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We report the exploration of all-inorganic perovskite photodetectors based on stabilized CsPb0.922Sn0.078I3 nanobelts, which exhibit overall excellent performance with an ultrahigh detectivity up to 6.43 × 1013 Jones.

In the present work, the exploration of photodetectors (PDs) based on CsPbI3 nanotubes are reported. The as‐prepared CsPbI3 nanotubes can be stable for more than 2 months under air conditions. It is found that, in comparison to the nanowires, nanobelts, and nanosheets, the nanotubes can be advantageous to be used as the functional units for PDs, which is mainly attributed to the enhanced light absorption ability induced by the light trapping effect within the tube cavity. As a proof of concept, the as‐constructed PDs based on CsPbI3 nanotube present an overall excellent performance with a responsivity (Rλ), external quantum efficiency (EQE) and detectivity of 1.84 × 103 A W−1, 5.65 × 105% and 9.99 × 1013 Jones, respectively, which are all comparable to state‐of‐the‐art ones for all‐inorganic perovskite PDs.

The popularly reported energy storage mechanisms of potassium-ion batteries (PIBs) are based on alloy-, de-intercalation-, and conversion-type processes, which inevitably lead to structural damage of the electrodes caused by intercalation/de-intercalation of K+ with a relatively large radius, which is accompanied by poor cycle stabilities. Here, we report the exploration of robust high-temperature PIBs enabled by a carboxyl functional group energy storage mechanism, which is based on an example of p-phthalic acid (PTA) with two carboxyl functional groups as the redox centers. In such a case, the intercalation/de-intercalation of K+ can be performed via surface reactions with relieved volume change, thus favoring excellent cycle stability for PIBs against high temperatures. As proof of concept, at the fixed working temperature of 62.5 °C, the initial discharge and charge specific capacities of the PTA electrode are ∼660 and 165 mA⋅h⋅g−1, respectively, at a current density of 100 mA⋅g−1, with 86% specific capacity retention after 160 cycles. Meanwhile, it delivers 81.5% specific capacity retention after 390 cycles under a high current density of 500 mA⋅g−1. The cycle stabilities achieved under both low and high current densities are the best among those of high-temperature PIBs reported previously.

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Photoelectrochemical (PEC) splitting of water into H2 and O2 by direct use of sunlight is an ideal strategy for the production of clean and renewable energy, which fundamentally relies on the exploration of advanced photoanodes with high performance. In the present work, we report that single-crystal integrated photoanodes, that is, 4H-SiC nanohole arrays (active materials) and SiC wafer substrate (current collector), are established into a totally single-crystal configuration without interfaces, which was based on a two-step electrochemical etching process. The as-fabricated SiC photoanode showed a rather low onset potential of −0.016 V vs reversible hydrogen electrode (RHE) and a high photocurrent density of 3.20 mA/cm2 vs RHE 1.23 V, which were both superior to those of all reported SiC ones. Furthermore, such a rationally designed photoanode exhibited a fast photoresponse, wide photoresponse wavelength range, and long-term stability, representing its overall excellent PEC performance.