A sulfur-modified pore-blocking method to enhance the electrocatalytic stability of carbon-supported platinum nanoparticles.

Currently, the durability of electrode materials remains a big obstacle to the widespread adoption of proton exchange membrane fuel cells (PEMFCs). Herein thiourea and sodium dodecyl benzene sulfonate (SDS) were employed as sulfur source and carbon source to modify the pristine carbon black (Ketjen black EC300 J). A highly durable carbon supported Pt nanosized catalyst with higher platinum utilization for oxygen reduction reaction (ORR) in PEMFCs was produced by doping elemental sulfur into carbon supports and decreasing the carbon pore sizes and volume through a successive impregnation technique. The catalyst exhibits an initial activity of 0.167 A mgPt -1 at 0.90 V and demonstrates minimal activity loss after acceleration stress test (30,000 cycles of AST). The half-wave potential loss for representative sample (Pt/S-C-3) is only 14 mV with only 21.8 % ECSA decrease, 27.5 % MA loss and 5.9 % SA loss. A sintering test at various temperature shows a minor average size increase for sulfur-doped carbon (S-C) supported one (from 2.09 to 2.52 nm). In single-cell test, the MEA sample employing the platinum catalyst on modified carbon as cathode exhibited almost negligible performance loss after 30,000 cycles of AST.

Formation of Nanodimensional NiCoO2 Encapsulated in Porous Nitrogen-Doped Carbon Submicrospheres from a Bimetallic (Ni, Co) Organic Framework toward Efficient Lithium Storage.

Recently, rock-salt NiCoO2 (NCO) with desirable electronic conductivity has drawn enormous interest worldwide for energy-related applications. However, the intrinsically sluggish kinetics and electrode aggregation/volumetric change/pulverization during Li-insertion/-extraction processes hugely limit its applications in Li-ion batteries (LIBs). In the contribution, we first devise a bottom-up method for scalable fabrication of the nanodimensional NCO particles encapsulated in porous nitrogen-doped carbon submicrospheres (NCS), which are derived from a bimetal (Ni, Co) metal-organic framework. The porous NCS, as a flexible conductive skeleton, can buffer distinct volume expansion as an efficient buffering phase, restrain agglomeration of nanoscaled NCO, and enhance electronic conductivity and wettability of the electrode. Benefiting from the synergistic functions between the nanodimensional NCO and porous NCS, the obtained NCO@NCS anode (∼74.5 wt % NCO) is endowed with remarkable high-rate reversible capacity (∼403.0 mAh g-1 at 1.0 A g-1) and cycling behaviors (∼371.4 mAh g-1 after being cycled for 1000 times at 1.0 A g-1) along with a high lithium diffusion coefficient and remarkable pseudocapacitive contribution. Furthermore, the NCO@NCS-based full LIBs exhibit competitive lithium-storage properties in terms of energy density (∼217.0 Wh kg-1) and cyclic stability. Furthermore, we believe that the methodology is highly promising in versatile design and construction of binary metal oxide/carbon hybrid anodes for advanced LIBs.

Spatially Self-Confined Formation of Ultrafine NiCoO2 Nanoparticles@Ultralong Amorphous N-Doped Carbon Nanofibers as an Anode towards Efficient Capacitive Li+ Storage.

The exploration of anode materials with a high degree of electrochemical utilization for Li-ion batteries (LIBs) still remains a huge challenge despite pioneering breakthroughs. Rational engineering of electrode structures/components by facile strategies would offer infinite possibilities for the development of LIBs. In this study, one-dimensional ultralong nanohybrids of ultrafine NiCoO2 nanoparticles dispersed in situ in and/or on the surface of amorphous N-doped carbon nanofibers (NCO@ANCNFs) were fabricated by a bottom-up electrospinning protocol. By virtue of synergistic structural/component features, the obtained ultralong NCO@ANCNFs with low NCO loading (≈33.6 wt %) show highly efficient Li+ storage performance with high reversible capacity, high rate capability, and long cycle life. The unusual reversible crystalline transformation during cycling was analyzed. Quantitative analysis revealed that the pseudocapacitive contribution mainly accounts for the superior lithium storage of the NCO@ANCNFs. Besides, the ability of the hybrid anode to deliver competitive Li-storage properties even without conductive carbon greatly enhances its commercial applicability. An NCO@ANCNFs//LiNi0.8 Co0.15 Al0.05 O2 full battery was assembled and exhibited striking electrochemical properties. This contribution offers a scalable methodology to fabricate highly efficient hybrid anodes for advanced next-generation LIBs.

Sustainable rose multiflora derived nitrogen/oxygen-enriched micro-/mesoporous carbon as a low-cost competitive electrode towards high-performance electrochemical supercapacitors.

Cost-efficient carbonaceous materials have been utilized extensively for advanced electrochemical supercapacitors. However, modest gravimetric/volumetric capacitances are the insuperable bottleneck in their practical applications. Herein, we develop a simple yet scalable method to fabricate low-cost micro-/mesoporous N/O-enriched carbon (NOC-K) by using natural rose multiflora as a precursor with KOH activation. The biomass-derived NOC-K is endowed with a large surface area of ∼1646.7 m2 g-1, micro-/mesoporosity with ∼61.3% microporosity, high surface wettability, and a high content of N (∼1.2 at%)/O (∼26.7 at%) species. When evaluated as an electroactive material for supercapacitors, the NOC-K electrode (5 mg cm-2) yields large gravimetric/volumetric specific capacitances of ∼340.0 F g-1 (∼238.0 F cm-3) at 0.5 A g-1, and even ∼200.0 F g-1 (∼140.0 F cm-3) at 5.0 A g-1, a low capacitance decay of ∼4.2% after 8200 consecutive cycles, and a striking specific energy of ∼8.3 W h kg-1 in aqueous KOH electrolyte, benefiting from its intrinsic structural and compositional superiorities. Moreover, a remarkable specific energy of ∼52.6 W h kg-1 and ∼96.6% capacitance retention over 6500 cycles for the NOC-K based symmetric cell are obtained with the organic electrolyte. More promisingly, the competitive NOC-K demonstrates enormous potential towards advanced supercapacitors both with aqueous and organic electrolytes as a sustainable electrode candidate.