Electrochemical energy storage devices that can harvest energy from the environment and store it are increasingly important to address both energy poverty in developing parts of the world, as well as powering off-grid autonomous devices. Currently, batteries or supercapacitors connected to solar cells are used for these applications, but these frequently suffer from voltage mismatches and inefficiencies in the device packaging. This paper presents an optically and electrochemically active electrode for photo-rechargeable zinc-ion capacitors using vanadium oxide nanofibers. These rely on photo-excited charge carrier separation to charge the capacitors without any external photovoltaic or electrical devices. We found that silver nanowires are better than carbon based conductive additives as they support photo-excited holes transport and provides light scattering centers that enhance visible light absorption. The proposed capacitors show a ~ 63% capacity increase under illumination, photo-recharge in 30 minutes and ~ 99% capacity retention over 4000 cycles.

Tin-based alloys (Sn-M, M = Fe, Co, Ni, and Cu) have been considered as promising alternatives for graphite anode in advanced Li-ion batteries, but their practical application is hindered by huge volume change-induced poor cycle life. We propose here a facile inorganic-organic double-network nanostructured hydrogel-enabled methodology for uniformly immobilizing ultrafine Sn-M alloys in hierarchical carbon frameworks. The double-network nanostructured gel, consisting of three-dimensional (3D) intertwined cyano-bridged Sn(IV)-Fe(II) inorganic gel and chitosan-glutaraldehyde organic polymer gel, can realize 3D space confinement in molecular scale and thus obtain ultrafine Sn-Fe alloy particles (average size ∼2.7 nm) uniformly embedded in hierarchical 1D to 3D carbon framework. These unique structural features enable the Sn-Fe@C framework electrodes to exhibit long cycle life (516 mA h g after 500 cycles at 0.1 A g) and high rate capability (491 and 270 mA h g at 1 and 10 A g, respectively). This work provides new insight into controlled synthesis of ultrafine alloys in hierarchical 3D carbon frameworks for improving energy storage properties.

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Traditional luminescent materials including fluorescent probes suffer from notorious aggregation‐caused quenching in aqueous solutions. Although several approaches such as the aggregation‐induced emission effect have been developed, it remains a significant challenge to identify an effective and efficient strategy to resolve this issue. Herein, quaternary ammonium salts Q8PBn and Q8PNap as a novel class of bright near infrared window II (NIR‐II, 1000–1700 nm) probes are designed and synthesized, and the twisted intramolecular charge transfer formation at the excited state can be effectively suppressed for the newly designed probes. Furthermore, Q8PNap complexation with fetal bovine serum (Q8PNap/FBS) significantly increases the quantum yield by ≈32‐fold compared with PEGylated tertiary amine Q8P, and Q8PNap/FBS is successfully used to achieve high spatial and temporal resolution imaging of hind limb vasculature, lymphatic system, and small tumor metastasis, as well as precise NIR‐II imaging‐guided tumor and lymph node surgery in small animal models for the first time.

Hierarchical flower-like Nb2O5 microspheres have been prepared via a facile hydrothermal approach without any additives.

Hollow and hybrid nanomaterials are excellent electrocatalysts on account of their novel electrocatalytic properties compared with homogeneous solid nanostructures. In this report, NiSe-Ni3Se2 hybrid nanostructure with morphology of hollow hexagonal nanodisk was synthesized in situ on graphene. A series of NiSe-Ni3Se2/RGO with different phase constitutions and nanostructures were obtained by controlling the durations of solvothermal treatment. Because of their unique hollow and hybrid structure, NiSe-Ni3Se2/RGO hollow nanodisks exhibited higher electrocatalytic performance than NiSe/RGO and solid NiSe-Ni3Se2/RGO nanostructure for reducing I3(-) as counter cell (CE) of dye-sensitized solar cells (DSSCs). Additionally, NiSe-Ni3Se2/RGO hollow nanodisks achieved much lower charge transfer resistance (Rct = 0.68 Ω) and higher power conversion efficiency (PCE) (7.87%) than those of Pt (Rct = 1.41 Ω, PCE = 7.28%).

Mesoporous Ni0.85Se nanospheres grown on graphene were synthesized via the hydrothermal approach. Because of the exceptional electron-transfer pathway of graphene and the excellent catalytic ability of the mesoporous Ni0.85Se nanospheres, the nanocomposites exhibited excellent electrocatalytic property as the counter electrode (CE) of dye-sensitized solar cells. More catalytic active sites, better charge-transfer ability and faster reaction velocity of Ni0.85Se@RGO (RGO = reduced graphene oxide) CE led to faster and more complete I3(-) reduction than Pt, Ni0.85Se, and RGO CEs. Furthermore, the power conversion efficiency of Ni0.85Se@RGO CE reached 7.82%, which is higher than that of Pt CE (7.54%). Electrochemical impedance spectra, cyclic voltammetry, and Tafel polarization were obtained to demonstrate positive synergetic effect between Ni0.85Se and RGO, as well as the higher catalytic activity and the better charge-transfer ability of Ni0.85Se@RGO compared with Pt CE.

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