TY - JOUR
T1 - Fast-response/stable Ni-Bi cells achieved using hollowed-out Bi@carbon nanospheres
T2 - A preferred electricity storage choice to couple with clean energy harvesting
AU - Yao, Jiajia
AU - Li, Linpo
AU - Li, Ning
AU - Jiang, Jian
AU - Wang, Yanlong
AU - Zhu, Jianhui
N1 - Publisher Copyright:
This journal is © the Partner Organisations.
PY - 2020/4
Y1 - 2020/4
N2 - Metallic bismuth (Bi) is a burgeoning choice of anode for rechargeable aqueous batteries given its large volumetric capacity, proper operating potential and highly reversible redox behavior. However, its further progress for full-cell implementation is unfortunately impeded due to the inferior anodic stability of Bi over long-term operation. Worse still, its low melting point (∼271 °C) prevents the use of conventional optimizing techniques (e.g., carbon modification) to alleviate tough anodic fading issues. We herein propose an unusual engineering protocol to enable Bi nanounits packaged into carbon sheaths using NH4Bi3F10 nanospheres as initiating materials. Of particular note is that the high electrovalent bond of Bi-F plays a key role in promoting the bismuth thermal durability beyond 400 °C. Such Bi@carbon hybrids have special hollowed-out nanoscale features, with highly accessible surface areas, smooth ionic transport channels and robust mechanical properties against electrode degradation. The as-built anodes possess impressive specific capacity and rate capability (∼53.9% capacity retention at 20 A g-1), as well as prolonged cyclic lifespan (beyond 80% capacity retention after 103 cycles). More significantly, we further affirm the unique anodic phase conversions of "Bi ↔ Bi(OH)3" on a real-time basis using characterizations/post-analysis at different cyclic stages. Our assembled Ni-Bi cells with notable peak energy/power densities of ∼82.32 W h kg-1/∼15.7 kW kg-1 and fast-response and stable behavior, may be fit for green energy-harvesting use.
AB - Metallic bismuth (Bi) is a burgeoning choice of anode for rechargeable aqueous batteries given its large volumetric capacity, proper operating potential and highly reversible redox behavior. However, its further progress for full-cell implementation is unfortunately impeded due to the inferior anodic stability of Bi over long-term operation. Worse still, its low melting point (∼271 °C) prevents the use of conventional optimizing techniques (e.g., carbon modification) to alleviate tough anodic fading issues. We herein propose an unusual engineering protocol to enable Bi nanounits packaged into carbon sheaths using NH4Bi3F10 nanospheres as initiating materials. Of particular note is that the high electrovalent bond of Bi-F plays a key role in promoting the bismuth thermal durability beyond 400 °C. Such Bi@carbon hybrids have special hollowed-out nanoscale features, with highly accessible surface areas, smooth ionic transport channels and robust mechanical properties against electrode degradation. The as-built anodes possess impressive specific capacity and rate capability (∼53.9% capacity retention at 20 A g-1), as well as prolonged cyclic lifespan (beyond 80% capacity retention after 103 cycles). More significantly, we further affirm the unique anodic phase conversions of "Bi ↔ Bi(OH)3" on a real-time basis using characterizations/post-analysis at different cyclic stages. Our assembled Ni-Bi cells with notable peak energy/power densities of ∼82.32 W h kg-1/∼15.7 kW kg-1 and fast-response and stable behavior, may be fit for green energy-harvesting use.
UR - http://www.scopus.com/inward/record.url?scp=85083221855&partnerID=8YFLogxK
U2 - 10.1039/d0qm00017e
DO - 10.1039/d0qm00017e
M3 - Article
AN - SCOPUS:85083221855
SN - 2052-1537
VL - 4
SP - 1249
EP - 1255
JO - Materials Chemistry Frontiers
JF - Materials Chemistry Frontiers
IS - 4
ER -