A precisely Assembled Wall-Like Architecture for High Lithium/Sodium Storage.

MXene nanosheets and ordered porous carbons both have their own advantages and disadvantages. Assembling and combining the advantages of the two will be a good choice for battery electrode hosts of active materials. In this work, an electrostatic separation-adsorption strategy is proposed to realize the ordered alternating self-assembly of MXene nanosheets and ordered porous carbon (MPOC), obtaining a unique wall-like porous material with a high conductivity and interconnected porous nanostructure, which strengthens the transfer rate of electrons and ions simultaneously. Meanwhile, the introduction of N-doping from porous carbon into MPOC prolongs the cycle life. When use red phosphorus (RP) as active materials, the MPOC@RP anode exhibited high-capacity output (2454.3 and 2408.1 mAh g-1 in lithium-ion batteries (LIBs) and sodium-ion batteries (SIBs) at 0.1 C) and long cycle life (the decay rates per cycle of 0.028% and 0.036% after 1500 and 1200 cycles at 2 C in LIBs and SIBs respectively). The successful application in RP anodes displays great potential in other electrode materials such as silicon, sulfur, selenium, and so on. Meanwhile, this strategy is also effective to design other composites materials like MXene and carbon nanotubes, MXene and Graphene, and so on.

Tailoring Ordered Porous Carbon Embedded with Cu Clusters for High-Energy and Long-Lasting Phosphorus Anode.

The natural insulating property and notorious pulverization of volume variation-induced materials during cycling pares the electrochemical activity of red phosphorous (RP) for lithium/sodium-ion batteries (LIBs/SIBs). To work out these issues, a tailored trimodal porous carbon support comprising highly ordered macropores and micro-mesoporous walls embedded with copper (Cu) nanoclusters (Cu-OMC) is proposed to confine RP. The construction of highly conductive copper-carbon wall facilitates fast electrons and ions transportation, while the interconnected and ordered porous structure not only creates enough space to resist the expansion effect of RP but also minimizes the ion diffusion length and enhances ion accessibility (the ion migration coefficient is ten times that of disordered porous carbon). Consequently, the resulting Cu-OMC@RP anode delivers a high reversible capacity (2498.7 mAh g-1 at 0.3 C for LIBs; 2454.2 mAh g-1 at 0.1 C for SIBs), superb rate properties (824.7 mAh g-1 at 10 C for LIBs; 774.2 mAh g-1 at 5 C for SIBs), and outstanding cycling stability (an ultralow decay rate of 0.057% per cycle after 1000 cycles at 10 C for LIBs and 0.048% per cycle at 5 C over 500 cycles for SIBs).

3D Ordered Porous Nanostructure Confers Fast Charge Transfer Rate and Reduces the Electrode Polarization in Thick Electrode.

Lithium batteries with high electrode thickness always possess a poor battery property due to electrode polarization along the thickness direction. Herein, a concept that the electrode polarization can be reduced through the fabrication of 3D ordered interconnected nanostructure in the electrode is put forward. A nitrogen-doped carbon photonic crystal (NCPC) with the ordered interconnected nanostructure is used in the electrode to prove the concept. NCPC can provide a fast charge transfer rate along the thickness direction and a uniform distribution for electrons and lithium ions, resulting in diminishing the concentration polarization and concentration gradient. When NCPC works for lithium-sulfur battery, the thick electrode achieves a fast charge transfer rate and a small voltage gap as well as the thin electrode. The 200 µm thick sulfur cathode obtains a specific capacity (87%) as high as 100 µm thick sulfur cathode. In contrast, the capacity ratio of the electrode made by the traditional coating method is only 45%.

Efficient Bifunctional Catalytic Electrodes with Uniformly Distributed NiN2 Active Sites and Channels for Long-Lasting Rechargeable Zinc-Air Batteries.

Freestanding bifunctional electrodes with outstanding oxygen reduction reaction (ORR) and oxygen evolution reaction (OER) properties are of great significance for zinc-air batteries, attributed to the avoided use of organic binder and strong adhesion with substrates. Herein, a strategy is developed to fabricate freestanding bifunctional electrodes from the predeposited nickel nanoparticles (Ni-NCNT) on carbon fiber paper. The steric effect of monodispersed SiO2 nanospheres limits the configuration of carbon atoms forming 3D interconnected nanotubes with uniformly distributed NiN2 active sites. The bifunctional electrodes (Ni-NCNT) demonstrate ideal ORR and OER properties. The zinc-air batteries assembled with Ni-NCNT directly exhibit extremely outstanding long term stability (2250 cycles with 10 mA cm-2 charge/discharge current density) along with high power density of 120 mV cm-2 and specific capacity of 834.1 mA h g-1 . This work provides a new view to optimize the distribution of active sites and the electrode structure.

Graphene/graphitic carbon nitride decorated with AgBr to boost photoelectrochemical performance with enhanced catalytic ability.

A novel graphene nanoplatelets (GNP) bridge between two semiconductors (AgBr and graphitic carbon nitride) was created to boost photoelectrochemical performance. The heterojunction created makes the whole system a Z-scheme catalyst. For the construction of this catalyst, the syringe pump methodology was adopted and different analytical techniques were used for the confirmation of structure and morphology. High angle annular dark field (HAADF), dark field (DF), DF-4 and DF-2 techniques, using Z-contrast phenomena, confirmed the heterostructure (ABGCN) and its composition. The constructed structure showed an enhanced photoelectrochemical and catalytic property against 'acute toxicity category-III (MM)' and 'category-IV (tetracycline hydrochloride (TH))' organic pollutants. The constructed catalyst degraded the MM in 57 min and the TH in 35 min with degradation rates of 0.01489 min-1 and 0.02387 min-1, respectively, due to the accumulation of photogenerated electrons on the conduction band (CB) of g-C3N4 and photogenerated holes on the valence band (VB) of AgBr by the transformation of charges through the graphene bridge. An ion trapping study also revealed that ·O2 and h+ were the active species which actively participated in the photocatalytic reaction.

Enhanced Charge Transfer by Passivation Layer in 3DOM Ferroelectric Heterojunction for Water Oxidation in HCO3 - /CO2 System.

Photoelectrochemical carbon dioxide conversion to fuels such as carbon monoxide, methanol, and ethylene exhibits great potential to solve energy issues. Unfortunately, CO2 conversion efficiency is still low due to violent charge recombination at the photoanode. Herein, a novel 3D macroporous ferroelectric heterojunction composed of BiFeO3 and LiNbO3 is developed by a template-assisted sol-gel method, aiming at facilitating charge transfer kinetics. As expected, a tremendous enhancement of photocurrent density (300 times vs bare planar BiFeO3 film) and charge transfer efficiency (up to 76%) is obtained in the HCO3 - /CO2 system without any cocatalyst. The photoelectrochemical performance is switchable by poling to form a depolarization electric field. Photoelectrochemical impedance spectroscopy reveals that the charge transfer resistance decreases due to the synergistic effect of BiFeO3 3D macroporous skeleton and LiNbO3 passivation layer by tuning surface states. These results suggest a novel strategy for enhancing photoelectrochemical water oxidation as the anodic reaction of CO2 reduction.

A Host-Configured Lithium-Sulfur Cell Built on 3D Nickel Photonic Crystal with Superior Electrochemical Performances.

The insulator of the sulfur cathode and the easy dendrites growth of the lithium anode are the main barriers for lithium-sulfur cells in commercial application. Here, a 3D NPC@S/3D NPC@Li full cell is reported based on 3D hierarchical and continuously porous nickel photonic crystal (NPC) to solve the problems of sulfur cathode and lithium anode at the same time. In this case, the 3D NPC@S cathode can not only offer a fast transfer of electron and lithium ion, but also effectively prevent the dissolution of polysulfides and the tremendous volume change during cycling, and the 3D NPC@Li anode can efficiently inhibit the growth of lithium dendrites and volume expansion, too. As a result, the cell exhibits a high reversible capacity of 1383 mAh g-1 at 0.5 C (the current density of 837 mA g-1 ), superior rate ability (the reversible capacity of 735 mAh g-1 at the extremely high current density of 16 750 mA g-1 ) with excellent coulombic efficiency of about 100% and an excellent cycle life over 500 cycles with only about 0.026% capacity loss per cycle.

Surface chemical polishing and passivation minimize non-radiative recombination for all-perovskite tandem solar cells.

All-perovskite tandem solar cells have shown great promise in breaking the Shockley-Queisser limit of single-junction solar cells. However, the efficiency improvement of all-perovskite tandem solar cells is largely hindered by the surface defects induced non-radiative recombination loss in Sn-Pb mixed narrow bandgap perovskite films. Here, we report a surface reconstruction strategy utilizing a surface polishing agent, 1,4-butanediamine, together with a surface passivator, ethylenediammonium diiodide, to eliminate Sn-related defects and passivate organic cation and halide vacancy defects on the surface of Sn-Pb mixed perovskite films. Our strategy not only delivers high-quality Sn-Pb mixed perovskite films with a close-to-ideal stoichiometric ratio surface but also minimizes the non-radiative energy loss at the perovskite/electron transport layer interface. As a result, our Sn-Pb mixed perovskite solar cells with bandgaps of 1.32 and 1.25 eV realize power conversion efficiencies of 22.65% and 23.32%, respectively. Additionally, we further obtain a certified power conversion efficiency of 28.49% of two-junction all-perovskite tandem solar cells.

Dendrite-Free and Ultra-Long-Life Lithium Metal Anode Enabled via a Three-Dimensional Ordered Porous Nanostructure.

Constructing a stable non-dendritic lithium metal anode is the key to the development of high-energy batteries in the future. Herein, we fabricated nitrogen-doped carbon photonic crystals in situ in the macropores of carbon papers as a porous skeleton and confined hosts for metallic lithium. The large specific surface area of the carbon photonic crystal reduces the current density of the electrode. The three-dimensional ordered microstructure promotes uniform charge distribution and uniform lithium deposition and inhibits the volume expansion of metallic lithium. The as-prepared lithium metal anode exhibits prominent electrochemical performance with a small hysteresis of less than 95 mV beyond 180 cycles at an extremely high current density of 15 mA cm-2. When the as-prepared lithium metal anode is coupled with the sulfur cathode, the obtained full cell displays enhanced capacitive properties and cycle life. Compared with the bare Li anode, the full cell exhibits more than 300 cycles of cell life and a 70 mA h g-1 higher discharge capacity.

Three-Dimensional Ordered Porous Nanostructures for Lithium-Selenium Battery Cathodes That Confer Superior Energy-Storage Performance.

Lithium-selenium (Li-Se) batteries suffer from the problems of polyselenides dissolution and volume expansion of active materials during the charge/discharge process. Moreover, the heavy atomic mass of selenium atoms limits the capacitive property of a Li-Se battery. Porous materials as the host for selenium particles reported by previous research studies are often disordered in pore structure and nonuniform in pore size. Herein, we report that a three-dimensional (3D) nitrogen-doped carbon photonic crystal (NCPC) with an ordered, interconnected structure was synthesized via a simple method to be the host of active materials. In addition, we prepared a Se-rich Se1-xSx by introducing a small amount of sulfur into a selenium ring to reduce the molecular mass but still keep the high electronic conductivity. As cathodes for a Li-Se battery, amorphous Se-rich Se1-xSx@NCPC composites exhibited high electrochemical performance with a specific capacity of 692 mA h g-1 at 0.1 Ag1-, an excellent rate capability of 526 mA h g-1 at 3 Ag1-, and an outstanding cycling property with an ultralow decay rate of 0.0132% per cycle at 0.6 Ag1- over 1000 cycles. Moreover, the pouch cell of Se1-xSx@NCPC composites also showed a good property with an energy of 253 Wh kg-1 at 0.1 Ag1- and an outstanding rate energy of 192 Wh kg-1 at 1.5 Ag1-, manifesting great potential in practical application.

Three-Dimensional-Ordered Porous Nanostructures for Lithium-Sulfur Battery Anodes and Cathodes Confer Superior Energy Storage Performance.

The nonuniformity of microscopic electrochemical reaction of electrodes essentially results in the partial reaction discrepancy and subsequent partial overheating, which is the most critical safety problem of the battery system in electric vehicles. Herein, we report a class of DLPC@S/DLPC@Li full cell based on a distinctly constructed double-layer photonic crystal (DLPC) with a three-dimensional-ordered interconnected structure. This full cell not only ensures the uniformity of microscopic electrochemical reaction but also solves common problems such as low conductivity of sulfur, poor cycle life, and lithium dendrite growth. Impressively, the full cell exhibits superior electrochemical performance pertaining to high reversible capacity of 703.3 mAh g-1 even at an extremely high rate of 10 C and excellent cycle performance with 1200 cycles with about 0.0317% capacity loss per cycle at 0.5 C.

Plasmonic nanoparticles tuned thermal sensitive photonic polymer for biomimetic chameleon.

Among many thermo-photochromic materials, the color-changing behavior caused by temperature and light is usually lack of a full color response. And the study on visible light-stimuli chromic response is rarely reported. Here, we proposed a strategy to design a thermo-photochromic chameleon biomimetic material consisting of photonic poly(N-isopropylacrylamide-co-methacrylic acid) copolymer and plasmonic nanoparticles which has a vivid color change triggered by temperature and light like chameleons. We make use of the plasmonic nanoparticles like gold nanoparticles and silver nanoparticles to increase the sensitivity of the responsive behavior and control the lower critical solution temperature of the thermosensitive films by tuning the polymer chain conformation transition. Finally, it is possible that this film would have colorimetric responses to the entire VIS spectrum by the addition of different plasmonic nanoparticles to tune the plasmonic excitation wavelength. As a result, this method provides a potential use in new biosensors, military and many other aspects.