Enhanced Thermoelectric Properties of Polyaniline Nanofilms Induced by Self‐Assembled Supramolecules

Polyaniline (PANI) is one of the most promising candidates for flexible organic thermoelectric (TE) applications owing to its relatively low cost and high stability. Herein, the self‐assembled supramolecule (SAS) (3,6‐dioctyldecyloxy‐1,4‐benzenedicarboxylic acid) was used as an additive and was introduced into PANI films as a template. Raman spectroscopy, X‐ray diffraction, and conductive atomic force microscopy analyses demonstrated that the highly ordered chain structure of PANI was achieved by chemical interactions between PANI and the SAS. Moreover, the ordered regions in the PANI‐SAS film increased with a decrease in the film thickness. Consequently, the TE properties of PANI‐SAS films were not only much higher than those of PANI films, but they also increased with a decrease in film thickness. The maximum TE power factor of the PANI‐SAS film reached 31 μW m^?1 K^?2, which is approximately six times higher than the power factor of a PANI film with a similar thickness. This work offers a promising way to prepare PANI thin films with enhanced TE properties.     

Tuning Optimum Temperature Range of Bi2Te3‐Based Thermoelectric Materials by Defect Engineering

Bi₂Te₃‐based solid solutions, which have been widely used as thermoelectric (TE) materials for the room temperature TE refrigeration, are also the potential candidates for the power generators with medium and low‐temperature heat sources. Therefore, depending on the applications, Bi₂Te₃‐based materials are expected to exhibit excellent TE properties in different temperature ranges. Manipulating the point defects in Bi₂Te₃‐based materials is an effective and important method to realize this purpose. In this review, we focus on how to optimize the TE properties of Bi₂Te₃‐based TE materials in different temperature ranges by defect engineering. Our calculation results of two‐band model revel that tuning the carrier concentration and band gap, which is easily realized by defects engineering, can obtain better TE properties at different temperatures. Then, the typical paradigms about optimizing the TE properties at different temperatures for n‐type and p‐type Bi₂Te₃‐based ZM ingots and polycrystals are discussed in the perspective of defects engineering. This review can provide the guidance to improve the TE properties of Bi₂Te₃‐based materials at different temperatures by defects engineering.     

添加La的Bi2Te3和Bi0.5Sb1.5Te3热电材料的电磁感应熔炼法制备及其热电性能

在N2气保护下,采用电磁感应法制备了添加La的Bi2Te3和Bi0.5Sb1.5Te3。运用X射线粉末衍射、电感耦合等离子光谱和扫描电子显微镜对材料的物相成分和形貌进行了表征。研究了La对Bi2Te3和Bi0.5Sb1.5Te3热电材料的电导率(σ)、Seebeck系数(S)和热导率(κ)的影响。实验结果表明,添加La明显降低了2种材料的热导率,提高了热电优值(ZT),添加La的Bi0.5Sb1.5Te3的热电优值在室温超过了1。     

Facile One‐Pot Synthesis of Tellurium Nanorods as Antioxidant and Anticancer Agents

Nanorods have been utilized in targeted therapy, controlled release, molecular diagnosis, and molecule imaging owing to their large surface area and optical, magnetic, electronic, and structural properties. However, low stability and complex synthetic methods have substantially limited the application of tellurium nanorods for use as antioxidant and anticancer agents. Herein, a facile one‐pot synthesis of functionalized tellurium nanorods (PTNRs) by using a hydrothermal synthetic system with a polysaccharide–protein complex (PTR), which was extracted from Pleurotus tuber‐regium, as a capping agent is described. PTNRs remained stable in water and in phosphate‐buffered saline and exhibited high hemocompatibility. Interestingly, these nanorods possessed strong antioxidant activity for scavenging 2,2′‐azinobis‐(3‐ethylbenzothiazoline‐6‐sulfonic acid radical cation (ABTS^.+) and 2,2‐diphenyl‐1‐picrylhydrazylhydrate (DPPH) free radicals and demonstrated novel anticancer activities. However, these nanorods exhibited low cytotoxicity toward normal human cells. In addition, the PTNRs effectively induced a decrease in the mitochondrial membrane potential in a dose‐dependent manner, which indicated that mitochondrial dysfunction might play an important role in PTNR‐induced apoptosis. Therefore, this study provides a one‐pot strategy for the facile synthesis of tellurium nanorods with novel antioxidant and anticancer application potentials.     

Fine-Tuning Bi2Te3-Copper Selenide Alloys Enables an Efficient n-Type Thermoelectric Conversion

Bismuth tellurides is one of the most promising thermoelectric (TE) material candidates in low-temperature application circumstances, but the n-type thermoelectric property is relatively low compared to the p-type counterpart and still needs to be improved. Herein, we incorporated different copper selenides (CuSe, Cu₃Se₂ and Cu_2−xSe) into a Bi₂Te₃ matrix to create the alloy by grinding and successive sintering to enable higher thermoelectric performance. The results demonstrated that all alloys achieved n-type TE characteristics and Bi₂Te₃-CuSe exhibited the best Seebeck coefficient and power factor among them. Along with the low thermal conductivity, the maximum dimensionless TE figure of merit (ZT) value of 1.64 at 573 K was delivered for Bi₂Te₃-CuSe alloy, which is among the best reported results in the n-type Bi₂Te₃-based TE materials to the best of our knowledge. The improved TE properties should be related to the co-doping process of Se and Cu. Our investigation shows a new method to enhance the performance of n-type TE materials by appropriate co-doping or alloying.     

含镧的Bi2Te3基化合物的溶剂热合成及微观结构

以BiCl3,LaCl3和Te粉为原料,用溶剂热合成法制备了含稀土元素的单相LaxBi4Te6(x≤1)热电材料纳米粉末.研究发现,三元化合物LaxBi4Te6具有与二元Bi2Te3化合物相同的晶体结构和相似的晶格常数。LaxBi4Te6中的La含量随合成温度升高而增加,但与反应时间没有显著关系。LaxBi4Te6合成粉末的颗粒尺寸在30nm左右,并且几乎与反应温度和反应时间没有关系。在120℃合成的粉末基本上为不规则多面体形状,在150℃及以上温度合成的粉末则趋向于薄片状．并存在一些直径在50～80nm之间的纳米管。     

A New Strategy for Realizing the Conversion of “Homo–Hetero–Homo” Heteroepitaxial Growth in Bi2Te3 and the Thermoelectric Performance

Uncovering the reason for structure‐dependent thermoelectric performance still remains a big challenge. A low‐temperature and easily scalable strategy for synthesizing Bi₂Te₃ nanostring hierarchical structures through solution‐phase reactions, during which there is the conversion of “homo–hetero–homo” in Bi₂Te₃ heteroepitaxial growth, is reported. Bi₂Te₃ nanostrings are obtained through the transformation from pure Bi₂Te₃ hexagonal nanosheets followed by Te?Bi₂Te₃ “nanotop” heterostructures to Bi₂Te₃ nanostrings. The growth of Bi₂Te₃ nanostrings appears to be a self‐assembly process through a wavy competition process generated from Te and Bi³⁺. The conversion of homo–hetero–homo opens up new platforms to investigate the wet chemistry of Bi₂Te₃ nanomaterials. Furthermore, to study the effect of morphologies and hetero/homo structures, especially with the same origin and uniform conditions on their thermoelectric properties, the thermoelectric properties of Bi₂Te₃ nanostrings and Te?Bi₂Te₃ heterostructured pellets fabricated by spark plasma sintering have been investigated separately.     

One‐Pot Hydrothermal Synthesis of Heterostructured ZnO/ZnS Nanorod Arrays with High Ethanol‐Sensing Properties

ZnO/ZnS heterostructured nanorod arrays with uniform diameter and length were synthesized from zinc substrates in a one‐pot procedure by using a simple hydrothermal method. Structural characterization by HRTEM indicated that the heterostructured nanorods were composed of parallel segments of wurtzite‐type ZnO and zinc‐blende ZnS, with a distinct interface along the axial direction, which revealed the epitaxial relationship, ZnO (10$\bar 1$ 0) and ZnS ($\bar 1$ 1$\bar 1$ ). The as‐prepared ZnO/ZnS nanorods showed only two green emissions at around 523 nm and 576 nm. We also found that the nanorods exhibited high sensitivity to ethanol at relatively low temperatures, owing to their smaller size and structure.     

All‐Inorganic Nanocrystals as a Glue for BiSbTe Grains: Design of Interfaces in Mesostructured Thermoelectric Materials

Nano‐ and mesostructuring is widely used in thermoelectric (TE) materials. It introduces numerous interfaces and grain boundaries that scatter phonons and decrease thermal conductivity. A new approach has been developed for the rational design of the interfaces in TE materials by using all‐inorganic nanocrystals (NCs) that serve as a “glue” for mesoscopic grains. For example, circa 10 nm Bi NCs capped with (N₂H₅)₄Sb₂Te₇ chalcogenidometallate ligands can be used as an additive to BiSbTe particles. During heat treatment, NCs fill up the voids between particles and act as a “glue”, joining grains in hot‐pressed pellets or solution‐processed films. The chemical design of NC glue allowed the selective enhancement or decrease of the majority‐carrier concentration near the grain boundaries, and thus resulted in doped or de‐doped interfaces in granular TE material. Chemically engineered interfaces can be used as to optimize power factor and thermal conductivity.     

Synthesis and growth mechanism of Bi2S3 nanoribbons

This article describes a facile solvothermal method by using mixed solvents for the large-scale synthesis of Bi(2)S(3) nanoribbons with lengths of up to several millimeters. These nanoribbons were formed by a solvothermal reaction between Bi(III)-glycerol complexes and various sulfur sources in a mixed solution of aqueous NaOH and glycerol. HRTEM (high-resolution transmission electron microscopy) and SAED (selective-area electron diffraction) studies show that the as-synthesized nanoribbons had predominately grown along the [001] direction. The Bi(2)S(3) nanoribbons prepared by the use of different sulfur sources have a common formation process: the initial formation of NaBiS(2) polycrystals, which serve as the precursors to Bi(2)S(3), the decomposition of NaBiS(2), and the formation of Bi(2)S(3) seeds in the solution through a homogeneous nucleation process; the growth of Bi(2)S(3) nanoribbons occurs at the expense of NaBiS(2) materials. The growth mechanism of millimeter-scale nanoribbons involves a special solid-solution-solid transformation as well as an Ostwald ripening process. Some crucial factors affect nanoribbon growth, such as, solvothermal temperature, volume ratio of glycerol to water, and the concentration of NaOH; these have also been discussed.     

Unexpected Room‐Temperature Ferromagnetism in Nanostructured Bi2Te3

There is an urgent need for the development in the field of the magnetism of topological insulators, owing to the necessity for the realization of the quantum anomalous Hall effect. Herein, we discuss experimentally fabricated nanostructured hierarchical architectures of the topological insulator Bi₂Te₃ without the introduction of any exotic magnetic dopants, in which intriguing room‐temperature ferromagnetism was identified. First‐principles calculations demonstrated that the intrinsic point defect with respect to the antisite Te site is responsible for the creation of a magnetic moment. Such a mechanism, which is different from that of a vacancy defect, provides new insights into the origins of magnetism. Our findings may pave the way for developing future Bi₂Te₃‐based dissipationless spintronics and fault‐tolerant quantum computation.     

Bottom‐Up On‐Surface Synthesis of Two‐Dimensional Graphene Nanoribbon Networks and Their Thermoelectric Properties

Graphene, the one‐atom‐thick two‐dimensional (2D) carbon material, has attracted tremendous interest in both academia and industry due to its outstanding electrical, mechanical, and thermal properties. For electronic applications, the challenging task is to make it as a semiconductor. The bottom‐up synthesis of semiconducting one‐dimensional (1D) nanometer‐wide graphene strips, namely, graphene nanoribbons (GNRs), has attracted much attention owing to its promising electronic, optical, and magnetic properties. In this regard, we report the fabrication of cove‐type 2D GNR networks (GNNs) via the interconnection of 1D self‐assembled GNRs on the surface of Au(111). The cove‐type 2D GNRs networks (GNNs) were fabricated from the GNR, 5‐CGNR‐1‐1 , synthesized using the precursor of DBSP . Annealing of high‐density self‐assembled GNRs on the surface of Au(111) through two‐zone chemical vapour deposition (2Z CVD) successfully generated a 2D interconnected structure with high yield via the fusion and ladder coupling reactions of GNR chains. In order to validate the later fusion reaction, we have also synthesized the GNR, 7‐AGNR‐1‐1 , using the precursor of DBBA . The GNNs, which consist of hybridized metallic‐like and semiconducting GNRs, are a new class of carbon‐based materials. Further, we applied this material for thermoelectric (TE) applications and found a very low cross‐plane thermal conductivity of 0.11 Wm^?1 K^?1, which is one of the lowest value among the carbon‐based materials as well as inorganic semiconductors, while maintaining the cross‐plane electrical conductivity of 188 S m^?1.     

One‐Pot Self‐Templating Synthesis of Pt Hollow Nanostructures and Their Catalytic Properties for CO Oxidation

Nanoporous Pt hollow nanostructures with octahedral and hexagonal frame‐like morphologies were prepared by a novel one‐pot self‐templating route with no assistance from a preformed template or shape‐directing agent. The hexagonal frame‐like Pt hollow structures exhibited significantly enhanced catalytic activity toward CO oxidation reaction compared to the octahedral Pt hollow nanostructures due to the higher oxidation state of Pt.     

Graphene–CdS Nanocomposites: Facile One‐Step Synthesis and Enhanced Photoelectrochemical Cytosensing

Graphene–CdS (GR–CdS) nanocomposites were prepared in a one‐step synthesis in aqueous solution. The synthetic approach was simple and fast, and it may be extended for the synthesis of other GR–metal‐sulfide nanocomposites. The as‐prepared GR–CdS nanocomposite films inherited the excellent electron‐transport properties of GR. In addition, the heteronanostructure of the GR–CdS nanocomposites facilitated the spatial separation of the charge carriers, thus resulting in enhanced photocurrent intensity, which makes it a promising candidate for photoelectrochemical applications. This strategy was used for the fabrication of an advanced photoelectrochemical cytosensor, based on these GR–CdS nanocomposites, by using a layer‐by‐layer assembly process. This photoelectrochemical cytosensor showed a good photoelectronic effect and cell‐capture ability, and had a wide linear range and low detection limit for Hela cells. The as‐synthesized GR–CdS nanocomposites exhibited obviously enhanced photovoltaic properties, which could be an efficient platform for many other high‐performance photovoltaic devices.     

Creating Zipper‐Like van der Waals Gap Discontinuity in Low‐Temperature‐Processed Nanostructured PbBi2nTe1+3n: Enhanced Phonon Scattering and Improved Thermoelectric Performance

Nanoengineered materials can embody distinct atomic structures which deviate from that of the bulk‐grain counterpart and induce significantly modified electronic structures and physical/chemical properties. The phonon structure and thermal properties, which can also be potentially modulated by the modified atomic structure in nanostructured materials, however, are seldom investigated. Employed here is a mild approach to fabricate nanostructured PbBi_2nTe_1+3n using a solution‐synthesized PbTe‐Bi₂Te₃ nano‐heterostructure as a precursor. The as‐obtained monoliths have unprecedented atomic structure, differing from that of the bulk counterpart, especially the zipper‐like van der Waals gap discontinuity and the random arrangement of septuple‐quintuple layers. These structural motifs break the lattice periodicity and coherence of phonon transport, leading to ultralow thermal conductivity and excellent thermoelectric z T.     

Synthesis of Bi2WO6/Bi2O3 Composite with Enhanced Photocatalytic Activity by a Facile One‐step Hydrothermal Synthesis Route

In this study, the characterization and photocatalytic activity of Bi₂WO₆/Bi₂O₃ under visible‐light irradiation was investigated in detail. The results suggested that Bi₂WO₆/Bi₂O₃ can be synthesized by a facile one‐pot hydrothermal route using a super big 200 mL Teflon‐lined autoclave with optimal sodium oleate/Bi molar ratio of 1.25. Through the characterization of Bi₂WO₆/Bi₂O₃ by X‐ray diffraction, scanning electron microscopy, X‐ray photoelectron spectroscopy, Fourier transform infrared, UV‐vis diffuse reflectance spectra and Photoluminescence spectra, it was found that the as‐prepared composite possessed smaller crystallite size and higher visible‐light responsive than the pure Bi₂WO₆. Moreover, it was expected that the as‐prepared composites exhibited enhanced photocatalytic activity for the degradation of Rhodamine B under visible‐light irradiation, which could be ascribed to their improved light absorption property and the reduced recombination of the photogenerated electrons and holes during the photocatalytic reaction. In general, this study could provide a principle method to synthesize Bi₂WO₆/Bi₂O₃ with enhanced photocatalytic activity by one‐step hydrothermal synthesis route for environmental purification.     

Assembly of Na3V2(PO4)3 Nanoparticles Confined in a One‐Dimensional Carbon Sheath for Enhanced Sodium‐Ion Cathode Properties

Structural and morphological control is an effective approach for improvement of electrochemical properties in rechargeable batteries. One‐dimensionally assembled structure composed of NASICON‐type Na₃V₂(PO₄)₃ nanoparticles were fabricated through an electrospinning method to meet the requirements for the development of efficient electrode materials in Na‐ion batteries. High‐temperature treatment of electrospun precursor fibers under an argon flow provides a nonwoven fabric of nanowires comprising crystallographically oriented nanoparticles of NASICON‐type Na₃V₂(PO₄)₃ within a carbon sheath. The mesostructure comprising NASICON‐type Na₃V₂(PO₄)₃ and carbon give a short sodium‐ion transport pass and an efficient electron conduction pass. Electrochemical properties of NASICON‐type Na₃V₂(PO₄)₃ are improved on the basis of one‐dimensional nanostructures designed in the present study.