In this study, the activation of peroxydisulfate (PS) by K2FeO4-activation biochar (KFeB) and acid-picking K2FeO4-activation biochar (AKFeB) was investigated to reveal the mechanism differences between iron site and graphitic structure in sulfadiazine (SDZ) degradation and ARB inactivation, respectively. KFeB/PS and AKFeB/PS systems had similar degradation property towards SDZ, but only KFeB/PS system showed excellent bactericidal property. The mechanism study demonstrated that dissolved SDZ was degraded through electron transfer pathway mediated by graphitic structure, while suspended ARB was inactivated through free radicals generated by iron-activated PS, accompanied by excellent removal on antibiotic resistance genes (ARGs). The significant decrease in conjugative transfer frequency indicated the reduced horizontal gene transfer risk of ARGs after treatment with KFeB/PS system. Transcriptome data suggested that membrane protein channel disruption and adenosine triphosphate synthesis inhibition were key reasons for conjugative transfer frequency reduction. Continuous flow reactor of KFeB/PS system can efficiently remove antibiotics and ARB, implying the potential application in practical wastewater purification. In conclusion, this study provides novel insights for classified and collaborative control of antibiotics and ARB by carbon-based catalysts driven persulfate advanced oxidation technology.

Multipores engineering composed of micro/mesopores is an effective strategy to improve potassium storage performance via providing enormous adsorption sites and shortened ions diffusion distance. However, a detailed exploration of the role played by macropores in potassium storage is still lacking and has been barely reported until now. Herein, a superstructure carbon hexahedron (DGN-900) is synthesized using poly tannic acid (PTA) as precursor. Due to the spatially confined two-step local contraction of PTA along different directions and dimensions during pyrolysis, defective nanosheets with macropores are formed, while realizing a balance between defects content and graphitization degree by regulating temperature. The presence of macropores is conducive to accelerating electrolyte ions rapid infiltration within electrode, and its pore volume can accommodate electrode structure fluctuation upon cycling, while the most suitable ratio of defects to graphitic provides rich ions adsorption sites and sufficient electrons transfer channels, simultaneously. These advantages enable a prominent electrochemical performance in DGN-900 electrode, including high rate (202.9 mAh g-1 at 2 A g-1 ) and long cycling stability over 2000 cycles. This unique fabrication strategy, that is, defects engineering coupled with macropores structure, makes fast and durable potassium storage possible.

Sweet potato-derived carbon with a unique solid core/porous layer core/shell structure is used as a conductive substrate for gradually immobilizing sulfur to construct a cathode for Li-S batteries. The first discharge specific capacity of the Li-S batteries with the C-10K@2S composite cathode at 0.1C is around 1645 mAh g-1, which is very close to the theoretical specific capacity of active sulfur. Especially, after 175 cycles at 0.5C, the maintained specific discharge capacities of the C-10K@2S cathode at -20, 0, 25, and 40 °C are about 184.9, 687.2, 795.5, and 758.3 mAh g-1, respectively, and the cathode is superior to most of the classical carbon form matrices. Working mechanisms of the cathodes under different temperatures are confirmed based on X-ray photoelectron spectroscopy (XPS) and in situ X-ray diffraction (XRD) characterizations. Distinctively, during the discharge stage, the widely proposed two-step cathodic reactions occur simultaneously rather than sequentially. In addition, the largely accelerated phase conversion efficiency of the cathode at a higher temperature (from room temperature to 40 °C) contributes to its enhanced charge/discharge specific capacity, while the byproduct Li2S2O7 or Li3N irreversibly formed during the cycles limits its application performance at 0 °C. These conclusions would be very significant and useful for designing cathodes for Li-S batteries with excellent wide working temperature performance.

Unlocking the effects of chemical structure and molecular weight of lignin on the properties of carbonized fiber can accelerate the development of lignin-based carbon fiber which was mainly limited by its complex structure. Hardwood kraft lignins (HKLs) with different structures and molecular weights prepared via heat treatment and fractionation processes were spun into ultrafine fibers using electrospinning technique at the assistance of 1 wt% polyoxyethylene (PEO), which was further removed during the carbonization process to eliminate the potential impacts. The structure and molecular weight of HKLs together with their influences on the thermal behavior, fiber morphology, crystal structure and mechanical performance of HKLs ultrafine fibers or carbonized ultrafine fibers were systemically investigated to provide an elaborate knowledge on the relationship between physico-chemical structure and properties of HKLs ultrafine fibers. Results suggest that a high molecular weight of HKL is beneficial to the formation of graphite-like crystallite, and the formed graphite-like crystallite and condensed structure of HKLs are crucial for the improvement of the mechanical performance of carbonized ultrafine fibers.

Continuous efforts have been made to achieve nanostructured carbon materials with highly ordered graphitic structures using facile synthetic methods. 3D graphite nanoballs (GNBs) are synthesized by the low-temperature pyrolysis of a non-graphitizable precursor, tannic acid (TA). Abundant phenol groups on TA bind to Ni2+ to form metal-phenolic coordination, which renders each Ni cation to be atomically distributed by the TA ligands. Even at low temperatures (1000 °C), highly ordered graphitic structure is promoted by the distributed Ni nanoparticles that act as a graphitization catalyzer. The crystallinity of the GNB is fully corroborated by the intense 2D peak observed in Raman spectroscopy. In particular, the graphitic layers have orientations pointing toward multidirections, which are beneficial for the rapid transport of Li-ions into graphite grains. The resulting materials exhibit outstanding electrochemical performance (120 mAh g-1 at 5 C and 282 mAh g-1 at 0.5 C after 500 cycles) when evaluated as a fast-chargeable negative electrode for lithium ion batteries.

Rosette-shaped graphitic carbon nitride (rosette-GCN) is described as a promising alternative to natural peroxidase for its application to fluorescence-based glucose assays. Rosette-GCN was synthesized via a rapid reaction between melamine and cyanuric acid for 10 min at 35 °C, followed by thermal calcination for 4 h. Importantly, rosette-GCN possesses a peroxidase-like activity, producing intense fluorescence from the oxidation of Amplex UltraRed in the presence of H2O2 over a broad pH-range of, including neutral pH; the peroxidase activity of rosette-GCN was ~ 10-fold higher than that of conventional bulk-GCN. This enhancement of peroxidase activity is presumed to occur because rosette-GCN has a significantly larger surface area and higher porosity while preserving its unique graphitic structure. Based on the high peroxidase activity of rosette-GCN along with the catalytic action of glucose oxidase (GOx), glucose was reliably determined down to 1.2 μM with a dynamic linear concentration range of 5.0 to 275.0 μM under neutral pH conditions. Practical utility of this strategy was also successfully demonstrated by determining the glucose levels in serum samples. This work highlights the advantages of GCNs synthesized via rapid methods but with unique structures for the preparation of enzyme-mimicking catalysts, thus extending their applications to the diagnostics field and other biotechnological fields. Graphical abstract.

Nanoporous carbons (NPCs) have large specific surface areas, good electrical and thermal conductivity, and both chemical and mechanical stability, which facilitate their use in energy storage device applications. In the present study, highly graphitized NPCs are synthesized by one-step direct carbonization of cobalt-containing zeolitic imidazolate framework-67 (ZIF-67). After chemical etching, the deposited Co content can be completely removed to prepare pure NPCs with high specific surface area, large pore volume, and intrinsic electrical conductivity (high content of sp(2) -bonded carbons). A detailed electrochemical study is performed using cyclic voltammetry and galvanostatic charge-discharge measurements. Our NPC is very promising for efficient electrodes for high-performance supercapacitor applications. A maximum specific capacitance of 238 F g(-1) is observed at a scan rate of 20 mV s(-1) . This value is very high compared to previous works on carbon-based electric double layer capacitors.