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Developing the technology for high yielding photocatalytic hydrogen evolution reactions is an important challenge. Development and optimization of photocatalytic junctions is a likely route for achieving this if heterojunctions with suitable band alignments can be achieved in sufficiently high‐density form. Here, a novel anatase‐TiO2/H‐rutile‐TiO2 heterophase homojunction system with near optimum energy band alignment is reported. The resulting as‐prepared catalyst exhibits an excellent photocatalytic hydrogen evolution rate of 29.63 mmol g–1 h–1 under UV–vis light irradiation and an outstanding apparent quantum efficiency of 45.6% at 365 nm. The significant improvement is ascribed to near perfect lattice matching in combination with the rapid separation and transfer of photogenerated carriers in anatase‐TiO2/H‐rutile‐TiO2 heterophase homojunctions. In situ X‐ray photoelectron spectroscopy, electron spin resonance spin‐trapping tests, femtosecond transient absorption spectroscopy, steady‐state surface photovoltage spectroscopy, and transient‐state surface photovoltage with additional ex situ characterizations and theoretical calculations show that the mechanism is enhanced transfer of photogenerated carriers in the anatase‐TiO2/H‐rutile‐TiO2 catalyst. This work provides a pathway for enhancing photocatalytic performance through optimization of heterojunctions. [ABSTRACT FROM AUTHOR]

Abstract: Metal organic frameworks (MOFs) are considered as promising candidates for supercapacitors because of high specific area and potential redox sites. However, their shuffled orientations and low conductivity nature lead to severely‐degraded performance. Designing an accessibly‐manipulated and efficient method to address those issues is of outmost significance for MOF application in supercapacitors. It is the common way that MOFs scarify themselves as templates or precursors to prepare target products. But to reversely think it, using target products to prepare MOF could be the way to unlock the bottleneck of MOFs' performance in supercapacitors. Herein, a novel strategy using Co(OH)2 as both the template and precursor to fabricate vertically‐oriented MOF electrode is proposed. The electrode shows a double high specific capacitance of 1044 Fg−1 and excellent rate capability compared to MOF in powder form. An asymmetric supercapacitor was also fabricated, which delivers a maximum energy density of 28.5 W h kg−1 at a power density of 1500 W kg−1, and the maximum of 24000 W kg−1 can be obtained with a remaining energy density of 13.3 W h kg−1. Therefore, the proposed strategy paves the way to unlock the inherent advantages of MOFs and also inspires for advanced MOF synthesis with optimum performance. [ABSTRACT FROM AUTHOR]

A delicate configuration of dual‐ion battery is proposed to achieve optimum energy/power density. High potential intercalation reaction of positive electrode contributes to high energy density and quick absorption/desorption of negative is beneficial for power density. Such novel designed electrochemical energy storage device enables access to optimum power/energy density. [ABSTRACT FROM AUTHOR]