کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
8955460 | 1646091 | 2019 | 9 صفحه PDF | دانلود رایگان |
عنوان انگلیسی مقاله ISI
ZnSxSe1-x/N-C (xâ¯=â¯0.24) hierarchical nanosphere with improved energy storage capability as sodium-ion battery anode
دانلود مقاله + سفارش ترجمه
دانلود مقاله ISI انگلیسی
رایگان برای ایرانیان
موضوعات مرتبط
مهندسی و علوم پایه
مهندسی مواد
فلزات و آلیاژها
پیش نمایش صفحه اول مقاله

چکیده انگلیسی
Anode materials are demonstrated to essentially affect the electrochemical performance of sodium-ion batteries (SIBs), which are considered as a promising large-scale energy storage device. In this work, alloying ZnSxSe1-x (xâ¯=â¯0.24) and N doped carbon composite (ZnSxSe1-x/N-C (xâ¯=â¯0.24)) hierarchical nanospheres are prepared by selenizing the ZnS precursor. The corresponding X-ray diffraction and high-resolution transmission electron microscopy results prove the formation of an alloyed phase, resulting in a wider lattice compared with ZnS. Benefitting from the coexistence of S2â and Se2â in the ZnSxSe1-x lattice, the weaker Zn-Se bonds and wider lattice spacing facilitate ultrafast pseudocapacitive sodium storage capability and enhanced cycling stability, when ZnSxSe1-x/N-C is used as anode material for SIBs. At current of 1.0â¯Aâ¯gâ1, it delivers a capacity of 378â¯mAh gâ1 after 130 cycles with capacity retention of 87.9%, which is much higher than 34.3% for the ZnS/N-C electrode. In addition, for the rate performance, it can maintain an impressive capacity of 233â¯mAh gâ1â¯at 10.0â¯Aâ¯gâ1 with a capacity retention of 55.9% in comparison with the capacity at 0.2â¯Aâ¯gâ1. This work provides us common thoughts to enhance the electrochemical performance of transition metal chalcogenide anode through anion substitution.
ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Journal of Alloys and Compounds - Volume 771, 15 January 2019, Pages 147-155
Journal: Journal of Alloys and Compounds - Volume 771, 15 January 2019, Pages 147-155
نویسندگان
Dongxu Cao, Yuyu Wang, Wenpei Kang, Chenxu Li, Dongwei Cao, Lili Fan, Rongming Wang, Daofeng Sun,