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181.
Abe K Abt I Ahn CJ Akagi T Allen NJ Ash WW Aston D Baird KG Baltay C Band HR Barakat MB Baranko G Bardon O Barklow T Bazarko AO Ben-David R Benvenuti AC Bienz T Bilei GM Bisello D Blaylock G Bogart JR Bolton T Bower GR Brau JE Breidenbach M Bugg WM Burke D Burnett TH Burrows PN Busza W Calcaterra A Caldwell DO Calloway D Camanzi B Carpinelli M Cassell R Castaldi R Castro A Cavalli-Sforza M Church E Cohn HO Coller JA Cook V Cotton R Cowan RF Coyne DG D'Oliveira A Damerell CJ Daoudi M 《Physical review D: Particles and fields》1995,52(7):4240-4244
182.
Bai JZ Bardon O Blum I Breakstone A Burnett T Chen GP Chen HF Chen J Chen SJ Chen SM Chen Y Chen YB Chen YQ Cheng BS Cowan RF Cui HC Cui XZ Ding HL Du ZZ Dunwoodie W Fan XL Fang J Fero M Gao CS Gao ML Gao SQ Gao WX Gratton P Gu JH Gu SD Gu WX Gu YF Guo YN Han SW Han Y Harris FA Hatanaka M He J He KR He M Hitlin DG Hu GY Hu HB Hu T Hu XQ Huang DQ Huang YZ Izen JM Jia QP Jiang CH Jin Y Jones L Kang SH Kelsey MH Kim BK Lai YF Lan HB Lang PF Lankford A Li F Li J Li PQ Li Q Li RB 《Physical review D: Particles and fields》1995,52(7):3781-3784
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186.
Abe K Abt I Ash WW Aston D Bacchetta N Baird KG Baltay C Band HR Barakat MB Baranko G Bardon O Barklow T Bazarko AO Ben-David R Benvenuti AC Bienz T Bilei GM Bisello D Blaylock G Bogart JR Bolton T Bower GR Brau JE Breidenbach M Bugg WM Burke D Burnett TH Burrows PN Busza W Calcaterra A Caldwell DO Calloway D Camanzi B Carpinelli M Cassell R Castaldi R Castro A Cavalli-Sforza M Church E Cohn HO Coller JA Cook V Cotton R Cowan RF Coyne DG D'Oliveira A Damerell CJ Dasu S De Sangro R De Simone P 《Physical review D: Particles and fields》1994,50(9):5580-5590
187.
Duan Bin Yanyan Du Beibei Yang Hongbin Lu Yao Liu Yongyao Xia 《Advanced functional materials》2023,33(8):2211765
Aqueous rechargeable zinc batteries (ARZBs) are recently prevailing devices that utilize the abundant Zn resources and the merits of aqueous electrolytes to become a competitive alternative for large-scale energy storage. Benefiting from the unique inductive effect and flexible structure, the past five years have experienced a diversiform of phosphate-based polyanion materials that are used as cathodes in ARZBs. In this review, the most recent advances in the Zn2+ storage mechanisms and electrolyte optimization of the phosphate-based cathodes of ARZBs, which mainly focus on vanadium/iron-based phosphates and their derivatives are presented. Furthermore, in addition to significant progress on polyanion phosphate-based cathode materials, the design strategies both for electrode materials and compatible electrolytes are also elaborated to improve the energy density and extend the cycling life of aqueous Zn/polyanion batteries. 相似文献
188.
Ying-Xia Du Qiao Yang Wang-Ting Lu Qing-Yu Guan Fei-Fei Cao Geng Zhang 《Advanced functional materials》2023,33(27):2300895
Single metal atom isolated in nitrogen-doped carbon materials (M N C) are effective electrocatalysts for oxygen reduction reaction (ORR), which produces H2O2 or H2O via 2-electron or 4-electron process. However, most of M N C catalysts can only present high selectivity for one product, and the selectivity is usually regulated by complicated structure design. Herein, a carbon black-supported Co N C catalyst (CB@Co N C) is synthesized. Tunable 2-electron/4-electron behavior is realized on CB@Co-N-C by utilizing its H2O2 yield dependence on electrolyte pH and catalyst loading. In acidic media with low catalyst loading, CB@Co N C presents excellent mass activity and high selectivity for H2O2 production. In flow cell with gas diffusion electrode, a H2O2 production rate of 5.04 mol h−1 g−1 is achieved by CB@Co N C on electrolyte circulation mode, and a long-term H2O2 production of 200 h is demonstrated on electrolyte non-circulation mode. Meanwhile, CB@Co N C exhibits a dominant 4-electron ORR pathway with high activity and durability in pH neutral media with high catalyst loading. The microbial fuel cell using CB@Co N C as the cathode catalyst shows a peak power density close to that of benchmark Pt/C catalyst. 相似文献
189.
Yiqian Du Zhikai Yan Wenbin You Qiaoqiao Men Guanyu Chen Xiaowei Lv Yuyang Wu Kaicheng Luo Biao Zhao Jincang Zhang Renchao Che 《Advanced functional materials》2023,33(34):2301449
Surface chemistry and interlayer engineering determines the electrical properties of 2D MXene. However, it remains challenging to regulate the surface and interfacial chemistry of MXene simultaneously. Herein, simultaneous modulation of Ti3C2Tx MXene surface termination and layer spacing by alkali treatment are achieved. The electrical and electromagnetic properties of Ti3C2Tx are investigated in detail with respect to KOH and ammonia concentration dependence. A high concentration of KOH caused the Ti3C2Tx layer spacing to expand to 13.7 Å and the surface O/F ratio to increase to 33.84. Because of its weaker ionization effect, ammonia provides finer tuning compared to the drastic intercalation of KOH with a thorough sweeping of the F-containing groups. Ti3C2Tx is enriched with conductive -OH termination after ammonia treatment, which achieves an effective balance with the increased interlayer resistance. Therefore, NH3H2O-Ti3C2Tx achieves broad-band impedance matching and exhibits an efficient microwave loss of −49.1 dB at a low thickness of 1.7 mm, with an effective frequency bandwidth of 3.9 GHz. The results herein optimize the electrical properties of Ti3C2Tx using surface and interfacial chemistry to achieve broad microwave absorption, providing a framework for enhancing the electromagnetic wave loss of intrinsic MXene. 相似文献
190.
Hao Hu Mingzhe Nie Massimiliano Galluzzi Xuefeng Yu Xuemin Du 《Advanced functional materials》2023,33(45):2304634
Artificial intelligent actuators are extensively explored for emerging applications such as soft robots, human-machine interfaces, and biomedical devices. However, intelligent actuating systems based on synthesized polymers suffer from challenges in renewability, sustainability, and safety, while natural polymer-based actuators show limited capabilities and performances due to the presence of abundant hydrogen-bond lockers. Here this study reports a new hydrogen bond-mediated strategy to develop mimosa-inspired starch actuators (SA). By harnessing the unique features of gelatinization and abundant hydrogen bonds, these SA enable high-sensitivity and multi-responsive actuation in various scenarios. The non-gelatinized SA can be irreversibly programmed into diverse shapes, such as artificial flowers, bowl shapes, and helix structures, using near-infrared light. Furthermore, the gelatinized SA exhibit reversibly multi-responsive actuation when exposed to low humidity (10.2%), low temperature (37 °C), or low-energy light (0.42 W cm−2). More importantly, the SA demonstrate robust applications in smart living, including artificial mimosa, intelligent lampshade, and morphing food. By overcoming the hydrogen-bond lockers inherent in natural polymers, SA open new avenues for next-generation recyclable materials and actuators, bringing them closer to practical applications. 相似文献