Energy Conversion Technologies Research Articles

Editorial on the Special Issue “Progresses in Electrochemical Energy Conversion and Storage—Materials, Structures and Simulation”—Towards Better Electrochemical Energy Conversion and Storage Technologies

Editorial on the Special Issue “Progresses in Electrochemical Energy Conversion and Storage—Materials, Structures and Simulation”—Towards Better Electrochemical Energy Conversion and Storage Technologies

Ni-Doped SFM Double-Perovskite Electrocatalyst for High-Performance Symmetrical Direct-Ammonia-Fed Solid Oxide Fuel Cells.

Ammonia has emerged as a promising fuel for solid oxide fuel cells (SOFCs) owing to its high energy density, high hydrogen content, and carbon-free nature. Herein, the electrocatalytic potential of a novel Ni-doped SFM double-perovskite (Sr1.9Fe0.4Ni0.1Mo0.5O6-δ) is studied, for the first time, as an alternative anode material for symmetrical direct-ammonia SOFCs. Scanning and transmission electron microscopy characterization has revealed the exsolution of Ni-Fe nanoparticles (NPs) from the parent Sr2Fe1.5Mo0.5O6 under anode conditions, and X-ray diffraction has identified the FeNi3 phase after exposure to ammonia at 800 °C. The active-exsolved NPs contribute to achieving a maximal ammonia conversion rate of 97.9% within the cell's operating temperatures (550-800 °C). Utilizing 3D-printed symmetrical cells with SFNM-GDC electrodes, the study demonstrates comparable polarization resistances and peak power densities of 430 and 416 mW cm-2 for H2 and NH3 fuels, respectively, with long-term stability and a negligible voltage loss of 0.48% per 100 h during ammonia-fed extended galvanostatic operation. Finally, the ammonia consumption mechanism is elucidated as a multistep process involving ammonia decomposition, followed by hydrogen oxidation. This study provides a promising avenue for improving the performance and stability of ammonia-based SOFCs for potential applications in clean energy conversion technologies.

Electrochemical synthesis of Mn–Ni–S on titania nanotubes as new dual-function electrodes for photo-assisted asymmetric supercapacitors

Photo-assisted energy storage systems, by which solar energy can be both converted and stored, have been of interest in the past few years. Novel energy conversion and storage technology is offered by photo-supercapacitors through the combination of an energy collecting unit and a supercapacitor. This dual-application system effectively generates and stores power in a single device, which makes it appropriate for various purposes. In this work, the electrochemical anodization-electrodeposition has been employed to fabricate manganese-nickel sulfide (Mn–Ni–S) nanostructures on titania nanotubes (TNs) and used them as photoelectrodes in photo-supercapacitors. The high surface area and improved properties make TNs considerably important for energy production and storage. Photoelectrochemical analysis was carried out in a three-electrode system under a xenon (Xe) lamp irradiation using the film prepared as the photoelectrode. The highest photocurrent and photovoltage were shown by MnNiS-3/TN electrode, indicating its superior photosensitivity. Upon illumination under a 0.7 mA/cm2 current density, the area-specific capacitance of MnNiS-3/TN electrode increased from 388.3 to 723.3 mF/cm2, which is 2.0, 3.6, and 12.8 times higher than the corresponding values for NiS/TN, MnS/TN, and bare TN electrodes under similar conditions, respectively. This indicates the considerable enhancement of the capacitance of this electrode induced by light. The desirable light-sensitive properties of MnNiS/TN make it capable of simultaneous solar energy harvesting and storage. Light sensitivity makes it possible to charge MnNiS/TN optically. More importantly, upon light irradiation, the capacity can be increased from 374.7 to 630.2 mF/cm2 (current density 0.5 mA/cm2) compared to the corresponding value in the dark. Using MnNiS-3/TN as the best photoelectrode and MnS/FTO, NiS/FTO, MnNiS-1/FTO, MnNiS-2/FTO, and MnNiS-3/FTO as the counter electrodes, photo-charged through light illumination on their surfaces, five asymmetric solid-state photo-supercapacitors (ASSPS) were prepared. MnNiS-3/TN//MnNiS-3/FTO device showed the largest CV curve area, which indicated its highest areal capacitance. High capacitance gain under irradiation (155.7% at 2.0 mA/cm2) and outstanding capacitance maintenance (97.9% over 10000 cycles) were shown by this ASSPS. Furthermore, a great energy density of 4855.4 mWh/cm2 was shown by the MnNiS-3/TN//MnNiS-3/FTO device under light irradiation. This research introduces a novel approach to the development of powerful solar energy conversion/storage devices.

Efficiently all-weather anti-icing and de-icing coatings enabled by polyaniline microcapsules encapsulated phase change materials

Photothermal superhydrophobic coatings are one of the most promising anti-icing/de-icing materials. However, the intermittence of light energy limits the application of photothermal energy conversion technologies when continuous de-icing is required. Herein, an innovative solution for the integration of photothermal effect and phase change thermal storage was proposed. In this work, an efficient anti-icing/de-icing coating was successfully fabricated based on multifunctional polyaniline microcapsule encapsulating butyl stearate (BS). Benefiting from the heat storage capacity of BS in the microcapsule, the coating could achieve all-weather anti-icing capability. Under the condition of −20 °C, the freezing time of water droplets on the coating with only 10 wt% microcapsules was delayed by about 12.6 times compared to the blank coating. At the same time, under simulated dark conditions, the freezing time of water droplets could be delayed by about 14.1 times. Moreover, owing to the thermal conductivity and high solar energy exploitation, polyaniline endowed the coating with outstanding photothermal de-icing performance, presenting the superiority of outdoor applications. Under NIR (200 mW/cm2) illumination, the melting time of water droplets was reduced to 18 s, which was nearly 10 times faster than that on the blank coating. Moreover, the polyaniline microcapsules also possessed outstanding anticorrosion property, which was particularly attractive for mental coating applications. The combined properties of this all-weather anti-icing and de-icing coating could render it a promising contender for challenging outdoor applications.

Thermodynamic investigation of biomass-steam gasification in converter vaporisation flue for synthesis gas production

Biomass gasification for hydrogen production is a highly promising technology for energy conversion and utilisation. This paper proposed a novel technology for the injection of biomass and steam into the flue of a converter vaporisation to produce hydrogen-rich syngas. The feasibility of hydrogen generation through gasification between biomass, steam, and carbon dioxide in the high-temperature flue gas was investigated based on the thermodynamic principle of Gibbs free energy minimisation. The influence of gasification parameters on the composition of syngas was also explored. The results indicate that in the gasification process, biomass and steam injected into the converter vaporisation flue can effectively inhibit the generation of by-products such as tar. As the steam volume increases, the volume fraction of hydrogen in the product also increases, while the concentration of carbon monoxide decreases. By adjusting the steam-to-biomass ratio, syngas with a hydrogen content exceeding 20% can be produced. At a reaction temperature of 1200 °C, with a steam addition of 5%, a biomass addition of 8 g/L, and a [Formula: see text] ratio of 3, the gas products are composed of 25% hydrogen and 67% carbon dioxide. The process has the potential to achieve a hydrogen yield of up to 90%, a syngas yield of 94%, and a CO2 conversion rate of 70%. Additionally, the lower heating value of the syngas is measured at 11.24 MJ/Nm3. The research results have confirmed the viability of the new technology, thus establishing a theoretical foundation for the industrial implementation of injecting biomass and steam into the converter vaporisation flue to produce hydrogen-rich syngas.

Construction of NiFe/MnNiCo-LDH heterostructure for enhanced oxygen evolution reaction for efficient water splitting

Developing highly efficient and cost-effective oxygen evolution reaction (OER) catalysts is pivotal for advancing sustainable energy storage and conversion technologies. Herein, NiFe/MnNiCo-LDH was successfully prepared by in-situ growth method. The OER performance of this composite material had been significantly enhanced through bimetallic atom modification and cation doping strategies. These modifications not only enhanced the electronic conductivity but also regulated the electron distribution within the catalyst structure. As a result, NiFe/MnNiCo-LDH can reach a current density of 10 mA cm−2 at an overpotential of only 227 mV in the OER reaction. Moreover, the catalyst exhibited remarkable durability and maintained its high performance over an extended period of 48 h during the water splitting reaction. In this work, the potential of dual modification methods for optimizing catalytic properties of OER materials was investigated.

Advancements in Amorphous Oxides For Electrocatalytic Carbon Dioxide Reduction

Electrocatalytic CO2 reduction (ECR) is a crucial energy conversion technology that transforms CO2 into value-added chemicals, reducing reliance on fossil fuels and advancing energy transitions. Designing high-performance catalysts is pivotal for widespread adoption of CO2 reduction reactions, aiming for high activity, selectivity, and stability. Amorphous oxides represent a burgeoning frontier in this field, attracting attention due to their abundant active sites that refine the catalyst structure-performance relationship. This paper aims to provide an overview of recent advances in using amorphous oxides for ECR. We begin by introducing the basic theory of electrocatalytic CO2 reduction, followed by discussing current synthesis approaches for amorphous oxides in CO2 reduction, focusing on optimization strategies for these catalysts. Finally, we address challenges and future perspectives of amorphous oxides in ECR, aiming to foster the development of more efficient catalyst designs.

Integrating NiSe2-MoSe2 heterojunctions with N-doped porous carbon substrate architecture for an enhanced electrocatalytic water splitting device

The development of sustainable energy technologies relies on the exploitation of efficient and durable electrocatalysts for water splitting at high current densities. Our work presents a novel bifunctional catalyst, denoted as NM@NC/CC, which combines the benefits of NiSe2-MoSe2 heterojunctions with nitrogen-enriched porous carbon derived from metal-organic frameworks (MOFs). The integration of these components is designed to harness their combined advantages, which include enhanced electron transfer, improved mass and gas evolution dynamics, and an increased number of catalytically active sites. These features collectively optimize the energetics for both the hydrogen evolution reaction (HER) and oxygen evolution reaction (OER). As a result, the catalyst facilitates rapid kinetics for the overall water-splitting process. The NM@NC/CC demonstrates low overpotentials, requiring only 91 mV for the HER and 280 mV for the OER to reach a current density of 10 mA cm−2. Even at higher current densities of 100 mA cm−2 for HER and 50 mA cm−2 for OER, the overpotentials are only 159 mV and 350 mV, respectively. Additionally, a two-electrode setup using this catalyst achieves a current density of 10 mA cm−2 with a minimal cell voltage of 1.56 V. The insights gained from this study will contribute to the advancement of electrocatalysts for energy conversion technologies.

Ultra-wideband solar absorber via vertically structured GDPT metamaterials

We explore a new solar absorber via vertically structured metamaterials integrating 2D graphene, dielectric layers of silica (SiO2), aluminum oxide (Al2O3), and phase-transition vanadium dioxide (VO2) graphene, dielectric, phase transition (GDPT), achieving broadband absorption and polarization independence. Applying the finite-difference time-domain (FDTD) method, the optical performance of the absorber is analyzed under the normal incidence of a plane wave spanning wavelengths from 250 to 4000 nm. Particularly, our investigation reveals a broad bandwidth exceeding 90 % absorption, spanning 3559 nm from 250 to 3809 nm, with an impressive average absorption efficiency of over 95.9 %. Significantly, the absorber demonstrates polarization independence and insensitivity to large angles of incidence, enhancing its practical capability. We illuminate the important role of Fabry-Perot resonance in absorption by precisely tuning layer thicknesses to induce interference effects. The integration of graphene, dielectric layers, and VO2, augmented by Fabry-Perot resonance, provides a vital foundation for high-performance solar energy conversion technology. This technology has important applications in efficient and broadband solar absorbers, and these absorbers can maintain high performance under different conditions. Our goal is to solve current technological challenges and contribute to the development of next-generation solar energy conversion for various photon technologies, such as energy harvesting, electromagnetic wave capture, and photovoltaic devices.

Effects of corrugation on convective heat transfer and power generation in a wavy walled triangular cavity equipped with inclined elastic fin and piezo-energy harvester assembly

Piezoelectric energy harvesters are one of the energy conversion technologies that can be used to convert a variety of external sources, including wind, fluid motion, and vibrations, into electrical energy. This work suggests a novel wall corrugation design in addition to an elastic fin piezo assembly arrangement for power generation and thermal management in a triangular cavity during turbulent forced convection of air. Using the finite element method with ALE, the analysis is conducted for different values of fin inclination (γ between 0 and 60), corrugation amplitude (Af between 0.01H and 0.06H), corrugation frequency (Nf between 1 and 20) and fin distance from the mid-point of the inclined wall in wall direction. The average Nusselt number (Nu) and generated power (PW) show a non-linear increasing trend with increasing fin tilt. Average Nu increment factor becomes 5.17 with the highest fin inclination while the power increments become 11.6 and 4.46 when rising inclination from 30 to 45 and from 45 to 60. The generated power rises with higher corrugation amplitude and wave number. However, increasing the wave number results in thermal performance degradation. Increment of average Nu becomes 1.17 with highest corrugation amplitude while it declines by a factor of 10.3 at the highest wave number. Power enhancement factors of 5.73 and 2.32 are obtained by increasing the corrugation amplitude from Af = 0.0714H to Af = 0.1786H and from Af = 0.1786H to Af = 0.2143H. When fin positions sf = 0.7143H and sf = -0.7143H are compared with the case of fin location at sf = 0, the power increment factors become 12.27 and 4.76, respectively. For the power produced by the piezo device, a polynomial type correlation is suggested by adjusting the parameters of the corrugated wall.

Polarization-dependent near-field coupling and far-field harmonic modulation in a graphene-based plasmonic nanostructure

The interplay between light and matter has fostered innovative research in surface plasmons, specifically in graphene, due to its tunable Fermi energy and reduced losses in the infrared and terahertz spectra. This study explores the anisotropic coupling of nonlocalized surface plasmons in graphene with localized magnetic polaritons (MP) in a silicon carbide (SiC) array. By adjusting graphene’s Fermi energy and polarization angle, we successfully achieved hybrid coupling, giving rise to three clearly distinguishable hybridized states. Using the coupled oscillator model as a framework, we conducted an analysis of the intricate multimode coupling and accurately ascertained the weighting efficiencies of the individual modes comprising the hybrids. By integrating the design principles of space-time coding metasurfaces, we successfully broadened the scope of the application, extending its reach from the near-field to the far-field. These novel discoveries pave new paths for advancements in thermal emitters, photonic systems, energy conversion technologies, and the creation of cutting-edge plasmonic devices.

A core-shell structured catalyst for enhanced oxygen evolution: NiFe double hydroxide coating over phosphorus -modified NiMoO4 nanorod cores

In this paper, we innovatively employed low-temperature phosphorization technology to successfully incorporate P doping into NiMoO4 nanorods. Subsequently, utilizing the electrodeposition method with a solution rich in Ni²⁺ and Fe³⁺ as the electrolyte, we delicately tuned the process to identify the optimal deposition time, achieving a uniform coating of NiFe LDH on the surface of the P-doped NiMoO4 nanorods. This led to the construction of a three-dimensional core-shell structured NiFe LDH@P-NiMoO4 composite material. To validate the performance of this composite, we conducted thorough structural characterization and electrochemical oxygen evolution reaction (OER) performance tests. The experimental results revealed that in a 1 M KOH electrolyte environment, when the current density reached 100 mA cm⁻², the composite exhibited exceptionally superior OER performance, with an overpotential of merely 267 mV and a Tafel slope as low as 93 mV dec⁻¹, firmly demonstrating its remarkable catalytic efficiency. Furthermore, the composite displayed good stability and durability during prolonged testing, providing a solid foundation for its practical application. In summary, this work not only paves a new way for the preparation of high-performance non-precious metal OER electrocatalysts but also provides robust support for the realization of efficient and stable energy conversion and storage technologies.

Enhanced ORR kinetics and stability through synergy of Pt-Ni clustering and porous N-doped C/Ca aerogel support

The oxygen reduction reaction (ORR) is fundamental in numerous electrochemical energy conversion technologies, necessitating efficient catalysts to enhance reaction kinetics and reduce precious metal usage. This study focuses strategic clustering of Pt-Ni on Calcium Oxide/activated carbon (C/Ca) aerogels. Electrochemical analyses confirmed that incorporating Ni into Pt matrices significantly enhanced ORR activities with Pt25Ni75-C/Ca composition emerged as optimum. A positive shift in half-wave potential (905 mV vs. RHE) and impressive mass activity (72.50 Ag−1 at 85 V) highlight the potential of this composite as a highly effective and stable ORR catalyst. Pt-C/Ca demonstrated performance fluctuation, while Pt25Ni75-C/Ca showed remarkable stability after 40,000 cycles. Furthermore, C/Ca aerogels exhibited a significantly increased BET surface area, and the presence of Pt-Ni/pyridinic-N species on its surface C/Ca aerogel provided supplementary active sites that facilitated the adsorption and reduction of O2 during ORR.

Trifunctional Graphene-Sandwiched Heterojunction-Embedded Layered Lattice Electrocatalyst for High Performance in Zn-Air Battery-Driven Water Splitting.

Zn-air battery (ZAB)-driven water splitting holds great promise as a next-generation energy conversion technology, but its large overpotential, low activity, and poor stability for oxygen reduction reaction (ORR), oxygen evolution reaction (OER), and hydrogen evolution reaction (HER) remain obstacles. Here, a trifunctional graphene-sandwiched, heterojunction-embedded layered lattice (G-SHELL) electrocatalyst offering a solution to these challenges are reported. Its hollow core-layered shell morphology promotes ion transport to Co3S4 for OER and graphene-sandwiched MoS2 for ORR/HER, while its heterojunction-induced internal electric fields facilitate electron migration. The structural characteristics of G-SHELL are thoroughly investigated using X-ray absorption spectroscopy. Additionally, atomic-resolution transmission electron microscopy (TEM) images align well with the DFT-relaxed structures and simulated TEM images, further confirming its structure. It exhibits an approximately threefold smaller ORR charge transfer resistance than Pt/C, a lower OER overpotential and Tafel slope than RuO₂, and excellent HER overpotential and Tafel slope, while outlasting noble metals in terms of durability. Ex situ X-ray photoelectron spectroscopy analysis under varying potentials by examining the peak shifts and ratios (Co2+/Co3+ and Mo4+/Mo6+) elucidates electrocatalytic reaction mechanisms. Furthermore, the ZAB with G-SHELL outperforms Pt/C+RuO2 in terms of energy density (797Wh kg-1) and peak power density (275.8mW cm-2), realizing the ZAB-driven water splitting.

Advancing flexible thermoelectrics for integrated electronics.

With the increasing demand for energy and the climate challenges caused by the consumption of traditional fuels, there is an urgent need to accelerate the adoption of green and sustainable energy conversion and storage technologies. The integration of flexible thermoelectrics with other various energy conversion technologies plays a crucial role, enabling the conversion of multiple forms of energy such as temperature differentials, solar energy, mechanical force, and humidity into electricity. The development of these technologies lays the foundation for sustainable power solutions and promotes research progress in energy conversion. Given the complexity and rapid development of this field, this review provides a detailed overview of the progress of multifunctional integrated energy conversion and storage technologies based on thermoelectric conversion. The focus is on improving material performance, optimizing the design of integrated device structures, and achieving device flexibility to expand their application scenarios, particularly the integration and multi-functionalization of wearable energy conversion technologies. Additionally, we discuss the current development bottlenecks and future directions to facilitate the continuous advancement of this field.

Manipulating the Electronic Properties of an Fe Single Atom Catalyst via Secondary Coordination Sphere Engineering to Provide Enhanced Oxygen Electrocatalytic Activity in Zinc-Air Batteries.

Oxygen reduction and evolution reactions are two key processes in electrochemical energy conversion technologies. Synthesis of nonprecious metal, carbon-based electrocatalysts with high oxygen bifunctional activity and stability is a crucial, yet challenging step to achieving electrochemical energy conversion. Here, an approach to address this issue: synthesis of an atomically dispersed Fe electrocatalyst (Fe1/NCP) over a porous, defect-containing nitrogen-doped carbon support, is described. Through incorporation of a phosphorus atom into the second coordination sphere of iron, the activity and durability boundaries of this catalyst are pushed to an unprecedented level in alkaline environments, such as those found in a zinc-air battery. The rationale is to delicately incorporate P heteroatoms and defects close to the central metal sites (FeN4P1-OH) in order to break the local symmetry of the electronic distribution. This enables suitable binding strength with oxygenated intermediates. In situ characterizations and theoretical studies demonstrate that these synergetic interactions are responsible for high bifunctional activity and stability. These intrinsic advantages of Fe1/NCP enable a potential gap of a mere 0.65V and a high power density of 263.8mWcm-2 when incorporated into a zinc-air battery. These findings underscore the importance of design principles to access high-performance electrocatalysts for green energy technologies.

Co/CoOx–N–C bifunctional nanocatalyst derived from carbothermally optimized graphene networks with in-situ formed zeolitic imidazolate framework for high performance zinc-air batteries

Rechargeable zinc-air batteries are underpinned by high-performance and durable bifunctional oxygen electrocatalysts. Among the platinum-group metals (PGMs)-free catalysts, the redox-active cobalt-nitrogen-carbon (Co/CoOx–N–C) based materials are promising, however require further structural improvements. This work utilises extremely porous graphene networks (EGO) of hierarchical porosity to in-situ grow ZIF-67 nanocrystals extensively and homogeneously within the porous structure. A simple carbonization of nanoZIF-67@EGO not only generates finely dispersed redox capable Co/CoOx–N–C active sites with the help of residual oxygen functional groups of EGO, but also produces 2-3 dimensional hierarchical porous and conducting structure, readily facilitating high electrochemical surface area. This characteristic structure synergistically contributes to rapid charge and mass transfer rates along with high activity and stability for both ORR and OER. Here, it is worth mentioning that to produce equivalent catalyst material involving different graphitic or template supports requires prolonged and multi-step synthesis routes. The optimized catalyst delivers low potential difference of 0.86 V for bifucntional activity by offering superb ORR half-wave potential of 0.83 V vs RHE and limiting current density of 5.85 mA cm−2 in 0.1 M KOH electrolyte. Zinc-air battery exhibits peak power density of ∼175 mW cm−2 and specific capacity of ∼767 mAh g−1, along with durable cycling round trip efficiency of >63 % (correspond to low voltage gap of ∼0.74 V). These characteristics are better than numerous M–N–C based catalysts reported in the literature. This new strategy holds a great potential to boost the development of diverse MOFs and carbon-based electrocatalysts for a wide range of energy storage and conversion technologies.

Vacancy-rich heterogeneous MnCo2O4.5@NiS electrocatalyst for highly efficient overall water splitting

Alkaline water electrolysis is regarded as a promising technology for sustainable energy conversion. Spinel oxides have attracted considerable attention as potential catalysts because of their diverse metal valence states. However, achieving the required current densities at low voltages is a challenge due to its limited active sites and suboptimal electron transport. In this study, we present a novel bifunctional catalyst composed of MnCo2O4.5 nanoneedles grown on NiS nanosheets for water electrolysis. Remarkably, MnCo2O4.5@NiS demonstrates exceptional catalytic activity, requiring 187 and 288 mV to achieve a current density of 100 mA cm−2 for hydrogen evolution reaction (HER) and oxygen evolution reaction (OER), respectively. The impressive performance of MnCo2O4.5@NiS is demonstrated by the lower value of voltage 1.44 V needed to deliver the current density of 10 mA cm−2, which outperformed the 1.66 V required for a commercial Pt/C||RuO2 system. Detailed structure analysis and density functional theory (DFT) calculations reveal that the MnCo2O4.5@NiS heterostructure enhances electron transfer at the interface, promotes the formation of oxygen vacancies and tunes the electronic structures of Mn and Co. These findings underscore the potential of MnCo2O4.5@NiS as an efficient and cost-effective electrocatalyst for hydrogen production.

Computational screening of transition metal atom doped ZnS and ZnSe nanostructures as promising bifunctional oxygen electrocatalysts.

The design of bifunctional oxygen electrocatalysts showing high catalytic performance for the oxygen evolution reaction (OER) and oxygen reduction reaction (ORR) is of great significance for developing new renewable energy storage and conversion technologies. Herein, based on the first principles calculations, we systematically explored the electrocatalytic activity of a series of transition metal atom (Fe, Co, Ni, Cu, Pd and Pt)-doped ZnS and ZnSe nanostructures for OER and ORR. The calculated results revealed that Ni- and Pt-doped ZnS and ZnSe nanostructures exhibit promising electrocatalytic performance for both OER and ORR in comparison to the pristine ZnS and ZnSe nanostructures. Especially, the OER/ORR overpotentials of Ni-doped ZnS and ZnSe nanostructures are estimated to be 0.28/0.30 and 0.31/0.31 V, respectively, disclosing their great potential as bifunctional oxygen electrocatalysts. Moreover, it is found that Ni-doped ZnS and ZnSe nanostructures for OER and ORR are on the top of the volcano plots, evincing promising catalytic performance. Our results provide theoretical insights into a feasible strategy to synthesize highly efficient ZnS- and ZnSe-based bifunctional oxygen electrocatalysts in the future.

An Evolving Blue Economy: Exploring the Future for Marine Renewable Energy

Abstract Offshore energy generation is one of the fastest-growing U.S. marine sectors, ranging from expanding deployment of offshore wind to rapid development and testing of technologies for energy conversion from waves, tides, ocean currents, and gradients in temperature, salinity, and pressure. Generating energy from the offshore environment creates expanded opportunities to improve upon the collection of ocean and coastal-derived data and information that will support economic and maritime growth, the management of resources, and solutions to address societal and climate issues. Despite its many promises and challenges, barriers remain for widespread implementation of offshore energy generation technologies that address the nation's energy needs and climate change. A town hall was convened to present a vision of the changing ocean-scape through the lens of marine renewable technologies and to explore innovative solutions that these technologies might offer to support the New Blue Economy.