Layer-by-Layer Electrode Fabrication for Improved Performance of Porous Polyimide-Based Supercapacitors

Nanoporous polymers are becoming increasingly interesting materials for electrochemical applications, as their large surface areas with redox-active sites allow efficient adsorption and diffusion of ions. However, their limited electrical conductivity remains a major obstacle in practical applications. The conventional approach that alleviates this problem is the hybridisation of the polymer with carbon-based additives, but this directly prevents the utilisation of the maximum capacity of the polymers. Here, we report a layer-by-layer fabrication technique where we separated the active (porous polymer, top) layer and the conductive (carbon, bottom) layer and used these “layered” electrodes in a supercapacitor (SC). Through this approach, direct contact with the electrolyte and polymer material is greatly enhanced. With extensive electrochemical characterisation techniques, we show that the layered electrodes allowed a significant contribution of fast faradic surface reactions to the overall capacitance. The electrochemical performance of the layered-electrode SC outperformed other reported porous polymer-based devices with a specific gravimetric capacitance of 388 F·g⁻¹ and an outstanding energy density of 65 Wh·kg⁻¹ at a current density of 0.4 A·g⁻¹. The device also showed outstanding cyclability with 90% of capacitance retention after 5000 cycles at 1.6 A·g⁻¹, comparable to the reported porous polymer-based SCs. Thus, the introduction of a layered electrode structure would pave the way for more effective utilisation of porous organic polymers in future energy storage/harvesting and sensing devices by exploiting their nanoporous architecture and limiting the negative effects of the carbon/binder matrix.     

GET4 is a novel driver gene in colorectal cancer that regulates the localization of BAG6, a nucleocytoplasmic shuttling protein

Colorectal cancer (CRC) is one of the most common types of cancer and a significant cause of cancer mortality worldwide. Further improvements of CRC therapeutic approaches are needed. BCL2‐associated athanogene 6 (BAG6), a multifunctional scaffold protein, plays an important role in tumor progression. However, regulation of BAG6 in malignancies remains unclear. This study showed that guided entry of tail‐anchored proteins factor 4 (GET4), a component of the BAG6 complex, regulates the intercellular localization of BAG6 in CRC. Furthermore, GET4 was identified as a candidate driver gene on the short arm of chromosome 7, which is often amplified in CRC, by our bioinformatics approach using the CRC dataset from The Cancer Genome Atlas. Clinicopathologic and prognostic analyses using CRC datasets showed that GET4 was overexpressed in tumor cells due to an increased DNA copy number. High GET4 expression was an independent poor prognostic factor in CRC, whereas BAG6 was mainly overexpressed in the cytoplasm of tumor cells without gene alteration. The biological significance of GET4 was examined using GET4 KO CRC cells generated with CRISPR‐Cas9 technology or transfected CRC cells. In vitro and in vivo analyses showed that GET4 promoted tumor growth. It appears to facilitate cell cycle progression by cytoplasmic enrichment of BAG6‐mediated p53 acetylation followed by reduced p21 expression. In conclusion, we showed that GET4 is a novel driver gene and a prognostic biomarker that promotes CRC progression by inducing the cytoplasmic transport of BAG6. GET4 could be a promising therapeutic molecular target in CRC.     

Ketoacidosis,Hypertriglyceridemia and Acute Pancreatitis Induced by Soft Drink Polydipsia in a Patient with Occult Central Diabetes Insipidus

A 21-year-old Japanese man without known diabetes mellitus had abdominal pain. The diagnosis was ketoacidosis and hypertriglyceridemia-induced acute pancreatitis. He had polydipsia and polyuria and had habitually drunk several soft drinks every day for two years. After hospitalization, despite adequate liquid intake, dehydration remained with hypotonic polyuria. Further examinations revealed the coexistence of central diabetes insipidus (CDI), possibly caused by lymphocytic infundibulo-neurohypophysitis, based on anti-rabphilin-3A antibody positivity. Although CDI had been undiagnosed for two years, over-consumption of sugar-rich soft drinks to ease thirst caused ketoacidosis, hypertriglyceridemia, and acute pancreatitis. There are no previous reports of this three-part combination of symptoms caused by CDI.     

Creating an appropriate access for endovascular repair by replacing a dissected femoral artery in aortic dissection

Transfemoral endovascular repair has been widely accepted as an effective treatment for type B aortic dissection. However, if the dissection extends to the femoral artery, the transfemoral approach increases the risk of access complications. We describe a case of acute complicated type B aortic dissection involving the dissected bilateral femoral arteries. Successful endovascular repair without access complications was performed through an appropriate access route created by a femoral arterial conduit. We believe that this approach results in reliable cannulation of the true lumen and the reduction of the risk for intimal injury in aortic dissection with the dissected femoral artery.     

The diagnostic value of dual-phase cone-beam CT during hepatic arteriography in transarterial chemoembolization for hepatocellular carcinoma

To evaluate the diagnostic value of dual-phase cone beam CT during hepatic arteriography (CBCTHA) for hepatocellular carcinoma (HCC).Thirty seven patients with unresectable HCC underwent the dual-phase CBCTHA prior to transarterial chemoembolization (TACE). Three blinded observers independently reviewed and compared the first phase CBCTHA images alone and the dual phase CBCTHA images. Diagnostic accuracy was evaluated by the alternative free-response receiver operating characteristic method (Area under the curve: Az value). Sensitivities were analyzed with the paired t test. The analysis was performed for overall HCCs, HCCs up to 1 cm and those larger than 1 cm.For all HCCs and HCCs up to 1 cm, Az value and sensitivity showed no significant difference between the first-phase CBCTHA alone and the dual-phase CBCTHA (Az: 0.81 vs 0.88, P = .07, 0.79 and 0.85, P = .14, sensitivity: 0.61 and 0.73, P = .11, 0.41 and 0.52, P = .33, respectively). For HCCs larger than 1 cm, the mean Az value and sensitivity for the dual-phase CBCTHA were significantly higher than those for the first phase CBCTHA alone (Az: 0.96 vs 0.92, P = .008, sensitivity: 0.85 vs 0.75, P = .013, respectively).The diagnostic accuracy of the dual-phase CBCTHA was superior to that of the first phase CBCTHA alone in the diagnosis of HCC larger than 1 cm.     

Preparation of a platinum nanoparticle catalyst located near photocatalyst titanium oxide and its catalytic activity to convert benzyl alcohols to the corresponding ethers

A novel platinum nanoparticle catalyst closely located near the surface of titanium oxide, PtNP/TiO₂, has been prepared. This catalyst has both the properties of a photocatalyst and a metal nanoparticle catalyst, and acquired environmentally friendly catalytic activity, which cannot be achieved by just one of these catalysts, to afford ethers from benzyl alcohols under the wavelength of 420 nm.

A novel platinum nanoparticle catalyst closely located near the surface of titanium oxide, PtNP/TiO₂, has been prepared. It has catalytic activity to afford ethers from benzyl alcohols under the wavelength of 420 nm.

The electrolysis of water by a heterogeneous metal oxide semiconductor (MOS) photocatalyst, called the Honda–Fujishima effect,¹ received considerable attention because it enables the conversion of solar energy. As a result, photoreactions by heterogeneous photocatalysts based on MOS have been reported until now, including numerous practical applications such as carbon dioxide reduction² and pollutant removal.³Research on photocatalytic reactions using visible light is progressing steadily. Among them, TiO₂ has been extensively studied due to its high catalytic activity, low cost, non-toxicity, and long-term stability.^4,5Titanium oxide has a very strong oxidizing power, but it does not have a strong reducing power.⁶ By using a transition metal such as platinum on titanium oxide as a support, its reducing power can be increased, and the amount of hydrogen generated in the electrolysis of water can be improved eight times compared to the case of titanium oxide alone.⁷Furthermore, when MOS contacts the metal, a potential barrier called Schottky barrier is formed at the interface. The basic characteristic of this Schottky barrier lies in the Schottky barrier height (Φ), which represents the difference between the CB of the MOS distorted by the contact with a metal and the Fermi level (E_F) of the metal. Although it has been studied for almost half a century, how to determine the barrier is still not well understood. Due to the formation of the Schottky barrier height, the energy required to move the electrons from the valence band of MOS to the conductor changes from E_g to Φ, and the energy becomes smaller and it changes to a longer wavelength. As a result, a photoreaction with titanium oxide using light with a wavelength longer than 387 nm has also been reported (Scheme 1)⁸Open in a separate windowScheme 1Effect of sunlight exposure on aerobic oxidation of alcohols with the Pt/TiO₂ catalysts.On the other hand, we have recently developed a sulfur-modified Au-supported Pd NP catalyst (SAPd) that is applicable in Suzuki–Miyaura coupling^9a,9b and C–H functionalization^9c (Scheme 2a). It was constructed by approximately 10 layers of self-assembled Pd(0) NPs (mean size: <5 nm) supported on a sulfur-modified Au surface. We speculated that the self-assembled Pd NPs, which were encapsulated in a sulfated p-xylene polymer matrix,^9d were formed using in situ metal NP and nanospace simultaneous organization (PSSO), as illustrated in Scheme 2b: (i) the reduction of a high-valence metal source, (ii) growth of transition metal NPs, (iii) growth of a matrix with appropriately sized nanopores, and (iv) encapsulation of the metal NPs in these nanopores. To prepare SARu,¹⁰ SANi,¹¹ SAFe(ii),¹² and SAFe(0)¹³ (Scheme 2a), the PSSO method involves the in situ reduction of a noble metal precursor to produce in situ metal NPs.Open in a separate windowScheme 2(a) Preparation of SAPd, SARu, SANi, SAFe(II) and SAFe(0) by combining in situ PSSO with an organic reductant, (b) in situ metal nanoparticle and nanospace simultaneous organization (PSSO) method and the image of the SAPd structure and (c) the preparation of PtNP/TiO₂.In this research project, we decided to create a novel metal NP catalyst having metal NPs near the surface of TiO₂ by substituting the gold-supported SAPd for gold with a titanium oxide (TiO₂) photocatalyst. Alternatively, by substituting the solid gold support for a photocatalyst, we thought that we could create a novel metal NPs catalyst with an unprecedented reactivity by combining the properties of both photocatalyst and metal nanoparticle catalyst (Scheme 2c).     

Structures and conductivities of stable and metastable Li5GaS4 solid electrolytes

Understanding the differences in the structures and defects in the stable crystalline phase and metastable phase is important for increasing the ionic conductivities of a solid electrolyte. The metastable phase often has higher conductivity than the stable phase. In this study, metastable lithium thiogallate, Li₅GaS₄, was synthesized via mechanochemistry and stable Li₅GaS₄ was obtained by heating the metastable phase. The metastable Li₅GaS₄ sample was found to have an antifluorite-type crystal structure with cationic disorder, while the stable phase was found to have a monoclinic crystal structure, similar to that of another solid electrolyte, Li₅AlS₄. In both the structures, the Ga³⁺ cations were surrounded by four S²⁻ anions in tetrahedral coordination. The conductivity of the metastable phase was determined to be 2.1 × 10⁻⁵ S cm⁻¹ at 25 °C, which is 1000 times greater than that of the monoclinic phase. The high conductivity of the metastable phase was achieved owing to cation disorder in the crystal structure.

A metastable antifluorite-type Li₅GaS₄ electrolyte prepared by a mechanochemical process exhibits the highest conductivity of 2.1 × 10⁻⁵ S cm⁻¹ at 25 °C, which is three orders of magnitude higher than that of the heated Li₅GaS₄ samples with the stable phase.     

Facile synthesis of ZnO nanobullets by solution plasma without chemical additives

ZnO nano-bullets were synthesized using solution plasma from only Zn electrode in water without any chemical agents. In this sustainable synthesis system, the rapid quenching reaction at the interface between the plasma/liquid phases facilitates the fast formation of nano-sized materials. The coil-to-pin type electrode geometry, which overcomes the discharge interruption owing to the electrode gap broadening of the typical pin-to-pin type enables the synthesis of numerous nanomaterials through a stable discharge for 1 h. The as-prepared samples exhibited a high crystalline ZnO structure without post calcination, and the length and width were 71.8 and 29.1 nm, respectively. The main exposed facet of ZnO nano-bullets was the (100) crystal facet, but interestingly, the (101) facet was confirmed at the inclined surfaces in the edges. The (101) crystal facet has an asymmetric Zn and O atom arrangement, and it could result in a focused electron density area with relatively high reactivity. Therefore, ZnO nano-bullets are promising materials for applications in advanced technologies.

ZnO nano-bullets were synthesized using only Zn electrode and water by solution plasma and new electrode geometry improved discharge time up to 1 h.