Practical semi-quantum key distribution with one-way key and one basis.

Semi-quantum key distribution (SQKD) protocols are used to distribute secret keys between a quantum party and a classical party. However, existing SQKD protocols rely on two-way communication, and may still be vulnerable to Trojan horse side-channel attacks where Eve sends her own photon into a receiver's apparatus and measures the reflected photon to estimate the key. In this paper, we propose a practical SQKD with one-way key. This requires that the single photons travelling through the one-way channel are used to encode bit information, and the returned photons are used to quantify Eve's information, thus reducing the security analysis of the Trojan horse attack in SQKD. Meanwhile, our protocol with one basis enjoys security advantage in practical SQKD systems when source flaws are taken into account. In particular, the present protocol is secure under practical conditions when weak coherent pulses (WCP) are used. Our simulation results show that the protocol using WCP can distribute secret keys over a distance of 110 km without decoy states.

Counterfactual quantum key distribution with untrusted detectors.

Compared with the traditional BB84 protocol, the counterfactual quantum key distribution (QKD) does not rely on any signal travelling in the quantum channel, and therefore can present a security advantage where Eve cannot fully access signal. However, the practical system may be damaged in a scenario where the devices are untrusted. In this paper, we analyze the security of counterfactual QKD in untrusted detectors scenario. We show that the requirement to disclose "which detector clicked" has become the main loophole in all counterfactual QKD versions. An eavesdropping scheme which is similar to the memory attack on device-independent QKD could break its security by exploiting detectors' imperfections. We consider two different counterfactual QKD protocols and analyze their security against this major loophole. One is a modified Noh09 protocol, which would be secure in untrusted detectors context. Another is a variant of counterfactual QKD with high efficiency (Phys. Rev. A 104 (2021) 022424) against a series of detectors side-channel attacks as well as against other attacks that exploit detectors imperfections.

An acid-base molecular assembly strategy toward N-doped Mo2C@C nanowires with mesoporous Mo2C cores and ultrathin carbon shells for efficient hydrogen evolution.

Molybdenum carbides are promising electrocatalysts for the hydrogen evolution reaction (HER). Rational design of morphology, composition and interfacial structure in Mo2C materials is essential to enhance their HER performance. Herein, an acid-base molecular assembly strategy is demonstrated for the synthesis of novel N-doped Mo2C@C core-shell nanowires (NWs) composed of mesoporous Mo2C cores with interconnected crystalline walls and ultrathin carbon shells. The strong interactions between the two precursors, adenine (Ade) and phosphomolybdic acid (PMA), lead to the formation of inter-molecular hybrid NWs during a hydrothermal process. The subsequent pyrolysis leads to confined growth of crystalline Mo2C NWs with inter-crystal mesopores (5 ~ 10 nm), formation of ultrathin carbon shells (~1.5 nm in thickness), and effective N doping. Such a structure architecture can provide abundant active sites, fast and diverse mass and electron transport paths, as well as stable reaction interfaces. The typical N-doped Mo2C@C NWs exhibit high HER performance with a low overpotential of 136 mV at 10 mA cm-2, a small Tafel slop of 58 mV dec-1, excellent durability and outstanding anti-poisoning performance against CO and H2S gases. Furthermore, the influences of several important factors, including the pyrolysis temperature, hydrothermal temperature and precursor mass ratio, on the morphology, composition and structural configuration of the resulted materials are elucidated and correlated with their HER performance. This work may provide a general strategy for the synthesis of other nanoscale metal carbides for various catalytic applications.

Study on the Stability, Evolution of Physicochemical Properties, and Postsynthesis of Metal-Organic Frameworks in Bubbled Aqueous Ozone Solution.

Metal-organic frameworks (MOFs) are highly promising in many areas. Their application and postsynthesis under strong oxidative environments are emerging. However, the stability, physicochemical property evolution, and possible postmodification and postsynthesis of MOFs in strong oxidative solutions are largely unknown. In this paper, the behaviors of a series of MOFs in bubbled aqueous ozone (O3) solutions are studied. The chosen MOFs are categorized into trimesic type including MIL-101(Fe) and MIL-96(Al); terephthalic type including MOF-74(Co), UiO-66(Zr), MIL-53(Al), and MIL-101(Cr); and imidazole type including ZIF-67(Co) and ZIF-8(Zn), based on the ligand structure. The intrinsic stability and evolution of the physicochemical properties of these MOFs during aqueous O3 treatment are elucidated using structural, morphological, textural, thermal, and spectroscopic analyses. Several stable, metastable, and instable MOFs are identified. The critical parameters that determine the stability and capability for postsynthesis of these MOFs in aqueous O3 solutions are discussed. The stability follows the general order of trimesic-type > terephthalic-type ≫ imidazole-type MOFs because of the distinct antioxidation capability of the ligands. The effects of the ligand, metal cation, and their coordination number on stability are discussed. MIL-100(Fe), MIL-96(Al), and MOF-74(Co) are stable in aqueous O3. UiO-66(Zr), MIL-53(Al), and MIL-101(Cr) are metastable that their porosity, particle size, and crystallinity can be postmodified. ZIF-67(Co) and ZIF-8(Zn) are instable and can be gradually and completely disassembled. Their particle size and morphology and surface groups can be tuned by controlling the treatment time. Postsynthesis of metal hydroxides from ZIF-67(Co) and gradual release of dissolved zinc ion from ZIF-8(Zn) are achievable. The stable MIL-96(Al) shows promising performance in catalytic ozonation for degrading 4-nitrophenol, and the α-Co(OH)2 derived from treating ZIF-67(Co) shows highly promising performance in the electrocatalytic oxygen evolution reaction (OER).

A Molecular Foaming and Activation Strategy to Porous N-Doped Carbon Foams for Supercapacitors and CO2 Capture.

Hierarchically porous carbon materials are promising for energy storage, separation and catalysis. It is desirable but fairly challenging to simultaneously create ultrahigh surface areas, large pore volumes and high N contents in these materials. Herein, we demonstrate a facile acid-base enabled in situ molecular foaming and activation strategy for the synthesis of hierarchically macro-/meso-/microporous N-doped carbon foams (HPNCFs). The key design for the synthesis is the selection of histidine (His) and potassium bicarbonate (PBC) to allow the formation of 3D foam structures by in situ foaming, the PBC/His acid-base reaction to enable a molecular mixing and subsequent a uniform chemical activation, and the stable imidazole moiety in His to sustain high N contents after carbonization. The formation mechanism of the HPNCFs is studied in detail. The prepared HPNCFs possess 3D macroporous frameworks with thin well-graphitized carbon walls, ultrahigh surface areas (up to 3200 m2 g-1), large pore volumes (up to 2.0 cm3 g-1), high micropore volumes (up to 0.67 cm3 g-1), narrowly distributed micropores and mesopores and high N contents (up to 14.6 wt%) with pyrrolic N as the predominant N site. The HPNCFs are promising for supercapacitors with high specific capacitances (185-240 F g-1), good rate capability and excellent stability. They are also excellent for CO2 capture with a high adsorption capacity (~ 4.13 mmol g-1), a large isosteric heat of adsorption (26.5 kJ mol-1) and an excellent CO2/N2 selectivity (~ 24).