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Metal-free carbon materials have emerged as cost-effective and high-performance catalysts for the production of hydrogen peroxide (H 2 O 2 ) through the two-electron oxygen reduction reaction (ORR). Here, we show that 3D crumpled graphene with controlled oxygen and defect configurations significantly improves the electrocatalytic production of H 2 O 2 . The crumpled graphene electrocatalyst with optimal defect structures and oxygen functional groups exhibits outstanding H 2 O 2 selectivity of 92–100% in a wide potential window of 0.05–0.7 V vs. reversible hydrogen electrode (RHE) and a high mass activity of 158 A g −1 at 0.65 V vs. RHE in alkaline media. In addition, the crumpled graphene catalyst showed an excellent H 2 O 2 production rate of 473.9 mmol gcat −1 h −1 and stability over 46 h at 0.4 V vs. RHE. Moreover, density functional theory calculations revealed the role of the functional groups and defect sites in the two-electron ORR pathway through the scaling relation between OOH and O adsorption strengths. These results establish a structure-mechanism-performance relationship of functionalized carbon catalysts for the effective production of H 2 O 2 . 

For decades, reports have suggested that photo-catalytic nitrogen fixation by titania in an aqueous environment is possible. Yet a consensus does not exist regarding how the reaction proceeds. Furthermore, the presence of an aqueous protonated solvent and the similarity between the redox potential for nitrogen and proton reduction suggest that ammonia production is unlikely. Here, we re-investigate photo-catalytic nitrogen fixation by titania in an aqueous environment through a series of photo-catalytic and electrocatalytic experiments. Photo-catalytic testing reveals that mineral phase and metal dopants play a marginal role in promoting nitrogen photofixation, with ammonia production increasing when the majority phase is rutile and with iron dopants. However, the presence of a trace amount of adsorbed carbonaceous species increased the rate of ammonia production by two times that observed without adsorbed carbon based species. This suggests that carbon species play a potential larger role in mediating the nitrogen fixation process over mineral phase and metal dopants. We also demonstrate an experimental approach aimed to detect low-level ammonia production from photo-catalysts using rotating ring disk electrode experiments conducted with and without illumination. Consistent with the photocatalysis, ammonia is only discernible at the ring with rutile phase titania, but not with mixed-phase titania. Rotating ring disk electrode experiments may also provide a new avenue to attain a higher degree of precision in detecting ammonia at low levels. 

The significant performance decay in conventional graphite anodes under low‐temperature conditions is attributed to the slow diffusion of alkali metal ions, requiring new strategies to enhance the charge storage kinetics at low temperatures. Here, nitrogen (N)‐doped defective crumpled graphene (NCG) is employed as a promising anode to enable stable low‐temperature operation of alkali metal‐ion storage by exploiting the surface‐controlled charge storage mechanisms. At a low temperature of −40 °C, the NCG anodes maintain high capacities of ≈172 mAh g⁻¹for lithium (Li)‐ion, ≈107 mAh g⁻¹for sodium (Na)‐ion, and ≈118 mAh g⁻¹for potassium (K)‐ion at 0.01 A g⁻¹with outstanding rate‐capability and cycling stability. A combination of density functional theory (DFT) and electrochemical analysis further reveals the role of the N‐functional groups and defect sites in improving the utilization of the surface‐controlled charge storage mechanisms. In addition, the full cell with the NCG anode and a LiFePO₄cathode shows a high capacity of ≈73 mAh g⁻¹at 0.5 °C even at −40 °C. The results highlight the importance of utilizing the surface‐controlled charge storage mechanisms with controlled defect structures and functional groups on the carbon surface to improve the charge storage performance of alkali metal‐ion under low‐temperature conditions.

 

Organic materials with redox‐active oxygen functional groups are of great interest as electrode materials for alkali‐ion storage due to their earth‐abundant constituents, structural tunability, and enhanced energy storage properties. Herein, a hybrid carbon framework consisting of reduced graphene oxide and oxygen functionalized carbon quantum dots (CQDs) is developed via the one‐pot solvothermal reduction method, and a systematic study is undertaken to investigate its redox mechanism and electrochemical properties with Li‐, Na‐, and K‐ions. Due to the incorporation of CQDs, the hybrid cathode delivers consistent improvements in charge storage performance for the alkali‐ions and impressive reversible capacity (257 mAh g⁻¹at 50 mA g⁻¹), rate capability (111 mAh g⁻¹at 1 A g⁻¹), and cycling stability (79% retention after 10 000 cycles) with Li‐ion. Furthermore, density functional theory calculations uncover the CQD structure‐electrochemical reactivity trends for different alkali‐ion. The results provide important insights into adopting CQD species for optimal alkali‐ion storage.

 

Sodium‐metal batteries (SMBs) are considered as a compliment to lithium‐metal batteries for next‐generation high‐energy batteries because of their low cost and the abundance of sodium (Na). Herein, a 3D nanostructured porous carbon particle containing carbon‐shell‐coated Fe nanoparticles (PC‐CFe) is employed as a highly reversible Na‐metal host. PC‐CFe has a unique 3D hierarchy based on sub‐micrometer‐sized carbon particles, ordered open channels, and evenly distributed carbon‐coated Fe nanoparticles (CFe) on the surface. PC‐CFe achieves high reversibility of Na plating/stripping processes over 500 cycles with a Coulombic efficiency of 99.6% at 10 mA cm^–2with 10 mAh cm^–2in Na//Cu asymmetric cells, as well as over 14 400 cycles at 60 mA cm^–2in Na//Na symmetric cells. Density functional theory calculations reveal that the superior cycling performance of PC‐CFe stems from the stronger adsorption of Na on the surface of the CFe, providing initial nucleation sites more favorable to Na deposition. Moreover, the full cell with a PC‐CFe host without Na metal and a high‐loading Na₃V₂(PO₄)₃cathode (10 mg cm^–2) maintains a high capacity of 103 mAh g^–1at 1 mA cm^–2even after 100 cycles, demonstrating the operation of anode‐free SMBs.

 

The energy and power performance of lithium (Li)‐ion batteries is significantly reduced at low‐temperature conditions, which is mainly due to the slow diffusion of Li‐ions in graphite anode. Here, it is demonstrated that the effective utilization of the surface‐controlled charge storage mechanism through the transition from layered graphite to 3D crumpled graphene (CG) dramatically improves the Li‐ion charge storage kinetics and structural stability at low‐temperature conditions. The structure‐controlled CG anode prepared via a one‐step aerosol drying process shows a remarkable rate‐capability by delivering ≈206 mAh g^–1at a high current density of 10 A g^–1at room temperature. At an extremely low temperature of −40 °C, CG anode still exhibits a high capacity of ≈154 mAh g^–1at 0.01 A g^–1with excellent rate‐capability and cycling stability. A combination of electrochemical studies and density functional theory (DFT) reveals that the superior performance of CG anode stems from the dominant surface‐controlled charge storage mechanism at various defect sites. This study establishes the effective utilization of the surface‐controlled charge storage mechanism through structure‐controlled graphene as a promising strategy to improve the charge storage kinetics and stability under low‐temperature conditions.