High-performance K-ion half/full batteries with superb rate capability and cycle stability.

SignificanceThe present work might be significant for exploring advanced K-ion batteries with superb rate capability and cycle stability toward practical applications. The as-assembled K-ion half cell exhibits an excellent rate capability of 428 mA h g-1 at 100 mA g-1 and a high reversible specific capacity of 330 mA h g-1 with 120% specific capacity retention after 2,000 cycles at 2,000 mA g-1, which is the best among those based on carbon materials. The as-constructed full cell delivers 98% specific capacity retention over 750 cycles at 500 mA g-1, superior to most of those based on carbon materials that have been reported thus far.

Robust high-temperature potassium-ion batteries enabled by carboxyl functional group energy storage.

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.

CsPbI3 Nanotube Photodetectors with High Detectivity.

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.

Hot Workability of the Multi-Size SiC Particle-Reinforced 6013 Aluminum Matrix Composites.

The size and distribution of ceramic particles in aluminum matrix composites have been reported to remarkably influence their properties. For a single ceramic particle, the particle size is too small and prone to agglomeration, which makes the mechanical properties of the composites worse. When the ceramic particle size is too large, the particles and alloy at the interface are not firmly bonded, and the effect of dispersion distribution is not achieved, which will also reduce the mechanical properties of the composites. The multi-size ceramic particles are expected to improve this situation, while their effect on hot workability is less studied. In this study, the hot deformation behavior, constitutive model, processing map and SEM microstructure were investigated to evaluate the hot workability of multi-size SiC particle-reinforced 6013 aluminum matrix composites. The results showed that the increased deformation temperature and decreased strain rate could decrease flow stresses. The flow stress behaviors of the composites can be described by the sine-hyperbolic Arrhenius equation with the deformation activation energy of Q = 205.863 kJ/mol. The constitutive equation of the composites is ε ˙=3.11592×1013sinh0.024909σ4.12413exp−205863RT. Then, the hot processing map of the SiCp/6013 composites was constructed and verified by SEM observations. The rheological instability zone was in the region of a high strain rate. The optimal processing zone for composites was 450~500 °C and 0.03~0.25 s−1. In addition, the strain level was found to increase both the Q value and the area of the instability zone.

Revealing the Influence of SiC Particle Size on the Hot Workability of SiCp/6013 Aluminum Matrix Composites.

SiC particle (SiCp) size has been found to significantly influence the hot workability of particle-reinforced aluminum matrix composites (AMC). In this work, therefore, three types of SiCp/6013 composites with different SiCp sizes (0.7, 5 and 15 µm) were prepared and then subjected to isothermal hot compression tests. In addition, constitutive analysis, processing maps and microstructural characterizations were used to reveal the influence of SiCp size on the hot workability of SiCp/6013 composite. The results showed that the values of hot deformation activation energy Q increased with decreasing SiCp size. Specifically, at lower temperatures (e.g., 350 and 400 °C), the highest peak stress was shown in the AMC with SiCp size of 0.7 µm (AMC-0.7), while in the AMC with SiCp size of 5 µm (AMC-5) at higher temperatures (e.g., 450 and 500 °C). This is because a finer SiCp size would lead to stronger dislocation pinning and grain refinement strengthening effects, and such effects would be weakened at higher temperatures. Further, dynamic softening mechanisms were found to transform from dynamic recovery to dynamic recrystallization with increasing SiCp size, and the dynamic recrystallization occurred more easily at higher temperatures and lower strain rates. Consequently, the instability zones of the composites are all mainly located in the deformation region with lower temperature and higher strain rate, and smaller SiCp results in larger instability zones.

Effect of Heat Treatments on the Corrosion Resistance of a High Strength Mg-Gd-Y-Zn-Zr Alloy.

Magnesium-rare earth (Mg-Re) alloys are very promising structural materials in lightweight industries, while the poor corrosion resistance limits their widespread application. In this work, to provide insights into the functions of precipitate characteristics on the corrosion behaviors of Mg-Re alloys, the influence of heat treatments on the corrosion behavior of Mg-11.46Gd-4.08Y-2.09Zn-0.56Zr alloy was investigated via an immersion test, electrochemical experiment and scanning electron microscope (SEM). The results showed that the corrosion rate of Mg-11.46Gd-4.08Y-2.09Zn-0.56Zr alloy specimens decreased by 17.58% and 20.44% after T5 and T6 heat treatment, respectively. In the heat-treated specimens, the corrosion did not extend further into the matrix but formed fine corrosion grooves along the extrusion direction. The improved homogeneity reduced the residual stress and the ß' precipitate introduced as a corrosion barrier after T5 and T6 heat treatment reduced the corrosion rate of the studied Mg alloy. In addition, the volume fraction of the long-period stacking-ordered (LPSO) phase decreased after heat treatment, which effectively reduced galvanic corrosion and enhanced the protective effect on the Mg matrix.

Effect of Grain Size on the Plastic Deformation Behaviors of a Fe-18Mn-1.3Al-0.6C Austenitic Steel.

Grain size is a microscopic parameter that has a significant impact on the macroscopic deformation behavior and mechanical properties of twinning induced plasticity (TWIP) steels. In this study, Fe-18Mn-1.3Al-0.6C steel specimens with different grain sizes were first obtained by combining cold rolling and annealing processes. Then the influence of grain size on the plastic deformation mechanisms was investigated by mechanical testing, X-ray diffraction-based line profile analysis, and electron backscatter diffraction. The experimental results showed that the larger grain size could effectively promote twinning during plastic straining, produce an obvious TWIP effect, and suppress the rate of dislocation proliferation. The continuous contribution of dislocation strengthening and twinning functions led to a long plateau in the work-hardening rate curve, and increased the work-hardening index and work-hardening ability. At the same time, the strain could be uniformly distributed at the grain boundaries and twin boundaries inside the grain, which effectively relieved the stress concentration at the grain boundaries and improved the plasticity of deformed samples.

High-Performance Potassium-Ion Batteries with Robust Stability Based on N/S-Codoped Hollow Carbon Nanocubes.

Currently, a big challenge for the practical use of potassium-ion batteries (PIBs) is their intrinsically poor cycling stability, due to the relatively large radius of K+ and sluggish kinetics for intercalation/deintercalation. Here we report the scalable fabrication of N/S-codoped hollow carbon nanocubes (NSHCCs), which have the potential as an electrode for advanced PIBs with robust stability. Their discharge and charge specific capacities are ∼560 mA h g-1 and 310 mA h g-1 at a current density of 50 mA g-1, respectively. Meanwhile, they exhibit 100% specific capacity retention after 620 cycles over 9 months at a low current density of 50 mA g-1, which is state-of-the-art among carbon materials. Moreover, they demonstrate nearly no sacrifice in specific capacities with 99.9% retention after 3000 cycles over 4 months under a high current density of 1000 mA g-1, superior to most carbon analogues for potassium storage previously reported. The improved electrochemical performance of NSHCC can be mainly attributed to the unique hollow carbon nanocubes with incorporated N and S dopants, which can expand the carbon layer spacing, facilitate K+ adsorption, and relieve the volume change during the intercalation/deintercalation of K+ ions.

Single-Crystal Integrated Photoanodes Based on 4H-SiC Nanohole Arrays for Boosting Photoelectrochemical Water Splitting Activity.

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.