摘要：The hydrogenation of CO_(2) into methanol has attracted much attention and In_(2)O_(3) is a promising *** metal elements into In_(2)O_(3)(M/In_(2)O_(3))is one of the main strategies to improve its ***,its mechanism and active sites remain unclear and need to be further ***,the noble‐metal‐free In_(x)‐Co_(y) oxides catalysts were ***‐improved performance and obvious product selectivity shift were *** optimized catalyst(In_(1)‐Co_(4))(9.7 mmol g_(cat)^(–1) h^(–1))showed five times methanol yields than pure In_(2)O_(3)(2.2 mmol g_(cat)^(–1) h^(–1))(P=4.0 MPa,T=300°C,GHSV=24000 cm^(3)_(STP) g_(cat)^(–1) h^(–1),H_(2):CO_(2)=3).And the cobalt‐catalyzed CO_(2) methanation activity was suppressed,although cobalt was most of the metal *** unravel this selectivity shift,detailed catalysts performance evaluation,together with several in‐situ and ex‐situ characterizations,were employed on cobalt and In‐Co for comparative *** results indicated CO_(2) hydrogenation on cobalt and In‐Co catalyst both followed the formate pathway,and In‐Co reconstructed and generated a surface In_(2)O_(3)‐enriched core‐shell‐like structure under a reductive *** enriched In_(2)O_(3) at the surface significantly enhanced CO_(2) adsorption capacity and well stabilized the intermediates of CO_(2) ***_(2) and carbon‐containing intermediates adsorbed much stronger on In‐Co than cobalt led to a feasible surface C/H ratio,thus allowing the*CH_(3)O to desorb to produce CH_(3)OH instead of being over‐hydrogenated to CH_(4).

摘要：Developing efficient electrocatalysts for the oxygen evolution reaction(OER)under neutral conditions is important for microbial electrolysis cells(MECs).However,the OER kinetics in neutral electrolytes at present are extremely sluggish,resulting in high overpotentials that greatly limit the energy conversion efficiencies of *** studies failed to probe the adsorbates on surface metal sites of catalysts at the atomic scale and elucidate their influence on the catalytic activities,which has impeded the rational design of efficient neutral OER catalysts with optimal surface ***,using in situ transmission electron microscopy(TEM),in situ X-ray photoelectron spectroscopy(XPS)and in situ low-energy ion scattering studies,we have identified,for the first time,that the electrochemically activated adsorbates on surface metal sites play a critical role in boosting the neutral OER activities of Ru-Ir binary oxide(RuxIryO2)*** adsorbate-activated RuxIryO2on a glassy carbon electrode achieved a low overpotential of 324 m V at10 m A cm-2in neutral electrolyte,with a 36-fold improvement in turnover frequency compared with that of Ir *** application in an MEC system,the resulting full cell showed a decreased voltage of 1.8 V,200 m V lower than the best value reported to date,facilitating efficient synthesis of poly(3-hydroxybutyrate)from bioelectrochemical *** functional theory(DFT)studies revealed that the enhanced OER activity of RuxIryO2catalyst arose from local structural distortion of adjacent adsorbate-covered Ru octahedra at the catalyst surface and the consequently decreased adsorption energies of OER intermediates on Ir active center.

摘要：The vicious cycle between tumor cell proliferation and bone resorption remarkably elevates the progression and metastasis of bone ***,we fabricated polyethylene glycol-conjugated alendronate-functionalized and chloroquine(CQ)-loaded polydopamine nanoparticles(PPA/CQ)for efficient treatment of bone tumors via breaking the vicious *** nanoparticles were efficiently accumulated to the bone tissues,especially the osteolytic lesions around *** released from PPA/CQ inhibited osteoclastogenesis via preventing the degradation of tumor necrosis factor(TNF)receptor-associated receptor 3 to attenuate the osteolysis in bone *** the other hand,CQ blocked the autophagy in cancer cells,resulting in improved photothermal killing of cancer ***,the in vivo experiment revealed that PPA/CQ-associated treatment efficiently inhibited both tumor growth and *** work suggests that autophagy inhibition-associated photothermal therapy could be a promising strategy for treating malignant bone tumors.

摘要：MXene is a variety of new two-dimensional(2D)materials with early transition metal carbides,nitrides,and *** chemical studies have been carried out on the geometries,electronic structures,stability and catalytic properties of a non-noble metal single-atom catalyst(SAC)with single Co atom anchored on MXene materials of Mo_(2)CS_(2).The Co adatom anchored on top of the Mo atom of this MXene is found to be rather stable,and this SAC is appropriate for CO *** charge transfers from the surface to the adsorbed CO and O2 play a significant role in the activation of these molecules on Co_(1)/Mo_(2)CS_(2).With this catalyst,the Eley-Rideal(ER),Langmuir-Hinshelwood(LH),and Termolecular Eley-Rideal(TER)mechanisms are explored for CO *** find that,while all the three mechanisms are feasible at low temperature,Co_(1)/Mo_(2)CS_(2) possesses higher catalytic activity for CO oxidation through the TER mechanism that features an intriguing OC(OO)CO intermediate(IM)adsorbed on Co single *** calculated activation energy barriers of the rate-limiting step are 0.67 eV(TER),0.78 eV(LH)and 0.88 eV(ER),*** present study illustrates that it is promising to develop and design low-cost,non-noble metal SACs using MXene types of 2D materials.

摘要：背景在糖尿病自我管理支持方面,智能手机应用程序越来越受欢迎。糖尿病自我管理的一个重要方面是恰当服药。本研究旨在系统地评估和描述糖尿病自我管理应用程序中的用药管理功能,及其与基于证据的最佳实践标准的一致性。方法 2018年6月,在Google Play和Apple应用程序商店中,使用英语搜索糖尿病相关术语。根据国际用药管理和糖尿病指南的评估标准,下载并评估具有用药和血糖管理功能的应用程序。结果共搜索到3 369个Android和1 799个iOS潜在相关的应用程序;其中,143个应用程序(81个Android,62个iOS)符合纳入标准,并已下载和评估。超过一半[58.0%(83/143)]的应用程序具有用药提醒功能;16.8%(24/143)的应用程序具有审查药物依从性的功能;39.9%(57/143)的应用程序允许进入服药指示;5.6%(8/143)的应用程序提供药物相关信息;4.2%(6/143)的应用程序显示鼓励服药的激励消息。只有两个应用程序鼓励用户采用辅助性疗法。在应用评估期间,观察到诸如有限的药物记录容量、错误的提醒功能、不明确的药物依从性评估,以及视觉上过度分散注意力的广告等问题。结论大部分糖尿病自我管理应用程序缺乏增强用药依从性和安全性的功能。应更加重视糖尿病应用程序中用药管理功能的设计,以提高其与基于证据的最佳实践标准的一致性。

摘要：Transition metal phosphides(TMPs)/carbonaceous matrices have gradually attracted attention in the field of energy *** this study,we presented nickel phosphide(Ni2P)nanoparticles anchored to nitrogen-doped carbon porous spheres(Ni2P/NC)by using metal-organic framework-Ni as the *** comprehensive encapsulation architecture provides closer contact among the Ni2P nanoparticles and greatly improves the structural integrity as well as the electronic conductivity,resulting in excellent lithium storage *** reversible specific capacity of 286.4 mA hg^-1 has been obtained even at a high current density of 3.0 Ag^-1 and 450.4 mA hg^-1 is obtained after 800 cycles at 0.5 Ag^-***,full batteries based on LiNi1/3Co1/3Mn1/3O2||Ni2P/NC exhibit both good rate capability and cycling *** study provides a powerful and indepth insight on new advanced electrodes in high-performance energy storage devices.

摘要：本文研究了一种新型低密度(~6.24 g cm^(-3))双相AlTiVCoNi高熵合金,其组织结构由有序L21高熵金属间化合物、无序体心立方结构和纳米L21相多层次结构构成.该合金在1200℃+24 h热处理下未发生相结构转变,在此条件下具有优异的高温相结构稳定性,其铸态和热处理态的压缩屈服强度相当,达到~1.6 GPa.另外,该合金在室温和600℃条件下表现出了优异的强塑性匹配和优异的比屈服强度,分别达到了约261和210 MPa g^(-1)cm^(3).该合金的超高强度主要源于有序L21相与体心立方相的半共格界面导致的一种强相结构稳定性和多层次结构的复合强化机制.该合金在800和1000℃压缩过程中出现了动态再结晶软化,使得其高温强度有所降低.这种“具有半共格界面L21+体心立方+纳米L21颗粒”的多层次结构设计为开发新型低密度耐高温高熵合金提供了一种新设计思路.

摘要：量子自旋霍尔绝缘体拥有具有带隙的体态和无能隙的一维拓扑边缘态.然而,由于拓扑边缘态局域在纳米尺度,所以很难用光学手段直接观测并区分体态和边缘态,这就限制了对拓扑边缘态独特的光学特性和光电响应等方面的研究和应用.Bi_(4)Br_(4)体材料的台阶存在一维非平庸的边缘态,多个台阶累加的效应使得通过较为宏观的光学和光电分析手段来研究一维边缘态成为可能.该工作利用中远红外显微吸收光谱和泵浦探测光谱,对比研究了Bi_(4)Br_(4)体和边缘的光学响应行为.研究发现Bi_(4)Br_(4)的边缘在小于带隙(约0.22 eV)的波段存在明显的强于体内的红外吸收,且该吸收呈现较强的各向异性.室温下的红外泵浦探测首次观察到边缘处载流子激发态超长的弛豫时间(1.5 ns),该激发态载流子寿命要比体内载流子寿命长两个量级.该工作证实体态和拓扑边缘态具有明显不同的光学和光电响应行为,为未来设计新型红外探测器提供了材料和物理基础.

摘要：Rapid and sensitive detection of various analytes is in high *** from its application in genome editing,CRISPR-Cas also shows promises in nucleic acid detection *** further exploit the potential of CRISPR-Cas for detection of diverse analytes,we present a versatile biosensing platform that couples the excellent affinity of aptamers for broad-range analytes with the collateral single-strand DNA cleavage activity of CRISPR-Cas12 *** demonstrated that the biosensors developed by this platform can be used to detect protein and small molecule in human serum with a complicated background,i.e.,the tumor marker alpha fetoprotein and cocaine with the detection limits of 0.07 fmol/L and 0.34 lmol/L,respectively,highlighting the advantages of simplicity,sensitivity,short detection time,and low cost compared with the state-of-the-art biosensing ***,this biosensing platform with plug-and-play design show great potential in the detection of diverse analytes.

摘要：三维(3D)狄拉克半金属因其独特的拓扑能带结构及优异的光电性能在中/远红外波段的宽光谱光电探测领域具有巨大的应用潜力.然而,由于较大的暗电流,构建具有高信噪比(SNR)的3D狄拉克半金属宽光谱光电探测器仍面临很大挑战.本工作基于分子束外延生长的(Cd_(1-x)Zn_(x))_(3)As_(2)薄膜发展了一种超低器件噪声的3 D狄拉克半金属(Cd_(1-x)Zn_(x))_(3)As_(2)/Sb_(2)Se_(3)背靠背异质结光电探测器线阵.得益于有效的双异质结设计策略,该探测器可以实现从可见光(450 nm)到中红外(4.5μm)波段的室温高性能宽光谱探测器目标,其峰值SNR和D*分别可达104和5.2×10^(12)Jones,并具有相对较快的响应速度(~87.5μs).此外,不同探测器线列单元之间呈现出的稳定性、均匀性特征表明了其在未来应用于光迹实时跟踪等光电子器件中的可行性.该研究为基于3D狄拉克半金属材料制备具有超高SNR的高速宽光谱光电探测器提供了参考策略,展示了半金属在高速非制冷红外焦平面成像阵列探测器中的广阔前景.