Microalgae-derived carbon quantum dots mediated formation of metal sulfide nano-adsorbents with exceptional cadmium removal performance.

Metal sulfides are regarded as efficient scavengers for heavy metals. However, the heavy metal adsorption capacity of metal sulfides is far from its theoretical values due to the insufficient exposure of adsorption sites. Surface modification of metal sulfides is considered one of the most effective strategies for improving heavy metal removal performance. Here, microalgae-derived carbon quantum dots (CQDs) were used as a green modifier for mediating nano-MnS/FeS formation to enhance Cd2+ removal. With the addition of 1 wt% CQDs, the Cd2+ adsorption capacity of 1 %CQDs-MnS reached 481 mg/g at 25 °C and 648.6 mg/g at 45 °C, which surpassed most of the previously reported metal sulfides. Furthermore, the CQDs-modified MnS displayed a better Cd2+ removal capacity than the commercial modifier sodium alginate. The mechanism analysis suggested that decreasing the particle size to expose more adsorption sites and providing additional chelating sites derived from the CQDs are two main reasons why CQDs enhance the Cd2+ adsorption capacity of metal sulfides. This study presents an exceptional cadmium nano-adsorbent of 1 %CQDs-MnS and provides a new perspective on the enhancement of heavy metal removal by using CQDs as a promising and universal green modifier that mediates the formation of metal sulfides.

Enrichment of sulfur-oxidizing bacteria using S-doped NiFe2O4 nanosheets as the anode in microbial fuel cell enhances power production and sulfur recovery.

Microbial fuel cells (MFCs) have great promise for power generation by oxidizing organic wastewater, yet the challenge to realize high efficiency in simultaneous energy production and resource recovery remains. In this study, we designed a novel MFC anode by synthesizing S-doped NiFe2O4 nanosheet arrays on carbon cloth (S10-NiFe2O4@CC) to build a three-dimensional (3D) hierarchically porous structure, with the aim to regulate the microbial community of sulfur-cycling microbes in order to enhance power production and elemental sulfur (S0) recovery. The S10-NiFe2O4@CC anode obtained a faster start-up time of 2 d and the highest power density of 4.5 W/m2 in acetate-fed and mixed bacteria-based MFCs. More importantly, sulfide removal efficiency (98.3 %) (initial concentration of 50 mg/L S2-) could be achieved within 3 d and sulfur (S8) could be produced. Microbial community analysis revealed that the S10-NiFe2O4@CC anode markedly enriched sulfur-oxidizing bacteria (SOB) and promoted enrichment of SOB and sulfate-reducing bacteria (SRB) in the bulk solution as well, leading to the enhancement of power generation and S0 recovery. This study shows how carefully designing and optimizing the composition and structure of the anode can lead to the enrichment of a multifunctional microbiota with excellent potential for sulfide removal and resource recovery.

S-Doped NiFe2O4 Nanosheets Regulated Microbial Community of Suspension for Constructing High Electroactive Consortia.

Iron-based nanomaterials (NMs) are increasingly used to promote extracellular electron transfer (EET) for energy production in bioelectrochemical systems (BESs). However, the composition and roles of planktonic bacteria in the solution regulated by iron-based NMs have rarely been taken into account. Herein, the changes of the microbial community in the solution by S-doped NiFe2O4 anodes have been demonstrated and used for constructing electroactive consortia on normal carbon cloth anodes, which could achieve the same level of electricity generation as NMs-mediated biofilm, as indicated by the significantly high voltage response (0.64 V) and power density (3.5 W m-2), whereas with different microbial diversity and connections. Network analysis showed that the introduction of iron-based NMs made Geobacter positively interact with f_Rhodocyclaceae, improving the competitiveness of the consortium (Geobacter and f_Rhodocyclaceae). Additionally, planktonic bacteria regulated by S-doped anode alone cannot hinder the stimulation of Geobacter by electricity and acetate, while the assistance of lining biofilm enhanced the cooperation of sulfur-oxidizing bacteria (SOB) and fermentative bacteria (FB), thus promoting the electroactivity of microbial consortia. This study reveals the effect of S-doped NiFe2O4 NMs on the network of microbial communities in MFCs and highlights the importance of globality of microbial community, which provides a feasible solution for the safer and more economical environmental applications of NMs.

Hierarchical Core-Shell Co2 N/CoP Embedded in N, P-doped Carbon Nanotubes as Efficient Oxygen Reduction Reaction Catalysts for Zn-air Batteries.

Projecting a cost-effective and highly efficient electrocatalyst for the oxygen reaction reduction (ORR) counts a great deal for Zn-air batteries. Herein, a hierarchical core-shell ORR catalyst (Co2 N/CoP@PNCNTs) is developed by embedding cobalt phosphides and/or cobalt nitrides as the core into N, P-doped carbon nanotubes (PNCNTs) as the shell via one-step carbonization, nitridation, and phosphorization of pyrolyzing Co-MOF precursor. The globally N, P-doped structure of Co2 N/CoP@PNCNTs demonstrates an outstanding electrocatalytic activity in the alkaline solution with the onset and half-wave potentials of 1.07 and 0.85 V respectively. Moreover, a Zn-air battery assembled from Co2 N/CoP@PNCNTs as the air cathode delivers an open circuit potential of 1.49 V, a maximum power density of 151.1 mW cm-2 and a specific capacity of 823.8 mAh kg-1 . It is reflected that Co2 N/CoP@PNCNTs provides a long-term durability with a slight decline of 15 h in the chronoamperometry measurement and an excellent charge-discharge stability with negligible voltage decay for 150 h at 10 mA cm-2 in Zn-air batteries. The results reveal that Co2 N/CoP@PNCNTs has superiority over most Co-Nx -C or Cox P@C catalysts reported so far. The excellent catalytic properties and stability of Co2 N/CoP@PNCNTs derive from synergistic effects between Co2 N/CoP and mesoporous N, P-doped carbon nanotubes.