Constructing a stable interface on Ni-rich LiNi_(0.8)Co_(0.1)Mn_(0.1)O_(2) cathode via lactic acid-assisted engineering strategy

Ni-rich layered oxides are potential cathode materials for next-generation high energy density Li-ion batteries due to their high capacity and low cost.However,the inherently unstable surface properties,including high levels of residual Li compounds,dissolution of transition metal cations,and parasitic side reactions,have not been effectively addressed,leading to significant degradation in their electrochemical performance.In this study,we propose a simple and effective lactic acid-assisted interface engineering strategy to regulate the surface chemistry and properties of Ni-rich LiNi_(0.8)Co_(0.1)Mr_(0.1)O_(2) cathode.This novel surface treatment method successfully eliminates surface residual Li compounds,inhibits structural collapse,and mitigates cathode-electrolyte interface film growth.As a result,the lactic acidtreated LiNi_(0.8)Co_(0.1)Mn_(0.1)O_(2) achieved a remarkable capacity retention of 91.7% after 100 cycles at 0.5 C(25℃) and outstanding rate capability of 149.5 mA h g^(-1) at 10 C,significantly outperforming the pristine material.Furthermore,a pouch-type full cell incorporating the modified LiNi_(0.8)Co_(0.1)Mn_(0.1)O_(2) cathode demonstrates impressive long-term cycle life,retaining 81.5% of its capacity after 500 cycles at 1 C.More importantly,the thermal stability of the modified cathode is also dramatically improved.This study offers a valuable surface modification strategy for enhancing the overall performance of Ni-rich cathode materials.

A facile solution processed ZnO@ZnS core–shell nanorods arrays for high-efficiency perovskite solar cells with boosted stability

Zinc Oxide(ZnO)has been extensively applied as electron transport material(ETM)in perovskite solar cells(PSCs)since the emergence of PSCs.However,some chemisorbed oxygen species on the surface of ZnO can cause the degradation of CH3NH3+(MA^(+))based perovskite.To avoid the destructive effect of ZnO,a facile solution strategy was proposed to produce a ZnS shell around the ZnO nanorods arrays(ZnO-NRs),i.e.ZnO@ZnS core-shell nanorods(ZnO-NRs@ZnS).The ZnO-NRs@ZnS cascade structure can not only facilitate carrier transport,but also enhance the stability of ZnO based PSCs.A power conversion efficiency(PCE)of 20.6%was finally yielded,which is the-state-of-the-art efficiency for PSCs with one-dimensional(1 D)ZnO electron transport materials(ETMs).Moreover,over 90%of the initial efficiency was retained for the unencapsulated device with ZnO-NRs@ZnS ETMs at 85℃for 500 h,demonstrating excellent stability.This work provides a simple and efficient avenue to simultaneously enhance the photovoltaic(PV)performance and stability of 1 D ZnO nanostructure-based PSCs.

Crystallization tailoring of cesium/formamidinium double-cation perovskite for efficient and highly stable solar cells

Achieving high-quality perovskite crystal films is a critical prerequisite in boosting solar cell efficiency and improving the device stability,but the delicate control of nucleation and growth of the perovskite film remains limited success.Herein,a facile but effective strategy has been developed to finely tailor the crystallization of thermally stable cesium/formamidinium(Cs/FA)based perovskite via partially replacing PbI2 with PbCl2 in the precursor solution.The incorporation of chlorine into the perovskite crystal lattice derived from PbCl2 changes the crystallization process and improves the crystal quality,which further results in the formation of larger crystal grains compared to the control sample.The larger crystal grains with high crystallinity lead to reduced grain boundaries,suppressed non-radiative recombination,and enhanced photoluminescence lifetime.Under the optimized conditions,the methylammonium free perovskite solar cells(PSCs)delivers a champion power conversion efficiency(PCE)of 21.30%with an open-circuit voltage as high as 1.18 V,which is one of the highest efficiencies for Cs/FA based PSCs up to now.Importantly,the unencapsulated PSC devices retain more than 95%and 81%of their original PCEs even after long-term(over one year)storage under ambient conditions or 2000 h’s thermal aging at 850C in a nitrogen atmosphere,respectively.

检察机关支持公益诉讼的制度体系——东莞市人民检察院支持东莞市环境科学学会诉袁某某等三人环境污染民事公益诉讼案评析

2016年6月至2017年1月期间,袁某某雇用陈某某作为其广州市增城区无牌电镀厂的司机,并指使陈某某驾驶货车将其电镀厂产生的废水运送至东莞市石碣镇何树朝经营的无牌废品收购店,经何某某同意后通过店内私设的暗管,将约700吨废水直接排放到市政下水道,电镀废水流入中心涌,并最终流向东江、中堂水道。经检测,倾倒点电镀废水各类重金属超出《电镀水污染排放标准》(DB44/1597—2015)排放限值700—8000多倍,偷排的废水被认定为有毒物质。

Effects of gradient concentration on the microstructure and electrochemical performance of LiNi0.6Co0.2Mn0.2O2 cathode materials

Nickel(Ni)-rich layered materials have attracted considerable interests as promising cathode materials for lithium ion batteries(LIBs)owing to their higher capacities and lower cost.Nevertheless,Mn-rich cathode materials usually suffer from poor cyclability caused by the unavoidable side-reactions between Ni^4+ions on the surface a nd electrolytes.The design of gradient concentration(GC)particles with Ni-rich inside and Mn-rich outside is proved to be an efficient way to address the issue.Herein,a series of LiNi0.6Co0.2Mn0.2O2(LNCM 622)materials with different GCs(the atomic ratio of Ni/Mn decreasing from the core to the outer layer)have been successfully synthesized via rationally designed co-precipitation process.Experimental results demonstrate that the GC of LNCM 622 materials plays an important role in their microstructure and electrochemical properties.The as-prepared GC3.5 cathode material with optimal GC can provide a shorter pathway for lithium-ion diffusion and stabilize the near-surface region,and finally achieve excellent electrochemical performances,delivering a discharge capacity over 176 mAh·g^-1 at 0.2 C rate and exhibiting capacity retention up to 94%after 100 cycles at 1 C.T h e rationally-designed co-precipitation process for fabricating the Ni-rich layered cathode materials with gradient composition lays a solid foundation for the preparation of high-performance cathode materials for LIBs.

THE EVOLUTION OF THE CIVIL PROCEDURE SYSTEM OF CHINA

This article reviews the initiation, stagnation, recovery and reformation of the Civil Procedure Law of China, and places an emphasis on the evolution of the Civil Procedure Law under the background of judicial reformation. This article observes the amendment of the Civil Procedure Law, the adjustment of the rules of civil procedure, the establishment of the basic principles of the Civil Procedure Law, the trend of the Civil Procedure Law that is based on the research of major litigation systems and the perfection of legislation.