Heng Jiang,Jessica J. Hong,Xianyong Wu,T. Wesley Surta,Yitong Qi,Shengyang Dong,Zhifei Li,Daniel P. Leonard,John Holoubek,Jane C. Wong,Joshua J. Razink,Xiaogang Zhang,Xiulei Ji
This study reveals the transport behavior of lattice water during proton (de)insertion in the structure of the hexagonal WO3·0.6H2O electrode. By monitoring the mass evolution of this electrode material via electrochemical quartz crystal microbalance, we discovered (1) WO3·0.6H2O incorporates additional lattice water when immersing in the electrolyte at open circuit voltage and during initial cycling; (2) The reductive proton insertion in the WO3 hydrate is a three-tier process, where in the first stage 0.25 H+ is inserted per formula unit of WO3 while simultaneously 0.25 lattice water is expelled; then in the second stage 0.30 naked H+ is inserted, followed by the third stage with 0.17 H3O+ inserted per formula unit. Ex situ XRD reveals that protonation of the WO3 hydrate causes consecutive anisotropic structural changes: it first contracts along the c-axis but later expands along the ab planes. Furthermore, WO3·0.6H2O exhibits impressive cycle life over 20 000 cycles, together with appreciable capacity and promising rate performance.