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:T548,To address the challenge of huge volume change and unstable solid electrolyte interface (SEI) of silicon in cycles, causing severe pulverization, this paper proposes a "double-shell" concept. This concept is designed to perform dual functions on encapsulating volume change of silicon and stabilizing SEI layer in cycles using double carbon shells. Double carbon shells coated Si nanoparticles (DCS-Si) are prepared. Inner carbon shell provides finite inner voids to allow large volume changes of Si nanoparticles inside of inner carbon shell, while static outer shell facilitates the formation of stable SEI. Most importantly, intershell spaces are preserved to buffer volume changes and alleviate mechanical stress from inner carbon shell. DCS-Si electrodes display a high rechargeable specific capacity of 1802 mAh g^-1 at a current rate of 0.2 C, superior rate capability and good cycling performance up to 1000 cycles. A full cell of DCS-Si//LiNi_0.45 Co_0.1 Mn_1.45 O₄ exhibits an average discharge voltage of 4.2 V, a high energy density of 473.6 Wh kg^-1 , and good cycling performance. Such double-shell concept can be applied to synthesize other electrode materials with large volume changes in cycles by simultaneously enhancing electronic conductivity and controlling SEI growth.1e:T42b,Abstract In this study, a straightforward coassembly strategy is demonstrated to synthesize Pt sensitized mesoporous WO 3 with crystalline framework through the simultaneous coassembly of amphiphilic poly(ethylene oxide)‐ b ‐polystyrene, hydrophobic platinum precursors, and hydrophilic tungsten precursors. The obtained WO 3 /Pt nanocomposites possess large pore size (≈13 nm), high surface area (128 m 2 g −1 ), large pore volume (0.32 cm 3 g −1 ), and Pt nanoparticles (≈4 nm) in situ homogeneously distributed in mesopores, and they exhibit excellent catalytic sensing response to CO of low concentration at low working temperature with good sensitivity, ultrashort response‐recovery time (16 s/1 s), and high selectivity. In‐depth study reveals that besides the contribution from the fast diffusion of gaseous molecules and rich interfaces in mesoporous WO 3 /Pt nanocomposites, the partially oxidized Pt nanoparticles that chemically and electronically sensitize the crystalline WO 3 matrix, dramatically enhance the sensitivity and selectivity.

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