Blue Energy Collection toward All‐Hours Self‐Powered Chemical Energy Conversion

The conversion and transmission of blue energy in the ocean are critical issues. By employing triboelectric nanogenerators (TENGs), blue energy can be harvested but the corresponding electricity transmission and storage are still great challenges. In this work, an automatic high‐efficiency self‐powered energy collection and conversion system is proposed that converts blue energy to chemical energy. A gear‐driven unidirectional acceleration TENG is designed to convert disordered and low‐frequency water wave energy to low voltage and high current DC output. The output bias from the TENG can be used to drive a Ti–Fe₂O₃/FeNiOOH based photoelectrochemical cell under sunlight to produce hydrogen. Moreover, under the situation without sunlight, the self‐powered system can be automatically switched to another working state to charge a Co₃O₄ based lithium‐ion battery. The hydrogen production rate reaches to 4.65 µL min^‐1 under sunlight at the rotation speed of 120 rpm. The conversion efficiency of the whole system is calculated to be 2.29%. The system triggered by photoswitches can automatically switch between two working states with or without sunlight and convert the blue energy to either hydrogen energy or battery energy for easy storage and transmission, which widens the future applications for blue energy.     

Opening Two‐Dimensional Materials for Energy Conversion and Storage: A Concept

The development of two‐dimensional (2D) materials is experiencing a renaissance since the adventure of graphene. 2D materials typically exhibit strong in‐plane covalent bonding and weak out‐of‐plane van der Waals interactions through the interlayer gap. Opening 2D materials is an effective way to alter the physical and chemical properties, such as band gap, conductivity, optical property, thermoelectric property, photovoltaic property and superconductivity. A larger interlayer distance means more accessible active sites for catalysis, an ion‐accessible surface in the interlayer space, which may greatly enhance the performance of 2D materials for energy conversion and storage. Moreover, opening 2D materials by intercalation can change the band filling state and the Fermi level. This review mainly focuses on the opening of 2D materials and their subsequent applications in energy conversion and storage fields, expecting to promote the development of such a new class of materials, namely expanded 2D materials. The exciting progresses of these expanded materials made in both energy conversion and storage devices including solar cells, thermoelectric devices, electrocatalyst, supercapacitors and rechargeable batteries, is presented and discussed in depth. Furthermore, prospects and further developments in these exciting fields of the expanded 2D materials are also commented.     

Earth‐Rich Transition Metal Phosphide for Energy Conversion and Storage

Low‐cost and resourceful transition metal phosphides (TMPs) have gradually received wide acceptance in the energy industry through exhibiting comparable catalytic activity and long‐term stability to traditional catalysts (e.g., Pt/C, LiCoO₂, LiFePO₄, etc.). With the emergence of the research hotspot of TMPs, probing their mechanism of catalytic energy conversion and storage inspired by the superb structure of metal‐phosphorus chelate is of great significance. To this end, recent developments in TMPs with various crystal structures and morphologies have attracted much attention. The design of TMPs ranging from the choice of different transition metals to phosphorus sources has been intensively explored. This research has indicated that multidimensional morphologies of TMPs prominently enrich the patterns of charge storage and electron transportation, and ultra‐nanoscaled TMPs obtained by multiple tools and techniques might challenge the threshold of electrocatalytic reactions. Here, recent developments in synthetic strategies of TMPs from different precursors are classified. The underlying mechanism between the structural and crystallographic characteristics and the tuned properties of TMPs in energy applications is also presented. Additionally, the key trends in structure and morphology characterization of TMPs are highlighted. Future perspectives on the challenges and opportunities facing TMPs catalysts are thereby proposed.     

Solar‐to‐Hydrogen Energy Conversion Based on Water Splitting

Artificial photosynthesis provides a blueprint to harvest solar energy to sustain the future energy demands. Solar‐driven water splitting, converting solar energy into hydrogen energy, is the prototype of photosynthesis. Various systems have been designed and evaluated to understand the reaction pathways and/or to meet the requirements of potential applications. In solar‐to‐hydrogen conversion, electrocatalytic hydrogen and oxygen evolution reactions are key research areas that are meaningful both theoretically and practically. To utilize hydrogen energy, fuel cell technology has been extensively investigated because of its high efficiency in releasing chemical energy. In this review, general concepts of the photosynthesis in green plants are discussed, different strategies for the light‐driven water splitting proposed in laboratories are introduced, the progress of electrocatalytic hydrogen and oxygen evolution reactions are reviewed, and finally, the reactions in hydrogen fuel cells are briefly discussed. Overall, the mass and energy circulation in the solar‐hydrogen‐electricity circle are delineated. The authors conclude that attention from scientists and engineers of relevant research areas is still highly needed to eliminate the wide disparity between the aspirations and realities of artificial photosynthesis.     

Biochemical and thermodynamic analyses of energy conversion in extremophiles

A variety of extreme environments, characterized by extreme values of various physicochemical parameters (temperature, pressure, salinity, pH, and so on), are found on Earth. Organisms that favorably live in such extreme environments are called extremophiles. All living organisms, including extremophiles, must acquire energy to maintain cellular homeostasis, including extremophiles. For energy conversion in harsh environments, thermodynamically useful reactions and stable biomolecules are essential. In this review, I briefly summarize recent studies of extreme environments and extremophiles living in these environments and describe energy conversion processes in various extremophiles based on my previous research. Furthermore, I discuss the correlation between the biological system of electrotrophy, a third biological energy acquisition system, and the mechanism underlying microbiologically influenced corrosion. These insights into energy conversion in extremophiles may improve our understanding of the “limits of life”.

Abbreviations: PPi: pyrophosphate; PPase: pyrophosphatase; ITC: isothermal titration microcalorimetry; SVNTase: Shewanella violacea 5?-nucleotidase; SANTase: Shewanella amazonensis 5?-nucleotidase     

An Approach to Design Highly Durable Piezoelectric Nanogenerator Based on Self‐Poled PVDF/AlO‐rGO Flexible Nanocomposite with High Power Density and Energy Conversion Efficiency

Till date, fabrication of piezoelectric nanogenerator (PNG) with highly durable, high power density, and high energy conversion efficiency is of great concern. Here a flexible, sensitive, cost effective hybrid piezoelectric nanogenerator (HPNG) developed by integrating flexible steel woven fabric electrodes into poly(vinylidene fluoride) (PVDF)/aluminum oxides decorated reduced graphene oxide (AlO‐rGO) nanocomposite film is reported where AlO‐rGO acts as nucleating agent for electroactive β‐phase formation. The HPNG exhibits reliable energy harvesting performance with high output, fast charging capability, and high durability compared with previously reported PVDF based PNGs. This HPNG is capable for harvesting energy from a variety and easy accessible biomechanical and mechanical energy sources such as, body movements (e.g., hand folding, jogging, heel pressing, and foot striking, etc.) and machine vibration. The HPNG exhibits high output power density and energy conversion efficiency, facilitating direct light on different color of several commercial light‐emitting diodes instantly and powers up many portable electronic devices like wrist watch, calculator, speaker, and mobile liquid crystal display (LCD) screen through capacitor charging. More importantly, HPNG retains its performance after long compression cycles (≈158 400), demonstrating great promise as a piezoelectric energy harvester toward practical applications in harvesting biomechanical and mechanical energy for self‐powered systems.     

Dynamically probing ATP‐dependent RNA helicase A‐assisted RNA structure conversion using single molecule fluorescence resonance energy transfer

RNA helicase A (RHA) as a member of DExH‐box subgroup of helicase superfamily II, participates in diverse biological processes involved in RNA metabolism in organisms, and these RNA‐mediated biological processes rely on RNA structure conversion. However, how RHA regulate the RNA structure conversion was still unknown. In order to unveil the mechanism of RNA structure conversion mediated by RHA, single molecule fluorescence resonance energy transfer was adopted to in our assay, and substrates RNA were from internal ribosome entry site of foot‐and‐mouth disease virus genome. We first found that the RNA structure conversion by RHA against thermodynamic equilibrium in vitro, and the process of dsRNA YZ converted to dsRNA XY through a tripartite intermediate state. In addition, the rate of the RNA structure conversion and the distribution of dsRNA YZ and XY were affected by ATP concentrations. Our study provides real‐time insight into ATP‐dependent RHA‐assisted RNA structure conversion at the single molecule level, the mechanism displayed by RHA may help in understand how RHA contributes to many biological functions, and the basic mechanistic features illustrated in our work also underlay more complex protein‐assisted RNA structure conversions.     

Skin‐Inspired Low‐Grade Heat Energy Harvesting Using Directed Ionic Flow through Conical Nanochannels

Low‐grade heat energies are ubiquitous, and most of these energies are untapped as heated river water or seawater. Therefore, it is meaningful and valuable to extract the stored energies in the context of the energy crisis by using a simple device with low‐cost effectiveness. Here, a simple thermoelectric conversion system is shown using directed ionic flow through the biomimetic smart nanochannels, inspired by the human skin. The obtained power density of the nanodevice can ideally be 88.8 W m^?2 with a membrane temperature gradient (ΔT) of 40 °C. As proof of concept, it is demonstrated that the principle can be introduced into simple and portable prototypes to harvest low‐grade heat. Such a thermoelectric conversion apparatus provides a new venue for low‐grade heat harvesting. In addition, this self‐powered system may extend the electronic skin field and find applications in skin prosthetics.     

Photoactivation studies of zinc porphyrin-myoglobin system and its application for light-chemical energy conversion

An artificial zinc porphyrin-myoglobin-based photo-chemical energy conversion system, consisting of ZnPP-Mb or ZnPE(1)-Mb as a photosensitizer, NADP(+) as an electron acceptor, and triethanolamine as an electron donor, has been constructed to mimic photosystem I. The photoirradiated product is able to reduce a single-electron acceptor protein cytochrome c, but cannot catalyze the two-electron reduction of acetaldehyde by alcohol dehydrogenase, thus demonstrating a single electron transfer mechanism. Furthermore, the artificial system can bifunctionally promote oxidoredox reactions, depending on the presence or absence of a sacrificial electron donor, thus suggesting its potential application in electrochemical regeneration steps involved in chemical transformation and/or energy conversion.     

成都麻羊种群能量流动态的初步研究

家畜的能量流和能量的转化效率是家畜生产力的重要指标。在草地生态系统中,草食动物是能量和物质转化的重要环节。草地生态系统的能流,从第一性生产(总初级生产)到第二性生产的最终产品(净次级生产)至少要经过六个转化阶段。要加速能流和提高能量的转     

Luminescence properties of Tm3+ ions single‐doped YF3 materials in an unconventional excitation region

According to the spectral distribution of solar radiation at the earth's surface, under the excitation region of 1150 to 1350 nm, the up‐conversion luminescence of Tm³⁺ ions was investigated. The emission bands were matched well with the spectral response region of silicon solar cells, achieved by Tm³⁺ ions single‐doped yttrium fluoride (YF₃) phosphor, which was different from the conventional Tm³⁺/Yb³⁺ ion couple co‐doped materials. Additionally, the similar emission bands of Tm³⁺ ions were achieved under excitation in the ultraviolet region. It is expected that via up‐conversion and down‐conversion routes, Tm³⁺‐sensitized materials could convert photons to the desired wavelengths in order to reduce the energy loss of silicon solar cells, thereby enhancing the photovoltaic efficiency.     

Heterogeneous Single Atom Electrocatalysis,Where “Singles” Are “Married”

There is an intensive search for heterogeneous single atom catalysts (SACs) of high activity, efficiency, durability, and selectivity for a wide variety of electrocatalytic conversion and chemical reactions, such as the hydrogen evolution reaction (HER), oxygen evolution/reduction reaction (OER and ORR), CO₂ reduction reaction (CO₂ RR), and nitrogen reduction reaction (NRR). With the downsizing from nanoparticles and clusters to single atoms, there are steady changes in the bond and coordination environment for each and every atom involved. Indeed, the single atoms in these electrocatalysts are not “singles”; they are “married” to the supporting surfaces, and their performance is controlled by the bonding and coordination with the substrate surfaces. Herein, an overview is presented on the brief history leading to the rapid development of SACs and their current status, by focusing on their synthesis, control of composition, strategies to realize single atoms with the desired bonds and coordination, and targeted performance in selected reactions. Their applications in the selected spectrum of energy conversion and chemical reactions are discussed, in relation to their structures at varying length scales down to the atomic level. A particular emphasis is placed on on‐going research activities, together with the future perspectives and particular challenges for SACs.     

A Portable and Efficient Solar‐Rechargeable Battery with Ultrafast Photo‐Charge/Discharge Rate

The solar‐rechargeable electric energy storage systems (SEESSs), which can simultaneously harvest and store solar energy, are considered a promising next‐generation renewable energy supply system. However, the difficulty in meeting the demands of higher overall photoelectric conversion and storage efficiency (PCSE) with both high power density and large energy density in the current SEESSs severely limit their practical application. Herein, a new class is demonstrated of portable and highly efficient SEESS that uniquely integrates a perovskite solar module (PSM) and an aluminum‐ion battery (AIB) directly on a bifunctional aluminum electrode without any external circuit. Such nanostructural design in the SEESS not only exhibits fast photo‐charge/discharge rate (less than one minute) with high power density (above 5000 W kg^?1), but also delivers a high energy density (above 43 Wh kg^?1). By rationally matching the maximum power point voltage of PSM with AIB charging voltage, an excellent solar‐charging efficiency of 15.2% and a high PCSE of 12.04% are achieved, which is among the best in all reported portable SEESSs. Moreover, enhanced PCSE is observed as the light intensity decreases, which makes such SEESS immune from the geographical location and climate limitations for diverse practical applications.     

3D Nanostructures for the Next Generation of High‐Performance Nanodevices for Electrochemical Energy Conversion and Storage

Among the different nanostructures that have been demonstrated as promising materials for various applications, 3D nanostructures have attracted significant attention as building blocks for constructing high‐performance nanodevices. Particularly over the last decade, considerable research efforts have been devoted to designing, fabricating, and evaluating 3D nanostructures as electrodes for electrochemical energy conversion and storage devices. Although remarkable progress has been achieved, the performance of electrochemical energy devices based on 3D nanostructures in terms of energy conversion efficiency, energy storage capability, and device reliability still needs to be significantly improved to meet the requirements for practical applications. Rather than simply outlining and comparing different 3D nanostructures, this article systematically summarizes the general advantages as well as the existing and future challenges of 3D nanostructures for electrochemical energy conversion and storage, focusing on photoelectrochemical water splitting, photoelectrocatalytic solar‐to‐fuels conversion from nitrogen and carbon dioxide, rechargeable metal‐ion batteries, and supercapacitors. A comprehensive understanding of these advantages and challenges shall provide valuable guidelines and enlightenments to facilitate the further development of 3D nanostructured materials, and contribute to the achieving more efficient energy conversion and storage technologies toward a sustainable energy future.     

Controllable ZnMgO Electron‐Transporting Layers for Long‐Term Stable Organic Solar Cells with 8.06% Efficiency after One‐Year Storage

Currently, one main challenge in organic solar cells (OSCs) is to achieve both good stability and high power conversion efficiencies (PCEs). Here, highly efficient and long‐term stable inverted OSCs are fabricated by combining controllable ZnMgO (ZMO) cathode interfacial materials with a polymer:fullerene bulk‐heterojunction. The resulting devices based on the nanocolloid/nanoridge ZMO electron‐transporting layers (ETLs) show greatly enhanced performance compared to that of the conventional devices or control devices without ZMO or with ZnO ETLs. The ZMO‐based OSCs maintain 84%–93% of their original PCEs over 1‐year storage under ambient conditions. An initial PCE of 9.39% is achieved for the best device, and it still retains a high PCE of 8.06% after 1‐year storage, which represents a record high value for long‐term stable OSCs. The excellent performance is attributed to the enhanced electron transportation/collection, reduced interfacial energy losses, and improved stability of the nanocolloid ZMO ETL. These findings provide a promising way to develop OSCs with high efficiencies and long device lifetime towards practical applications.     

Solvent-Mediated Synthesis of Functional Powder Materials from Deep Eutectic Solvents for Energy Storage and Conversion: A Review

Developing advanced electrochemical energy storage and conversion (ESC) technologies based on renewable clean energy can alleviate severe global environmental pollution and energy crisis. The efficient preparation of functional electrode materials via a simple, green, and safe synthesis process is the key to the commercial feasibility of these ESC systems. Deep eutectic solvents (DESs) with easy-tunable solvent properties and recyclable features have emerged as novel solvent systems for designing and synthesizing various functional powder materials for ESC devices. In this paper, the application of DESs in the synthesis of energy-related functional powder materials is systematically reviewed. After briefly introducing the classification and synthesis of DESs, their critical roles in synthesizing powder materials are discussed. Then, the recent advances of DES-derived powder materials in ESC, including batteries, fuel cells, supercapacitors, and water splitting, are described in detail from the perspective of preparation-structure-activity. Finally, some challenges and development directions of the DESs-mediated synthesis of powder materials with high electrochemical performance for ESC applications are outlined.     

Spectral‐converting study of Ba9–3(m+n)/2ErmYbnY2Si6O24 (m = 0.005 – 0.2, n = 0 – 0.3) orthosilicate phosphors

Optical materials composed of Ba_9–3(m+n)/2Er_mYb_nY₂Si₆O₂₄ (m = 0.005–0.2, n = 0–0.3) were prepared using a solid‐state reaction. The X‐ray diffraction patterns of the obtained phosphors were examined to index the peak positions. The photoluminescence (PL) excitation and emission spectra of the Er³⁺‐activated phosphors and the critical emission quenching as a function of Er³⁺ content in the Ba_9–3m/2Er_mY₂Si₆O₂₄ structure were monitored. The spectral conversion properties of Er³⁺ and Er³⁺–Yb³⁺ ions doped in Ba₉Y₂Si₆O₂₄ phosphors were elucidated under diode‐laser irradiation at 980 nm. Up‐conversion emission spectra and the dependence of the emission intensity on pump power for the Ba_8.55Er_0.1Yb_0.2Y₂Si₆O₂₄ phosphor were investigated. The desired up‐conversion of the emitted light, which passed through the green, yellow, orange and red regions of the spectrum, was achieved through the use of appropriate Er³⁺ and/or Yb³⁺ concentrations in the host structure and 980 nm excitation light. The up‐conversion mechanism in the phosphors is described by an energy‐level schematic. Copyright © 2015 John Wiley & Sons, Ltd.     

Photo‐Rechargeable Electric Energy Storage Systems

The global energy demand is increasing at the same time as fossil fuel resources are dwindling. Consequently, the search for alternative energy sources is a major topic worldwide. Solar energy is one of the most promising, effective and emission‐free energy sources. However, the energy has to be stored to compensate the fluctuating availability of the sun and the actual energy demand. Photo‐rechargeable electric energy storage systems may solve this problem by immediately storing the generated electricity. Different combinations of solar cells and storage devices are possible. High efficiencies can be achieved by the combination of dye‐sensitized solar cells (DSSC) and capacitors. However, other hybrid devices including DSSCs or organic photovoltaic systems and redox flow batteries, lithium ion batteries and metal air batteries are playing an increasing role in this research field. This Progress Report reviews the state of the art research of photo‐rechargeable batteries based on organic solar cells, as well as storage modules.     

Elucidating the Irreversible Mechanism and Voltage Hysteresis in Conversion Reaction for High‐Energy Sodium–Metal Sulfide Batteries

Irreversible electrochemical behavior and large voltage hysteresis are commonly observed in battery materials, in particular for materials reacting through conversion reaction, resulting in undesirable round‐trip energy loss and low coulombic efficiency. Seeking solutions to these challenges relies on the understanding of the underlying mechanism and physical origins. Here, this study combines in operando 2D transmission X‐ray microscopy with X‐ray absorption near edge structure, 3D tomography, and galvanostatic intermittent titration techniques to uncover the conversion reaction in sodium–metal sulfide batteries, a promising high‐energy battery system. This study shows a high irreversible electrochemistry process predominately occurs at first cycle, which can be largely linked to Na ion trapping during the first desodiation process and large interfacial ion mobility resistance. Subsequently, phase transformation evolution and electrochemical reaction show good reversibility at multiple discharge/charge cycles due to materials' microstructural change and equilibrium. The origin of large hysteresis between discharge and charge is investigated and it can be attributed to multiple factors including ion mobility resistance at the two‐phase interface, intrinsic slow sodium ion diffusion kinetics, and irreversibility as well as ohmic voltage drop and overpotential. This study expects that such understandings will help pave the way for engineering design and optimization of materials microstructure for future‐generation batteries.     

高产大豆品种的高光效特性

利用荧光射光谱技术及荧光诱导动力学技术,研究了不同基因型大豆,高产大豆黑农４０和黑农４１及你燕大豆黑农３７的光能吸收,传递和转化等特性。结果表明,高产大豆的叶绿素（Ｃｈｌ）和类胡萝卜素（Ｃａｒ）的含量增高于黑农３７,但不同的品种种差异幅度有所不同。吸收光谱表明高产大豆叶经体对光能有更强的吸收能力;Ｍｇ＾２＋对高产大豆叶绿体ＰＳＩ和ＰＳⅡ之间激发能分配的有力均高于低产品种;高产大豆叶片ＰＳⅡ原初光能