The arrangement of (NH4)2V6O16 crystals is composed of VO5 square cone units and twisted VO6 octahedra, which collectively form a convoluted zigzag layer structure that aligns with the (00l) plane [129]. Meanwhile, (NH4)2V3O8 exhibits a layered and tunneled architecture consisting of VO5 square pyramids with shared vertices and VO4 tetrahedra. Such structures that possess laminar or tunneling features are capable of furnishing two-dimensional interstitial spaces for NH4+ intercalation, mitigating mechanical stresses arising from volumetric changes, as well as shortening diffusion distances [130, 131]. From an atomic configuration perspective, all singly-bonded oxygen atoms present in the NH4V4O10 and (NH4)2V3O8 layers can strongly interact with NH4+, whereby the stable and firmly anchored NH4+ ions function as robust “pillars” that consolidate the framework. Conversely, (NH4)2V6O16 comprises both single- and triple-bonded oxygen atoms on its surface layer. The triple-bonded oxygen atoms are unable to foster strong interactions with NH4+, leading to structural instability [132].
![驱动代码
void kalRxTaskletSchedule(struct GLUE_INFO *pr)
{
static unsigned int num = 0;
tasklet_hi_schedule(&pr->rRxTask[(num++)%NR_CPUS]);
// tasklet_hi_schedule(&pr->rRxTask);
DBGLOG(HAL, ERROR,](https://linuxcpp.0voice.com/zb_users/upload/2023/05/202305162226144313964.png)
