Enhancing the Output Performance of a Triboelectric Nanogenerator Based on Modified Polyimide and Sandwich-Structured Nanocomposite Film.

Recently, scientists have been facing major obstacles in terms of improving the performances of dielectric materials for triboelectric nanogenerators. The triboelectric nanogenerator (TENG) is one of the first green energy technologies that can convert random mechanical kinetic energy into electricity. The surface charge density of TENGs is a critical factor speeding up their commercialization, so it is important to explore unique methods to increase the surface charge density. The key to obtaining a high-performance TENG is the preparation of dielectric materials with good mechanical properties, thermal stability and output performance. To solve the problem of the low output performance of PI-based triboelectric nanogenerators, we modified PI films by introducing nanomaterials and designed a new type of sandwich-shaped nanocomposite film. Herein, we used polyimide (PI) with ideal mechanical properties, excellent heat resistance and flexibility as the dielectric material, prepared an A-B-A sandwich structure with PI in the outer layer and modified a copper calcium titanate/polyimide (CCTO/PI) storage layer in the middle to improve the output of a TENG electrode. The doping amount of the CCTO was tailored. The results showed that at 8 wt% CCTO content, the electrical output performance was the highest, and the open-circuit voltage of CCTO/PI was 42 V. In the TENG, the open-circuit voltage, short-circuit current and transfer charge of the prepared sandwich-structured film were increased by 607%, 629% and 672% compared to the TENG with the PI thin film, respectively. This study presents a novel strategy of optimizing dielectric materials for triboelectric nano-generators and has great potential for the future development of high output-performance TENGs.

Step-doped disulfide vacancies and functional groups synergistically enhance photocatalytic activity of S-scheme Cu3SnS4/L-BiOBr towards ciprofloxacin degradation.

Development of efficient photocatalysts for efficient recalcitrant organic pollutants degradation is of great significance. Herein, the step-doped disulfide vacancies S-scheme Cu3SnS4/L-BiOBr (CTS/L-BiOBr) heterojunction photocatalyst was prepared for ciprofloxacin (CIP) degradation. X-ray photoelectron spectroscopy (XPS) analysis, ultraviolet photo-electron spectroscopy (UPS) analysis, band structure and dominant radicals' identification together verified that the transfer of photogenerated carriers conformed to the S-scheme mechanism. Benefited from the interfacial electric field (IEF) of the S-scheme heterojunction and incorporation of L-cysteine with introducing S-vacancies and surface functional groups (-NH2, -COO-), photogenerated charges generation and separation of the CTS/L-BiOBr(10) were greatly improved. With ·OH and h+ as dominant reactive species, CIP removal reached 93% using CTS/L-BiOBr(10) within 180 min of visible light irradiation, which was 3.5 times and 2.6 times of pristine Cu3SnS4 and L-BiOBr, respectively. Moreover, possible CIP degradation pathways were proposed and the degradation intermediates ecotoxicity were evaluated. This study could provide reference for designing efficient S-scheme photocatalysts for recalcitrant wastewater treatment.

Hydroxyl radical and carbonate radical facilitate chlortetracycline degradation in the bio-photoelectrochemical system with a bioanode and a Bi2O3/CuO photocathode using bicarbonate buffer.

The single-chamber bio-photoelectrochemical system (BPES) with a bioanode and a Bi2O3/CuO photocathode is developed for chlortetracycline (CTC) degradation under simulated solar irradiation, using phosphate buffer solution (PBS) or NaHCO3 as buffer solution. The optimized Bi2O3/CuO photocathode possesses rich vacancies, great photoresponse capability, and exhibits great photocatalytic activity toward CTC degradation due to its Z-scheme structure. Electron spin-resonance spectroscopy (ESR) and reactive species trapping experiments reveal that superoxide radicals/hydroxyl radicals are both the main radicals contributing to CTC degradation. Moreover, carbonate radical plays a more effective role toward CTC degradation, resulting in 40% improvement for CTC degradation in the BPES within 2 h. Higher current density (maximum of 137.6 A m-2) and more negative cathode potential are obtained from the illuminated BPES with NaHCO3 buffer. Possible mechanism and pathways of CTC degradation are proposed. This study contributes to the development of BPESs for antibiotics degradation.

N, S co-doped carbon quantum dots anchoring on copper-vacancy-rich Cu nanowires/Cu foam as the cathode in microbial fuel cells: Role of C-S-Cu active site.

Oxygen reduction reaction (ORR) electrocatalysts have been considered as one of the key components in microbial fuel cells (MFCs). Heteroatom-doped carbon quantum dots (CQDs) derived from biomass have attracted wide attention due to their rich functional groups, excellent properties, and environmental friendliness. Herein, orange-peels-derived N, S co-doped carbon quantum dots (N, S-CQDs) are in-situ anchored on copper-vacancy-rich Cu nanowires/Cu foam (V-Cu NWs/CF), obtaining the N, S-CQDs/Cu2O-Cu NWs, to catalyze ORR in MFCs. The interaction between N, S-CQDs and V-Cu NWs/CF from the N, S-CQDs/Cu2O-Cu NWs is bridged by the C-S-Cu bond, which is demonstrated to be the active site towards ORR and plays an important role in promoting electron transfer by in-situ Raman and X-ray photoelectron spectroscopy characterizations. In MFCs, the maximum power density (924.5 ± 32.5 mW·m-2) of N, S-CQDs/Cu2O-Cu NWs is 1.34 times that of Pt/C (686.5 ± 28.0 mW·m-2), and its long-term stability also outperforms the Pt/C. This study provides inspiration for synthesis of efficient ORR electrocatalysts with metal-ligand active sites creating by heteroatom-doped CQDs and cationic-metal-vacancy-rich materials.

B-doped graphene quantum dots implanted into bimetallic organic framework as a highly active and robust cathodic catalyst in the microbial fuel cell.

Developing efficient and durable oxygen reduction reaction (ORR) cathodic catalysts plays an essential role in application of microbial fuel cells (MFCs). Herein, the B-doped graphene quantum dots implanted into bimetallic organic framework (BGQDs/MOF-t) are fabricated by a facile electro-deposition. Results show that, the in-situ growth of FeCoMOF on nickel foam can effectively assist construction of nanoflowers with compact connections, thus improves the conductivity. More importantly, this nano-network can serve as the template for the implantation of BGQDs through powerful interface of M-O-C bonding, avoiding π-π rearrangement and providing efficient charge transfer and abundant edge active sites. Benefitting from the enhanced electrode/electrolyte transport interface, abundant catalytic sites and low charge transfer resistance, the BGQDs/MOF-15 exhibits excellent ORR activity, superior to commercial Pt/C catalyst. In the MFC with the BGQDs/MOF-15 cathode, the maximum power density of 703.55 mW m-2 is achieved, which is 1.53 times of that of the Pt/C cathode. In addition, the BGQDs/MOF-15 cathode maintains great stability over 800 h, while that of Pt/C reduces to 61% of the initial voltage. This work opens new opportunities for developing efficient and durable MOF-derived ORR catalyst.

Visible-light-driven Z-scheme Zn3In2S6/AgBr photocatalyst for boosting simultaneous Cr (VI) reduction and metronidazole oxidation: Kinetics, degradation pathways and mechanism.

It is urgently needed to develop high-performance materials that can synchronously remove heavy metals and organic pollutants. Herein, the visible-light responsive Zn3In2S6/AgBr composites were prepared for concurrent removals of metronidazole (MNZ) and Cr (VI). In the Cr (VI)-MNZ coexisting system, the removals of MNZ and Cr (VI) using the optimized Zn3In2S6/AgBr-15 photocatalyst reached 98.2% and 94.8% within 2 h, respectively; higher than those using counterparts. The radical species trapping and electron spin resonance (ESR) results demonstrated that ·OH was the most dominated species for MNZ oxidation, and photo-generated electrons were responsible for Cr (VI) reduction. Besides, slight competition for ·O2- during the simultaneous MNZ degradation and Cr (VI) reduction occurred. Energy band structure analysis, ESR and the outstanding photocatalytic performance for MNZ and Cr (VI) removals demonstrated that the Zn3In2S6/AgBr-15 was a Z-scheme photocatalyst, which promoted photo-induced carrier's separation. Possible MNZ degradation pathways and mechanism over the Z-scheme Zn3In2S6/AgBr were also proposed based on the identified intermediates. This study could inspire new ideas for design of efficient Z-scheme photocatalysts for wastewater treatment.

Different refractory organic substances degradation and microbial community shift in the single-chamber bio-photoelectrochemical system.

The single-chamber bio-photoelectrochemical system (BPES) with a BiOBr photocathode was developed for acid orange 7 (AO7), 2,4 dichlorophenol (2,4-DCP) and chloramphenicol (CAP) degradation under solar irradiation. Photoelectrochemical characterizations showed that the optimized BiOBr-photocathode exhibited great light-response property and excellent electrochemcial performance. Moreover, desired TOC removals were achieved for various organic pollutants, with the values of 90.97% (AO7), 81.41% (2,4-DCP) and 78.47% (CAP). Besides, the lower cathode potentials in the illuminated BPESs were favorable to efficient pollutants degradation. Significant microbial community shifts were observed among the inoculation and anodic biofilms from the BPES, and the most dominated species in anodic biofilms acclimated to various pollutants were Geobacter and Pseudomonas, which have the abilities of extracellular electrons transfer and organics degradation. Some other species that different from the inoculation were also identified from the BPES biofilms. This study suggested that BPES had great potential for refractory organics degradation.