High performance of electrochemical energy storage devices depends on the smart structure engineering of electrodes, including the tailored nanoarchitectures of current collectors and subtle hybridization of active materials. To improve the anode supercapacitive performance of Fe2O3 for high‐voltage asymmetric supercapacitors, here, a hybrid core‐branch nanoarchitecture is proposed by integrating Fe2O3 nanoneedles on ultrafine Ni nanotube arrays (NiNTAs@Fe2O3 nanoneedles). The fabrication process employs a bottom‐up strategy via a modified template‐assisted method starting from ultrafine ZnO nanorod arrays, ensuring the formation of ultrafine Ni nanotube arrays with ultrathin tube walls. The novel developed NiNTAs@Fe2O3 nanoneedle electrode is demonstrated to be a highly capacitive anode (418.7 F g−1 at 10 mV s−1), matching well with the similarly built NiNTAs@MnO2 nanosheet cathode. Contributed by the efficient electron collection paths and short ion diffusion paths in the uniquely designed anode and cathode, the asymmetric supercapacitors exhibit an excellent maximum energy density of 34.1 Wh kg−1 at the power density of 3197.7 W kg−1 in aqueous electrolyte and 32.2 Wh kg−1 at the power density of 3199.5 W kg−1 in quasi‐solid‐state gel electrolyte.

In this work, a series of novel biobased copolymers, poly(propylene sebacate-co-isosorbide sebacate) (P(PSe-co-IS)), were synthesized by melt-polycondensation from sebacic acid (SA) and isosorbide (IS) with 1,3-propanediol (PD). In order to analyze the effects of isosorbide on the relative properties of poly(propylene sebacate) (PPSe), the composition, crystal structure, crystallization behavior, multiple melting behavior, and spherulitic morphology of these copolymers were investigated by 1 H-NMR, WAXD, DSC, TMDSC and POM, respectively. Results of 1 H-NMR indicated that IS have been successfully introduced into the PPSe main chains with the designed molar ratio. DSC data showed that crystallization ability of P(PSe-co-IS) copolymers was retarded with the introduction of IS. With the increment of IS, the overall crystallization rate decreased gradually. Furthermore, crystallization temperature (T c ), crystallization enthalpy (DH c ), melting temperature (T m ), and equilibrium melting temperature (T o m ) of P(PSe-co-IS) copolymers also decreased apparently with the increase of IS content. WAXD suggested that crystal structure of PPSe was not affected by IS, and POM revealed that all spherulites possess the typical "Maltese Cross" image. Furthermore, no obvious ring-banded spherulites could be detected for P(PSe-co-IS) copolymers in the wide temperature range except neat PPSe due to the hindrance of IS. With the increment of IS and crystallization temperature, the number of spherulites decreased rapidly and the size of spherulites increased, respectively.

It is an effective method to synthesize the functionalized sequence-controlled polymers by utilizing 1,1-diphenylethylene (DPE) derivatives in living anionic polymerization. Considering the capacity of sequence information and the diversify of...