Covalent的CQT质押迁移比率在以太坊上升至13%,超Moonbeam记录

Covalent Network(CQT)作为领先的结构化模块化数据基础设施层,目前其在以太坊上的 CQT 质押比率已超过之前在 Moonbeam 上达到的历史最高水平。自从将质押合约迁移到以太坊不到一个月的时间里,超过总供应量的 13% 的 CQT 代币已被锁定在质押合约中,目前的历史年化收益率约为 18%。这一重要里程碑凸显了 Covalent Network(CQT)日益增长的信心和参与度,并凸显了 Covalent Network(CQT)持续致力于提升其质押基础设施,并为所有用户提高质押流程的效率和可访问性的决心。

迁移到以太坊提升质押参与度

迁移至以太坊推动了质押参与度的提升,同时也鼓励了质押者通过 Wormhole 将代币从Moonbeam 迁移到以太坊。Covalent Network(CQT)用户可以利用其直观的质押仪表盘,将现已解锁的代币质押到新的以太坊质押合约中。因此,当前的质押量已经达到总供应量约 13% 的水平,超过之前在 Moonbeam 上进行质押时 11% 的比例水平。

这一增长不仅标志着成功迁移,还反映了现有和新加入的质押者对 Covalent Network(CQT)长期愿景日益增长的信任。如果所有之前在 Moonbeam 上质押的 11% 的 CQT 都转移到以太坊,那么上升到13% 的增长就表明有额外的利益相关者加入,这显示出人们对于以太坊质押过程更为信任,也可能是因为对即将启动的以太坊时光机(Ethereum Wayback Machine )充满期待,该机制将为以太坊带来长期数据可用性。

此前,在 Moonbeam 上进行 CQT 代币质押需要使用 GLMR 和 ETH 进行操作,在迁移到以太坊后只需使用 ETH 即可,大大简化了操作流程并降低了不熟悉该领域用户所面临复杂性。全新设计优化的资产管理面板进一步简化了流程,使得现有持有者能轻松完成迁移,并让新用户只需点击几下即可进行委托。这些改进很可能是参与度增加和新委托者涌入的主要原因。

结论

Covalent Network(CQT)向以太坊迁移并随之而来的CQT质押比例的增加,凸显了 Covalent Network(CQT)致力于为社区提供无缝高效的质押体验的承诺,早期参与质押的持币者有望获得更高年化收益率。随着 Covalent Network(CQT)接近其在以太坊上质押20%总CQT供应量的目标,这一比率将逐渐调整至约 12%。

展望未来,Covalent Network(CQT)致力于部署各种策略和更新,进一步加强网络,并确保为所有用户提供更安全、高效、可扩展的基础设施。代币持有者可以期待 Covalent Network(CQT)的不断改进和提升,以创建一个强大且去中心化的生态系统。

行动号召

对于尚未质押 CQT 或正在考虑加入 Covalent Network(CQT)社区的人来说,现在是最佳时机,前往我们的质押仪表板,开始在以太坊上质押您的 CQT。

关于共价网络(CQT)

Covalent Network(CQT)正在为去中心化生态系统提供数据基础设施,解决以太坊的长期数据可用性问题——这种基础设施可以重新执行数据块并塑造人工智能。随着 CQT 质押现已重新回到以太坊上,通往以太坊时光机的网络扩展的新曙光开始来临。这意味着AI、DeFi和其他用例可以无障碍地访问来自225多个区块链的结构化链上数据,并且这一数字还在不断增长。

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润色下面英文:The controlled drug delivery systems, due to their precise control of drug release in spatiotemporal level triggered by specific stimulating factors and advantages such as higher utilization ratio of drug, less side-effects to normal tissues and so forth, provide a new strategy for the precise treatment of many serious diseases, especially tumors. The materials that constitute the controlled drug delivery systems are called “smart materials” and they can respond to the stimuli of some internal (pH, redox, enzymes, etc.) or external (temperature, electrical/magnetic, ultrasonic and optical, etc.) environments. Before and after the response to the specific stimulus, the composition or conformational of smart materials will be changed, damaging the original balance of the delivery systems and releasing the drug from the delivery systems. Amongst them, the photo-controlled drug delivery systems, which display drug release controlled by light, demonstrated extensive potential applications, and received wide attention from researchers. In recent years, photo-controlled drug delivery systems based on different photo-responsive groups have been designed and developed for precise photo-controlled release of drugs. Herein, in this review, we introduced four photo-responsive groups including photocleavage groups, photoisomerization groups, photo-induced rearrangement groups and photocrosslinking groups, and their different photo-responsive mechanisms. Firstly, the photocleavage groups represented by O-nitrobenzyl are able to absorb the energy of the photons, inducing the cleavage of some specific covalent bonds. Secondly, azobenzenes, as a kind of photoisomerization groups, are able to convert reversibly between the apolar trans form and the polar cis form upon different light irradiation. Thirdly, 2-diazo-1,2-naphthoquinone as the representative of the photo-induced rearrangement groups will absorb specific photon energy, carrying out Wolff rearrangement reaction. Finally, coumarin is a promising category photocrosslinking groups that can undergo [2+2] cycloaddition reactions under light irradiation. The research progress of photo-controlled drug delivery systems based on different photo-responsive mechanisms were mainly reviewed. Additionally, the existing problems and the future research perspectives of photo-controlled drug delivery systems were proposed.
02-06

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