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For lithium ion batteries (LIBs), low electronic conductivity of CuO leads to rapid capacity decay and poor structural stability. Herein, we successfully fabricate three-dimensional CuO nanoflake arrays coated Cu foam by facile and efficient electrochemical oxidation. When being applied as anode material for LIBs, the CuO electrodes deliver stable reversible capacities of 523.9 mA h g −1 at 0.5 A g −1 , 376.1 mA h g −1 at 1.0 A g −1 and 322.7 mA h g −1 at 2.0 A g −1 with high coulombic efficiency (>99%) after 100 cycles. A long cycle life of up to 400 cycles at 2.0 A g −1 is also achieved with the retention capacity of 193.5 mA h g −1 . Moreover, the electrode exhibits excellent rate capability and can regain its original capacities as reversing to the low current densities. Noticeably, on-line differential electrochemical mass spectrometry and in situ Raman measurements confirm the formation of solid electrolyte interface film and the conversion mechanism for the CuO electrodes, respectively. The superior lithium storage performance can be attributed to the favorable nanoflake structures with high surface area and the perfect electrical contact between CuO and Cu substrate. [ABSTRACT FROM AUTHOR]

Understanding the sodium (Na) chemistry is crucial for development of high-performance sodium ion batteries (SIBs). Nanostructured bismuth (Bi) has shown great potentials as an anode in SIBs, however, the Na storage mechanisms of Bi are still unclear. Herein, the operando X-ray diffraction (XRD) technique was utilized to probe the Na storage mechanisms of three Bi anodes (sputtered Bi film, nanoporous Bi and commercial Bi). Despite different morphologies and sizes, all the Bi anodes follow the same two-step reversible alloying/dealloying mechanisms (Bi ↔ NaBi ↔ Na 3 Bi) during the discharge/charge processes, associated with two voltage plateaus. As for the intercalation/deintercalation mechanism proposed for nanostructured Bi anodes in SIBs, we rationalize the reason why only the Bi phase is detected in the discharged/charged samples under ex-situ XRD conditions through addressing the stability issue of the Na-Bi system (NaBi and Na 3 Bi). [ABSTRACT FROM AUTHOR]

Low electronic conductivity and drastic volume change during cycling of transition metal oxides, as anodes for lithium ion batteries (LIBs), lead to rapid capacity decay and poor structural stability. Herein, nanostructured NiCo 2 O 4 anchored on carbon sheets was synthesized by a facile hydrothermal method with following thermal treatment. The wrinkled carbon substrate in the composite derives from the carbonization of pomelo peels, which can be mass-produced for the large-scale application. This composite shows mesoporous structures with high specific surface areas and intimate NiCo 2 O 4 /carbon interfaces, which favors the alleviation of the volume expansion/shrink during charging/discharging process and improves the electron/mass transport, enhancing the capability and stability for LIBs. This composite delivers a high reversible capacity of 473.7 mA h g−1 after 210 cycles at a current density of 500 mA g−1. A long cycle life of up to 1100 cycles at 2000 mA g−1 is achieved with the retention capacity of 363 mA h g−1. The electrode also exhibits excellent rate capability and can regain its original capacities as reversing to the low current densities. This work highlights the biomass-derived carbon-supported metal oxides as an environmentally friendly and economic strategy for advanced LIBs. • Carbon substrate as buffer for anode materials can be derived from pomelo peels. • Cycling stability of NiCo 2 O 4 is improved by depositing it on carbon substrate. • Faster Li+ diffusion coefficients are obtained with the existence of carbon. [ABSTRACT FROM AUTHOR]

Transition metal oxalate materials have shown huge competitive advantages for applications in supercapacitors. Herein, nanostructured cobalt oxalate supported on cobalt foils has been facilely fabricated by anodization, and could directly serve as additive/binder-free electrodes for supercapacitors. The as-prepared cobalt oxalate electrodes present superior specific capacitance of 1269 F g −1 at the current density of 6 A g −1 in the galvanostatic charge/discharge test. Moreover, the retained capacitance is as high as 87.2% as the current density increases from 6 A g −1 to 30 A g −1 . More importantly, the specific capacitance of cobalt oxalate retains 91.9% even after super-long cycling of 100,000 cycles. In addition, an asymmetric supercapacitor assembled with cobalt oxalate (positive electrode) and activated carbon (negative electrode) demonstrates excellent capacitive performance with high energy density and power density. [ABSTRACT FROM AUTHOR]