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:T4f8,A sweat-based flexible supercapacitor (SC) for self-powered smart textiles and wearable systems is presented. The developed SC uses sweat as the electrolyte and poly(3,4-ethylenedioxythiophene):poly(styrenesulfonate) (PEDOT:PSS) as the active electrode. With PEDOT:PSS coated onto cellulose/polyester cloth, the SC shows specific capacitance of 8.94 F g^-1 (10 mF cm^-2 ) at 1 mV s^-1 . With artificial sweat, the energy and power densities of the SC are 1.36 Wh kg^-1 and 329.70 W kg^-1 , respectively for 1.31 V and its specific capacitance is 5.65 F g^-1 . With real human sweat the observed energy and power densities are 0.25 Wh kg^-1 , and 30.62 W kg^-1 , respectively. The SC performance is evaluated with different volumes of sweat (20, 50, and 100 µL), bending radii (10, 15, 20 mm), charging/discharging stability (4000 cycles), and washability. With successful on-body testing, the first demonstration of the suitability of a sweat-based SC for self-powered cloth-based sensors to monitor sweat salinity is presented. With attractive performance and the use of body fluids, the presented approach is a safe and sustainable route to meet the power requirements in wearable systems.1e:T493,Battery-type materials for supercapacitors have attracted increasing research interest owing to their high energy density. However, their poor electrode kinetics severely limit the utilization of redox-active sites on the electrode surface, resulting in subpar electrochemical performance. Herein, we incorporate both Cu dopants and O vacancies into Co3O4 nanocrystals confined in a carbon matrix (Ov-Cu-Co3O4@C) which are assembled into nanowires. This heterostructured architecture with multifunctional nanogeometries provides a high intercomponent synergy, enabling high accessibility to active species. Moreover, the Cu dopants and O vacancies in Ov-Cu-Co3O4@C synergistically manipulate the electronic states and provide more accessible active sites, resulting in enhanced electrical conductivity and enriched redox chemistry. The Ov-Cu-Co3O4@C achieves a significantly improved specific capacity and rate performance, exceeding those of Co3O4@C. The asymmetric supercapacitors with Ov-Cu-Co3O4@C deliver a high energy density of 64.1 W h kg–1 at 800 W kg–1, exhibiting good flexibility without significant performance degradation under different bending states.1f:T56f,Abstract Developing low‐cost and high‐efficiency catalysts for sustainable hydrogen production through electrocatalytic hydrogen evolution reaction (HER) is crucial yet remains challenging. Here, a strategy is proposed to fill Ni‐vacancy (Ni v ) sites of dual‐deficient NiO (D‐NiO‐Pt) deliberately created by Ar plasma with homogeneously distributed Pt atoms driven by oxygen vacancies (O v ). The incorporated Pt atoms filling the Ni v reduce the formation energy to increase crystal stability, and subsequently combine with additional O v to tune the electronic structure of the surrounding Ni sites. Thus, a more ideal hydrogen adsorption free energy (Δ G H* ) closer to 0 of Ni sites and Pt sites can be achieved. As a result, the D‐NiO‐Pt electrode achieves superior mass activity of ≈1600 mA mg −1 (normalized by platinum) and nearly negligible loss of activity during long‐term operation, which is much better than as‐prepared Pt‐containing NiO catalysts without plasma treatment. A low overpotential of 20 mV i

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