有效控制的半量子秘密共享协议的密码分析与纠状态共享协议
Shuang Li1,2, Xiao-Qiu Cai3, Shuai-Jia Song1,2
1School of Mathematical Science, Luoyang Normal University, Luoyang, 471934, China.
Scientific reports
|April 29, 2025
概括
这项研究揭示了最近量子秘密共享协议中的安全漏洞. 控制器可以访问秘密,攻击者可以引入未检测到的错误,损害数据完整性和机密性.
科学领域:
- 量子密码学 量子密码学
- 信息安全 信息安全
背景情况:
- 量子秘密共享对于安全的密钥管理和多方计算至关重要.
- 最近的进展包括使用纠状态的受控半量子秘密共享协议.
研究的目的:
- 执行一个高效控制的半量子秘密共享协议的加密分析.
- 识别漏洞并评估协议的安全保证.
主要方法:
- 拟议协议的加密分析.
- 模拟攻击场景,包括勾结和拒绝服务.
主要成果:
- 控制者可以与单一参与者勾结,以恢复秘密.
- 外部对手可以通过拒绝服务攻击注入未被检测到的错误 (虚假的秘密).
结论:
- 该协议未能满足基本的安全要求.
- 它并不能确保未经授权的当事人无法获取有关秘密的信息.
- 对已识别的攻击,不能保证协议的正确性.
相关概念视频
The Quantum-Mechanical Model of an Atom
41.5K
Shortly after de Broglie published his ideas that the electron in a hydrogen atom could be better thought of as being a circular standing wave instead of a particle moving in quantized circular orbits, Erwin Schrödinger extended de Broglie’s work by deriving what is now known as the Schrödinger equation. When Schrödinger applied his equation to hydrogen-like atoms, he was able to reproduce Bohr’s expression for the energy and, thus, the Rydberg formula governing...
41.5K
Crystal Field Theory - Tetrahedral and Square Planar Complexes
40.7K
Tetrahedral Complexes
Crystal field theory (CFT) is applicable to molecules in geometries other than octahedral. In octahedral complexes, the lobes of the dx2−y2 and dz2 orbitals point directly at the ligands. For tetrahedral complexes, the d orbitals remain in place, but with only four ligands located between the axes. None of the orbitals points directly at the tetrahedral ligands. However, the dx2−y2 and dz2 orbitals (along the Cartesian axes) overlap with the ligands less than...
Crystal field theory (CFT) is applicable to molecules in geometries other than octahedral. In octahedral complexes, the lobes of the dx2−y2 and dz2 orbitals point directly at the ligands. For tetrahedral complexes, the d orbitals remain in place, but with only four ligands located between the axes. None of the orbitals points directly at the tetrahedral ligands. However, the dx2−y2 and dz2 orbitals (along the Cartesian axes) overlap with the ligands less than...
40.7K
Molecular Orbital Theory I
31.0K
Overview of Molecular Orbital Theory
31.0K
Interpreting ¹H NMR Signal Splitting: The (n + 1) Rule
1.1K
In the AX proton spin system, proton A can sense the two spin states of a coupled proton X, resulting in a doublet NMR signal with two peaks of equal (1:1) intensity. When proton A is coupled to two equivalent protons (AX2 spin system), the spin states of each X can be aligned with or against the external field, creating three possible scenarios. This results in a 1:2:1 triplet signal, where the central peak corresponds to the chemical shift of A and is twice as large or intense as the...
1.1K
Complexation Equilibria: The Chelate Effect
392
In complexation reactions, metal atoms or cations interact with ligands to form donor-acceptor adducts called metal complexes. Ligands that bind through one donor site are monodentate, ligands with two donor sites are bidentate, and those with more than two donor sites are polydentate ligands. For example, ethylene diamine is a bidentate ligand that binds through two nitrogen donor atoms, forming a five-membered ring. EDTA is a polydentate ligand that binds through four oxygen and two nitrogen...
392
Valence Bond Theory
8.3K
Coordination compounds and complexes exhibit different colors, geometries, and magnetic behavior, depending on the metal atom/ion and ligands from which they are composed. In an attempt to explain the bonding and structure of coordination complexes, Linus Pauling proposed the valence bond theory, or VBT, using the concepts of hybridization and the overlapping of the atomic orbitals. According to VBT, the central metal atom or ion (Lewis acid) hybridizes to provide empty orbitals of suitable...
8.3K


