Interface engineering enabled by sodium dodecyl sulfonate surfactant for stable Zn metal batteries.

Aqueous zinc-ion batteries are emerging as powerful candidates for large-scale energy storage, due to their inherent high safety and high theoretical capacity. However, the inevitable hydrogen evolution and side effects of the deposition process limit their lifespan, which requires rational engineering of the interface between anode and aqueous electrolyte. In this paper, an anionic surfactant as electrolyte additive, sodium dodecyl sulfonate (SDS), is introduced to deliver highly reversible zinc metal batteries.

Achieving Dendrite-Free Zinc Metal Anodes via Molecule Anchoring and lon-Transport Pumping.

The potential for scale-up application has been acknowledged by researchers for rechargeable aqueous zinc-ion batteries (ZIBs). Nonetheless, the progress of the development is significantly impeded due to the instability of the interface between the zinc anode and electrolyte. Herein, efficient and environmentally benign valine (Val) were introduced as aqueous electrolyte additive to stabilize the electrode/electrolyte interface (EEI) via functional groups in additive molecules, thus achieving reversible dendrite-free zinc anode.

Nitroxyl radical triggered the construction of a molecular protective layer for achieving durable Zn metal anodes.

The issues of dendrite growth, hydrogen evolution reaction, and zinc anode corrosion have significantly hindered the widespread implementation of aqueous zinc-ion batteries (AZIBs). Herein, trace amounts of 2,2,6,6-tetramethylpiperidine-1-oxyl (TEMPO) additive is introduced into AZIBs to protect the zinc metal anode. Trace amounts of the TEMPO additive with nitroxyl radical can provide fast Zn transport and anode protection ability by forming an adsorbed molecular layer via Zn-O bond.

Interface Engineering for Aqueous Aluminum Metal Batteries: Current Progresses and Future Prospects.

Aqueous aluminum metal batteries (AMBs) have attracted numerous attention because of the abundant reserves, low cost, high theoretical capacity, and high safety. Nevertheless, the poor thermodynamics stability of metallic Al anode in aqueous solution, which is caused by the self-corrosion, surface passivation, or hydrogen evolution reaction, dramatically limits the electrochemical performance and hampers the further development of AMBs. In this comprehensive review, the key scientific challenges of Al anode/electrolyte interface (AEI) are highlighted.

An efficient and multifunctional S-scheme heterojunction photocatalyst constructed by tungsten oxide and graphitic carbon nitride: Design and mechanism study.

The design of multifunctional photocatalyst with strong redox performance is the key to achieve sustainable utilization of solar energy. In this study, an elegant S-scheme heterojunction photocatalyst was constructed between metal-free graphitic carbon nitride (g-CN) and noble-metal-free tungsten oxide (WO). As-established S-scheme heterojunction photocatalyst enabled multifunctional photocatalysis behavior, including hydrogen production, degradation (Rhodamine B) and bactericidal (Escherichia coli) properties, which represented extraordinary sustainability.

Rechargeable Aqueous Aluminum-Ion Battery: Progress and Outlook.

The high cost and scarcity of lithium resources have prompted researchers to seek alternatives to lithium-ion batteries. Among emerging "Beyond Lithium" batteries, rechargeable aluminum-ion batteries (AIBs) are yet another attractive electrochemical storage device due to their high specific capacity and the abundance of aluminum. Although the current electrochemical performance of nonaqueous AIBs is better than aqueous AIBs (AAIBs), AAIBs have recently gained attention due to their low cost and enhanced safety.

Reversible Al Metal Anodes Enabled by Amorphization for Aqueous Aluminum Batteries.

Aqueous aluminum metal batteries (AMBs) are regarded as one of the most sustainable energy storage systems among post-lithium-ion candidates, which is attributable to their highest theoretical volumetric capacity, inherent safe operation, and low cost. Yet, the development of aqueous AMBs is plagued by the incapable aluminum plating in an aqueous solution and severe parasitic reactions, which results in the limited discharge voltage, thus making the development of aqueous AMBs unsuccessful so far. Here, we demonstrate that amorphization is an effective strategy to tackle these critical issues of a metallic Al anode by shifting the reduction potential for Al deposition.

A Defect Engineered Electrocatalyst that Promotes High-Efficiency Urea Synthesis under Ambient Conditions.

Synthesizing urea from nitrate and carbon dioxide through an electrocatalysis approach under ambient conditions is extraordinarily sustainable. However, this approach still lacks electrocatalysts developed with high catalytic efficiencies, which is a key challenge. Here, we report the high-efficiency electrocatalytic synthesis of urea using indium oxyhydroxide with oxygen vacancy defects, which enables selective C-N coupling toward standout electrocatalytic urea synthesis activity.

Machine Learning: An Advanced Platform for Materials Development and State Prediction in Lithium-Ion Batteries.

Lithium-ion batteries (LIBs) are vital energy-storage devices in modern society. However, the performance and cost are still not satisfactory in terms of energy density, power density, cycle life, safety, etc. To further improve the performance of batteries, traditional "trial-and-error" processes require a vast number of tedious experiments.

Architecting a Stable High-Energy Aqueous Al-Ion Battery.

Aqueous Al-ion batteries (AAIBs) are the subject of great interest due to the inherent safety and high theoretical capacity of aluminum. The high abundancy and easy accessibility of aluminum raw materials further make AAIBs appealing for grid-scale energy storage. However, the passivating oxide film formation and hydrogen side reactions at the aluminum anode as well as limited availability of the cathode lead to low discharge voltage and poor cycling stability.

A 1D Honeycomb-Like Amorphous Zincic Vanadate for Stable and Fast Sodium-Ion Storage.

Developing nanomaterials with synergistic effects of various structural merits is considered to be an effective strategy to improve the sluggish ion kinetics and severe structural degradation of sodium-ion battery (SIB) anodes. Herein, honeycomb-like amorphous Zn V O (ZVO-AH) nanofibers as SIBs anode material with plentiful defective sites, complex cavities, and good mechanical flexibility are reported. The fabrication strategy relies on the expansive and volatile nature of the organic vanadium source, based on a simple electrospinning with subsequent calcination.

Significantly Improving Lithium-Ion Transport via Conjugated Anion Intercalation in Inorganic Layered Hosts.

Layered hydroxides (LHs) have emerged as an important class of functional materials owing to their unusual physicochemical properties induced by various intercalated species. While both the electrochemistry and interlayer engineering of the materials have been reported, the role of interlayer engineering in improving the Li-ion storage of these materials remains unclear. Here, we rationally introduce pillar ions with conjugated anion dicarboxylate groups, cobalt oxalate ions ([CoOx]), into the interlayers of Co(OH) nanosheets [denoted as I-Co(OH) NSs].

Defect Engineering Metal-Free Polymeric Carbon Nitride Electrocatalyst for Effective Nitrogen Fixation under Ambient Conditions.

Electrocatalytic nitrogen reduction reaction (NRR) under ambient conditions provides an intriguing picture for the conversion of N into NH . However, electrocatalytic NRR mainly relies on metal-based catalysts, and it remains a grand challenge in enabling effective N activation on metal-free catalysts. Here we report a defect engineering strategy to realize effective NRR performance (NH yield: 8.

An Amorphous Noble-Metal-Free Electrocatalyst that Enables Nitrogen Fixation under Ambient Conditions.

N fixation by the electrocatalytic nitrogen reduction reaction (NRR) under ambient conditions is regarded as a potential approach to achieve NH production, which still heavily relies on the Haber-Bosch process at the cost of huge energy and massive production of CO . A noble-metal-free Bi V O /CeO hybrid with an amorphous phase (BVC-A) is used as the cathode for electrocatalytic NRR. The amorphous Bi V O contains significant defects, which play a role as active sites.

Structural Engineering of 2D Nanomaterials for Energy Storage and Catalysis.

Research on 2D nanomaterials is rising to an unprecedented height and will continue to remain a very important topic in materials science. In parallel with the discovery of new candidate materials and exploration of their unique characteristics, there are intensive interests to rationally control and tune the properties of 2D nanomaterials in a predictable manner. Considerable attention is focused on modifying these materials structurally or engineering them into designed architectures to meet requirements for specific applications.

Engineering 2D Nanofluidic Li-Ion Transport Channels for Superior Electrochemical Energy Storage.

Rational surface engineering of 2D nanoarchitectures-based electrode materials is crucial as it may enable fast ion transport, abundant-surface-controlled energy storage, long-term structural integrity, and high-rate cycling performance. Here we developed the stacked ultrathin Co O nanosheets with surface functionalization (SUCNs-SF) converted from layered hydroxides with inheritance of included anion groups (OH , NO , CO ). Such stacked structure establishes 2D nanofluidic channels offering extra lithium storage sites, accelerated Li-ion transport, and sufficient buffering space for volume change during electrochemical processes.

Metallic Transition Metal Selenide Holey Nanosheets for Efficient Oxygen Evolution Electrocatalysis.

Catalysts for oxygen evolution reaction (OER) are pivotal to the scalable storage of sustainable energy by means of converting water to oxygen and hydrogen fuel. Designing efficient electrocatalysis combining the features of excellent electrical conductivity, abundant active surface, and structural stability remains a critical challenge. Here, we report the rational design and controlled synthesis of metallic transition metal selenide NiCoSe-based holey nanosheets as a highly efficient and robust OER electrocatalyst.

Engineering Mesoporous Single Crystals Co-Doped FeO for High-Performance Lithium Ion Batteries.

To achieve high-efficiency lithium ion batteries (LIBs), an effective active electrode material is vital. For the first time, mesoporous single crystals cobalt-doped FeO (MSCs Co-FeO) is synthesized using formamide as a pore forming agent, through a solvothermal process followed by calcination. Compared with mesoporous single crystals FeO (MSCs FeO) and cobalt-doped FeO (Co-FeO), MSCs Co-FeO exhibits a significantly improved electrochemical performance with high reversible capacity, excellent rate capability, and cycling life as anode materials for LIBs.

Two-Dimensional Holey CoO Nanosheets for High-Rate Alkali-Ion Batteries: From Rational Synthesis to in Situ Probing.

A general template-directed strategy is developed for the controlled synthesis of two-dimensional (2D) assembly of CoO nanoparticles (ACN) with unique holey architecture and tunable hole sizes that enable greatly improved alkali-ion storage properties (demonstrated for both Li and Na ion storage). The as-synthesized holey ACN with 10 nm holes exhibit excellent reversible capacities of 1324 mAh/g at 0.4 A/g and 566 mAh/g at 0.

A novel anode comprised of C&N co-doped Co3O4 hollow nanofibres with excellent performance for lithium-ion batteries.

C&N co-doped Co3O4 hollow nanofibres are prepared by combining the electrospinning technique and the hydrothermal method, which show a high reversible capacity and excellent cycling stability as anode materials for Li-ion batteries. DFT calculations give a good explanation for the experimentally enhanced conductivity in C&N co-doped Co3O4 hollow nanofibres.