The study of geomagnetic jerk from 2010 to 2021 based on hourly mean data from global geomagnetic observatories

The secular variation in the global geomagnetic field was analyzed in terms of the annual differences in monthly means by using the hourly mean data from 18 foreign(outside China)observatories of the World Data Center(WDC)for Geomagnetism from January 2010 to January 2020 as well as 9 observatories in the Geomagnetic Network of China from January 2015 to April 2021.In addition,according to the correlation of noisy components from the observatories,a covariance matrix was constructed based on residuals between observations and the CHAOS-7.4 model to remove external contamination.Through a comparison before and after denoising,we found that the overall average standard deviations were reduced by 29.97%in China and by 41.4%outside China.Results showed the correlation coefficient between external noise(mainly the magnetosphere ring current)and the Dst index was 0.82,and the correlation coefficient between external noise and the Ring Current(RC)index reached 0.94.A geomagnetic jerk was globally discovered around 2018.0 on the geomagnetic eastward component Y.The jerk timing in China was around 2020.0,and the earliest one was in2018.75,whereas the timing outside China was around 2018.0,and the earliest one was in 2017.67.This 2-year lag may have been caused by the higher electrical conductivity of the deep mantle.After more data were added,this jerk event was found to occur in an orderly manner in the northern hemisphere as the longitude increased and the intensity gradually increased as well.The variations in location of the jerk center were analyzed according to the CHAOS-7.4 model.Results revealed six extreme points distributed nearby the equator.The strongest was near the equator,at 170°E,and the strength gradually decreased as it extended to the northern and southern hemispheres.Another extreme point with the opposite sign was located at the equator,at 20°W,in the south-central part of the Atlantic,and the strength gradually decreased as it extended into Europe.The covariance matrix method can be used to analyze data from the Macao Science Satellite-1 mission in the future,and this method is expected to play a positive role in modeling and separating the large-scale external field.

Inconsistency of changes in uniaxial compressive strength and P-wave velocity of sandstone after temperature treatments

It is generally accepted that the uniaxial compressive strength(UCS)and P-wave velocity of rocks tend to decrease simultaneously with increasing temperature.However,based on a great number of statistical data and systematic analysis of the microstructure variation of rocks with temperature rising and corresponding propagation mechanism of elastic wave,the results show that(1)There are three different trends for the changes of UCS and P-wave velocity of sandstone when heated from room temperature(20C or 25C)to 800C:(i)Both the UCS and P-wave velocity decrease simultaneously;(ii)The UCS increases initially and then decreases,while the P-wave velocity decreases continuously;and(iii)The UCS increases initially and then fluctuates,while the P-wave velocity continuously decreases.(2)The UCS changes at room temperaturee400C,400Ce600C,and 600Ce800C are mainly attributed to the discrepancy of microstructure characteristics and quartz content,the transformation plasticity of clay minerals,and the balance between the thermal cementation and thermal damage,respectively.(3)The inconsistency in the trends of UCS and P-wave velocity changes is caused by the change of quartz content,phase transition of water and certain minerals.

Sandstone-concrete interface transition zone (ITZ) damage and debonding micromechanisms under freeze-thaw

The sufficient bond between concrete and rock is an important prerequisite to ensure the effect of shotcrete support. However, in cold regions engineering protection system, the bond condition of rock and concrete surface is easily affected by freeze-thaw cycles, resulting in interface damage, debonding and even supporting failure. Understanding the micromechanisms of the damage and debonding of the rock-concrete interface is essential for improving the interface protection.Therefore, the micromorphology, micromechanical properties, and microdebonding evolution of the sandstone-concrete interface transition zone(ITZ) under varying freeze-thaw cycles(0, 5, 10, 15, 20) were studied using scanning electron microscope, stereoscopic microscope, and nano-indentation. Furthermore, the distribution range and evolution process of ITZ affected by freeze-thaw cycles were defined. Major findings of this study are as follows:(1) The microdamage evolution law of the ITZ under increasing freeze-thaw cycles is clarified, and the relationship between the number of cracks in the ITZ and freeze-thaw cycles is established;(2) As the number of freeze-thaw cycles increases, the ITZ's micromechanical strength decreases, and its development width tends to increase;(3) The damage and debonding evolution mechanisms of sandstone-concrete ITZ under freeze-thaw cycles is revealed, and its micromechanical evolution model induced by freeze-thaw cycles is proposed.

消防减阻用聚合物/表面活性剂复配体系实验探索

在全球能源紧张的背景下,“过程节能”手段的探索具有重要意义。消防工作在国民经济和社会发展中占据重要地位,将添加剂湍流减阻技术引进到消防系统,在不额外增大能耗的前提下能直接提高消防水的射出速度和射程,在提高灭火效率的同时节省水泵功耗。根据消防水流特点,初步选定聚氧乙烯/十八烷基三甲基氯化铵/水杨酸钠的聚合物/表面活性剂复配体系作为研究对象,通过测试该体系的减阻性能和表面张力,证实此体系可以用作消防系统减阻添加剂,但需控制聚合物浓度。研究发现复配体系的减阻性能及表面张力表现主要依赖于聚、表分子之间的相互作用,因此聚、表分子间相互作用强的体系,才更适合用作消防减阻聚/表复配添加剂。

18.55% Efficiency Polymer Solar Cells Based on a Small Molecule Acceptor with Alkylthienyl Outer Side Chains and a Low-Cost Polymer Donor PTQ10

The development of A-DA′D-A type small molecule acceptors(SMAs)has promoted the rapid progress of polymer solar cells(PSCs)in recent years.The outer side chains on the terminal thiophene ring and inner side chains on nitrogen atoms of the pyrrole ring of the DA′D fused ring play important roles in the photovoltaic performance of the SMAs.Here,we synthesized two new SMAs,2,2′-((2Z,2′Z)-((12,13-bis(2-ethylhexyl)-3,9-bis(4-(2-ethylhexyl)thiophen-2-yl)-12,13-dihydro-[1,2,5]thiadiazolo[3,4-e]thieno[2″,3″:4′,5′]thieno[2′,3′:4,5]pyrrolo[3,2-g]thieno[2′,3′:4,5]thieno[3,2-b]indole-2,10-diyl)bis(methaneylylidene))bis(5,6-difluoro-3-oxo-2,3-dihydro-1H-indene-2,1-diylidene))dimalononitrile(T2EH)and 2,2′-((2Z,2′Z)-((12,13-bis(2-ethylhexyl)-3,9-bis(3-(2-ethylhexyl)phenyl)-12,13-dihydro-[1,2,5]thiadiazolo[3,4-e]thieno[2″,3″:4′,5′]thieno[2′,3′:4,5]pyrrolo[3,2-g]thieno[2′,3′:4,5]thieno[3,2-b]indole-2,10-diyl)bis(methaneylylidene))bis(5,6-difluoro-3-oxo-2,3-dihydro-1H-indene-2,1-diylidene)(P2EH),with 2-ethylhexylβ-substituted thienyl or phenyl as the outer side chains,respectively,to improve the photovoltaic properties of the SMAs.Compared with P2EH,T2EH exhibits closerπ−πstacking,slightly red-shifted absorption,and higher electron mobility.Moreover,the active layer of T2EH blended with the low-cost polymer donor poly[(thiophene)-alt-(6,7-difluoro-2-(2-hexyldecyloxy)quinoxaline)](PTQ10)possesses higher mobilities,a longer lifetime,and less recombination of the charge carriers in comparison with that of the PTQ10:P2EH active layer.Eventually,the PTQ10:T2EH-based PSCs showed an outstanding power conversion efficiency(PCE)of 18.55%,while the PSC based on PTQ10:P2EH displayed a PCE of 17.50%.Importantly,18.55%is the highest PCE in the PTQ10-based binary PSCs so far.The results indicate that T2EH is one of the best SMAs for the PTQ10-based PSCs and is a promising SMA for the application of PSCs.

High-Performance D-A Copolymer Donor Based on Difluoroquinoxaline A-Unit with Alkyl-Chlorothiophene Substituents for Polymer Solar Cells

Side chain engineering with fluorine substitution is widely used to enhance photovoltaic performance of polymer donors in the research field of polymer solar cells(PSCs).However,fluorine substitution has disadvantages of complicated synthesis and high cost.Herein,we synthesized a novel D-A copolymer donor PBQ9 based on difluoroquinoxaline A-unit with chlorine substitution on its alkyl-thiophene side chains instead of fluorine substitution in the polymer donor PBQ6,which greatly shortens the synthetic route and reduces the cost.Interestingly,the optimized binary PSC with PBQ9 as polymer donor and m-TEH as acceptor demonstrated a high power conversion efficiency(PCE)of 18.81%(certified PCE of 18.33%by National Institute of Metrology,China)with a high fill factor of 80.59%,and the photovoltaic performance of the PSCs is insensitive to the different batches of the polymer donor.The results indicate that PBQ9 is a high-performance polymer donor and that chlorine substitution is an effective strategy to improve photovoltaic performance and reduce the cost of polymer donors.

Chlorinated polymerized small molecule acceptor enabling ternary all-polymer solar cells with over 16.6% efficiency

Recently,all-polymer solar cells(all-PSCs) based on polymerized small molecule acceptors(PSMAs) have achieved significant progress.Ternary blending has proven to be an effective strategy to further boost the power conversion efficiency(PCE) of the all-PSCs.Herein,a new A-DA′D-A small-molecule acceptor-based PSMA(named as PYCl-T) was designed and synthesized,which possesses similar polymer backbone with the widely used PY-IT,but with chlorine substitution on the A-end groups in the A-DA′D-A structure.PYCl-T was then employed as the third component into the PM6:PY-IT system and the ternary all-PSCs based on PM6:PY-IT:PYCl-T demonstrated a high PCE of 16.62%(certified value of 16.3%).Moreover,the PCE of 15.52% was realized in the enlarged ternary all-PSCs with effective area of 1 cm^(2),indicating the great potential in large-scale applications.Moreover,the optimized ternary blend films of PM6:PY-IT:PYCl-T show excellent thermal stability at 150 ℃.This work demonstrates that the utilization of a ternary blend system involving two well-compatible PSMA polymer acceptors is an effective strategy to boost the performance of the all-PSCs.

Stable perovskite solar cells with efficiency of 22.6%via quinoxaline-based polymeric hole transport material

Poor stability of spiro-OMe TAD hole transport materials(HTMs)with dopant is a major obstacle for the commercialization of perovskite solar cells(pero-SCs).Herein,we demonstrate a series of quinoxaline-based D-A copolymers PBQ5,PBQ6 and PBQ10 as the dopant-free polymer HTMs for high performance pero-SCs.The D-A copolymers are composed of fluorothienyl benzodithiophene(BDTT)as D-unit,difluoroquinoxaline(DFQ)with different side chains as A-unit,and thiophene asπ-bridge,where the side chains on the DFQ unit are bi-alkyl for PBQ5,bi-alkyl-fluorothienyl for PBQ6,and alkoxyl for PBQ10.All the three copolymers are adopted as the dopant-free HTM in the pero-SCs.The planar n-i-p structured pero-SCs based on(FAPb I_(3))_(0.98)(MAPb Br_(3))_(0.02)with PBQ6 HTM demonstrated the high power conversion efficiency(PCE)of 22.6%with Vocof1.13 V and FF of 80.8%,which is benefitted from the suitable energy level and high hole mobility of PBQ6.The PCE of 22.6%is the highest efficiency reported in the n-i-p structured pero-SCs based on dopant-free D-A copolymer HTM.In addition,the peroSCs show significantly enhanced ambient,thermal and light-soaking stability compared with the devices with traditional spiroOMe TAD HTM.

基于苯并三氮唑π-桥单元协同高效率和低能量损失的全小分子有机太阳电池

降低电压损失(V_(loss))是有机光伏电池未来商业化应用面临的关键挑战之一.V_(loss)一般由活性层材料的光学带隙和器件的开路电压(V_(oc))之差定义,而V_(oc)则由给受体之间的最低未占据分子轨(LUMO)和最高占据分子轨道(HOMO)之间的能级差决定.本文通过引入苯并三唑(BTz)π-桥单元,利用末端调控策略合成了两种A-π-D-π-A型小分子给体SMBTz-1和SM-BTz-2.结果显示,BTzπ-桥单位显著降低了小分子给体的HOMO能级,使其具有较高的Voc和载流子迁移率,实现了高效率与低能量损失(小于0.5 eV)之间的平衡.最终,以SM-BTz-2为给体,Y6为受体的全小分子有机太阳能电池V_(o c)为0.91 V,短路电流密度(J_(sc))为22.8 mA cm^(−2),填充因子为68%,能量转化效率为14.12%.此外,该工作也进一步说明了苯并三唑π-桥单元是提高载流子迁移率,降低能量损失的有效构建单元.

Non-equivalent D-A copolymerization strategy towards highly efficient polymer donor for polymer solar cells

D-A copolymerization is a broadly utilized molecular design strategy to construct high efficiency photovoltaic materials for polymer solar cells(PSCs),and all the D-A copolymer donors reported till now are the alternate D-A copolymers with equal D-and A-units.Here,we first propose a non-equivalent D-A copolymerization strategy with unequal D-and A-units,and develop three novel non-equivalent D-A copolymer donors(PM6-D1,PM6-D2 and PM6-D3 with D/A unit ratio of 1.1:0.9,1.2:0.8 and1.3:0.7,respectively)by inserting more D units into the alternate D-A copolymer PM6 backbone to finely tune the physicochemical and photovoltaic properties of the polymers.The three non-equivalent D-A copolymers show the down-shifted highest occupied molecular orbital(HOMO)energy levels,higher hole mobility,higher degree of molecular self-assembly and higher molecular crystallinity with the increase of D-unit ratio in comparison with the alternate D-A copolymer PM6.As a result,all the three non-equivalent D-A copolymer-based PSCs with Y6 as acceptor achieve improved power conversion efficiency(PCE)with higher V_(oc),larger J_(sc)and higher FF simultaneously.Particularly,the PM6-D1:Y6 based PSC achieved a high PCE of17.71%,which is significantly higher than that(15.82%)of the PM6:Y6 based PSC and is one of the highest performances in the binary PSCs.

Low-Cost and High-Performance Polymer Solar Cells with Efficiency Insensitive to Active-Layer Thickness

The power conversion efficiency(PCE)of polymer solar cells(PSCs)has recently increased quickly,propelling PSCs closer to large-scale commercialization.However,several critical issues,such as the cost of materials and the sensitivity of the PCE to active-layer thickness,must be addressed before industrial application can be realized on a large scale.Here,we fabricated a high-performance ternary PSC based on a low-cost polymer donor PTQ10 and an A-DA’D-A-type small molecule acceptor(SMA)2,2'-((2Z,2'Z)-((12,13-bis(2-butyloctyl)-3,9-bis(4-(2-ethylhexyl)thiophen-2-yl)-12,13-dihydro-[1,2,5]thiadiazolo[3,4-e]thieno[2'',3'':4',5']thieno[2',3':4,5]pyrrolo[3,2-g]thieno[2',3':4,5]thieno[3,2-b]indole-2,10-diyl)bis(methaneylylidene))bis(5,6-difluoro-3-oxo-2,3-dihydro-1H-indene-2,1-diylidene))dimalononitrile(m-TEH)with a newA-DA’D-A-type SMA 2,2'-((2Z,2'Z)-((12,13-bis(2-butyloctyl)-3,9-bis(3-(2-ethylhexyl)phenyl)-12,13-dihydro-[1,2,5]thiadiazolo[3,4-e]thieno[2'',3'':4',5']thieno[2',3':4,5]pyrrolo[3,2-g]thieno[2',3':4,5]thieno[3,2-b]indole-2,10-diyl)bis(methaneylylidene))bis(5,6-difluoro-3-oxo-2,3-dihydro-1H-indene-2,1-diylidene))dimalononitrile(m-PEH)(with phenyl outer side chains)as the third component.Benefitting from the good compatibility and the unique alignment of the energy levels between PTQ10 and the two SMAs,the ternary system showed favorable phase separation and dominant face-on orientation,exhibiting suitable film morphology and enhanced charge transport.Therefore,the optimized ternary PSCs based on PTQ10∶m-TEH∶m-PEH(1.0∶0.9∶0.3,w/w/w)demonstrated an outstanding PCE of 19.34%,which is one of the highest PCEs reported for the single junction PSCs to date.More importantly,the ternary PSCs demonstrated superior tolerance to the active-layer thickness and showed a high PCE of 18.02% with a high fill factor(FF)of 76.56% for the devices with the active-layer thickness even reaching 300 nm.These results indicate that the ternary devices based on PTQ10∶m-TEH∶m-PEH are highly promising for future large-area fabrication and commercial application of PSCs.