1c:I[419806,["/_next/static/chunks/bb923814e1f4d2e9.js","/_next/static/chunks/dd3ee9f5b7716ca6.js","/_next/static/chunks/4204a0ae82542ca8.js","/_next/static/chunks/1270dead247da766.js","/_next/static/chunks/6e1aa89a642f40be.js","/_next/static/chunks/2d7aa753e81324a8.js","/_next/static/chunks/8ffd0b71567920d8.js","/_next/static/chunks/67ea6dfd21f16c5f.js","/_next/static/chunks/24eb4379f68013fd.js","/_next/static/chunks/b8cd775ffdf935bd.js","/_next/static/chunks/983103cd9eb7b428.js","/_next/static/chunks/263f2cdcb9aa2341.js","/_next/static/chunks/294b9525248c8e5f.js"],"default"] 1d:T46c,Abstract Carbonaceous materials have been accepted as a promising family of anode materials for lithium‐ion batteries (LIBs) owing to optimal overall performance. Among various emerging carbonaceous anode materials, hard carbons have recently gained significant attention for high‐energy LIBs. The most attractive features of hard carbons are the enriched microcrystalline structure, which not only benefits the uptake of more Li + ions but also facilitates the Li + ions intercalation and deintercalation. However, the booming application of hard carbons is significantly slowed by the low initial Coulombic efficiency, large initial irreversible capacity, and voltage hysteresis. Many efforts have been devoted to address these challenges toward practical applications. This paper focuses on an up‐to‐date overview of hard carbons, with an emphasis on the lithium storage fundamentals and material classification of hard carbons as well as present challenges and potential solutions. The future prospects and perspectives on hard carbons to enable practical application in next‐generation batteries are also highlighted.1e:T41b,Large-area phosphorus-doped carbon nanosheets (P-CNSs) are first obtained from carbon dots (CDs) through self-assembly driving from thermal treatment with Na catalysis. This is the first time to realize the conversion from 0D CDs to 2D nanosheets doped with phosphorus. The sodium storage behavior of phosphorus-doped carbon material is also investigated for the first time. As anode material for sodium-ion batteries (SIBs), P-CNSs exhibit superb performances for electrochemical storage of sodium. When cycled at 0.1 A g^-1, the P-CNSs electrode delivers a high reversible capacity of 328 mAh g^-1, even at a high current density of 20 A g^-1, a considerable capacity of 108 mAh g^-1 can still be maintained. Besides, this material also shows excellent cycling stability, at a current density of 5 A g^-1, the reversible capacity can still reach 149 mAh g^-1 after 5000 cycles. This work will provide significant value for the development of both carbon materials and SIBs anode materials.1f:T501,MoSe 2 grown on N,P‐co‐doped carbon nanosheets is synthesized by a solvothermal reaction followed with a high‐temperature calcination. This composite has an interlayer spacing of MoSe 2 expanded to facilitate sodium‐ion diffusion, MoSe 2 immobilized on carbon nanosheets to improve charge‐transfer kinetics, and N and P incorporated into carbon to enhance its interaction with active species upon cycling. These features greatly improve the electrochemical performance of this composite, as compared to all the controls. It presents a specific capacity of 378 mAh g −1 after 1000 cycles at 0.5 A g −1 , corresponding to 87% of the capacity at the second cycle. Ex situ Raman spectra and high‐resolution transmission electron microscopy images confirm that it is element Se, rather than MoSe 2 , formed after the charging process. The interaction of the active species with modified carbon is simulated using density functional theory to explain this excellent stability. The superior rate capability, where the capacity at 15 A g −1 equals ≈55% of that at 0.5 A g −1 , could be associated with the significant contribution of pseudocapacitance. By pairing with homemade Na 3 V 2 (PO 4 ) 3 /C, this composite also exhibits excellent performances in full cells.20:T528,Abstract The low

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