Mn^(2+)-doped CsPbCl_(3)(Mn^(2+):CsPbCl_(3)) nanocrystals(NCs) have attracted considerable attention due to their unique strong and broad orange-red emission band,presenting promising applications in the field of phot...Mn^(2+)-doped CsPbCl_(3)(Mn^(2+):CsPbCl_(3)) nanocrystals(NCs) have attracted considerable attention due to their unique strong and broad orange-red emission band,presenting promising applications in the field of photoelectric devices.However,pristine Mn^(2+):CsPbCl_(3)NCs commonly suffer from low photoluminescence quantum yield(PL QY) and stability issues.Herein,we introduced europium ions(Eu^(3+))into Mn^(2+):CsPbCl_(3)NCs via the thermal injection synthesis method to obtain high performance Eu^(3+)and Mn^(2+)codoped CsPbCl_(3)(Eu^(3+)/Mn^(2+):CsPbCl_(3)) NCs.The maximum PL QY of the resulting Eu^(3+)/Mn^(2+):CsPbCl_(3)NCs reaches up to 90.92%.It is found that the doping of Eu^(3+)ions significantly reduces the non-radiative recombination caused by high defect states,and improves the energy transfer efficiency from exciton to Mn^(2+),thereby boosting the PL performance.Moreover,doping Eu^(3+)ions notably improves the UV-light and water stability of Mn^(2+):CsPbCl_(3)NCs.We further demonstrate the application versatility of Eu^(3+)/Mn^(2+):CsPbCl_(3)NCs in white light emitting diodes(WLEDs) and optical anticounterfeiting applications.This work provides a valuable perspective for the attainment of high performance Mn^(2+):CsPbCl_(3)NCs and lays a foundation for the codoping of other lanthanide ions to adjust the luminescence properties of Mn^(2+):CsPbCl_(3)NCs.展开更多
Non-precious metal cobalt-based oxide inevitably dissolves for acid oxygen evolution reaction(OER).Designing an efficient deposition channel for leaching cobalt species is a promising approach.The dissolution-depositi...Non-precious metal cobalt-based oxide inevitably dissolves for acid oxygen evolution reaction(OER).Designing an efficient deposition channel for leaching cobalt species is a promising approach.The dissolution-deposition equilibrium of Co is achieved by doping Mn in the lattice of LaCo_(1-x)Mn_(x)O_(3),prolonging the lifespan in acidic conditions by 14 times.The lattice doping of Mn produces a strain that enhances the adsorption capacity of OH^(-).The self-catalysis of Mn causes the leaching Co to be deposited in the form of CoO_(2),which ensures that the long-term stability of LaCo_(1-x)Mn_(x)O_(3)is 70 h instead of 5 h for LaCoO_(3).Mn doping enhances the deprotonation of^(*)OOH→O_(2)in acidic environments.Notably,the over-potential of optimized LaCo_(1-x)Mn_(x)O_(3)is 345 mV at 10 mA cm^(-2)for acidic OER.This work presents a promising method for developing noble metal-free catalysts that enhance the acidic OER activity and stability.展开更多
采用高温固相法制备了SrZrSi_(2)O_(7):Ce^(3+),Mn^(2+)荧光粉。通过X射线衍射(X-ray Power Diffractometer,XRD)、激发和发射光谱及电子显微分析对材料的分子结构、显微形貌、发光特性和能量传递机理进行了研究。结果表明,荧光粉的主...采用高温固相法制备了SrZrSi_(2)O_(7):Ce^(3+),Mn^(2+)荧光粉。通过X射线衍射(X-ray Power Diffractometer,XRD)、激发和发射光谱及电子显微分析对材料的分子结构、显微形貌、发光特性和能量传递机理进行了研究。结果表明,荧光粉的主晶相是单斜晶系的SrZrSi_(2)O_(7),Ce^(3+)离子和Mn^(2+)离子占据一部分Sr^(2+)离子的晶体学格位。在296 nm激发下,可以观察到来自Ce^(3+)离子的蓝光发射峰,归属于Ce^(3+)离子的5d→4f能级跃迁。在544 nm处,有来自Mn^(2+)离子的绿光发射峰,归因于Mn^(2+)离子的^(4)T_(1)(4G)-^(6)A_(1)(6S)自旋禁止跃迁,表明发生了从Ce^(3+)离子到Mn^(2+)离子的能量传递过程,为设计蓝光到绿光之间可控制备的新型荧光粉提供了理论和实验的信息。展开更多
Lead-free Bi_(_(0.5))Na_(_(0.5))TiO_(3)(BNT)piezoelectric ceramics have the advantages of large coercive fields and high Curie temperatures.But the improvement of piezoelectric coefficient(d 33)is usually accompanied ...Lead-free Bi_(_(0.5))Na_(_(0.5))TiO_(3)(BNT)piezoelectric ceramics have the advantages of large coercive fields and high Curie temperatures.But the improvement of piezoelectric coefficient(d 33)is usually accompanied by a huge sacrifice of depolarization temperature(T d).In this work,a well-balanced performance of d 33 and T d is achieved in MnO_(2)-doped 0.79(Bi_(_(0.5))Na_(_(0.5))TiO_(3))-0.14(Bi_(0.5)K_(0.5)TiO_(3))-0.07BaTiO_(3)ternary ceramics.The in-corporation of 0.25 mol%MnO_(2)enhances the d 33 by more than 40%,while T d remains almost unchanged(i.e.,d 33=181 pC/N,T d=184℃).X-ray diffraction(XRD)shows that an appropriate fraction of the small axis-ratio ferroelectric phase(pseudo-cubic,P c)coexists with the long-range ferroelectric phase(tetrag-onal,T)under this MnO_(2)doping.Piezoelectric force microscopy(PFM)has revealed a special domain configuration,namely large striped and layered macro domains embedded with small nanodomains.This study provides a distinctive avenue to design BNT-based piezoelectric ceramics with high piezoelectric performance and temperature stability.展开更多
Reducing the cost of RuO_(2)/TiO_(2)catalysts is still one of the urgent challenges in catalytic HCl oxidation.In the present work,a Ce-doped TiO_(2)supported RuO_(2)catalyst with a low Ru loading was developed,showin...Reducing the cost of RuO_(2)/TiO_(2)catalysts is still one of the urgent challenges in catalytic HCl oxidation.In the present work,a Ce-doped TiO_(2)supported RuO_(2)catalyst with a low Ru loading was developed,showing a high activity in the catalytic oxidation of HCl to Cl_(2).The results on some extensive characterizations of both Ce-doped TiO_(2)carriers and their supported RuO_(2)catalysts show that the doping of Ce into TiO_(2)can effectively change the lattice parameters of TiO_(2)to improve the dispersion of the active RuO_(2)species on the carrier,which facilitates the production of surface Ru species to expose more active sites for boosting the catalytic performance even under some harsh reaction conditions.This work provides some scientific basis and technical support for chlorine recycling.展开更多
This paper reports that the radio frequency magnetron sputtering is used to fabricate ZnO and Mn-doped ZnO thin films on glass substrates at 500 ℃. The Mn-doped ZnO thin films present wurtzite structure of ZnO and ha...This paper reports that the radio frequency magnetron sputtering is used to fabricate ZnO and Mn-doped ZnO thin films on glass substrates at 500 ℃. The Mn-doped ZnO thin films present wurtzite structure of ZnO and have a smoother surface, better conductivity but no ferromagnetism. The x-ray photoelectron spectroscopy results show that the binding energy of Mn2p3/2 increases with increasing Mn content slightly, and the state of Mn in the Mn-doped ZnO thin films is divalent. The chemisorbed oxygen in the Mn-doped ZnO thin films increases with increasing Mn doping concentration. The photoluminescence spectra of ZnO and Mmdoped ZnO thin films have a similar ultraviolet emission. The yellow green emissions of 4 wt.% and 10 wt.% Mn-doped thin films are quenched, whereas the yellow green emission occurs because of abundant oxygen vacancies in the Mn-doped ZnO thin films after 20 wt.% Mn doping. Compared with pure ZnO thin film, the bandgap of the Mn-doped ZnO thin films increases with increasing Mn content.展开更多
The V-based body-centered cubic(BCC)-type hydrogen storage alloys have attracted significant attention due to their high theoretical hydrogen storage capacity of3.80 wt%.However,their practical application faces chall...The V-based body-centered cubic(BCC)-type hydrogen storage alloys have attracted significant attention due to their high theoretical hydrogen storage capacity of3.80 wt%.However,their practical application faces challenges related to low dehydriding capacity and poor activation performance.To overcome these challenges,a BCC-type Ti-V-Cr-Mn-Mo-Ce high-entropy alloy(HEA)with an effectively dehydriding capacity of 2.5 wt% above 0.1 MPa was prepared.By introduction of Mo and conducting heat treatment,the precipitation of Ti-rich phase in HEA was successfully suppressed,resulting in improved compositional uniformity and dehydriding capacity.Consequently,the effective dehydriding capacity increased significantly from 0.60 wt% to 2.50 wt% at 65℃,surpassing that of other types of hydrogen storage alloys under the same conditions.Moreover,the addition of 1 wt%Ce enabled initial hydrogen absorption at 25℃ without the need for activation at 400℃.Furthermore,Ce doping reduced the dehydriding activation energy of the Ti-V-Cr-Mn-Mo-Ce HEA from 52.71 to 42.82 kJ·mol^(-1)Additionally,the enthalpy value of dehydrogenation decreased from 46.89 to 17.96 k J·mol^(-1),attributed to a decrease in the hysteresis factor from 0.68 to 0.52.These findings provide valuable insights for optimizing the hydrogen storage property of HEA.展开更多
本研究提出了一种尚未见报道的CO_(2)还原电催化剂及其构造,由MnCe作为活性位点,三聚氰胺泡沫(MS)作为载体前驱体的新型电极材料——MnCe-CMS(碳化MS)和MnCe-GOMS(氧化石墨烯活化MS),用于电催化CO_(2)还原研究.结果发现,MnCe-MS具有较...本研究提出了一种尚未见报道的CO_(2)还原电催化剂及其构造,由MnCe作为活性位点,三聚氰胺泡沫(MS)作为载体前驱体的新型电极材料——MnCe-CMS(碳化MS)和MnCe-GOMS(氧化石墨烯活化MS),用于电催化CO_(2)还原研究.结果发现,MnCe-MS具有较宽的电位范围(-0.2~-3 V vs.RHE)及较好的产甲酸能力.对比以常用的碳布(CC)为载体的MnCe-CC,MnCe-CMS和MnCe-GOMS的甲酸生成速率分别提高到2.3、2.8倍,法拉第效率分别提高到2.3、2.5倍(MnCe-CC的最佳电位-0.4 V条件下),并且MnCe-GOMS在-0.6 V表现出最佳甲酸法拉第效率(75.72%).这归因于MS材料丰富的孔隙结构、较大的电化学表面积、易形成碳缺陷的特点,分析表明GO的掺入可以进一步增大这些优势;此外,在Mn、Ce共同作用下,有效促进电子传输、抑制析氢竞争反应、形成氧空位,有利于CO_(2)的吸附、活化与转化,从而促进甲酸生成.展开更多
基金Project supported by the National Natural Science Foundation of China (12174075)the Scientific and Technological Bases and Talents of Guangxi (Guike AD21220016)+1 种基金Guangxi Science and Technology Major Project(AA23073018)the special fund for Guangxi Bagui Scholars。
文摘Mn^(2+)-doped CsPbCl_(3)(Mn^(2+):CsPbCl_(3)) nanocrystals(NCs) have attracted considerable attention due to their unique strong and broad orange-red emission band,presenting promising applications in the field of photoelectric devices.However,pristine Mn^(2+):CsPbCl_(3)NCs commonly suffer from low photoluminescence quantum yield(PL QY) and stability issues.Herein,we introduced europium ions(Eu^(3+))into Mn^(2+):CsPbCl_(3)NCs via the thermal injection synthesis method to obtain high performance Eu^(3+)and Mn^(2+)codoped CsPbCl_(3)(Eu^(3+)/Mn^(2+):CsPbCl_(3)) NCs.The maximum PL QY of the resulting Eu^(3+)/Mn^(2+):CsPbCl_(3)NCs reaches up to 90.92%.It is found that the doping of Eu^(3+)ions significantly reduces the non-radiative recombination caused by high defect states,and improves the energy transfer efficiency from exciton to Mn^(2+),thereby boosting the PL performance.Moreover,doping Eu^(3+)ions notably improves the UV-light and water stability of Mn^(2+):CsPbCl_(3)NCs.We further demonstrate the application versatility of Eu^(3+)/Mn^(2+):CsPbCl_(3)NCs in white light emitting diodes(WLEDs) and optical anticounterfeiting applications.This work provides a valuable perspective for the attainment of high performance Mn^(2+):CsPbCl_(3)NCs and lays a foundation for the codoping of other lanthanide ions to adjust the luminescence properties of Mn^(2+):CsPbCl_(3)NCs.
基金financially supported by the Shandong Provincial Natural Science Foundation(ZR2023LFG005)the National Natural Science Foundation of China(Nos.22479161,52274308 and U22B20144)the Fundamental Research Funds for the Central Universities(No.24CX03012A)。
文摘Non-precious metal cobalt-based oxide inevitably dissolves for acid oxygen evolution reaction(OER).Designing an efficient deposition channel for leaching cobalt species is a promising approach.The dissolution-deposition equilibrium of Co is achieved by doping Mn in the lattice of LaCo_(1-x)Mn_(x)O_(3),prolonging the lifespan in acidic conditions by 14 times.The lattice doping of Mn produces a strain that enhances the adsorption capacity of OH^(-).The self-catalysis of Mn causes the leaching Co to be deposited in the form of CoO_(2),which ensures that the long-term stability of LaCo_(1-x)Mn_(x)O_(3)is 70 h instead of 5 h for LaCoO_(3).Mn doping enhances the deprotonation of^(*)OOH→O_(2)in acidic environments.Notably,the over-potential of optimized LaCo_(1-x)Mn_(x)O_(3)is 345 mV at 10 mA cm^(-2)for acidic OER.This work presents a promising method for developing noble metal-free catalysts that enhance the acidic OER activity and stability.
文摘采用高温固相法制备了SrZrSi_(2)O_(7):Ce^(3+),Mn^(2+)荧光粉。通过X射线衍射(X-ray Power Diffractometer,XRD)、激发和发射光谱及电子显微分析对材料的分子结构、显微形貌、发光特性和能量传递机理进行了研究。结果表明,荧光粉的主晶相是单斜晶系的SrZrSi_(2)O_(7),Ce^(3+)离子和Mn^(2+)离子占据一部分Sr^(2+)离子的晶体学格位。在296 nm激发下,可以观察到来自Ce^(3+)离子的蓝光发射峰,归属于Ce^(3+)离子的5d→4f能级跃迁。在544 nm处,有来自Mn^(2+)离子的绿光发射峰,归因于Mn^(2+)离子的^(4)T_(1)(4G)-^(6)A_(1)(6S)自旋禁止跃迁,表明发生了从Ce^(3+)离子到Mn^(2+)离子的能量传递过程,为设计蓝光到绿光之间可控制备的新型荧光粉提供了理论和实验的信息。
基金supported by the Natural Science Foundation of Heilongjiang Province(No.LH2021A012).
文摘Lead-free Bi_(_(0.5))Na_(_(0.5))TiO_(3)(BNT)piezoelectric ceramics have the advantages of large coercive fields and high Curie temperatures.But the improvement of piezoelectric coefficient(d 33)is usually accompanied by a huge sacrifice of depolarization temperature(T d).In this work,a well-balanced performance of d 33 and T d is achieved in MnO_(2)-doped 0.79(Bi_(_(0.5))Na_(_(0.5))TiO_(3))-0.14(Bi_(0.5)K_(0.5)TiO_(3))-0.07BaTiO_(3)ternary ceramics.The in-corporation of 0.25 mol%MnO_(2)enhances the d 33 by more than 40%,while T d remains almost unchanged(i.e.,d 33=181 pC/N,T d=184℃).X-ray diffraction(XRD)shows that an appropriate fraction of the small axis-ratio ferroelectric phase(pseudo-cubic,P c)coexists with the long-range ferroelectric phase(tetrag-onal,T)under this MnO_(2)doping.Piezoelectric force microscopy(PFM)has revealed a special domain configuration,namely large striped and layered macro domains embedded with small nanodomains.This study provides a distinctive avenue to design BNT-based piezoelectric ceramics with high piezoelectric performance and temperature stability.
基金supported by Zhejiang Provincial Key R&D Project(No.2021C01056)the Programme of Introducing Talents of Discipline to Universities(No.D17008).
文摘Reducing the cost of RuO_(2)/TiO_(2)catalysts is still one of the urgent challenges in catalytic HCl oxidation.In the present work,a Ce-doped TiO_(2)supported RuO_(2)catalyst with a low Ru loading was developed,showing a high activity in the catalytic oxidation of HCl to Cl_(2).The results on some extensive characterizations of both Ce-doped TiO_(2)carriers and their supported RuO_(2)catalysts show that the doping of Ce into TiO_(2)can effectively change the lattice parameters of TiO_(2)to improve the dispersion of the active RuO_(2)species on the carrier,which facilitates the production of surface Ru species to expose more active sites for boosting the catalytic performance even under some harsh reaction conditions.This work provides some scientific basis and technical support for chlorine recycling.
基金Project supported by the State Key Development Program for Basic Research of China (Grant No 2004CB619302)
文摘This paper reports that the radio frequency magnetron sputtering is used to fabricate ZnO and Mn-doped ZnO thin films on glass substrates at 500 ℃. The Mn-doped ZnO thin films present wurtzite structure of ZnO and have a smoother surface, better conductivity but no ferromagnetism. The x-ray photoelectron spectroscopy results show that the binding energy of Mn2p3/2 increases with increasing Mn content slightly, and the state of Mn in the Mn-doped ZnO thin films is divalent. The chemisorbed oxygen in the Mn-doped ZnO thin films increases with increasing Mn doping concentration. The photoluminescence spectra of ZnO and Mmdoped ZnO thin films have a similar ultraviolet emission. The yellow green emissions of 4 wt.% and 10 wt.% Mn-doped thin films are quenched, whereas the yellow green emission occurs because of abundant oxygen vacancies in the Mn-doped ZnO thin films after 20 wt.% Mn doping. Compared with pure ZnO thin film, the bandgap of the Mn-doped ZnO thin films increases with increasing Mn content.
基金supported by National Key R&D Program of China(No.2022YFB3504700)the National Natural Science Foundation of China(No.92061125)Jiangxi Natural Science Foundation(No.20212ACB213009)。
文摘The V-based body-centered cubic(BCC)-type hydrogen storage alloys have attracted significant attention due to their high theoretical hydrogen storage capacity of3.80 wt%.However,their practical application faces challenges related to low dehydriding capacity and poor activation performance.To overcome these challenges,a BCC-type Ti-V-Cr-Mn-Mo-Ce high-entropy alloy(HEA)with an effectively dehydriding capacity of 2.5 wt% above 0.1 MPa was prepared.By introduction of Mo and conducting heat treatment,the precipitation of Ti-rich phase in HEA was successfully suppressed,resulting in improved compositional uniformity and dehydriding capacity.Consequently,the effective dehydriding capacity increased significantly from 0.60 wt% to 2.50 wt% at 65℃,surpassing that of other types of hydrogen storage alloys under the same conditions.Moreover,the addition of 1 wt%Ce enabled initial hydrogen absorption at 25℃ without the need for activation at 400℃.Furthermore,Ce doping reduced the dehydriding activation energy of the Ti-V-Cr-Mn-Mo-Ce HEA from 52.71 to 42.82 kJ·mol^(-1)Additionally,the enthalpy value of dehydrogenation decreased from 46.89 to 17.96 k J·mol^(-1),attributed to a decrease in the hysteresis factor from 0.68 to 0.52.These findings provide valuable insights for optimizing the hydrogen storage property of HEA.
文摘本研究提出了一种尚未见报道的CO_(2)还原电催化剂及其构造,由MnCe作为活性位点,三聚氰胺泡沫(MS)作为载体前驱体的新型电极材料——MnCe-CMS(碳化MS)和MnCe-GOMS(氧化石墨烯活化MS),用于电催化CO_(2)还原研究.结果发现,MnCe-MS具有较宽的电位范围(-0.2~-3 V vs.RHE)及较好的产甲酸能力.对比以常用的碳布(CC)为载体的MnCe-CC,MnCe-CMS和MnCe-GOMS的甲酸生成速率分别提高到2.3、2.8倍,法拉第效率分别提高到2.3、2.5倍(MnCe-CC的最佳电位-0.4 V条件下),并且MnCe-GOMS在-0.6 V表现出最佳甲酸法拉第效率(75.72%).这归因于MS材料丰富的孔隙结构、较大的电化学表面积、易形成碳缺陷的特点,分析表明GO的掺入可以进一步增大这些优势;此外,在Mn、Ce共同作用下,有效促进电子传输、抑制析氢竞争反应、形成氧空位,有利于CO_(2)的吸附、活化与转化,从而促进甲酸生成.
