MatterPub Date : 2026-08-25DOI: 10.1016/j.matt.2026.102970
Huanjie He,Tao Liu,Ziyi Ye,Xue Cui,Rongrong Liang,Kang Yu,Xiangjiang Meng,Chenchen Cai,Shuangxi Nie
{"title":"Triboelectric E-Fibers: Toward energy-autonomous wearable electronics","authors":"Huanjie He,Tao Liu,Ziyi Ye,Xue Cui,Rongrong Liang,Kang Yu,Xiangjiang Meng,Chenchen Cai,Shuangxi Nie","doi":"10.1016/j.matt.2026.102970","DOIUrl":"https://doi.org/10.1016/j.matt.2026.102970","url":null,"abstract":"Triboelectric electronic fibers (E-Fibers) combine wearability with electronic functionality, offering broad prospects in self-powered and sustainable wearable electronics and finding extensive applications in biomedical, sports health, and industrial manufacturing fields. However, due to research disparities between materials science and textile engineering, the intrinsic relationship between fiber structural advantages and advanced performance remains unclear, posing significant challenges for the development of wearable electronic devices. This review systematically discusses the fundamental fiber structures and fabrication methods, and summarizes the pathways through which these unique one-dimensional fibers transform into two- and three-dimensional morphologies. Subsequently, performance enhancement strategies are examined from the perspective of structural advantages, alongside an exploration of recent advances in triboelectric E-Fiber-based electronic devices, including energy harvesting, wearable sensors, physiological monitoring, and human-machine interaction. Finally, remaining challenges and future prospects are discussed, aiming to provide a theoretical reference for the development of the next generation of E-Fibers.","PeriodicalId":388,"journal":{"name":"Matter","volume":"134 1","pages":""},"PeriodicalIF":18.9,"publicationDate":"2026-08-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"148821515","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"Sequential guidance-derived custom interphase configuration for zinc anodes with deep reversibility and versatility","authors":"Yining Chen,Congge Lu,Shuang Zhou,Shaoxing Li,Weihang Li,Jingkang Ma,Xiaodong Shi,Shangyong Lin,Quan Zong,Xiaobo Ji,Anqiang Pan","doi":"10.1016/j.matt.2026.102973","DOIUrl":"https://doi.org/10.1016/j.matt.2026.102973","url":null,"abstract":"The practical deployment of zinc metal anodes is severely strangled by inevitable issues of dendrite growth and water-induced side reactions, which collectively degrade zinc utilization and cycling durability. Herein, a sequential guidance-derived solid electrolyte interphase (SEI) design concept is proposed to resolve the inherent trade-offs among Zn2+ deposition regulation, corrosion inhibition, deep-discharge adaptability, and long-term robustness. The advanced Zn||Zn symmetric cells operate steadily for 3,800 h, and sustain 680-h lifespan even at 96.6% zinc utilization. Meanwhile, this design criteria demonstrates universal full-cell compatibility and scalable production potential. High-mass-loading full cells using vanadium and iodine cathodes deliver exceptional cycling stability over 1,200 and 2,500 cycles with negligible capacity decay. Notably, a pouch cell with a low N/P ratio achieved highly stable cycling for 600 cycles. This work establishes a sustainable design paradigm for other burgeoning “beyond-lithium” aqueous battery technologies.","PeriodicalId":388,"journal":{"name":"Matter","volume":"3 1","pages":""},"PeriodicalIF":18.9,"publicationDate":"2026-08-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"148821624","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"Multidimensional chiroptical physical unclonable functions based on chiral photonic crystal film","authors":"Jiang Huang,Xuefeng Yang,Xue Jin,Dong Liu,Pengfei Duan","doi":"10.1016/j.matt.2026.102974","DOIUrl":"https://doi.org/10.1016/j.matt.2026.102974","url":null,"abstract":"Randomness underpins optical physical unclonable functions (PUFs), yet most systems rely on simple intensity or spectral variations with limited entropy and susceptibility to artificial intelligence (AI)-driven attacks. Advanced spectroscopic methods raise security, but their reliance on specialized instrumentation hinders practical deployment. Here, we present user-friendly, easily verifiable chiroptical PUFs (CP-PUFs) based on chiral photonic crystal films, where relief-structured surfaces and intrinsic chiral architectures generate structural color and vectorial optical modulation, enabling broadband chiroptical encoding. This stochastic architecture generates multidimensional challenge-response encoding within a single pixel, jointly defined by real-space optical patterns and chiral-space polarization states. The interplay between dye distribution and polarization modulation is systematically elucidated for practical authentication. These CP-PUFs intrinsically encode highly unpredictable, high-entropy chiroptical signals for reliable identity verification. Leveraging stable light-structure chiral interactions, CP-PUFs offer a robust, low-cost, reusable, and portable platform with large encoding capacity for next-generation information security.","PeriodicalId":388,"journal":{"name":"Matter","volume":"19 1","pages":""},"PeriodicalIF":18.9,"publicationDate":"2026-08-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"148769083","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
MatterPub Date : 2026-08-19DOI: 10.1016/j.matt.2026.102968
Xiangyu Liu,Qingdong He,Fang Guo,Jinfang Wu,Jie Qi,Feilong Gong,Jian Liu,Wenbo Wang
{"title":"Ultradense metal-chelated nanoconfined network hydrogels enable tough, anti-swelling, and cryogenic electrolyte performance","authors":"Xiangyu Liu,Qingdong He,Fang Guo,Jinfang Wu,Jie Qi,Feilong Gong,Jian Liu,Wenbo Wang","doi":"10.1016/j.matt.2026.102968","DOIUrl":"https://doi.org/10.1016/j.matt.2026.102968","url":null,"abstract":"Hydrogels that are simultaneously tough, swelling resistant, and ionically conductive at subzero temperatures are crucial for soft devices in harsh environments, but are limited by trade-offs between network integrity, water mobility, and energy dissipation. Here, we address these constraints by engineering hydrogel network topology to nanoconfined water. We construct ultradense metal-chelated poly(acrylic acid) networks with uniform Zr–O nodes and sub-100 nm pores, yielding ∼0.3% dangling chains and a 16.99-fold higher crosslinking density than conventional gels, thereby eliminating network heterogeneity. This architecture converts most free water into bound water, establishing a “nanoscaffold-confined aqueous state” that suppresses swelling and freezing. Despite high water content (70%), the hydrogel achieves high strength (69 MPa) and toughness (6 MJ·m−3), while retaining cryo-resistant mechanics down to −40°C. As an electrolyte, it maintains high ionic conductivity from 25°C to −65°C, enabling quasi-solid-state Zn-air batteries to operate over 20,000 cycles at −65°C without capacity decay.","PeriodicalId":388,"journal":{"name":"Matter","volume":"125 25 1","pages":""},"PeriodicalIF":18.9,"publicationDate":"2026-08-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"148769084","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"26.31%-efficiency TOPCon solar cells enabled by synergistic metallization with reduced optical shading and contact resistance losses","authors":"Sheshicheng Chen,Zhenhai Yang,Cuiwen Guo,Jiwei Feng,Huiyun Gu,Shanshan Yang,Ziqiang Sun,Pengfei Lv,Xiaopeng Zhang,Ruihao An,Haojiang Du,Zunke Liu,Wei Liu,Xiulin Jiang,Yuheng Zeng,Jichun Ye","doi":"10.1016/j.matt.2026.102965","DOIUrl":"https://doi.org/10.1016/j.matt.2026.102965","url":null,"abstract":"Although tunnel oxide passivated contact (TOPCon) solar cells have become dominant in the crystalline silicon photovoltaic market, conventional TOPCon metallization relies on Al-containing Ag pastes and high-temperature firing, causing severe passivation degradation and optical shading. To address this, this study proposes a synergistic metallization strategy combining Al-free Ag paste with a tailored laser-enhanced contact optimization (LECO) process. LECO enables an advanced, low-penetration Pb-Ag/Si contact configuration with low resistivity, eliminating Al-induced alloying. Simultaneously, the low-corrosivity, highly rheological Al-free paste preserves surface passivation and reduces shading, achieving a high gridline aspect ratio of 0.55 and an exceptional open-circuit voltage (Voc) gain of 10.2 mV. Notably, the enhanced spectral response boosts the short-circuit current density (Jsc) to a high value of 41.98 mA cm–2, representing the highest certified Jsc reported to date for large-area TOPCon solar cells and contributing to a high certified efficiency of 26.31%.","PeriodicalId":388,"journal":{"name":"Matter","volume":"1 1","pages":""},"PeriodicalIF":18.9,"publicationDate":"2026-08-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"148692887","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"Atomic-level etching enables black phosphorus-based electrocatalysts with tuned high-loading single-atom/nanocluster microdomains","authors":"Yijie Fan, Zhuo Wang, Cong Liu, Bowen Guo, Wen Wang, Shenggeng Zhao, Jingning Zhang, Wei Liu, Chang Zhu, Kailiang Ren, Zhou Li, Dan Luo, Dingsheng Wang","doi":"10.1016/j.matt.2026.102857","DOIUrl":"10.1016/j.matt.2026.102857","url":null,"abstract":"<div><div>Single-atom and nanocluster (SA/NC) catalysts represent the forefront of SA catalysis due to their synergistic catalytic active sites while maintaining exceptional atomic efficiency. However, the intrinsically high surface energy of both SAs and NCs drives their aggregation on carriers, typically resulting in the formation of stable nanoparticles rather than isolated atomic species. In this work, we proposed a biphasic interfacial atomic etching strategy (BIAES) to construct atomically defective black phosphorus nanosheet (ad-BP NS) carriers, enabling the universal high-density loading of metal SAs and NCs on ad-BP NSs (M-SA/NC@ad-BP, M = Co, Fe, Ni, Cu). Experimental and theoretical calculations indicated that the high reactivity and spatial confinement of the atomic-scale defective sites in ad-BP NSs were crucial for the synthesis of M-SA/NC@ad-BP. Strong metal-support interactions, coupled with NC-induced electronic modulation of SA, confer exceptional electrocatalytic activity across multiple reactions. This strategy lays the foundation for the design of high-performance 2D carrier-based SA/NC electrocatalysts.</div></div>","PeriodicalId":388,"journal":{"name":"Matter","volume":"9 8","pages":"Article 102857"},"PeriodicalIF":15.7,"publicationDate":"2026-08-05","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"148693922","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"Electrostatic amplification of ferroelectric tunneling in van der Waals heterostructures","authors":"Yu-Ching Kuo, Feng-Shou Yang, Che-Yi Lin, Huynh-Uyen-Phuong Nguyen, Chi-Chun Cheng, Yuan-Ming Chang, Mu-Pai Lee, Chen-Yu Hsu, Yu-Chuan Tsao, Wei-Cheng Tsai, Kenji Watanabe, Takashi Taniguchi, Yen-Jung Chen, Sheng-Yao Hung, Wen-Wei Wu, Jan-Chi Yang, Mario Hofmann, Chang-Hong Shen, Yu-Lun Chueh, Po-Wen Chiu, Yen-Fu Lin","doi":"10.1016/j.matt.2026.102878","DOIUrl":"10.1016/j.matt.2026.102878","url":null,"abstract":"<div><div>Ferroelectric tunnel junctions promise energy-efficient non-volatile memories, but their scalability is limited by an electrostatic dilemma: ultrathin ferroelectric barriers enhance tunneling modulation yet suffer from severe leakage, whereas thicker barriers suppress leakage but reduce electroresistance. Here, we identify an electrostatic regime in a van der Waals heterostructure that is enabled by a low-density-of-states electrode and overcomes this trade-off by decoupling polarization control, tunneling modulation, and charge screening. Using a ferroelectric-semiconductor tunnel memory based on Bi<sub>2</sub>O<sub>2</sub>Se, hexagonal boron nitride, and graphene, we achieve ultra-low leakage and tunneling electroresistance exceeding 10<sup>5</sup>. Low-bias readout is dominated by polarization-modulated tunneling, while higher bias programming may involve additional field-assisted carrier redistribution. Systematic variation of graphene thickness reveals an exponential decay of electroresistance governed by Thomas-Fermi screening, establishing a screening-based design rule for van der Waals ferroelectric tunneling heterostructures.</div></div>","PeriodicalId":388,"journal":{"name":"Matter","volume":"9 8","pages":"Article 102878"},"PeriodicalIF":15.7,"publicationDate":"2026-08-05","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"148311608","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
MatterPub Date : 2026-08-05DOI: 10.1016/j.matt.2026.102946
Sheng Wu, Meifang Zhu, Shan Jiang
{"title":"An all-hydrogel fiber neural electrode array shrinks to the scale of neurons","authors":"Sheng Wu, Meifang Zhu, Shan Jiang","doi":"10.1016/j.matt.2026.102946","DOIUrl":"10.1016/j.matt.2026.102946","url":null,"abstract":"<div><div>The chronic performance of implantable neural electrodes is often compromised by multidimensional mismatches with living brain tissue, including geometric size, mechanical compliance, three-dimensional topology, and biochemical properties. Here, this preview highlights a study by Wang et al. that shrinks all-hydrogel fiber electrodes to the scale of neurons, advancing tissue-matched neural interfaces for stable long-term recording with minimal immune response.</div></div>","PeriodicalId":388,"journal":{"name":"Matter","volume":"9 8","pages":"Article 102946"},"PeriodicalIF":15.7,"publicationDate":"2026-08-05","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"148692850","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
MatterPub Date : 2026-08-05Epub Date: 2026-06-05DOI: 10.1016/j.matt.2026.102858
Jounghyun Yoo, Jinmyoung Joo, Wei Gao
{"title":"Bridging the barrier: Micro- and nanorobotics for active brain delivery","authors":"Jounghyun Yoo, Jinmyoung Joo, Wei Gao","doi":"10.1016/j.matt.2026.102858","DOIUrl":"10.1016/j.matt.2026.102858","url":null,"abstract":"<div><div>Micro- and nanorobots are emerging as an active transport modality for brain delivery, but the central question is when active control provides a meaningful advantage rather than a more elaborate route to the same endpoint. In the brain, therapeutic failure often reflects coupled bottlenecks at the vascular interface and after entry, where limited redistribution confines exposure to perivascular regions. This perspective asks when active control can meaningfully overcome these coupled transport bottlenecks. We organize the field around how actuation interacts with defined barrier-engagement mechanisms and post-entry redistribution across major brain disease contexts. We further propose quantitative benchmarks for evidencing blood-brain barrier (BBB) traversal, distinguishing parenchymal exposure from vascular retention, and defining exposure, safety, and reporting standards required for translation. By centering transport physics and compartment-resolved validation, we outline a roadmap for transforming active brain delivery from proof-of-concept demonstrations into clinically credible platforms.</div></div>","PeriodicalId":388,"journal":{"name":"Matter","volume":"9 8","pages":"Article 102858"},"PeriodicalIF":15.7,"publicationDate":"2026-08-05","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"148693925","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}