We present herein a facile one-step low-temperature hydrothermal approach for in situ growth of metal selenides (Co(0.85)Se and Ni(0.85)Se) on conductive glass substrates. The as-prepared metal selenides on conductive substrates can be used directly as transparent counter electrodes for dye-sensitized solar cells (DSSCs) without any post-treatments. It is found that graphene-like Co(0.85)Se exhibits higher electrocatalytic activity than Pt for the reduction of triiodide. As a consequence, the DSSC with Co(0.85)Se generates higher short-circuit photocurrent and power conversion efficiency (9.40%) than that with Pt.

The durability and reactivity of catalysts can be effectively and precisely controlled through the careful design and engineering of their surface structures and morphologies. Herein, we develop a novel "adsorption-calcination-reduction" strategy to synthesize spinel transitional metal oxides with a unique necklace-like multishelled hollow structure exploiting sacrificial templates of carbonaceous microspheres, including NiCoO (NCO), CoMnO, and NiMnO. Importantly, benefiting from the unique structures and reduction treatment to offer rich oxygen vacancies, the unique reduced NCO (R-NCO) as a bifunctional electrocatalyst exhibits the dual characteristics of good stability as well as high electrocatalytic activity for both the hydrogen evolution reaction (HER) and oxygen evolution reaction (OER). At 1.61 V cell voltage, a 10 mA cm water splitting current density is obtained from the dual-electrode, alkaline water electrolyzer. Calculations based on density functional theory (DFT) reveal a mechanism for the promotion of the catalytic reactions based on a decrease in the energy barrier for the formation of intermediates resulting from the introduction of oxygen vacancies through the reduction process. This method could prove to be an effective general strategy for the preparation of complex, hollow structures and functionalities.

Metal wires suffer from corrosion in fiber-shaped dye-sensitized solar cells (DSSCs). We report herein that stable, ultrastrong, and highly flexible aligned carbon nanotube fibers can be used not only as catalytic counter electrodes but also as conductive materials to support dye-loaded TiO(2) nanoparticles in DSSCs. The power conversion efficiency of this fiber solar cell can achieve 2.94%. These solar power fibers, exhibiting power conversion efficiency independent of incident light angle and cell length, can be woven into textiles via a convenient weaving technology.

A sandwich-like 2D-mesoporous-carbon/MoS -nanosheet heterostructure is fabricated for the first time. The hybrid structure is composed of three well-stacked monolayers: an ordered-mesoporous-carbon monolayer, a MoS monolayer, and a further ordered-mesoporous-carbon monolayer. This unique heterostructure exhibits excellent electrochemical performance as an anode material for lithium-ion batteries.

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