Ramakrishnan Prakash, Shanmugam Sangaraju, Kim Jae Hyun
Division of Nano and Energy Convergence Research, Daegu Gyeongbuk Institute of Science and Technology (DGIST), 333, Techno Jungang Daero, Hyeonpung-myeon, Dalseong-gun, Daegu, 42988, Republic of Korea.
Department of Energy Systems Engineering, Daegu Gyeongbuk Institute of Science and Technology (DGIST), 333, Techno Jungang Daero, Hyeonpung-myeon, Dalseong-gun, Daegu, 42988, Republic of Korea.
ChemSusChem. 2017 Apr 10;10(7):1554-1562. doi: 10.1002/cssc.201601810. Epub 2017 Mar 2.
Cost-effective dual heteroatom-doped 3D carbon nanofoam-wrapped FeS nanoparticles (NPs), FeS-C, act as efficient bifunctional catalysts for Li-O batteries. This cathode exhibits a maximum deep discharge capacity of 14 777.5 mA h g with a 98.1 % columbic efficiency at 0.1 mA cm . The controlled capacity (500 mA h g ) test of this cathode delivers a minimum polarization gap of 0.73 V at 0.1 mA cm and is sustained for 100 cycles with an energy efficiency of approximately 64 % (1st cycle) and 52 % (100th cycle) at 0.3 mA cm , under the potential window of 2.0-4.5 V. X-ray photoelectron spectroscopy reveals the substantial reversible formation and complete decomposition of Li O . The excellent recharging ability, high rate performance, and cycle stability of this catalyst is attributed to the synergistic effect of FeS catalytic behavior and textural properties of heteroatom-doped carbon nanostructures.
具有成本效益的双杂原子掺杂三维碳纳米泡沫包裹硫化亚铁纳米颗粒(FeS-C)可作为锂氧电池的高效双功能催化剂。这种阴极在0.1 mA cm 时表现出最大深度放电容量为14777.5 mA h g,库仑效率为98.1%。该阴极的控制容量(500 mA h g )测试在0.1 mA cm 时提供最小极化间隙为0.73 V,并在2.0 - 4.5 V的电位窗口下,于0.3 mA cm 时可持续100个循环,首次循环能量效率约为64%,第100次循环能量效率约为52%。X射线光电子能谱揭示了Li O 的大量可逆形成和完全分解。这种催化剂优异的充电能力、高倍率性能和循环稳定性归因于FeS催化行为与杂原子掺杂碳纳米结构的织构性质的协同效应。