanoparticles. C@SiO2 nanoparticles were coupled on the surface of silk fabric with the silane coupling agent KH570 to form C@SiO2 nanosilk fabric. The silk fabric that was subjected to such surface modification was endowed with a special photothermal function. The results obtained with scanning electron microscopy (SEM), energy dispersive spectrometer (EDS), and infrared spectroscopy (FTIR) showed that C@SiO2 nanoparticles were successfully modified on the surface of the silk fabric. In addition, under the irradiation of near-infrared light with a power of 20 W and a wavelength of 808 nm, the C@SiO2 nanosilk fabric experienced rapid warming from 23 °C to 60 °C within 30 s. After subjecting the functional fabric to hundreds of photothermal experiments and multiple washes, the photothermal efficiency remained largely unchanged and proved to be durable and stable. In addition, the thermogravimetric (TG) analysis results showed that the C@SiO2 nanoparticles contributed to the thermal stability of the silk fabric. The UV transmittance results indicated that C@SiO2 nanofabric is UV-resistant. The silk modification method developed in this study is low-cost, efficient, and environmentally friendly. It has some prospects for future applications in the textile industry.