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The addition of PLZST nanoparticles improves the dielectric constant and breakdown strength, reduces loss, thus improves the energy storage performance of PLZST/P(VDF-HFP) nanocomposites.

The sandwich-structured KNN-BZT/P(VDF-HFP) nanocomposites were prepared by solution casting method. When the breakdown strength reached 565 MV m−1, the excellent energy storage performance (Ud = 21.39 J cm−3, η = 70.54%) was obtained.

Zr-Mn mixed oxides with various Zr/Mn molar ratios were synthesized by redox-precipitation method and applied to benzene catalytic combustion. The results showed that the addition of Zr to MnO2 could improve the benzene combustion activity, among which Zr/MnO2-0.2 catalyst performed the best catalytic activity with T50 and T90 of 171 °C and 195 °C (1000 ppm benzene, GHSV = 60,000 ml · g−1 · h−1, 0% RH (relative humidity), 20 vol% O2/N2), respectively. A series of characterizations were used to investigate the structure–activity relationship of Zr–Mn mixed oxides, which demonstrated that the larger specific surface area, more surface reactive oxygen species, higher low-temperature reduction and acidity contributed to the enhanced catalytic activity of Zr–Mn mixed oxides. Finally, the possible pathways of benzene combustion over Zr–Mn mixed oxides were explored by in-situ DRIFTS spectra and the possible intermediates generated under different conditions were also revealed.

The radioactive sludges formed at the bottom of high-level liquid waste (HLW) storage tanks pose challenges when the HLWs are vitrified. This study aims to determine the influence of the sludge content (enriched in Na2O, Al2O3, NiO, Fe2O3, and BaSO4) on the structure and properties of waste glasses in order to find the optimal ratio of sludges to HLW during vitrification. In the experiments, the simulated sludge and simulated HLW were mixed at different ratios from 0:8 to 4:4, with an overall waste content of 16 wt %, in a borosilicate glass wasteform. It is found that the glass density, molar volume, sulfur retention, and glass transition temperature changed little when increasing the sludge content of the glasses, while the viscosity, chemical durability, and crystallization features of the glasses varied notably. The crystals formed in the glasses during the thermal treatment were exclusively Fe-substituted diopside (Ca, Mg, Fe)2Si2O6. An increase in the Al2O3 and NiO content of the glasses may have been responsible for the increased crystallinity at high temperatures. The leaching rate of Si, B, Na, and Cs from the glasses declined with the increasing addition of sludge to the glasses. Although all the glasses fulfilled the requirements for vitrification processing and glass-product performance, it is recommended that the sludge content of the whole waste should not exceed 25 wt %. This study guides further research on the immobilization of high-level sludges.

In this work, a lithiophilic Ni-Al@LDH interlayer is engineered at the Li6.4La3Zr1.4Ta0.6O12 (LLZTO) electrolyte and Li anode interface. The Ni-Al@LDH interlayer can significantly reduce the interfacial resistance as well as give excellent cycling performance both in a symmetric Li//Li cell and solid full lithium metal batteries.

Background: Tumor-associated macrophages (TAM) are the most abundant stromal cells in the tumor microenvironment. Turning the TAM against their host tumor cells is an intriguing therapeutic strategy particularly attractive for patients with immunologically “cold” tumors. This concept was mechanistically demonstrated on in vitro human and murine lung cancer cells and their corresponding TAM models through combinatorial use of nanodiamond-doxorubicin conjugates (Nano-DOX) and a PD-L1 blocking agent BMS-1. Nano-DOX are an agent previously proved to be able to stimulate tumor cells’ immunogenicity and thereby reactivate the TAM into the anti-tumor M1 phenotype. Results: Nano-DOX were first shown to stimulate the tumor cells and the TAM to release the cytokine HMGB1 which, regardless of its source, acted through the RAGE/NF-κB pathway to induce PD-L1 in the tumor cells and PD-L1/PD-1 in the TAM. Interestingly, Nano-DOX also induced NF-κB-dependent RAGE expression in the tumor cells and thus reinforced HMGB1’s action thereon. Then, BMS-1 was shown to enhance Nano-DOX-stimulated M1-type activation of TAM both by blocking Nano-DOX-induced PD-L1 in the TAM and by blocking tumor cell PD-L1 ligation with TAM PD-1. The TAM with enhanced M1-type repolarization both killed the tumor cells and suppressed their growth. BMS-1 could also potentiate Nano-DOX’s action to suppress tumor cell growth via blocking of Nano-DOX-induced PD-L1 therein. Finally, Nano-DOX and BMS-1 achieved synergistic therapeutic efficacy against in vivo tumor grafts in a TAM-dependent manner. Conclusions: PD-L1/PD-1 upregulation mediated by autocrine and paracrine activation of the HMGB1/RAGE/NF-κB signaling is a key response of lung cancer cells and their TAM to stress, which can be induced by Nano-DOX. Blockade of Nano-DOX-induced PD-L1, both in the cancer cells and the TAM, achieves enhanced activation of TAM-mediated anti-tumor response.

Carbon-based materials with great adsorption performance are of importance to meet the needs of industrial gas adsorption. Being massive agricultural wastes of sugarcane bagasse, China could use this waste into wealth. However, the comprehensive utilization of sugarcane bagasse as precursors for biochar that can be used as adsorbent has not been extensively explored. In this study, a series of in-situ sulfuric acid modified biochar were prepared by hydrothermal carbonization process. The prepared biochar (SBAC-7) is combined of two main advantages that are high microporosity (micropore surface area = 1106 m 2 /g) and rich in S-containing functional groups on the surface. In particular, SBAC-7 showed an excellent adsorption capacity of toluene (771.1 mg/g) at 30 o C, which is nearly 3 times as high as the commercial activated carbons. Meanwhile, it showed great stability and cyclic regeneration performance with five toluene adsorption-desorption test cycles. This study provides a high-performance biochar for adsorption-desorption cycle in practical engineering applications, and would contribute to the sustainable “sugarcane production - bagasse utilization” circular economy.

Struvite-K (MgKPO

Ceramic dielectrics are reported with superior energy storage performance for applications, such as power electronics in electrical vehicles. A recoverable energy density (Wrec) of ∼4.55 J cm–3 with η ∼ 90% is achieved in lead-free relaxor BaTiO3-0.06Bi2/3(Mg1/3Nb2/3)O3 ceramics at ∼520 kV cm–1. These ceramics may be co-fired with Ag/Pd, which constitutes a major step forward toward their potential use in the fabrication of commercial multilayer ceramic capacitors. Compared to stoichiometric Bi(Mg2/3Nb1/3)O3-doped BaTiO3 (BT), A-site deficient Bi2/3(Mg1/3Nb2/3)O3 reduces the electrical heterogeneity of BT. Bulk conductivity differs from the grain boundary only by 1 order of magnitude which, coupled with a smaller volume fraction of conducting cores due to enhanced diffusion of the dopant via A-site vacancies in the A-site sublattice, results in higher breakdown strength under an electric field. This strategy can be employed to develop new dielectrics with improved energy storage performance.

Lead-free dielectric ceramics 0.75SrTiO3-0.25BiFeO3 (ST-BF) with an extra amount of bismuth (Bi) are synthesized by the conventional solid-state reaction method. The crystal structures of ST-BF retain pseudo-cubic phase as Bi content increases. The grain size is found to significantly increase from 1.8 to 4.9 µm and then fall to 3.3 µm in the presence of excess Bi, exhibiting a distinct heterogeneous core–shell microstructure. Impedance spectroscopy data indicates that with increasing excess Bi content to 2 mol%, the shell resistivity increases significantly to ∼ 9 MΩ cm with the largest volume fraction of the shell/core area, and both the core and shell activation energies are increased, resulting in reduced dielectric loss of ∼ 0.08 at 1 kHz and high breakdown strength of ∼ 140 kV cm−1. This work provides a potential strategy for further improvement of ST-BF for capacitor applications.

Aqueous supercapacitors have the superiorities of high safety, environmental friendliness, inexpensive, etc. High energy density supercapacitors are not conducive to manufacturing due to the limitation of water thermodynamic decomposition potential, resulting in a narrow working voltage window. To address such challenges, a great endeavor has started to investigate high voltage aqueous supercapacitors as well as making some progress. This review summarizes key strategies regarding the realization of wide working voltage of aqueous supercapacitors and analyzes the involved mechanism, including the optimization of electrodes, electrolytes, diaphragms, and supercapacitor structures. From the perspective of extending the theoretical voltage window, electrode functionalization, heteroatom doping, neutral electrolyte, water-in-salt electrolyte, introducing redox mediators into electrolyte, and designing asymmetric structure are effective strategies for achieving this goal. Further, the actual voltage window can be maximized by optimizing the electrode mass ratio, adjusting potential of zero voltage, and electrode functionalization. The challenge and future of expanding working voltage of aqueous supercapacitors are further discussed. Importantly, this review provides inspiration for the development of supercapacitors with high energy density.

Correction for ‘Engineering lithiophilic Ni-Al@LDH interlayers on a garnet-type electrolyte for solid-state lithium metal batteries’ by Wei Liu et al., Chem. Commun., 2021, 57, 10214–10217, DOI: 10.1039/D1CC02932K.

The mechanical and tribological properties of three types of diamond like carbon (DLC) coatings, i.e., non-doped, Si-doped, and W-doped DLC, are evaluated. Dry reciprocating sliding wear tests were performed to evaluate the effect of sliding frequency/velocity on friction, adhesion, and wear. The degree of graphitization of non-doped and W-doped DLC increases with sliding velocity, which results in a lower coefficient of friction (COF), and a decrease in wear rate. Si-doped DLC, however, exhibits distinct friction behaviour, with increasing COF and severe fluctuations in friction at higher sliding velocities. In Si-DLC frictional heating drives the formation of an oxide-rich tribofilm and large amounts of Si-rich oxide wear debris that are both adhesive and abrasive. The oxide-rich tribofilm, and lack of surface graphitization, result in the severe fluctuations of Si-DLC friction via stick-slip and surface fracture/wear mechanisms, and significantly increased COF and wear rates at higher sliding velocities.

Graphical abstract, Highlights • Industrial waste silica fume (SF) is used to improve the performance of basic magnesium sulfate cement (BMSC). • Incorporation of SF can enhance the mechanical properties of BMSC significantly. • Hydration behavior and process of BMSC influenced by SF are studied. • Microstructure and phase evolution of BMSC are characterized and analyzed., Silica fume (SF) as an important supplementary cementitious material has been widely used in Portland cement, but few published articles have reported on the effect of SF on the performance and hydration mechanism of basic magnesium sulfate cement (BMSC). In the present work, the properties, microstructure and hydration mechanism of BMSC influenced by SF was studied systematically. The results show that the setting time and compressive strength of BMSC may increase with the increase of SF content, while the hydration heat will decrease with the increase of SF content. Mercury intrusion porosimetry (MIP), X-ray computed tomography (X-CT), scanning electron microscope- Energy dispersive spectrometer (SEM-EDS) results show that SF exhibits filling effect in the BMSC matrix, which makes the microstructure of BMSC matrix with SF more compact. In addition, solid-state magnetic resonance (NMR) and SEM-EDS analysis indicate that the activity of SF was excited in the BMSC matrix, resulting in the formation of M−S−H gel.