Showing papers by "Wuhan University of Technology published in 2019"

Ultrathin 2D/2D WO3/g-C3N4 step-scheme H2-production photocatalyst

Abstract: The appropriate interfacial contact of heterojunction photocatalysts plays a critical role in transfer/separation of interfacial charge carriers. Design of two-dimensional (2D)/2D surface-to-surface heterojunction is an effective method for improving photocatalytic activity since greater contact area can enhance interfacial charge transfer rate. Herein, ultrathin 2D/2D WO3/g-C3N4 step-like composite heterojunction photocatalysts were fabricated by electrostatic self-assembly of ultrathin tungsten trioxide (WO3) and graphitic carbon nitride (g-C3N4) nanosheets. The ultrathin WO3 and g-C3N4 nanosheets were obtained by electrostatic-assisted ultrasonic exfoliation of bulk WO3 and a two-step thermal-etching of bulk g-C3N4, respectively. The thickness of ultrathin WO3 and g-C3N4 nanosheets are 2.5–3.5 nm, which is equivalent to 5–8 atomic or molecular layer thickness. This ultrathin layered heterojunction structure can enhance surface photocatalytic rate because photogenerated electrons and holes at heterogeneous interface more easily transfer to surface of photocatalysts. Therefore, the obtained ultrathin 2D/2D WO3/g-C3N4 step-scheme (S-scheme) heterojunction photocatalysts exhibited better H2-production activity than pure g-C3N4 and WO3 with the same loading amount of Pt as cocatalyst. The mechanism and driving force of charge transfer and separation in S-scheme heterojunction photocatalysts are investigated and discussed. This investigation will provide new insight about designing and constructing novel S-scheme heterojunction photocatalysts.

Cocatalysts for Selective Photoreduction of CO2 into Solar Fuels.

Abstract: Photoreduction of CO2 into sustainable and green solar fuels is generally believed to be an appealing solution to simultaneously overcome both environmental problems and energy crisis. The low selectivity of challenging multi-electron CO2 photoreduction reactions makes it one of the holy grails in heterogeneous photocatalysis. This Review highlights the important roles of cocatalysts in selective photocatalytic CO2 reduction into solar fuels using semiconductor catalysts. A special emphasis in this review is placed on the key role, design considerations and modification strategies of cocatalysts for CO2 photoreduction. Various cocatalysts, such as the biomimetic, metal-based, metal-free, and multifunctional ones, and their selectivity for CO2 photoreduction are summarized and discussed, along with the recent advances in this area. This Review provides useful information for the design of highly selective cocatalysts for photo(electro)reduction and electroreduction of CO2 and complements the existing reviews on various semiconductor photocatalysts.

In Situ Irradiated X-Ray Photoelectron Spectroscopy Investigation on a Direct Z-Scheme TiO2 /CdS Composite Film Photocatalyst.

Abstract: Inspired by nature, artificial photosynthesis through the construction of direct Z-scheme photocatalysts is extensively studied for sustainable solar fuel production due to the effectiveness in enhancing photoconversion efficiency. However, there is still a lack of thorough understanding and direct evidence for the direct Z-scheme charge transfer in these photocatalysts. Herein, a recyclable direct Z-scheme composite film composed of titanium dioxide and cadmium sulfide (TiO2 /CdS) is prepared for high-efficiency photocatalytic carbon dioxide (CO2 ) reduction. In situ irradiated X-ray photoelectron spectroscopy (ISI-XPS) confirms the direct Z-scheme charge-carrier migration pathway in the photocatalytic system. Furthermore, density functional theory simulation identifies the intrinsic cause for the formation of the direct Z-scheme heterojunction between the TiO2 and the CdS. Thanks to the significantly enhanced redox abilities of the charge carriers in the direct Z-scheme system, the photocatalytic CO2 reduction performance of the optimized TiO2 /CdS is 3.5, 5.4, and 6.3 times higher than that of CdS, TiO2 , and commercial TiO2 (P25), respectively, in terms of methane production. This work is a valuable guideline in preparation of highly efficient recyclable nanocomposite for photoconversion applications.

Dual Cocatalysts in TiO 2 Photocatalysis.

Abstract: Semiconductor photocatalysis is recognized as a promising strategy to simultaneously address energy needs and environmental pollution. Titanium dioxide (TiO2 ) has been investigated for such applications due to its low cost, nontoxicity, and high chemical stability. However, pristine TiO2 still suffers from low utilization of visible light and high photogenerated-charge-carrier recombination rate. Recently, TiO2 photocatalysts modified by dual cocatalysts with different functions have attracted much attention due to the extended light absorption, enhanced reactant adsorption, and promoted charge-carrier-separation efficiency granted by various cocatalysts. Recent progress on the component and structural design of dual cocatalysts in TiO2 photocatalysts is summarized. Depending on their components, dual cocatalysts decorated on TiO2 photocatalysts can be divided into the following categories: bimetallic cocatalysts, metal-metal oxide/sulfide cocatalysts, metal-graphene cocatalysts, and metal oxide/sulfide-graphene cocatalysts. Depending on their architecture, they can be categorized into randomly deposited binary cocatalysts, facet-dependent selective-deposition binary cocatalysts, and core-shell structural binary cocatalysts. Concluding perspectives on the challenges and opportunities for the further exploration of dual cocatalyst-modified TiO2 photocatalysts are presented.

Direct Z-scheme ZnO/CdS hierarchical photocatalyst for enhanced photocatalytic H2-production activity

Abstract: Herein, ZnO/CdS hierarchical composite was prepared through a hydrothermal and chemical bath deposition (CBD) process. Its photocatalytic H2-production performance was tested. Mass ratio of CdS acted a pivotal part in light absorption and photocatalytic properties. Noticeably, promoted photocatalytic H2-production activity of 4134 μmol g−1 h-1 was achieved by the sample with optimal CdS content. Significantly, the photoluminescence (PL) detection of hydroxyl radicals, as well as the in-situ XPS measurements was selected to verify the direct Z-scheme charge migration mechanism. This mechanism endowed the composite with strong capability for hydrogen evolution and elucidated the improved photocatalytic performance. The improvement of photocatalytic activity was due to hierarchical structure, extended visible light response and direct Z-scheme mechanism. This work will give an innovative vision in constructing direct Z-scheme photocatalytic system with great photocatalytic H2-production activity.

Silicon oxides: a promising family of anode materials for lithium-ion batteries

Abstract: Silicon oxides have been recognized as a promising family of anode materials for high-energy lithium-ion batteries (LIBs) owing to their abundant reserve, low cost, environmental friendliness, easy synthesis, and high theoretical capacity. However, the extended application of silicon oxides is severely hampered by the intrinsically low conductivity, large volume change, and low initial coulombic efficiency. Significant efforts have been dedicated to tackling these challenges towards practical applications. This Review focuses on the recent advances in the synthesis and lithium storage properties of silicon oxide-based anode materials. To present the progress in a systematic manner, this review is categorized as follows: (i) SiO-based anode materials, (ii) SiO2-based anode materials, (iii) non-stoichiometric SiOx-based anode materials, and (iv) Si-O-C-based anode materials. Finally, future outlook and our personal perspectives on silicon oxide-based anode materials are presented.

FCC-ee: The Lepton Collider: Future Circular Collider Conceptual Design Report Volume 2

Abstract: In response to the 2013 Update of the European Strategy for Particle Physics, the Future Circular Collider (FCC) study was launched, as an international collaboration hosted by CERN. This study covers a highest-luminosity high-energy lepton collider (FCC-ee) and an energy-frontier hadron collider (FCC-hh), which could, successively, be installed in the same 100 km tunnel. The scientific capabilities of the integrated FCC programme would serve the worldwide community throughout the 21st century. The FCC study also investigates an LHC energy upgrade, using FCC-hh technology. This document constitutes the second volume of the FCC Conceptual Design Report, devoted to the electron-positron collider FCC-ee. After summarizing the physics discovery opportunities, it presents the accelerator design, performance reach, a staged operation scenario, the underlying technologies, civil engineering, technical infrastructure, and an implementation plan. FCC-ee can be built with today’s technology. Most of the FCC-ee infrastructure could be reused for FCC-hh. Combining concepts from past and present lepton colliders and adding a few novel elements, the FCC-ee design promises outstandingly high luminosity. This will make the FCC-ee a unique precision instrument to study the heaviest known particles (Z, W and H bosons and the top quark), offering great direct and indirect sensitivity to new physics.

In Situ Grown Monolayer N-Doped Graphene on CdS Hollow Spheres with Seamless Contact for Photocatalytic CO2 Reduction.

Abstract: Photocatalytic CO2 reduction is an effective way to simultaneously mitigate the greenhouse effect and the energy crisis. Herein, CdS hollow spheres, on which monolayer nitrogen-doped graphene is in situ grown by chemical vapor deposition, are applied for realizing effective photocatalytic CO2 reduction. The constructed photocatalyst possesses a hollow interior for strengthening light absorption, a thin shell for shortening the electron migration distance, tight adhesion for facilitating separation and transfer of carriers, and a monolayer nitrogen-doped graphene surface for adsorbing and activating CO2 molecules. Achieving seamless contact between a photocatalyst and a cocatalyst, which provides a pollution-free and large-area transport interface for carriers, is an effective strategy for improving the photocatalytic CO2 reduction performance. Therefore, the yield of CO and CH4 , as dominating products, can be increased by four and five times than that of pristine CdS hollow spheres, respectively. This work emphasizes the importance of contact interface regulation between the photocatalyst and the cocatalyst and provides new ideas for the seamless and large-area contact of heterojunctions.

FCC-hh: The Hadron Collider

Abstract: Particle physics has arrived at an important moment of its history. The discovery of the Higgs boson, with a mass of 125 GeV, completes the matrix of particles and interactions that has constituted the “Standard Model” for several decades. This model is a consistent and predictive theory, which has so far proven successful at describing all phenomena accessible to collider experiments. However, several experimental facts do require the extension of the Standard Model and explanations are needed for observations such as the abundance of matter over antimatter, the striking evidence for dark matter and the non-zero neutrino masses. Theoretical issues such as the hierarchy problem, and, more in general, the dynamical origin of the Higgs mechanism, do likewise point to the existence of physics beyond the Standard Model. This report contains the description of a novel research infrastructure based on a highest-energy hadron collider with a centre-of-mass collision energy of 100 TeV and an integrated luminosity of at least a factor of 5 larger than the HL-LHC. It will extend the current energy frontier by almost an order of magnitude. The mass reach for direct discovery will reach several tens of TeV, and allow, for example, to produce new particles whose existence could be indirectly exposed by precision measurements during the earlier preceding e+e– collider phase. This collider will also precisely measure the Higgs self-coupling and thoroughly explore the dynamics of electroweak symmetry breaking at the TeV scale, to elucidate the nature of the electroweak phase transition. WIMPs as thermal dark matter candidates will be discovered, or ruled out. As a single project, this particle collider infrastructure will serve the world-wide physics community for about 25 years and, in combination with a lepton collider (see FCC conceptual design report volume 2), will provide a research tool until the end of the 21st century. Collision energies beyond 100 TeV can be considered when using high-temperature superconductors. The European Strategy for Particle Physics (ESPP) update 2013 stated “To stay at the forefront of particle physics, Europe needs to be in a position to propose an ambitious post-LHC accelerator project at CERN by the time of the next Strategy update”. The FCC study has implemented the ESPP recommendation by developing a long-term vision for an “accelerator project in a global context”. This document describes the detailed design and preparation of a construction project for a post-LHC circular energy frontier collider “in collaboration with national institutes, laboratories and universities worldwide”, and enhanced by a strong participation of industrial partners. Now, a coordinated preparation effort can be based on a core of an ever-growing consortium of already more than 135 institutes worldwide. The technology for constructing a high-energy circular hadron collider can be brought to the technology readiness level required for constructing within the coming ten years through a focused R&D programme. The FCC-hh concept comprises in the baseline scenario a power-saving, low-temperature superconducting magnet system based on an evolution of the Nb3Sn technology pioneered at the HL-LHC, an energy-efficient cryogenic refrigeration infrastructure based on a neon-helium (Nelium) light gas mixture, a high-reliability and low loss cryogen distribution infrastructure based on Invar, high-power distributed beam transfer using superconducting elements and local magnet energy recovery and re-use technologies that are already gradually introduced at other CERN accelerators. On a longer timescale, high-temperature superconductors can be developed together with industrial partners to achieve an even more energy efficient particle collider or to reach even higher collision energies.The re-use of the LHC and its injector chain, which also serve for a concurrently running physics programme, is an essential lever to come to an overall sustainable research infrastructure at the energy frontier. Strategic R&D for FCC-hh aims at minimising construction cost and energy consumption, while maximising the socio-economic impact. It will mitigate technology-related risks and ensure that industry can benefit from an acceptable utility. Concerning the implementation, a preparatory phase of about eight years is both necessary and adequate to establish the project governance and organisation structures, to build the international machine and experiment consortia, to develop a territorial implantation plan in agreement with the host-states’ requirements, to optimise the disposal of land and underground volumes, and to prepare the civil engineering project. Such a large-scale, international fundamental research infrastructure, tightly involving industrial partners and providing training at all education levels, will be a strong motor of economic and societal development in all participating nations. The FCC study has implemented a set of actions towards a coherent vision for the world-wide high-energy and particle physics community, providing a collaborative framework for topically complementary and geographically well-balanced contributions. This conceptual design report lays the foundation for a subsequent infrastructure preparatory and technical design phase.

An Isolated Zinc–Cobalt Atomic Pair for Highly Active and Durable Oxygen Reduction

Abstract: A competitive complexation strategy has been developed to construct a novel electrocatalyst with Zn-Co atomic pairs coordinated on N doped carbon support (Zn/CoN-C). Such architecture offers enhanced binding ability of O2 , significantly elongates the O-O length (from 1.23 A to 1.42 A), and thus facilitates the cleavage of O-O bond, showing a theoretical overpotential of 0.335 V during ORR process. As a result, the Zn/CoN-C catalyst exhibits outstanding ORR performance in both alkaline and acid conditions with a half-wave potential of 0.861 and 0.796 V respectively. The in situ XANES analysis suggests Co as the active center during the ORR. The assembled zinc-air battery with Zn/CoN-C as cathode catalyst presents a maximum power density of 230 mW cm-2 along with excellent operation durability. The excellent catalytic activity in acid is also verified by H2 /O2 fuel cell tests (peak power density of 705 mW cm-2 ).

FCC Physics Opportunities: Future Circular Collider Conceptual Design Report Volume 1

Abstract: We review the physics opportunities of the Future Circular Collider, covering its e+e-, pp, ep and heavy ion programmes. We describe the measurement capabilities of each FCC component, addressing the study of electroweak, Higgs and strong interactions, the top quark and flavour, as well as phenomena beyond the Standard Model. We highlight the synergy and complementarity of the different colliders, which will contribute to a uniquely coherent and ambitious research programme, providing an unmatchable combination of precision and sensitivity to new physics.

Self-smoothing anode for achieving high-energy lithium metal batteries under realistic conditions

Abstract: Despite considerable efforts to stabilize lithium metal anode structures and prevent dendrite formation, achieving long cycling life in high-energy batteries under realistic conditions remains extremely difficult due to a combination of complex failure modes that involve accelerated anode degradation and the depletion of electrolyte and lithium metal. Here we report a self-smoothing lithium–carbon anode structure based on mesoporous carbon nanofibres, which, coupled with a lithium nickel–manganese–cobalt oxide cathode with a high nickel content, can lead to a cell-level energy density of 350–380 Wh kg−1 (counting all the active and inactive components) and a stable cycling life up to 200 cycles. These performances are achieved under the realistic conditions required for practical high-energy rechargeable lithium metal batteries: cathode loading ≥4.0 mAh cm−2, negative to positive electrode capacity ratio ≤2 and electrolyte weight to cathode capacity ratio ≤3 g Ah−1. The high stability of our anode is due to the amine functionalization and the mesoporous carbon structures that favour smooth lithium deposition. Metallic lithium wets a functionalized mesoporous carbon film to create a self-smoothing anode that, in conjunction with a standard lithium nickel–manganese–cobalt cathode, delivers long cycling life, 350 Wh kg−1 high-energy cells under realistic conditions.

Review on Metal Sulphide-based Z-scheme Photocatalysts

Abstract: Semiconductor‐based Z‐scheme heterojunction photocatalysts have received considerable attention for solar energy conversion and environmental purification due to their spatially separated reduction and oxidation sites, effective separation and transportation of photo‐excited charge carriers and strong redox ability. With their wide visible‐light responsive range and high photocatalytic activity, metal sulphide is an important material in developing photocatalysts. This review summarizes and highlights recent research progress in sulphide‐based direct Z‐scheme photocatalysts, followed by analysis on the limitations over all‐solid‐state Z‐scheme photocatalyst. Furthermore, the applications and characterization methods of sulphide‐based direct Z‐scheme photocatalyst are summarized. Finally, the challenges and perspectives of sulphide‐based Z‐scheme photocatalyst are discussed.

A universal synthesis strategy for P-rich noble metal diphosphide-based electrocatalysts for the hydrogen evolution reaction

Abstract: Highly efficient, stable and cost-efficient electrocatalysts for hydrogen generation via water splitting have become in increasing demand for future energy systems. Hitherto, P-rich noble metal polyphosphides which can decrease noble metal (such as Rh, Pd, or Ir) dosage are important to probe potential high-performance HER electrocatalysts. Nevertheless, they are difficult to synthesize at ambient pressure and moderate temperatures. Herein, for the first time, we report a novel iridium diphosphide (IrP2) electrocatalyst embedded within an ultrathin nitrogen-doped carbon (NC) layer (IrP2@NC) synthesized at ambient pressure and moderate temperature (900 °C). Subsequent electrochemical tests revealed that such a P-rich IrP2@NC catalyst possesses the highest hydrogen evolution reaction (HER) activity among all the documented transition metal phosphide electrocatalysts, including the commercial Pt/C, with ultralow overpotentials of 8 and 28 mV to achieve 10 mA cm−2 in 0.5 M H2SO4 and 1.0 M KOH, respectively. Combined density functional theory (DFT) computational studies suggest that the introduction of phosphorus into iridium can weaken the H adsorption strength of IrP2, beneficial for boosting HER activity. More importantly, this synthetic strategy for P-rich IrP2@NC can also be applied to other noble metal diphosphides (RhP2@NC and Pd5P2@NC, etc.). This work presents a particularly efficient and stable P-rich transition metal polyphosphide with advanced HER performance and beyond.

Comprehensive Learning Particle Swarm Optimization Algorithm With Local Search for Multimodal Functions

Abstract: A comprehensive learning particle swarm optimizer (CLPSO) embedded with local search (LS) is proposed to pursue higher optimization performance by taking the advantages of CLPSO’s strong global search capability and LS’s fast convergence ability. This paper proposes an adaptive LS starting strategy by utilizing our proposed quasi-entropy index to address its key issue, i.e., when to start LS. The changes of the index as the optimization proceeds are analyzed in theory and via numerical tests. The proposed algorithm is tested on multimodal benchmark functions. Parameter sensitivity analysis is performed to demonstrate its robustness. The comparison results reveal overall higher convergence rate and accuracy than those of CLPSO, state-of-the-art particle swarm optimization variants.

Additive manufacturing of functionally graded materials: A review

Abstract: Functionally graded materials (FGMs) represent a class of novel materials in which compositions/constituents and/or microstructures gradually change along single or multiple spatial directions, resulting in a gradual change in properties and functions which can be tailored for enhanced performance. FGMs can be fabricated using a variety of well-established processing methods; however, it is also known that there are inherent drawbacks to existing synthesis methods. As an emerging technology that provides a high degree of control over spatial resolution, additive manufacturing (AM) provides an intriguing pathway to circumvent the drawbacks of currently available methods. AM involves the selective deposition of individual layers of single or multiple materials, and as such it offers the potential of local control of composition and microstructure in multiple dimensions; such process conditions, in principle, can be tailored to construct complex FGMs with multi-dimensional and directional gradient structures. In this review paper, our current understanding of important issues, such as modeling, processing, microstructures and mechanical properties, as related to FGMs produced via AM, are described and discussed in an effort to assess the state of the art in this field as well as to provide insight into future research directions.

Review on Recent Progress of All-Inorganic Metal Halide Perovskites and Solar Cells.

Abstract: All-inorganic perovskites are considered to be one of the most appealing research hotspots in the field of perovskite photovoltaics in the past 3 years due to their superior thermal stability compared to their organic-inorganic hybrid counterparts. The power-conversion efficiency has reached 17.06% and the number of important publications is ever increasing. Here, the progress of inorganic perovskites is systematically highlighted, covering materials design, preparation of high-quality perovskite films, and avoidance of phase instabilities. Inorganic perovskites, nanocrystals, quantum dots, and lead-free compounds are discussed and the corresponding device performances are reviewed, which have been realized on both rigid and flexible substrates. Methods for stabilization of the cubic phase of low-bandgap inorganic perovskites are emphasized, which is a prerequisite for highly efficient and stable solar cells. In addition, energy loss mechanisms both in the bulk of the perovskite and at the interfaces of perovskite and charge selective layers are unraveled. Reported approaches to reduce these charge-carrier recombination losses are summarized and complemented by methods proposed from our side. Finally, the potential of inorganic perovskites as stable absorbers is assessed, which opens up new perspectives toward the commercialization of inorganic perovskite solar cells.