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The practical application of lithium-sulfur (Li-S) batteries is hampered by the insulative nature of sulfur, sluggish electrochemical kinetics, and large volume variation, which result in capacity-fading at a large current density and poor cycling stability. Herein, a three-dimensional (3D) aluminum photonic crystal encapsulating sulfur (APC@S) composite as a binder-free cathode for Li-S battery is reported. The 3D APC@S cathode can deliver a fantastic capacity of 1,517.8 mAh·g−1 at 0.5 C, and retains 712.7 mAh·g−1 after 1,500 cycles at 2 C with a decay rate of 0.02% per cycle. Even at a high rate of 5 C, the reversible capacity can still maintain at 680.7 mAh·g−1 after 1,000 cycles with a capacity retention of 74.8%. Furthermore, the assembled soft-packaged Li-S battery also exhibits high reversible capacity and stable cycling performance. The excellent electrochemical performance is attributed to the 3D hierarchical and continuously porous structure and high conductive aluminum-wall, which can effectively trap polysulfides, confine the volume expansion on cycling, and accelerate electron/ion transfer. It is expected that this high conductive metal cathode has a great future for the application of energy storage devices.

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.

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

TiO2 nanostructures with different morphologies were successfully synthesized via a solvothermal reaction of titanium isopropoxide and acetic acid. The synthesized TiO2 nanostructures were characterizated in detail by powder X-ray diffractometry, scanning electron microscopy, Fourier transform infrared spectroscopy and Raman etc. technologies. The effect of growth time on the composition, morphology and crystal phase of synthesized TiO2 nanostructures were studied, and corresponding photovoltaic performance of dye-sensitized solar cell (DSSC) fabricated from TiO2 nanorice was also investigated. The DSSC based on the 24 h anatase TiO2 nanorice photoelectrode shows an overall light-to-electricity conversion efficiency of 7.45% accompanying a short-circuit current density of 18.83 mA cm−2, an open-circuit voltage of 788 mV and fill factor of 0.5, which is much higher than that of 12 h (5.25%), 16 h (5.73%) and 20 h (6.20%) samples. The significant enhancement of short-circuit current density and power conversion efficiency for the 24 h nanorice-based DSSC is mainly attributed to its larger dye loading amount.

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.

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.

Novel jujube-like hierarchical TiO2 microspheres (HTMs) were synthesized by an alkali-corrosion process of titanium phosphate (Ti2O3(H2PO4)2 · 2H2O) microspheres. The hierarchical titanium phosphate microsphere (HTPM) intermediates consisting of nanoflakes with a thickness of 20 nm were firstly prepared by a facile hydrothermal method. After reacting with diluted NaOH at low temperature and atmospheric pressure, followed by subsequent acid washing and a calcination process, the HTPM intermediates were transformed to TiO2 with the microsphere morphology well retained, while the nanoflakes became porous, and some new nanowires were formed between the nanoflakes. Finally, HTMs consisting of porous nanoflakes and nanowires were obtained. The possible growth mechanisms of HTPMs and HTMs are discussed. The HTMs demonstrate high specific surface area and excellent light-scattering ability. The performance of the dye sensitized solar cells (DSSCs) of the HTMs synthesized under different conditions is studied, and a total conversion efficiency of up to 8.93% was obtained. The improved DSSC performance was attributed to the enhanced dye loading, light-scattering, and charge transporting ability of the HTMs with a unique hierarchical nanostructure.

A hierarchically porous anatase TiO2 coated-WO3 2D inverse opal (IO) bilayer film was fabricated on ITO glass using a layer by layer route with a hierarchically porous TiO2 top layer and an ordered super-macroporous WO3 2D IO bottom layer. This novel TiO2 coated-WO3 2D IO bilayer film was evaluated for photochromic applications.