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Binary metal niobium oxides can offer a higher specific capacity compared to niobium pentoxide (Nb2O5) and thus are ideal anode candidates for lithium ion capacitors (LICs). However, their lower electronic conductivity limits their ability to achieve high energy and power densities. In this paper, one-dimensional (1D) copper niobate (CuNb2O6) nanowires are successfully prepared by electrospinning technology and then immobilized on two-dimensional (2D) reduced graphene oxide (rGO) nanosheets to form a unique 1D nanowire/2D nanosheet CuNb2O6/rGO structure. The 1D/2D CuNb2O6/rGO electrode exhibits a high specific capacity of 312.2 mAh g−1 at 100 mA g−1 as the anode of LICs. The proposed Li+ storage mechanism of the CuNb2O6 anode involves CuNb2O6 decomposition into lithium niobate (Li3NbO4) and copper (Cu) during the initial lithium insertion process. The intercalation-type Li3NbO4 will further serve as the host to Li+ and the inactive Cu phase will act as a conductive network for electron transportation. Furthermore, the energy density of the assembled CuNb2O6/rGO//activated carbon (CuNb2O6/rGO//AC) device could achieve a value as high as 92.1 Wh kg−1 and could thus be considered as a possible alternative electrode material for high energy and power LICs.

Electrocatalytic water splitting used for generating clean and sustainable hydrogen (H2) can be very promising to address current energy shortage and associated environmental issues. However, this methodology is severely impeded by the tardy oxygen evolution reaction (OER). Hence, designing a preferable kinetics and thermodynamics oxidation reaction that supersede OER is very significant for the energy-saving production of H2. Herein, hollow needle-like copper cobalt sulfide was constructed on carbon cloth (CuCo2S4/CC) as a bifunctional electrocatalyst to accelerate H2 generation and simultaneously convert ethanol into value-added acetic acid. Thanks to the synergistic effect and unique structure of Cu and Co, CuCo2S4/CC displays superior catalytic activity and durability in ethanol oxidation reaction (EOR) with a low potential of 1.38 V vs. RHE (@10 mA cm−2). Meanwhile, it exhibits excellent hydrogen evolution reaction (HER) performance. The homemade CuCo2S4/CC//CuCo2S4/CC ethanol–water electrolyser only demands a voltage of 1.59 V to deliver 10 mA cm−2, 150 mV less than that used for ordinary water splitting. This shows that the ethanol–water electrolyser elaborated here holds encouraging potential in the energy-saving production of H2 and oxidation of ethanol into value-added acetic acid. This present work may open the way for the rational design of other electrocatalysts for efficient biomass oxidation reaction and relevant H2 production applications.