Nanoscale Liquid Research Articles

Salivary peptidomic profiling of chronic gingivostomatitis in cats by matrix-assisted laser desorption/ionization-time-of-flight mass spectrometry and nanoscale liquid chromatography-tandem mass spectrometry.

Chronic gingivostomatitis in cats (FCGS) is a moderately to severely painful condition, potentially caused by inadequate immune response to oral antigenic stimulation. Salivary peptidome analysis can identify inflammatory protein mediators and pathways involved in oral mucosal immune activation and may indicate potential therapeutic options for FCGS. Evaluate the diversity and abundance of salivary peptides in cats with FCGS using matrix-assisted laser desorption/ionization-time-of-flight mass spectrometry (MALDI-TOF MS) and nanoscale liquid chromatography-tandem mass spectrometry (nano LC-MS/MS). Thirty-two cats with FCGS and 18 healthy controls. Case-control cross-sectional study. We compared the salivary peptide profiles of diseased and healthy cats. The diagnosis of FCGS was confirmed by histopathology. Saliva samples were analyzed for viral infections using polymerase chain reaction (PCR), peptide mass fingerprint (PMF) using MALDI-TOF MS, and peptide identification using nano LC-MS/MS. Distinct clusters of peptide profiles were observed between groups. In FCGS, 26 salivary peptides were altered, including apolipoprotein A1, nuclear receptor subfamily 1 group I member 3, fibrinogen alpha chain, interleukin 2 receptor gamma, interleukin 23 receptor, hemoglobin subunit alpha, and serpin peptidase inhibitor clade A (alpha-1 antiproteinase, antitrypsin) member 12, protein-tyrosine-phosphatase, and cholinergic receptor nicotinic alpha 10 subunit. Protein-anti-inflammatory drug interaction networks were observed. Peptide mass fingerprint and peptide profiles identified distinct clusters between FCGS and healthy cats. The 9 novel salivary peptide markers were associated with the JAK/STAT and PI3K/Akt pathways and immune responses. These potentially noninvasive biomarkers may facilitate understanding of FCGS pathophysiology and guide future therapeutic research.

Mechanism of Friction Enhancement Induced by Nanoscale Liquid Film: A Brief Review

Mechanism of Friction Enhancement Induced by Nanoscale Liquid Film: A Brief Review

Treatment of Refractory Mucosal Leishmaniasis Is Associated with Parasite Overexpression of HSP70 and ATPase and Reduced Host Hydrogen Peroxide Production (Brief Report).

Mucosal leishmaniasis (ML) is a deforming type of American Tegumentary Leishmaniasis caused by Leishmania (Viannia) braziliensis that frequently does not respond to treatment. Despite its relapsing clinical course, few parasites are usually found in mucosal lesions. Host and parasite factors may be responsible for this paradox in the pathogenesis of the disease, allowing for both a low parasite burden and the inability of the host to clear and eliminate the disease. In this work, we present a clinical case of relapsing ML that was treated for 25 years without success with SbV, N-methyl glucamine, sodium stibogluconate, amphotericin B deoxycholate, gabromycin, antimonial plus thalidomide, liposomal amphotericin B, Leishvacin (a vaccine made in Brazil) and miltefosine. In a comparative analysis using nanoscale liquid chromatography coupled with tandem mass spectrometry of protein extracts of L. (V.) braziliensis promastigotes isolated from the patient and from the reference strain (MHOM/BR/94/M15176), we observed increases in ATPase and HSP70 protein levels in the parasite. We also observed an impairment in the production of hydrogen peroxide by peripheral mononuclear blood monocytes (PBMCs), as assessed by the horseradish peroxidase-dependent oxidation of phenol red. We hypothesise that these parasite molecules may be linked to the impairment of host parasiticidal responses, resulting in Leishmania persistence in ML patients.

Hyphenation of microflow chromatography with electrospray ionization mass spectrometry for bioanalytical applications focusing on low molecular weight compounds: A tutorial review.

Benefits of miniaturized chromatography with various detection modes, such as increased sensitivity, chromatographic efficiency, and speed, were recognized nearly 50 years ago. Over the past two decades, this approach has experienced rapid growth, driven by the emergence of mass spectrometry applications serving -omics sciences and the need for analyzing minute volumes of precious samples with ever higher sensitivity. While nanoscale liquid chromatography (flow rates <1 μL/min) has gained widespread recognition in proteomics, the adoption of microscale setups (flow rates ranging from 1 to 100 μL/min) for low molecular weight compound applications, including metabolomics, has been surprisingly slow, despite the inherent advantages of the approach. Highly heterogeneous matrices and chemical structures accompanied by a relative lack of options for both selective sample preparation and user-friendly equipment are usually reported as major hindrances. To facilitate the wider implementation of microscale analyses, we present here a comprehensive tutorial encompassing important theoretical and practical considerations. We provide fundamental principles in micro-chromatography and guide the reader through the main elements of a microflow workflow, from LC pumps to ionization devices. Finally, based on both our literature overview and experience, illustrated by some in-house data, we highlight the critical importance of the ionization source design and its careful optimization to achieve significant sensitivity improvement.

A highly sensitive approach for the analysis of tyrosine phosphoproteome in primary T cells

Tyrosine phosphorylation, a common post-translational modification process for proteins, is involved in a variety of biological processes. However, the abundance of tyrosine-phosphorylated proteins is very low, making their identification by mass spectrometry (MS) is difficult; thus, milligrams of the starting material are often required for their enrichment. For example, tyrosine phosphorylation plays an important role in T cell signal transduction. However, the number of primary T cells derived from biological tissue samples is very small, and these cells are difficult to culture and expand; thus, the study of T cell signal transduction is usually carried out on immortalized cell lines, which can be greatly expanded. However, the data from immortalized cell lines cannot fully mimic the signal transduction processes observed in the real physiological state, and they usually lead to conclusions that are quite different from those of primary T cells. Therefore, a highly sensitive proteomic method was developed for studying tyrosine phosphorylation modification signals in primary T cells. To address the issue of the limited T cells numbers, a comprehensive protocol was first optimized for the isolation, activation, and expansion of primary T cells from mouse spleen. CD3+ primary T cells were successfully sorted; more than 91% of the T cells collected were well activated on day 2, and the number of T cells expanded to over 7-fold on day 4. Next, to address the low abundance of tyrosine-phosphorylated proteins, we used SH2-superbinder affinity enrichment and immobilized Ti4+affinity chromatography (Ti4+-IMAC) to enrich the tyrosine-phosphorylated polypeptides of primary T cells that were co-stimulated with anti-CD3 and anti-CD28. These polypeptides were resolved using nanoscale liquid chromatography-tandem mass spectrometry (nanoLC-MS/MS). Finally, 282 tyrosine phosphorylation sites were successfully identified in 1 mg of protein, including many tyrosine phosphorylation sites on the immunoreceptor tyrosine-based activation motif (ITAM) in the intracellular region of the T cell receptor membrane protein CD3, as well as the phosphotyrosine sites of ZAP70, LAT, VAV1, and other proteins related to signal transduction under costimulatory conditions. In summary, to solve the technical problems of the limited number of primary cells, low abundance of tyrosine-phosphorylated proteins, and difficulty of detection by MS, we developed a comprehensive proteomic method for the in-depth analysis of tyrosine phosphorylation modification signals in primary T cells. This protocol may be applied to map signal transduction networks that are closely related to physiological states.

A mesoscopic approach for nanoscale evaporation heat transfer characteristics

We propose a mesoscopic approach for investigating steady/transient nanoscale evaporation heat transfer characteristics, whose kinetic nature makes it an ideal tool to model the evaporation kinetics at the liquid-vapor interface and the microscopic wall-fluid interactions. Simulation of the evaporation of a flat nanoscale thin liquid film demonstrates its capability of resolving kinetically limited evaporation and liquid film adsorption. For the simulation of an evaporating meniscus in a nanochannel, our proposed mesoscopic approach considers the conservation of mass, momentum and energy of both liquid and vapor phases, thereby naturally incorporating both the multi-dimensional heat transfer effect and vapor transport resistance in nano-confined space. We demonstrate that solid-fluid interaction plays dominant roles on the interfacial transport during nanoscale evaporation, and vapor transport resistance has nonnegligible influences on the evaporation heat/mass transport in nano-confined spaces. By handling statistical behavior of molecule ensembles, this mesoscopic approach not only preserves microscopic physics but also has high computational efficiencies, enabling the simulation of space and time domains on the practical application level. This work paves the way for quantitative investigations of steady/transient nanoscale evaporation heat transfer characteristics using mesoscopic approach.

Olive Pomace Extract Contains Low Molecular Weight Peptides and Possesses ACE Inhibitory Activity.

The aim of the present study was to determine the ACE inhibitory activity of aqueous extracts of olive pomace and to understand whether they represent a good source of bioactive LMW peptides for nutritional and pharmacological applications. We produced a water extract from olive pomace (var. Picual) and obtained its low molecular weight (LMW) fraction (<3 kDa). The calculated yield of extraction was 100.2 ± 7.9 mg of LMW peptides per 100 g of olive pomace. The olive pomace LMW fraction possessed strong ACE inhibitory activity (IC50 = 3.57 ± 0.22 µg prot/mL). The LMW fraction (<3 kDa) was analysed by nanoscale liquid chromatography-Orbitrap coupled with tandem mass spectrometry and de novo sequencing. Thirty new peptides, containing between 7-17 amino acids and molecular masses ranging 778-1354 Da, were identified by the Peaks database algorithm using the available Olea europaea (cv. Farga) genome database. Ten new peptides were also identified by Peaks de novo sequencing. The protein sources of twelve peptides detected in the database by Peaks DB were identified by BLAST search. The ACE inhibitory activity of the identified peptides was predicted by BIOPEP software. We conclude that olive pomace possesses ACE inhibitory activity and contains low molecular weight peptides with (predicted) biological activity. Olive pomace may represent a good source of peptides for nutritional and pharmaceutical applications. In our study, it has been shown that olive pomace possesses ACE inhibitory activity and contains low molecular weight peptides with (predicted) biological activity. Olive pomace may represent a good source of peptides for nutritional and pharmaceutical applications. More research is needed in order to identify the in vivo effects of olive pomace bioactive peptides.

Fungal and bacterial species richness in biodeteriorated seventeenth century Venetian manuscripts

Historical paper documents are susceptible to complex degradation processes, including biodeterioration, which can progressively compromise their aesthetic and structural integrity. This study analyses seventeenth century handwritten historical letters stored at the Correr Museum Library in Venice, Italy, exhibiting pronounced signs of biodeterioration. The techniques used encompassed traditional colony isolation on agar plates and proteomics analyses, employing nanoscale liquid chromatography coupled with high-resolution mass spectrometry (nano-LC–MS). Fluorescence microscopy was used for the first time in the historical paper biodeterioration context to supplement the conventional stereoscopic, optical, and scanning electron microscopic imaging techniques. This method enables the visualisation of microorganisms beyond and beneath the paper’s surface through their natural intrinsic autofluorescence in a non-invasive and non-destructive way. The results demonstrate a diverse, complex, and abundant microbiota composed of coexisting fungal and bacterial species (Ascomycota, Mucoromycota, Basidiomycota, Proteobacteria, and Actinobacteria), along with mite carcasses, insects, parasites, and possibly protists. Furthermore, this study reveals certain species that were not previously documented in the biodeterioration of historical paper, including human pathogens, such as Histoplasma capsulatum, Brucella, Candida albicans, and species of Aspergillus (A. flavus, A. fumigatus, A. oryzae, A. terreus, A. niger) known to cause infections or produce mycotoxins, posing substantial risk to both artefacts and humans.

Chemically robust superhydrophobic surfaces with a self‐replenishing nanoscale liquid coating

AbstractDue to poor chemical robustness, superhydrophobic surfaces become susceptible to failure, especially in a highly oxidative environment. To ensure the long‐term efficacy of these surfaces, a more stable and environmentally friendly coating is required to replace the conventional salinization layers. Here, soot‐templated surfaces with re‐entrant nanostructures are precoated with polydimethylsiloxane (PDMS) brushes. An additional nanometer‐thick lubricant layer of PDMS was then applied to increase chemical stability. The surface is superhydrophobic with a nanoscale liquid coating. Since the lubricant layer is thin, ridge formation is suppressed, which leads to low drop sliding friction and fast drop shedding. By introducing a bottom “reservoir” of a free lubricant as an oil source for self‐replenishing to the upper layer, the superhydrophobic surface becomes more stable and heals spontaneously in response to alkali erosion and O2 plasma exposure. This design also leads to a higher icing delay time and faster removal of impacting cooled water drops than for uncoated surfaces, preventing icing at low temperatures.

Nanoscale liquid Al phase formation through beam heating of MgAl2O4 in TEM.

In this study, electron-beam irradiation of a MgAl2O4 single-crystalline thin-film specimen in a transmission electron microscope reveals an unexpected formation of nanoscale liquid Al droplets. Despite the comparable melting temperatures of Mg and Al, the resulting liquid phase is predominantly composed of Al. This predominant presence of Al in the liquid phase is attributed to the selective evaporation of Mg, driven by its higher vapor pressure at elevated temperatures. Our observations suggest a correlation between electron-beam irradiation and a subsequent rise in specimen temperature. In particular, the observed melting of Al defies explanation by the widely accepted mechanism that attributes specimen heating to electron-energy loss, given the negligible energy deposited as determined by the collision stopping power. Instead, we suggest that the significant specimen heating is due to Auger excitation, a process known to deposit substantial energy. This contention is supported by a quantitative heat-transfer finite element analysis.

Alpha-synuclein promotes PRMT5-mediated H4R3me2s histone methylation by interacting with the BAF complex.

α-Synuclein (αS) is a key molecule in the pathomechanism of Parkinson's disease. Most studies on αS to date have focused on its function in the neuronal cytosol, but its action in the nucleus has also been postulated. Indeed, several lines of evidence indicate that overexpressed αS leads to epigenomic alterations. To clarify the functional role of αS in the nucleus and its pathological significance, HEK293 cells constitutively expressing αS were used to screen for nuclear proteins that interact with αS by nanoscale liquid chromatography/tandem mass spectrometry. Interactome analysis of the 229 identified nuclear proteins revealed that αS interacts with the BRG1-associated factor (BAF) complex, a family of multi-subunit chromatin remodelers important for neurodevelopment, and protein arginine methyltransferase 5 (PRMT5). Subsequent transcriptomic analysis also suggested a functional link between αS and the BAF complex. Based on these results, we analyzed the effect of αS overexpression on the BAF complex in neuronally differentiated SH-SY5Y cells and found that induction of αS disturbed the BAF maturation process, leading to a global increase in symmetric demethylation of histone H4 on arginine 3 (H4R3me2s) via enhanced BAF-PRMT5 interaction. Chromatin immunoprecipitation sequencing confirmed accumulated H4R3me2s methylation near the transcription start site of the neuronal cell adhesion molecule (NRCAM) gene, which has roles during neuronal differentiation. Transcriptional analyses confirmed the negative regulation of NRCAM by αS and PRMT5, which was reconfirmed by multiple datasets in the Gene Expression Omnibus (GEO) database. Taken together, these findings suggest that the enhanced binding of αS to the BAF complex and PRMT5 may cooperatively affect the neuronal differentiation process.

Metastable liquid immiscibility in the 2018–2021 Fani Maoré lavas as a mechanism for volcanic nanolite formation

Nanoscale liquid immiscibility is observed in the 2018–2021 Fani Maoré submarine lavas (Comoros archipelago). Heat transfer calculations, Raman spectroscopy, scanning and transmission electron microscopy reveal that in contrast to thin (500 µm) outer rims of homogeneous glassy lava (rapidly quenched upon eruption, >1000 °C s−1), widespread liquid immiscibility is observed in thick (1 cm) inner lava rims (moderately quenched, 1–1000 °C s−1), which exhibit a nanoscale coexistence of Si- and Al-rich vs. Ca-, Fe-, and Ti-rich melt phases. In this zone, rapid nanolite crystallization contrasts with the classical crystallization process inferred for the slower cooled ( < 1 °C s−1) lava interiors. The occurrence of such metastable liquid immiscibility at eruptive conditions controls physicochemical characteristics of nanolites and residual melt compositions. This mechanism represents a common yet frequently unobserved feature in volcanic products, with the potential for major impacts on syn-eruptive magma degassing and rheology, and thus on eruptive dynamics.

Identification of novel umami peptides from yeast extract and the mechanism against T1R1/T1R3.

Yeast extract was separated by using ultrafiltration, gel filtration chromatography, and preparative high-performance liquid chromatography for analyzing the umami mechanism. 13 kinds of umami peptides were screened out from 73 kinds of peptides which were identified in yeast extract using nanoscale ultra-performance liquid chromatography-tandem mass spectrometry and virtual screening. The umami peptides were found to have a threshold range of 0.07-0.61mM. DWTDDVEAR exhibited a strong umami taste with a pronounced enhancement effect for monosodium glutamate. Molecular docking studies revealed that specific amino acid residues in the T1R1 subunit, including Arg316, Ser401, and Asp315, played a critical role in the umami perception with these peptides. Overall, the study highlights the potential of natural flavor enhancers and provides insights into the mechanism of umami taste perception.

Safety evaluation, hydrolysis activity of Kluyveromyces marxianus JY-1 and its application to obtain immunomodulatory peptide from bovine casein

Except in vitro enzymolysis, there are few studies on the production of casein-derived immunomodulatory peptides by microbial fermentation technology. In this study, the ability of a strain of Kluyveromyces marxianus JY-1 isolated from traditional fermented milk in Xinjiang District (China) to release casein-derived immunomodulatory peptides was evaluated. Results showed that this strain was safe and with high protease activity, which could highly hydrolyze casein. The hydrolysate of casein hydrolyzed by Kluyveromyces marxianus JY-1 could promote the proliferation of RAW264.7 macrophages and the production of cytokines (IL-6, IL-1β, and TNF-α) compared with the control group, showing obvious immunomodulatory activity. A nanoscale liquid chromatography-quadrupole time-of-flight tandem mass spectrometry (Nano LC-Q-TOF-MS/MS) was used to determine the amino acid sequences of bioactive peptides in casein hydrolysate of Kluyveromyces marxianus. According to the structural characteristics of immunomodulatory peptides, 3 peptides (HPHPHLSF, PFPEVFG, and SPAQILQW) with immunomodulatory activity were selected from 55 identified peptides by using in silico methods. This study demonstrates that Kluyveromyces marxianus JY-1 has a wide range of potential applications in the production of immunomodulatory peptides from casein and other food proteins.

Mesoscopic Model for Disjoining Pressure Effects in Nanoscale Thin Liquid Films and Evaporating Extended Meniscuses.

Disjoining pressure effect is the key to describe contact line dynamics, micro/nanoscale liquid-vapor phase change heat transfer, and liquid transport in nanopores. In this paper, by combining a mesoscopic approach for nanoscale liquid-vapor interfacial transport and a mean-field approximation of the long-range solid-fluid molecular interaction, a mesoscopic model for the disjoining pressure effect in nanoscale thin liquid films is proposed. The capability of this model to delineate the disjoining pressure effect is validated. We demonstrate that the Hamaker constant determined from our model agrees very well with molecular dynamics (MD) simulation and that the transient evaporation/condensation mass flux predicted by this mesoscopic model is also consistent with the kinetic theory. Using this model, we investigate the characteristics of the evaporating extended meniscus in a nanochannel. The nonevaporating film region, the evaporating thin-film region, and the intrinsic meniscus region are successfully captured by our model. Our results suggest that the apparent contact angle and thickness of the nonevaporating liquid film are self-tuned according to the evaporation rate, and a higher evaporation rate results a in larger apparent contact angle and thinner nonevaporating liquid film. We also show that disjoining pressure plays a dominant role in the nonevaporating film region and suppresses the evaporation in this region, while capillary pressure dominates the intrinsic meniscus region. Strong evaporation takes place in the thin-film region, and both the disjoining pressure and capillary pressure contribute to the total pressure difference that delivers the liquid from the intrinsic meniscus region to the evaporating thin-film region, compensating for the liquid mass loss due to strong evaporation. Our work provides a new avenue for investigating thin liquid film spreading, liquid transport in nanopores, and microscopic liquid-vapor phase change heat/mass transfer mechanisms near the three-phase contact line region.

Screening of Exosome-Derived Proteins and Their Potential as Biomarkers in Diagnostic and Prognostic for Pancreatic Cancer.

In the oncological area, pancreatic cancer is one of the most lethal diseases, with 5-year survival rising just 10% in high-development countries. This disease is genetically characterized by KRAS as a driven mutation followed by SMAD4, CDKN2, and TP53-associated mutations. In clinical aspects, pancreatic cancer presents unspecific clinical symptoms with the absence of screening and early plasmatic biomarker, being that CA19-9 is the unique plasmatic biomarker having specificity and sensitivity limitations. We analyzed the plasmatic exosome proteomic profile of 23 patients with pancreatic cancer and 10 healthy controls by using Nanoscale liquid chromatography coupled to tandem mass spectrometry (NanoLC-MS/MS). The pancreatic cancer patients were subdivided into IPMN and PDAC. Our findings show 33, 34, and 7 differentially expressed proteins when comparing the IPMN vs. control, PDAC-No treatment vs. control, and PDAC-No treatment vs. IPMN groups, highlighting proteins of the complement system and coagulation, such as C3, APOB, and SERPINA. Additionally, PDAC with no treatment showed 11 differentially expressed proteins when compared to Folfirinox neoadjuvant therapy or Gemcitabine adjuvant therapy. So here, we found plasmatic exosome-derived differentially expressed proteins among cancer patients (IPMN, PDAC) when comparing with healthy controls, which could represent alternative biomarkers for diagnostic and prognostic evaluation, supporting further scientific and clinical studies on pancreatic cancer.

Proteomic Analysis of Dysfunctional Liver Sinusoidal Endothelial Cells Reveals Substantial Differences in Most Common Experimental Models of Chronic Liver Diseases.

Molecular markers of dedifferentiation of dysfunctional liver sinusoidal endothelial cells (LSEC) have not been fully elucidated. We aimed at deciphering the molecular profile of dysfunctional LSEC in different pathological scenarios. Flow cytometry was used to sort CD11b-/CD32b+ and CD11b-/CD32b- LSEC from three rat models of liver disease (bile duct ligation-BDL; inhaled carbon tetrachloride-CCl4; and high fat glucose/fructose diet-HFGFD). A full proteomic profile was performed applying nano-scale liquid chromatography tandem mass spectrometry (nLC-MS) and analyzed with PEAKS software. The percentage of CD32b- LSEC varied across groups, suggesting different capillarization processes. Both CD32+ and CD32b- LSEC from models are different from control LSEC, but differently expressed proteins in CD32b- LSEC are significantly higher. Heatmaps evidenced specific protein expression patterns for each model. Analysis of biological significance comparing dysfunctional CD32b- LSEC with specialized CD32b+ LSEC from controls showed central similarities represented by 45 common down-regulated proteins involved in the suppression of the endocytic machinery and 63 common up-regulated proteins associated with the actin-dependent cytoskeleton reorganization. In summary; substantial differences but also similarities in dysfunctional LSEC from the three most common models of liver disease were found, supporting the idea that LSEC may harbor different protein expression profiles according to the etiology or disease stage.

Fluctuation-driven instability of nanoscale liquid films on chemically heterogeneous substrates

The instability and dewetting of bounded liquid films at the nanoscale are shown to strongly depend on thermal fluctuations. In this work, this fluctuation-driven instability of films on a chemically heterogeneous substrate is investigated both by a stochastic lubrication equation (SLE), which models thermal fluctuations with white noise, and by molecular dynamics (MD). Linear instability analysis for the SLE, considering slip and intermolecular forces of the heterogeneous substrates, is employed to derive a spectrum of the thermal capillary waves and their corresponding interface roughness, which are then quantitatively confirmed by numerical solutions for the SLE and MD. The fluctuation-driven instability is found to be enhanced by the slip and intermolecular forces, with the latter becoming dominant toward the final rupture. Moreover, the results suggest that a heterogeneous substrate can be approximated as a homogeneous one with effective (averaged) slip lengths and Hamaker constants for the intermolecular forces. The gradients of the slip and intermolecular forces due to the heterogeneities are shown not to affect the instability significantly.

Molecular dynamics simulation of the evaporation of thin liquid sodium film on the conical nanostructure surface

Deeply understanding the evaporation of the nanoscale thin liquid film on the nanostructure substrates is significant for further constructing the novel wick structure with nanostructure surfaces, which would be used in the optimal design of the sodium heat pipe. For this purpose, this paper investigates the evaporation of thin liquid film on conical nanostructured surfaces by the molecular dynamics method. A cuboid evaporation system is constructed. It consists of the bottom solid substrate and thin liquid sodium film. A flat solid wall is set as the reference. By changing the nanoscale cone's number and height, five conical nanostructure surfaces are built. The number of gas atoms and the total energy of fluid atoms are observed respectively. The evaporation rate and the average heat flux (q) of six cases are compared. The conical nanostructure suppresses evaporation. With the roughness of the conical nanostructures, the evaporation rate decrement maximum can reach 83% and the q decrement maximum can reach 58%. Based on the thermal resistances in the solid-liquid contact region, the D (Self-diffusion coefficient), and the peak values of RDF (Radial distribution function), the mechanisms of the conical nanostructure surfaces are analyzed. The suppressing effects of the conical nanostructure surfaces are achieved by weakening the heat conduction in the solid-liquid contact region and mitigating the collision heat transfer of liquid atoms.

Humidity-Controlled Molecular Assembly and Photoisomerization Behavior with a Bubble-Assisted Patterning Approach.

Precise control of molecular assembly is of great significance in the application of functional molecules. This work has systematically investigated the humidity effect in bubble-assisted molecular assembly. This work finds humidity is critical in the evolution of the soft confined space, leading to the formation of microscale liquid confined space under high humidity, and nanoscale liquid confined space under low humidity. It is also revealed that the differences in surface wettability and adhesion play the key role. Consequently, a flat pattern with thermodynamically favorable ordered structure and a sharp pattern with dynamically favorable disordered structure are achieved, which show different solid-state photoisomerization behaviors and photoresponsiveness. Interestingly, conductivity of sharp pattern with disordered structure is higher than that of flat pattern with layered ordered structure due to electronic transport mechanism of different spatial dimensions. This work opens a new way for manipulating the molecular self-assembly to control the morphology and function of molecular patterns.