期刊
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
卷 58, 期 46, 页码 16474-16479出版社
WILEY-V C H VERLAG GMBH
DOI: 10.1002/anie.201909202
关键词
electrochemistry; fast kinetics; inorganic open-framework; low strain; potassium-ion batteries
资金
- National Natural Science Foundation of China [21771180, 21971239, 51702318, 21703036]
- Natural Science Foundation of Fujian Province [2018J01031]
A key challenge for potassium-ion batteries is to explore low-cost electrode materials that allow fast and reversible insertion of large-ionic-size K+. Here, we report an inorganic-open-framework anode (KTiOPO4), which achieves a reversible capacity of up to 102mAhg(-1) (307mAhcm(-3)), flat voltage plateaus at a safe average potential of 0.82V (vs. K/K+), a long lifespan of over 200 cycles, and K+-transport kinetics approximate to 10 times faster than those of Na-superionic conductors. Combined experimental analysis and first-principles calculations reveal a charge storage mechanism involving biphasic and solid solution reactions and a cell volume change (9.5%) even smaller than that for Li+-insertion into graphite (approximate to 10%). KTiOPO4 exhibits quasi-3D lattice expansion on K+ intercalation, enabling the disintegration of small lattice strain and thus high structural stability. The inorganic open-frameworks may open a new avenue for exploring low-cost, stable and fast-kinetic battery chemistry.
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