Improving the ionic conductivity of polymer electrolytes induced by ceramic nanowire fillers with abundant lithium vacancies.

The addition of ceramic fillers is regarded as an effective strategy for enhancing the ionic conductivity of polymer electrolytes. However, particulate fillers typically fail to provide continuous conductive pathways and effective reinforcement. Herein, we report a ceramic nanowire filler with long-range interfacial conductivity and abundant lithium vacancies for a poly(ethylene oxide) (PEO)-based all-solid-state polymer electrolyte. LLZO nanowires (LLZO NWs) with a high aspect ratio are synthesized by combining sol-gel electrospinning and the multi-step process involving pre-oxidation, pre-sintering, and secondary sintering, resulting in a high tensile strength of the composite electrolyte (6.87 MPa). Notably, tantalum-aluminum co-substituted LLZO NWs (TALLZO NWs) release abundant lithium vacancies, further enhancing the Lewis acid-base properties, leading to a rapid ion migration speed (Li+ transfer number = 0.79) and significantly high ionic conductivity (3.80 × 10-4 S cm-1). Due to the synergistic effect of nanostructure modification and heteroatom co-doping, the assembled all-solid-state lithium-sulfur battery exhibits a high initial discharge capacity (776 mA h g-1 at 25 °C), remarkable rate capability, and excellent cycling performance (81% capacity retention after 200 cycles at 0.1C).

LINC00330/CCL2 axis-mediated ESCC TAM reprogramming affects tumor progression.

BACKGROUND: Tumor-associated macrophages (TAMs) significantly influence the progression, metastasis, and recurrence of esophageal squamous cell carcinoma (ESCC). The aberrant expression of long noncoding RNAs (lncRNAs) in ESCC has been established, yet the role of lncRNAs in TAM reprogramming during ESCC progression remains largely unexplored. METHODS: ESCC TAM-related lncRNAs were identified by intersecting differentially expressed lncRNAs with immune-related lncRNAs and performing immune cell infiltration analysis. The expression profile and clinical relevance of LINC00330 were examined using the TCGA database and clinical samples. The LINC00330 overexpression and interference sequences were constructed to evaluate the effect of LINC00330 on ESCC progression. Single-cell sequencing data, CIBERSORTx, and GEPIA were utilized to analyze immune cell infiltration within the ESCC tumor microenvironment and to assess the correlation between LINC00330 and TAM infiltration. ESCC-macrophage coculture experiments were conducted to investigate the influence of LINC00330 on TAM reprogramming and its subsequent effect on ESCC progression. The interaction between LINC00330 and C-C motif ligand 2 (CCL2) was confirmed through transcriptomic sequencing, subcellular localization analysis, RNA pulldown, silver staining, RNA immunoprecipitation, and other experiments. RESULTS: LINC00330 is significantly downregulated in ESCC tissues and strongly associated with poor patient outcomes. Overexpression of LINC00330 inhibits ESCC progression, including proliferation, invasion, epithelial-mesenchymal transition, and tumorigenicity in vivo. LINC00330 promotes TAM reprogramming, and LINC00330-mediated TAM reprogramming inhibits ESCC progression. LINC00330 binds to the CCL2 protein and inhibits the expression of CCL2 and downstream signaling pathways. CCL2 is critical for LINC00330-mediated TAM reprogramming and ESCC progression. CONCLUSIONS: LINC00330 inhibited ESCC progression by disrupting the CCL2/CCR2 axis and its downstream signaling pathways in an autocrine fashion; and by impeding CCL2-mediated TAM reprogramming in a paracrine manner. The new mechanism of TAM reprogramming mediated by the LINC00330/CCL2 axis may provide potential strategies for targeted and immunocombination therapies for patients with ESCC.

A Conductive Binder Based on Mesoscopic Interpenetration with Polysulfides Capturing Skeleton and Redox Intermediates Network for Lithium Sulfur Batteries.

The practical application of lithium-sulfur batteries with high theoretical energy density and readily available cathode active materials is hampered by problems such as sulfur insulation, dramatic volume changes, and polysulfide shuttling. The targeted development of novel binders is the most industrialized solution to the problem of sulfur cathodes. Herein, an aqueous conductive emulsion binder with the sulfonate-containing hard elastic copolymer core and the conjugate polymer shell, which is capable of forming a bicontinuous mesoscopic interpenetrating polymer network, is synthesized and investigated. Not only can the elastic skeleton formed by the copolymer bind the active substance under drastic volume changes, but also the rich ester and cyanide groups in it can effectively capture lithium polysulfide. Meanwhile, the conducting skeleton consisting of poly(3,4-ethylenedioxythiophene) both provides the additional charge conduction pathways and acts as the redox intermediates, significantly accelerating the kinetic process of lithium polysulfide conversion. Based on the synergistic effect of the above mechanisms, the use of the prepared binder on the sulfur carbon cathode significantly improves the rate performance and cycle stability of lithium sulfur batteries.

Long-lifespan Zinc-ion Capacitors Enabled by Anodes Integrated with Interconnected Mesoporous Chitosan Membranes through Electrophoresis-driven Phase Separation.

The advancement of highly secure and inexpensive aqueous zinc ion energy storage devices is impeded by issues, including dendrite growth, hydrogen evolution and corrosion of zinc anodes. It is essential to modify the interface of zinc anodes that homogenizes ion flux and facilitates highly reversible zinc planarized deposition and stripping. Herein, by coupling zinc ion coordination with acid-base neutralization under the driving of electrophoresis, manageable mesoscopic phase separation for constructing chitosan frameworks was achieved, thereby fabricating interconnected mesoporous chitosan membranes based heterogeneous quasi-solid-state electrolytes integrated with anodes. The framework is constructed by twisted chitosan nanofiber bundles, forming a three-dimensional continuous spindle-shaped pore structure. With this framework, the electrolyte provides exceptional ion conductivity of 25.1 mS cm-1 , with a puncture resistance strength of 2.3 GPa. In addition, the amino groups of chitosan molecule can make the surface of the framework positively charged. Thus, reversible zinc planarized deposition is successfully induced by the synergistic effect of stress constraint and electrostatic modulation. As a result, as-assembled zinc ion capacitor has an excellent cycle life and sustains the capacity by over 95 % after 20000 cycles at a current density of 5 A g-1 . This research presents a constructive strategy for stable electrolytes-integrated zinc anodes.

Integrated Construction Improving Electrochemical Performance of Stretchable Supercapacitors Based on Ant-Nest Amphiphilic Gel Electrolytes.

Aqueous integrated stretchable supercapacitors (ISSCs) have attracted extensive attention due to the intrinsic safety in future wearable electronics. However, aqueous ISSCs usually suffer from low energy density and poor dynamic deformation stability owing to the conventional hydrogel electrolytes' narrow electrochemical stability window (ESW) and dissatisfied interface bonding. Herein, an ant-nest amphiphilic polyurethane hydro/organogel electrolyte (sAPUGE) with a wide ESW (≈2.2 V) and superb self-adhesion is prepared by electrospinning, which interacts with carbon-based stretchable electrodes for the construction of flame-retardant PU-based sAPUGE-ISSC. Benefitting from the synergistic effect of chemical bonding and mechanical meshing between the electrode and gel electrolyte interface, as-assembled sAPUGE-ISSC delivers a high energy density of 13.7 mWh cm-3 (at a power density of 0.126 W cm-3 ) and outstanding dynamic deformation stability (98.3% capacitance retention after 500 stretching cycles under 100% strain). This unique hydro/organogel electrolyte provides a pathway toward the next generation of wearable energy products in modern electronics.

Super-Coordinated Nickel N4 Ni1 O2 Site Single-Atom Catalyst for Selective H2 O2 Electrosynthesis at High Current Densities.

Electrochemical production of hydrogen peroxide (H2 O2 ) from O2 on single-atom catalysts has attracted great attention, yet the quest for robust catalysts is driven by achieving >90 % Faradaic efficiency (FE) under industrial-relevant current densities (>100 mA cm-2 ). Herein we synthesize a catalyst that contains single nickel site coordinated by four nitrogen and two oxygen atoms (i.e., N4 Ni1 O2 ) via involving carboxyl functionalized multiwall carbon nanotubes as a substrate to provide extra O coordination to the regular NiN4 site. It has a cathodic energy efficiency of approximately 82 % and a H2 O2 FE of around 96 % at 200 mA cm-2 current density, outperforming the reported single-atom catalysts for H2 O2 electrosynthesis.

Effectiveness of a school-based, lay counselor-delivered cognitive behavioral therapy for Chinese children with posttraumatic stress symptoms: a randomized controlled trial.

Background: Improving children's access to mental health services need more innovative solutions, especially in low- and middle-income countries. School-based psychosocial interventions delivered by lay counselors may be an efficient way to improve children's access to mental health services. But few studies were conducted to examine the effectiveness of these interventions. Therefore, this study is to evaluate the effectiveness of trauma-focused cognitive behavioral therapy (TF-CBT) in a group format delivered by lay counselors to children with trauma-related symptoms in China. Methods: A total of 234 children (aged 9-12 years) with full or subthreshold posttraumatic stress disorder (PTSD) were randomly assigned to group-based TF-CBT or treatment as usual (TAU). In the intervention group, 118 children received 10-12 sessions of group-based TF-CBT delivered by lay counselors for 9 consecutive weeks. In the TAU group, 116 children received the usual school services provided by psychology teachers. The primary outcome was the reduction in PTSD severity, which was assessed with the UCLA PTSD reaction index for DSM-5 (PTSD-RI-5). The secondary outcomes included the reduction in PTSD severity and the remission of PTSD, both of which were measured with the PTSD checklist-5 (PCL-5). Secondary outcomes also included the reduction in depression severity and the reduction in generalized anxiety severity. Blinded assessments were collected at baseline, posttreatment (primary endpoint), and 3-month follow-up. This trial is registered with Chinese Clinical Trial Registry, ChiCTR1900027131. Findings: At posttreatment, the intervention group scored significantly lower than the TAU group on PTSD-RI-5 PTSD (30.98 vs. 39.22; adjusted mean difference [AMD], -7.35; 95% CI, -11.66 to -3.04), PCL-5 PTSD (28.78 vs. 38.04; AMD, -8.49; 95% CI, -13.23 to -3.75), depression (5.52 vs. 7.96; AMD, -1.63; 95% CI, -2.50 to -0.76), and generalized anxiety (7.23 vs. 8.64; AMD, -1.21; 95% CI, -2.20 to -0.23). The remission of PCL-5 PTSD was also significantly higher in the intervention group (42.86% vs. 13.54%, χ 2  = 13.10, P < 0.001). These two groups showed a similar level of symptoms at the 3-month follow-up. Interpretation: The group-based TF-CBT can significantly alleviate PTSD, depression, and generalized anxiety right after treatment in Chinese children who suffer from different types of trauma. But the long-term effects of this intervention need to be further tested. This intervention can be delivered by trained lay counselors in low- and middle-income countries. Funding: None.

A Heterostructured Gel Polymer Electrolyte Modified by MoS2 for High-Performance Lithium-Sulfur Batteries.

In Li-S batteries, the shuttle effect of polysulfide lithium (LiPS) on the cathode side and the growth of lithium dendrites on the anode side are two major problems that lead to an insufficient cycle life. Herein, in light of the challenges brought on by the different chemical environments on both sides of Li-S batteries, a heterostructured poly(ethyl acrylate-co-ionic liquid) gel electrolyte with a single-sided electrocatalytic reduced graphene oxide/MoS2 coating (MoS2@rGO-GPE) was developed in order to assemble a high-performance Li-S battery with a self-supporting graphene sulfur cathode. In such a device architecture, there is multiposition suppression of the shuttle effect; that is, the confinement of the graphene foam, the catalysis of the MoS2 composite, and the capture of the gel polymer electrolyte. Our results show that the ionic conductivity of the heterostructured electrolyte is 1.98 mS cm-1, and the Li ion transference number reaches 0.81. The assembled lithium-sulfur battery displays a high initial discharge capacity of 1027 mAh g-1 at 0.1 C, superior cycle stability (80% capacity retention after 500 cycles), and excellent rate performance. This design strategy provides a valuable route for the development of high-performance lithium-sulfur batteries.

Integrated Construction of a Long-Life Stretchable Zinc-Ion Capacitor.

The major challenge in achieving high-performance stretchable zinc-ion energy-storage devices is the combination of stretchable dendrite-free zinc negative electrodes and sufficient bonding between components (current collector, electrode, separator, and package). Herein, based on a series of physicochemically tunable self-healing polyurethanes, an elastic current collector is prepared through a swelling-induced wrinkling method, and then a stretchable zinc negative electrode prepared through in situ confined electroplating. The elastic current collector has a nano-network structure with polyurethane encapsulation, and exhibits both geometric and intrinsic stretchability. The stretchable zinc negative electrode formed in situ has high electrochemical activity and exhibits an excellent cycle life under the protection of a Zn2+ -permeable coating. Furthermore, fully polyurethane-based stretchable zinc-ion capacitors are assembled through in situ electrospinning and hot-pressing techniques. Due to the high stretchability of the components and the interfusion of the matrixes, the integrated device exhibits excellent deformability and desirable electrochemical stability. This work provides a systematic construction plan for stretchable zinc-ion energy-storage devices in three aspects: material synthesis, component preparation, and device assembly.

Stretchable sodium-ion capacitors based on coaxial CNT supported Na2Ti3O7 with high capacitance contribution.

Stretchable sodium-ion capacitors (SSICs) are promising energy storage devices for wearable electronic devices, and the development bottleneck is the realization of stretchable battery-type electrodes with desirable electrochemical properties during dynamic deformation. Herein, we find that electrostatic modification of acidified carbon nanotubes with polyamines can introduce active sites and modulate the surface pH microenvironment, thereby developing a route to realize the in situ coaxial nanometerization of sodium titanate (nCNT@NTO). The nCNT@NTO anode material has a fast Na+ transport and the high capacitive contribution, which can deliver a high specific capacity (206.5 mA h g-1 at 0.1 A g-1) and high rate performance (maintain 51% capacity at 10 A g-1), and the ideal cycle stability (∼93% capacity retention after 1000 cycles at 5 A g-1). In addition, acrylate-rubber with high stickiness and stretchability are served as the elastic matrix both of the stretchable electrodes and quasi-solid-state electrolytes, which endows strong adhesion between electrodes and electrolytes. Thus, the accordingly assembled SSIC delivers high energy density of 8.8 mW h cm-3 (at a power density of 0.024 W cm-3), and excellent deformation stability (89% capacitance retention after 500 stretching cycles under 100% strain).

High-Performance-Integrated Stretchable Supercapacitors Based on a Polyurethane Organo/Hydrogel Electrolyte.

Stretchable supercapacitors (SSCs) are promising energy storage devices for emerging wearable electronics. However, the low-energy density and poor deformation performance are still a challenge. Herein, an amphiphilic polyurethane-based organo/hydrogel electrolyte (APUGE) with a H2O/AN-in-salt (H2O/AN-NaClO4) is prepared for the first time. The as-prepared APUGE shows a wide voltage window (∼2.3 V), good adhesion, and excellent resilience. In addition, the intrinsically stretchable electrodes are prepared by coating the activated carbon slurry onto the PU/carbon black/MWCNT conductive elastic substrate. Based on the strong interface adhesion of the PU matrix, the as-assembled SSC delivers high-energy density (5.65 mW h cm-3 when the power density is 0.0256 W cm-3) and excellent deformation stability with 94.5% capacitance retention after 500 stretching cycles at 100% strain. This fully integrated construction concept is expected to be extended to multisystem stretchable metal ion batteries, stretchable lithium-sulfur batteries, and other stretchable energy storage devices.

In Vivo Genome-Wide CRISPR Activation Screening Identifies Functionally Important Long Noncoding RNAs in Hepatocellular Carcinoma.

BACKGROUND & AIMS: Long noncoding RNAs (lncRNAs) are found to have profound impacts on diverse cellular processes. Although high-throughput sequencing studies have shown the differential lncRNA expression profiles between hepatocellular carcinoma (HCC) and nontumor livers, the functional impacts of lncRNAs on HCC development await further investigation. Herein, we sought to address the functional roles of lncRNAs in HCC pathogenesis by in vivo functional screening. METHODS: We performed genome-wide clustered regularly interspaced short palindromic repeats (CRISPR)/dead CRISPR-associated protein 9 (dCas9) lncRNA activation screening in HCC xenografts. We characterized the clinical relevance of positively selected lncRNAs using transcriptomic data sets. We used CRISPR-based gene activation and knockdown approaches to show the functional roles of positively selected lncRNAs including Cancer Susceptibility 11 (CASC11) in HCC. RNA sequencing and chromatin isolation by RNA purification sequencing were used to investigate the molecular mechanisms of CASC11 in HCC progression. RESULTS: The in vivo functional screening identified 1603 positively selected lncRNAs, 538 of which were overexpressed in HCC patients. Systematic transcriptomic data analysis and clinical investigation showed that patients with high expression of these lncRNA candidates correlated with aggressive tumor behaviors. Overexpression of these lncRNAs aggravated HCC cell growth. Detailed characterization of a lncRNA candidate, CASC11, showed its pivotal role in cell proliferation and tumor growth. Mechanistically, chromatin isolation by RNA purification sequencing showed that CASC11 was bound to the CASC11/MYC proto-oncogene shared promoter region on chromosome 8q24. CASC11 modulated the transcriptional activity of MYC in a cis-regulatory manner, which affected the expression of MYC downstream target genes, consequently promoting G1/S progression. CONCLUSIONS: Our study showed the power of in vivo CRISPR screening, which comprehensively investigated the functionality of lncRNAs in HCC progression, providing a rationale for targeting these lncRNAs clinically.

Histone chaperone FACT complex coordinates with HIF to mediate an expeditious transcription program to adapt to poorly oxygenated cancers.

Cancer cells adapt to hypoxia through HIFs (hypoxia-inducible factors), which initiate the transcription of numerous genes for cancer cell survival in the hypoxia microenvironment. In this study, we find that the FACT (facilitates chromatin transcription) complex works cooperatively with HIFs to facilitate the expeditious expression of HIF targets for hypoxia adaptation. Knockout (KO) of the FACT complex abolishes HIF-mediated transcription by impeding transcription elongation in hypoxic cancer cells. Interestingly, the FACT complex is post-translationally regulated by PHD/VHL-mediated hydroxylation and proteasomal degradation, in similar fashion to HIF-1/2α. Metabolic tracing confirms that FACT KO suppresses glycolytic flux and impairs lactate extrusion, leading to intracellular acidification and apoptosis in cancer cells. Therapeutically, hepatic artery ligation and anti-angiogenic inhibitors adversely induce intratumoral hypoxia, while co-treatment with FACT inhibitor curaxin remarkably hinders the growth of hypoxic tumors. In summary, our findings suggest that the FACT complex is a critical component of hypoxia adaptation and a therapeutic target for hypoxic tumors.

Rearrangement of Ion Transport Path on Nano-Cross-linker for All-Solid-State Electrolyte with High Room Temperature Ionic Conductivity.

The low room temperature ionic conductivity (RTσ) of polyethylene oxide (PEO)-based solid-state polymer electrolyte (SPE) severely restricts its application for lithium batteries. Herein, acrylamide (AM) has been introduced into the poly(ethylene glycol) methyl ether methacrylate-poly(ethylene glycol) diacrylate (P-P). The multiple hydrogen bonds of AM expand the original single lithium environment (Li···O-C) to three types (Li···O-C, Li···N-H, and Li···O═C), which accelerates the conduction of lithium ions. In addition, the double bond modification of nanosilica (═SiO2) not only improves the mechanical properties but also brings a high-speed orderly vehicular transport mechanism. The multiple-lithium-ions environment is rearranged on the surface of the ═SiO2 to play a more significant role, making the RTσ of SPE reach 2.6 × 10-4 S cm-1, and the Li-ion transfer number reaches 0.84. The results show that the assembled all-solid-state lithium-sulfur battery has a high initial discharge capacity of 707 mAh g-1 at 30 °C when the sulfur loading is 4.3 mg cm-2, good cycle stability (capacity retention rate of 89% after 100 cycles at 0.1 C), and excellent rate performance. This SPE with high RTσ, stable interface engineering, and broad potential window (5.1 V) is expected to be used in other lithium/lithium-ion batteries that require high-voltage tolerance.

Transcriptomic analysis identifies a tumor subtype mRNA classifier for invasive non-functioning pituitary neuroendocrine tumor diagnostics.

Rationale: The invasive behavior of non-functioning pituitary neuroendocrine tumors (NF-PitNEts) presents obstacles for complete surgical resection and is indicative of poor prognosis. Therefore, developing reliable diagnostic tools for identifying invasive PitNEts would be helpful in guiding surgical decisions and, in particular, the follow-up treatment. Methods: We analyzed differential gene expression profiles between 39 non-invasive and 22 invasive NF-PitNEts by high-throughput sequencing, gene co-expression, and functional annotation. Twenty-one transcripts were further validated by Taqman-qPCR in another 143 NF-PitNEt samples. The histological expression and serum-exosomal mRNA of three candidate genes were examined by tissue microarray and droplet digital PCR. Results: Non-invasive and invasive NF-PitNEts were clustered into distinct groups with a few outliers because of their gonadotroph, corticotroph, or null cell lineages. The gene signature with strong invasive potential was enriched in 'Pathways in cancers' and 'MAPK pathway', with significantly higher in situ INSM1 and HSPA2 protein expression in invasive NF-PitNEts. Further integration of the 20 qPCR-validated differentially expressed genes and pituitary cell lineages provided a gene-subtype panel that performed 80.00-90.24% diagnostic accuracy for the invasiveness of NF-PitNEts. Conclusion: Our approach defined new characteristics in the core molecular network for patients at risk for invasive NF-PitNEt, representing a significant clinical advance in invasive PitNEt diagnostics.

Altered gut microbiota in Parkinson's disease patients/healthy spouses and its association with clinical features.

INTRODUCTION: Increasing evidence shows that gut microbiota dysbiosis may play important roles in the occurrence and progression of Parkinson's disease (PD), but the findings are inconsistent. Besides, the effect of family environment on gut microbiota dysbiosis remains unclear. METHODS: We characterized the gut microbial compositions of 63 PD patients, 63 healthy spouses (HS) and 74 healthy people (HP) using 16S rRNA sequencing. Clinical phenotypes and microbial composition were analyzed comprehensively. RESULTS: There were markedly different microbial compositions among PD, HS and HP samples by alpha/beta diversity. We also found differential microbial compositions among Hoehn & Yahr stage/disease duration. Eight inflammation-associated microbial genera shared a continuously increase trend with increased Hoehn & Yahr stage and disease duration, indicating characteristic bacteria associated with deterioration in PD. Additionally, seven bacterial markers were identified for accurately differentiating PD patients from the controls (area under the curve [AUC]: 0.856). CONCLUSIONS: Our study shows altered gut microbiota in PD patients. Importantly, inflammation-associated microbial genera may play roles in PD progression. Differential microbial compositions in HS and HP samples demonstrate that the gut microbiota are also affected by family environment. Disease-associated metagenomics studies should consider the family environmental factor. Our research provides an important reference and improves the understanding of gut microbiota in PD patients.

Poly(ionic liquid)-Based Quasi-Solid-State Copolymer Electrolytes for Dynamic-Reversible Adsorption of Lithium Polysulfides in Lithium-Sulfur Batteries.

The shuttle of the long-chain lithium polysulfides (LiPSs) is the main obstacle to the practical application of lithium-sulfur batteries. Herein, a poly(butyl acrylate/1-ethyl-3-vinylimidazole bis[(trifluoromethyl)sulfonyl]imide)-based quasi-solid-state copolymer electrolyte poly(ethylene glycol) diacrylate (PEGDA-P(BA-co-[EVIm]TFSI) QPE-IL) was prepared for lithium-sulfur batteries. The butyl acrylate component with abundant ester groups ensures the strong chemical capture for LiPSs. What is more, the introduction of ionic liquid ([EVIm]TFSI) can greatly improve the ionic conductivity and lithium-ion migration rate. More importantly, the dynamic-reversible adsorption of LiPSs was realized by chemical adsorption of ester-rich groups and electrostatic repulsion of free-moving negatively charged ions. As a result, the lithium-sulfur battery assembled by a reduced graphene oxide/carbon nanotube film@sulfur (rGOCTF@S) self-supporting cathode and QPE-IL displayed a high initial discharge capacity of 1179 mA h g-1, good cycling stability (72% capacity retention after 200 cycles at 0.5 C), and superior rate performance.

Surface modification of polyaniline using tetraethyl orthosilicate.

A well-dispersible conducting polyaniline/silica hybrid is prepared by the hydrolysis and condensation of tetraethyl orthosilicate (TEOS) on the surface of polyaniline in water/ethanol solution. It provides a simple and environmentally sound route for preparing the processable conducting polyaniline/silica hybrid at the nanometre level. The conductivity of polyaniline/silica hybrid is 2.43 S cm(-1) at 25 degrees C, and its powder is easily dispersed in the anhydrous ethanol or aqueous solution without any stabilizer. In addition, the structure, morphology and cyclic voltammorgram of this hybrid are also reported.

Poly(aniline-2-sulfonic acid) modified multiwalled carbon nanotubes with good aqueous dispersibility.

Poly(aniline-2-sulfonic acid) (PASA)-modified multiwalled carbon nanotubes (MWNTs) were prepared by in situ oxidative polymerization. HRTEM images show that the PASA-modified MWNTs (PASANTs) are core (MWNT)-shell (PASA) tubular structures with a shell thickness of several nanometers. The strong interaction between the surface of the MWNTs and the conjugated structure of the PASA shell layer was proven by FTIR spectra. It was found that the aqueous dispersibility and dispersion stability of PASANTs were significantly improved compared to those of the raw MWNTs. Furthermore, when the PASA content is greater than 30 wt%, no precipitation is found for the dispersions of modified MWNTs after sedimentation for 500 h, exhibiting an excellent stability. The electrical conductivity of these modified MWNTs is 2-5 times higher than that of raw MWNTs and is 10(3) times higher than that of PASA.

Distinct Photovoltaic Performance of Hierarchical Nanostructures Self-Assembled from Multiblock Copolymers.

We applied a multiscale approach coupling dissipative particle dynamics method with a drift-diffusion model to elucidate the photovoltaic properties of multiblock copolymers consisting of alternating electron donor and acceptor blocks. A series of hierarchical lamellae-in-lamellar structures were obtained from the self-assembly of the multiblock copolymers. A distinct improvement in photovoltaic performance upon the morphology transformation from lamella to lamellae-in-lamella was observed. The hierarchical lamellae-in-lamellar structures significantly enhanced exciton dissociation and charge carrier transport, which consequently contributed to the improved photovoltaic performance. On the basis of our theoretical calculations, the hierarchical nanostructures can achieve much enhanced energy conversion efficiencies, improved by around 25% compared with that of general ones, through structure modulation on the number and size of the small-length-scale domains via the molecular design of multiblock copolymers. Our findings are supported by recent experimental evidence and provide guidance for designing advanced photovoltaic materials with hierarchical structures.