Scalable Synthesis of SiOx-TiON Composite As an Ultrastable Anode for Li-Ion Half/Full Batteries.

Among various anode materials, SiOx is regarded as the next generation of promising anode due to its advantages of high theoretical capacity with 2680 mA h g-1, low lithium voltage platform, and rich natural resources. However, the pure SiOx-based materials have slow lithium storage kinetics attributed to their low electron/ion conductive properties and the large volume change during lithiation/delithiation, restricting their practical application. Optimizing the SiOx material structures and the fabricating methods to mitigate these fatal defects and adapt to the market demand for energy density is critical. Hence, SiOx material with TiO1-xNx phase modification has been prepared by simple, low-cost, and scalable ball milling and then combined with nitridation. Consequently, based on the TiO1-xNx modified layer, which boosts high ionic/electronic conductivity, chemical stability, and excellent mechanical properties, the SiOx@TON-10 electrode shows highly stable lithium-ion storage performance for lithium-ion half/full batteries due to a stable solid-electrolyte interface layer, fast Li+ transport channel, and alleviative volumetric expansion, further verifying its practical feasibility and universal applicability.

Low cost and highly dispersed Ce/Na-ZSM-5 catalysts close to atomic dispersion for enhancing formaldehyde oxidation.

Formaldehyde oxidation at room temperature with low-cost catalysts is one of the main development directions of environmental governance. Herein, we developed a low-cost and superior performance highly dispersed Ce on Na-ZSM-5 (Ce/Na-ZSM-5) catalyst, which is close to atomic dispersion for indoor formaldehyde (HCHO) oxidation at low temperature. The highly dispersed catalyst that was similar to atomic dispersion was characterized by EXAFS and AC HAADF-STEM. The optimal Ce/Na-ZSM-5 displays high HCHO removal performance (95%, at room temperature), as well as 100 h stable testing (∼90% HCHO removal). In addition, a reasonable reaction mechanism of the HCHO catalytic oxidation is proposed based on the in situ DRIFT spectra and DFT calculation. This work provides a new way to design an efficient catalyst for the complete oxidation of formaldehyde.

Promoting Plasmonic Hot Hole Extraction and Photothermal Effect for the Oxygen Evolution Reactions.

Boosting oxygen evolution reaction by local surface plasmon resonance (LSPR) provides breakthrough opportunities for the promotion of solar energy conversion; the potential of LSPR, however, has rarely been tapped and investigated. Here, we report the precise regulation of commercial Au nanoparticles plasmonic nanomaterial and OER electrocatalysts, viz., the NiCoOx electrocatalytic layer with hole transport ability and photothermal effect is prepared on the surface of Au nanoparticles by photoelectrodeposition. The NiCoOx layer not only increases the transmission distance of holes generated by plasmonic Au nanoparticles, but also reduce the agglomeration of plasmonic Au nanoparticles during long-time OER reaction, which greatly improves the OER catalytic ability. The current density of NiCoOx /Au anode achieves 16.58 mA cm-2 at 2.0 V versus RHE, which is about 6.5 times of pristine NiCoOx anode (2.56 mA cm-2 ) and 47 times of pristine Au anode (0.35 mA cm-2 ). More importantly, with the LSPR and photothermal effect of plasmonic Au nanoparticles, the NiCoOx /Au anode provides additional current density of 7.01 mA cm-2 after illumination, and maintains no attenuation for more than 2000 s. Benefiting from the solution of agglomeration problem of plasmonic Au nanoparticles in the long-time OER process and the effective utilization of generated holes of plasmonic Au nanoparticles, this design can provide guidance for the application of plasmonic materials in the field of electrocatalysis.

Heterogeneity between and within Single Hematite Nanorods as Electrocatalysts for Oxygen Evolution Reaction.

Understanding the structural nature of the active sites in electrocatalysis is central to discovering general design rules for better catalysts in fuel cells and electrolyzers. Nanostructures are widely used as electrocatalysts, but the location and structure of the active sites within the nanostructure are often unknown. This information is hidden in conventional bulk measurements due to ensemble averaging, hindering direct structure-activity correlation. Herein, we use a single-entity electrochemical approach to reveal the heterogeneity in electrocatalysts via scanning electrochemical cell microscopy (SECCM). Using hematite (α-Fe2O3) nanorods as the model catalyst for oxygen evolution reaction (OER), the electrocatalytic activity is measured at individual nanorods. Finer mapping within a single nanorod shows that the OER activity is consistently higher at the body portion vs the tip of the nanorod. Our results directly suggest the benefit of synthesizing longer hematite nanorods for better OER performance. The origin of the enhanced local activity is explained by the larger fraction of {001} facet exposed on the body compared to the tip. The finding goes beyond OER on hematite nanorods, highlighting the critical role of single-entity activity mapping and colocalized structural characterization in revealing active sites in electrocatalysis.

Atomically Thin Materials for Next-Generation Rechargeable Batteries.

Atomically thin materials (ATMs) with thicknesses in the atomic scale (typically <5 nm) offer inherent advantages of large specific surface areas, proper crystal lattice distortion, abundant surface dangling bonds, and strong in-plane chemical bonds, making them ideal 2D platforms to construct high-performance electrode materials for rechargeable metal-ion batteries, metal-sulfur batteries, and metal-air batteries. This work reviews the synthesis and electronic property tuning of state-of-the-art ATMs, including graphene and graphene derivatives (GE/GO/rGO), graphitic carbon nitride (g-C3N4), phosphorene, covalent organic frameworks (COFs), layered transition metal dichalcogenides (TMDs), transition metal carbides, carbonitrides, and nitrides (MXenes), transition metal oxides (TMOs), and metal-organic frameworks (MOFs) for constructing next-generation high-energy-density and high-power-density rechargeable batteries to meet the needs of the rapid developments in portable electronics, electric vehicles, and smart electricity grids. We also present our viewpoints on future challenges and opportunities of constructing efficient ATMs for next-generation rechargeable batteries.

Atomically thin photoanode of InSe/graphene heterostructure.

Achieving high-efficiency photoelectrochemical water splitting requires a better understanding of ion kinetics, e.g., diffusion, adsorption and reactions, near the photoelectrode's surface. However, with macroscopic three-dimensional electrodes, it is often difficult to disentangle the contributions of surface effects to the total photocurrent from that of various factors in the bulk. Here, we report a photoanode made from a InSe crystal monolayer that is encapsulated with monolayer graphene to ensure high stability. We choose InSe among other photoresponsive two-dimensional (2D) materials because of its unique properties of high mobility and strongly suppressing electron-hole pair recombination. Using the atomically thin electrodes, we obtained a photocurrent with a density >10 mA cm-2 at 1.23 V versus reversible hydrogen electrode, which is several orders of magnitude greater than other 2D photoelectrodes. In addition to the outstanding characteristics of InSe, we attribute the enhanced photocurrent to the strong coupling between the hydroxide ions and photo-generated holes near the anode surface. As a result, a persistent current even after illumination ceased was also observed due to the presence of ions trapped holes with suppressed electron-hole recombination. Our results provide atomically thin materials as a platform for investigating ion kinetics at the electrode surface and shed light on developing next-generation photoelectrodes with high efficiency.

Enhancing photoelectrochemical water splitting by combining work function tuning and heterojunction engineering.

We herein demonstrate the unusual effectiveness of two strategies in combination to enhance photoelectrochemical water splitting. First, the work function adjustment via molybdenum (Mo) doping significantly reduces the interfacial energy loss and increases the open-circuit photovoltage of bismuth vanadate (BiVO4) photoelectrochemical cells. Second, the creation and optimization of the heterojunction of boron (B) doping carbon nitride (C3N4) and Mo doping BiVO4 to enforce directional charge transfer, accomplished by work function adjustment via B doping for C3N4, substantially boost the charge separation of photo-generated electron-hole pairs at the B-C3N4 and Mo-BiVO4 interface. The synergy between the above efforts have significantly reduced the onset potential, and enhanced charge separation and optical properties of the BiVO4-based photoanode, culminating in achieving a record applied bias photon-to-current efficiency of 2.67% at 0.54 V vs. the reversible hydrogen electrode. This work sheds light on designing and fabricating the semiconductor structures for the next-generation photoelectrodes.

Combining Bulk/Surface Engineering of Hematite To Synergistically Improve Its Photoelectrochemical Water Splitting Performance.

One of the most promising candidates for photoelectrochemical (PEC) water splitting photoanode is hematite (α-Fe2O3) due to its narrow bandgap and chemical stability. However, the poor bulk/surface kinetics of hematite limits its PEC performance. Herein, a facile two-step approach is reported to synergistically improve the PEC performance of Fe2O3. First, through bulk engineering of Ti doping, the photocurrent density of Ti-Fe2O3 photoanode (1.68 mA cm(-2) at 1.23 VRHE) shows a 3-fold increase compared with that of pure Fe2O3 photoanode (0.50 mA cm(-2) at 1.23 VRHE). Second, the photocurrent density of Ti-Fe2O3 photoanode could be further enhanced to 2.31 mA cm(-2) by surface engineering of FeOOH. The enhanced PEC water splitting performance is proposed to be the synergistic effect of bulk and surface engineering, which can be mainly attributed to the great increase of charge separation efficiency and surface transfer efficiency.

Au-NiCo2O4 supported on three-dimensional hierarchical porous graphene-like material for highly effective oxygen evolution reaction.

A three-dimensional hierarchical porous graphene-like (3D HPG) material was synthesized by a one-step ion-exchange/activation combination method using a cheap metal ion exchanged resin as carbon precursor. The 3D HPG material as support for Au-NiCo2O4 gives good activity and stability for oxygen evolution reaction (OER). The 3D HPG material is induced into NiCo2O4 as conductive support to increase the specific area and improve the poor conductivity of NiCo2O4. The activity of and stability of NiCo2O4 significantly are enhanced by a small amount of Au for OER. Au is a highly electronegative metal and acts as an electron adsorbate, which is believed to facilitate to generate and stabilize Co(4+) and Ni(3+) cations as the active centres for the OER.