Institute of Applied Technology

Abstract The aqueous zinc ion battery has emerged as a promising alternative technology for large-scale energy storage due to its low cost, natural abundance, and high safety features. However, the sluggish kinetics stemming from the strong electrostatic interaction of divalent zinc ions in the host crystal structure is one of challenges for highly efficient energy storage. Oxygen vacancies (VO••), in the present work, lead to a larger tunnel structure along the b axis, which improves the reactive kinetics and enhances Zn-ion storage capability in VO2 (B) cathode. DFT calculations further support that VO•• in VO2 (B) result in a narrower bandgap and lower Zn ion diffusion energy barrier compared to those of pristine VO2 (B). VO••-rich VO2 (B) achieves a specific capacity of 375 mAh g–1 at a current density of 100 mA g–1 and long-term cyclic stability with retained specific capacity of 175 mAh g–1 at 5 A g–1 over 2000 cycles (85% capacity retention), higher than that of VO2 (B) nanobelts (280 mAh g–1 at 100 mA g–1 and 120 mAh g–1 at 5 A g–1, 65% capacity retention).

Principal component analysis (PCA) has been widely applied in the area of computer science. It is well-known that PCA is a popular transform method and the transform result is not directly related to a sole feature component of the original sample. However, in this paper, we try to apply principal components analysis (PCA) to feature selection. The proposed method well addresses the feature selection issue, from a viewpoint of numerical analysis. The analysis clearly shows that PCA has the potential to perform feature selection and is able to select a number of important individuals from all the feature components. Our method assumes that different feature components of original samples have different effects on feature extraction result and exploits the eigenvectors of the covariance matrix of PCA to evaluate the significance of each feature component of the original sample. When evaluating the significance of the feature components, the proposed method takes a number of eigenvectors into account. Then it uses a reasonable scheme to perform feature selection. The devised algorithm is not only subject to the nature of PCA but also computationally efficient. The experimental results on face recognition show that when the proposed method is able to greatly reduce the dimensionality of the original samples, it also does not bring the decrease in the recognition accuracy.

Due to the malicious attacks in wireless networks, physical layer security has attracted increasing concerns from both academia and industry. The research on physical layer security mainly focuses either on the secrecy capacity/achievable secrecy rate/capacity-equivocation region from the perspective of information theory, or on the security designs from the viewpoints of optimization and signal processing. Because of its importance in security designs, the latter research direction is surveyed in a comprehensive way in this paper. The survey begins with typical wiretap channel models to cover common scenarios and systems. The topics on physical-layer security designs are then summarized from resource allocation, beamforming/precoding, and antenna/node selection and cooperation. Based on the aforementioned schemes, the performance metrics and fundamental optimization problems are discussed, which are generally adopted in security designs. Thereafter, the state of the art of optimization approaches on each research topic of physical layer security is reviewed from four categories of optimization problems, such as secrecy rate maximization, secrecy outrage probability minimization, power consumption minimization, and secure energy efficiency maximization. Furthermore, the impacts of channel state information on optimization and design are discussed. Finally, the survey concludes with the observations on potential future directions and open challenges.

Abstract With the potential of achieving high efficiency and low production costs, perovskite solar cells (PSCs) have attracted great attention. However, their unstableness under moist condition has retarded the commercial development. Recently, 2D perovskites have received a lot of attention due to their high moisture resistance. In this work, four quasi 2D quasi perovskites are prepared, then their stability under moist condition is investigated. The surface morphology, crystal structure, optical properties, and photovoltaic performance are measured. Among the four quasi‐2D perovskites, (C6H5CH2NH3)2(FA)8Pb9I28 has the best performance: uniform and dense film, extremely well‐oriented crystal structure, strong absorption, and a high power conversion efficiency (PCE) of 17.40%. The aging tests show that quasi‐2D perovskites are more stable under moist conditions than FAPbI3 is. The (C6H5CH2NH3)2(FA)8Pb9I28 quasi‐2D perovskite devices exhibit high humidity stability, maintaining 80% of the starting PCE after 500 h under 80% relative humidity. Compared with other quasi‐2D perovskites, (C6H5CH2NH3)2(FA)8Pb9I28 has the highest humidity stability, due to their strongest hydrophobicity from C6H5CH2NH3+. This work demonstrates that the properties of perovskite materials can be modified by adding different ammonium salts into FAPbI3. Thus, by introducing ammonium salts with high hydrophobic properties the fabrication of highly efficient and stable 2D PSCs may be possible.

Aqueous Zn-ion batteries (ZIBs) are a potential electrochemical energy storage device because of their highly intrinsic safety, low cost, and large capacity. However, it is still in the primary stage because of the limited selection of cathode materials with high rate and long-life cycling stability. In addition, the energy storage mechanisms of ZIBs have not been well established. In this work, we report the synthesis of porous V 2 O 3 @C materials with high conductivity and further illustrate its application as the intercalation cathode for aqueous zinc-ion batteries. The unique channel and appropriate pore size distribution of corundum-type V 2 O 3 are beneficial to the rapid zinc ion intercalation and removal, leading to a high rate capability. Also, the carbon framework structure achieves a high cyclic stability. The porous V 2 O 3 @C cathode delivers high capacities of 350 mA h g –1 at 100 mA g –1, an excellent rate capability (250 mA h g –1 at 2 A g –1 ), and an impressive long-life cycling stability with 90% capacity retention over 4000 cycles at 5 A g –1 . The storage mechanism of zinc ions in the Zn/V 2 O 3 system was studied by various analytical methods and first-principles calculation.

Portable electronic devices and wireless communication systems enable a broad range of applications such as environmental and food safety monitoring, personalized medicine and healthcare management. Particularly, hybrid smartphone and microfluidic devices provide an integrated solution for the new generation of mobile sensing applications. Such mobile sensing based on microfluidic devices (broadly defined) and smartphones (MS(2)) offers a mobile laboratory for performing a wide range of bio-chemical detection and analysis functions such as water and food quality analysis, routine health tests and disease diagnosis. MS(2) offers significant advantages over traditional platforms in terms of test speed and control, low cost, mobility, ease-of-operation and data management. These improvements put MS(2) in a promising position in the fields of interdisciplinary basic and applied research. In particular, MS(2) enables applications to remote in-field testing, homecare, and healthcare in low-resource areas. The marriage of smartphones and microfluidic devices offers a powerful on-chip operating platform to enable various bio-chemical tests, remote sensing, data analysis and management in a mobile fashion. The implications of such integration are beyond telecommunication and microfluidic-related research and technology development. In this review, we will first provide the general background of microfluidic-based sensing, smartphone-based sensing, and their integration. Then, we will focus on several key application areas of MS(2) by systematically reviewing the important literature in each area. We will conclude by discussing our perspectives on the opportunities, issues and future directions of this emerging novel field.

A mesoporous SnO 2 electrode is firstly introduced in the CH 3 NH 3 PbI 3 perovskite solar cell as the electron-transporting material and scaffold layer with over 10% power conversion efficiency.

Various types of chronic diseases (CD) are the leading causes of disability and death worldwide. While those diseases are chronic in nature, accurate and timely clinical decision making is critically required. Current diagnosis procedures are often lengthy and costly, which present a major bottleneck for effective CD healthcare. Rapid, reliable and low-cost diagnostic tools at point-of-care (PoC) are therefore on high demand. Owing to miniaturization, lab-on-chip (LoC) technology has high potential to enable improved biomedical applications in terms of low-cost, high-throughput, ease-of-operation and analysis. In this direction, research toward developing new LoC-based PoC systems for CD diagnosis is fast growing into an emerging area. Some studies in this area began to incorporate digital and mobile technologies. Here we review the recent developments of this area with the focus on chronic respiratory diseases (CRD), diabetes, and chronic kidney diseases (CKD). We conclude by discussing the challenges, opportunities and future perspectives of this field.

Abstract The organic–inorganic halide CH3NH3PbI3 (MAPbI3) has been the most commonly used light absorber layer of perovskite solar cells (PSCs); however, solution‐processed MAPbI3 films usually suffer from random crystal orientation and high trap density, resulting in inferior power conversion efficiency (PCE) with open circuit voltage (Voc) being typically below 1.2 V for PSC devices. Herein, for the first time an imidazole sulfonate zwitterion, 4‐(1H‐imidazol‐3‐ium‐3‐yl)butane‐1‐sulfonate (IMS), is applied as a bifunctional additive in regular‐structure planar heterojunction PSC devices to regulate the crystal orientation, yielding highly ordered MAPbI3 film and passivating the trap states of the film. Such a dual effect of IMS is fulfilled via coordination interactions between the sulfonate moiety of IMS with the Pb2+ ion and the electrostatic interaction between the imidazole of IMS with the I– ion of MAPbI3. As a result, under a optimized IMS doping ratio of 0.5 wt%, the PSC device exhibits a significant increase in PCE from 18.77% to 20.84%, with suppressed current–voltage hysteresis and promoted ambient stability. Moreover, a high Voc of 1.208 V is achieved under a higher IMS doping ratio of 1.2 wt%, which is the highest Voc for regular‐structure MAPbI3 planar PSC devices based on TiO2 electron transport layer.

The nucleation stage has an important influence on the lead halide perovskite film morphology, and therefore the solar cell performance.

One of the limitations of TiO2 based perovskite solar cells is the poor electron mobility of TiO2. Here, perovskite oxide BaSnO3 is used as a replacement. It has a higher electron mobility and the same perovskite structure as the light harvesting materials. After optimization, devices based on BaSnO3 showed the best performance of 12.3% vs. 11.1% for TiO2.

The orientation of ultrahigh aspect ratio thermally conductive fillers can construct a heat transfer path to enhance the thermal conductivity of composite materials effectively with low filler loading. Nevertheless, single orientation (vertical or horizontal) limited the application of these materials when there was the need for isotropic heat transferring. Here we report a novel strategy to prepare thermally conductive flexible cycloaliphatic epoxy resin nanocomposites with an oriented three-dimensional staggered interconnected network of vertically aligned h-BN (hexagonal boron nitride) platelets and randomly dispersed CNT-NH 2 (aminated carbon nanotubes). In this structure, h-BN platelets coated with magnetic particles could respond to the external magnetic field; however, the CNT-NH 2 couldn’t. The obtained composites exhibited both through-plane (0.98 ± 0.037 W/m·K) and in-plane (0.99 ± 0.001 W/m·K) thermal conductivity enhancement at low h-BN loading of 30 wt %, and also presented excellent electrical insulating properties (<1.2 × 10 –12 S/cm). In addition, the equal value of thermal conductivity of two directions (in-plane and through-plane) was shown when the content of h-BN was about 26.43 wt % and of CNT-NH 2 was 2 wt %, displaying no difference between the thermal conductivity of two directions (in-plane and through-plane). The infrared imaging tests showed the outstanding heat dissipation capability of the composites by capturing the surface temperature variations of a heater with the composites as the heat dissipating material.

We demonstrate a novel simplified close space sublimation (CSS) deposition for growing a high quality CH 3 NH 3 PbI 3 thin film in a low-vacuum and even non-vacuum oven.

With the increasing concerns on security breaches and transaction fraud, highly reliable and convenient personal verification and identification technologies are more and more requisite in our social activities and national services. Biometrics, used to recognize the identity of an individual, are gaining ever-growing popularity in an extensive array of governmental, military, forensic, and commercial security applications. This book focuses on two kinds of advanced biometric recognition technologies, biometric data discrimination and multi-biometrics, while systematically introducing recent research in developing effective biometric recognition technologies. Organized into three main sections, this cutting-edge book explores advanced biometric data discrimination technologies, describes tensor-based biometric data discrimination technologies, and develops the fundamental conception and categories of multi-biometrics technologies

Heterogeneous Internet of Things (IoT) and multi-access mobile edge computing (MA-MEC) are believed as supporting technologies for building a smart city. The advancement and flourish of IoT are facilitating the entry of human society into the Internet of Everything era, which lay the foundation of the smart city. To address the conflict between computation capability and low-cost mobile devices in IoT, the MA-MEC is available for supporting the resource-limited and computation-sensitive services and applications by computation offloading and distributed content delivery/caching. However, deploying cloud computing capability within the radio access network may face serious security threats, which stem from not only the existing technologies and networks but also the MA-MEC-based IoT itself. Therefore, in this paper, the solutions to address the security threats are investigated from physical layer perspectives, since physical layer security technologies have the advantages of achieving perfect secrecy, low-computational complexity, and resource consumption, and good adaptation for channel changes. Specifically, we investigate the secure wiretap coding, resource allocation, signal processing, and multi-node cooperation, along with physical layer key generation and authentication, to cope with the emerging security challenges. Finally, the paper is concluded with some possible future research directions.

Yolk-shell TiO2 microspheres were synthesized via a one-pot template-free solvothermal method building on the aldol condensation reaction of acetylacetone. This unique structure shows superior light scattering ability resulting in power conversion efficiency as high as 11%. This work provided a new synthesis system for TiO2 microspheres from solid to hollow and a novel material platform for high performance solar cells.

Abstract Perovskite solar cells (PSCs) have witnessed astonishing improvement in power conversion efficiency (PCE), more recently, with advances in long‐term stability and scalable fabrication. However, the presence of an anomalous hysteresis behavior in the current density–voltage characteristic of these devices remains a key obstacle on the road to commercialization. Herein, sol–gel‐processed mesoporous boron‐doped TiO2 (B‐TiO2) is demonstrated as an improved electron transport layer (ETL) for PSCs for the reduction of hysteresis. The incorporation of boron dopant in TiO2 ETL not only reduces the hysteresis behavior but also improves PCE of the perovskite device. The simultaneous improvements are mainly ascribed to the following two reasons. First, the substitution of under‐coordinated titanium atom by boron species effectively passivates oxygen vacancy defects in the TiO2 ETL, leading to increased electron mobility and conductivity, thereby greatly facilitating electron transport. Second, the boron dopant upshifts the conduction band edge of TiO2, resulting in more efficient electron extraction with suppressed charge recombination. Consequently, a methylammonium lead iodide (MAPbI3) photovoltaic device based on B‐TiO2 ETL achieves a higher efficiency of 20.51% than the 19.06% of the pure TiO2 ETL based device, and the hysteresis is reduced from 0.13% to 0.01% with the B‐TiO2 based device showing negligible hysteresis behavior.

Abstract Organic–inorganic lead halide perovskites have shown great future for application in solar cells owing to their exceptional optical and electronic properties. To achieve high‐performance perovskite solar cells, a perovskite light absorbing layer with large grains is desirable in order to minimize grain boundaries and recombination during the operation of the device. Herein, a simple yet efficient approach is developed to synthesize perovskite films consisting of monolithic‐like grains with micrometer size through in situ deposition of octadecylamine functionalized single‐walled carbon nanotubes (ODA‐SWCNTs) onto the surface of the perovskite layer. The ODA‐SWCNTs form a capping layer that controls the evaporation rate of organic solvents in the perovskite film during the postthermal treatment. This favorable morphology in turn dramatically enhances the short‐circuit current density of the perovskite solar cells and almost completely eliminates the hysteresis. A maximum power conversion efficiency of 16.1% is achieved with an ODA‐SWCNT incorporated planar solar cell using (FA0.83MA0.17)0.95Cs0.05Pb(I0.83Br0.17)3 as light absorber. Furthermore, the perovskite solar cells with ODA‐SWCNT demonstrate extraordinary stability with performance retention of 80% after 45 d stability testing under high humidity (60–90%) environment. This work opens up a new avenue for morphology manipulation of perovskite films and enhances the device stability using carbon material.

TiO2 microspheres are of great interest for a great deal of applications, especially in the solar cell field. Because of their unique microstructure and light-scattering effect, TiO2 microsphere-based solar cells often exhibit superior photovoltaic performance. Hence, exploring new suitable TiO2 microspheres for high-efficiency solar cells is essential. In this work, we demonstrate a facile one-pot solvothermal approach for synthesis of TiO2 microspheres using acetone as solvent. The as-prepared TiO2 microspheres are composed of densely interconnected nanocrystals and possess a high specific surface area up to 138.47 m(2) g(-1). As the photoanode, the TiO2 microsphere-based DSSC gives higher dye loading and light adsorption ability as well as longer electron lifetime, resulting in higher short-circuit current value and superior power conversion efficiency (PCE) compared with Dyesol 18 nm TiO2 nanoparticle paste. Finally, the TiO2 microsphere-based DSSC were optimized by adding a TiO2 nanocrystal underlayer and TiCl4 post-treatment, giving a high PCE of 10.32%.

The promising candidate La-BaSnO 3 provides a novel perspective on the application and investigation of doped materials in PSCs.