摘要：设计实验研究了以无机镍盐和NaOH为原料,利用水热法制备Ni(OH)2纳米线,OH-和SO24-对于产物形貌的影响,并利用X射线衍射(XRD),傅立叶变换红外光谱(FTIR),透射电镜(TEM)等对材料结构、形貌和成分进行了表征,研究了Ni(OH)2纳米线形成的相关机理.结果表明,低的OH-浓度与高纯的SO24-水热环境是α-Ni(OH)2纳米线形成的关键因素.SO24-能够加速α-Ni(OH)2晶体沿[001]方向的生长,而OH-含量较低时,较低的库伦斥力不足以阻碍晶体沿[001]方向生长过程的进行.

摘要：氢气是一种清洁高效的能源载体,通过海水电解规模化制备氢气能够为应对全球能源挑战提供新的机遇。然而,缺乏高活性、高选择性和高稳定性的理想电极材料是在腐蚀性海水中连续电解过程的一个巨大挑战。为了缓解这一困境,需要从基础理论和实际应用两方面对材料进行深入研究。近年来,人们围绕电极材料的催化活性、选择性和耐腐蚀性进行了大量的探索。本文重点总结了高选择性和强耐腐蚀性材料的设计合成与作用机制。其中详细介绍了多种电极材料(如多金属氧化物、Ni/Fe/Co基复合材料、氧化锰包覆异质结构等)对氧气生成选择性的研究进展;系统论述了各种材料的抗腐蚀工程研究成果,主要讨论了本征抗腐蚀材料、外防护涂层和原位产生抗腐蚀物种三种情况。此外,提出了海水电解过程中存在的挑战和潜在的机遇。先进纳米材料的设计有望为解决海水电解中的氯化学问题提供新思路。

摘要：The Pt-based catalyst tends to be poisoned by carbon monoxide(CO)-like intermediates produced in fuel cell reactions,which seriously deteriorates its catalytic ***,noble metal Au with the capacity of resistance to CO-like intermediates poisoning was employed to construct multi-element Pt-based *** trimetallic NiPtAu hollow nanocrystals(HNCs)with different surface Au contents were synthesized to explore the role of Au in electrocatalysis for alkaline methanol oxidation reaction(MOR).The trimetallic NiPtAu-SRAu HNCs catalyst with the relative rich Au content(15.17 at%)on surface exhibits a much lower CO oxidation peak potential than the other HNCs counterpart and 20 wt%Pt/C,which indicates the more exceptional CO-resisting ***,the MOR specific activity of NiPtAu-SRAu HNCs(31.52 mA cm^−2)is 7 times higher than that of 20wt%Pt/C(4.50 mA cm^−2).This enhancement in catalytic activity as well as anti-CO poisoning capability for NiPtAu-SRAu HNCs can be mainly ascribed to the weakened CO adsorption due to the exposure of Au atoms on NiPt surface evidenced by the experimental data and density functional theory *** study not only investigates the role of Au in MOR catalysis but also could be helpful for designing and optimizing the electrocatalysts for high-active and robust fuel cell applications.

摘要：Sluggish water dissociation kinetics severely limits the rate of alkaline electrocatalytic hydrogen evolution reaction(HER).Therefore,finding highly active electrocatalysts and clarifying the mechanism of water dissociation are challenging but *** this study,we report an integrated nanoporous nickel(np-Ni)catalyst with high alkaline HER performance and the origin of the corresponding enhanced catalytic *** 1 mol L^(-1) KOH solution,this np-Ni electrode shows an HER overpotential of 20 mV at 10 mA cm^(-2),along with fast water dissociation *** excellent performance is not only attributed to the large surface area provided by the three-dimensional interconnected conductive network but also from the enhanced intrinsic activity induced by the unique surface *** studies reveal that the types of oxygen species that naturally form on the Ni surface play a key role in water ***,when the lattice oxygen almost disappears,the Ni surface terminates with_(ads)orbed oxygen(O_(ads)),exhibiting the fastest water dissociation *** functional theory calculation suggests that when O_(ads)acts as the surface termination of Ni metal,the orientation and configuration of polar water molecules are strongly affected by O_(ads).Finally,the H–OH bond of interfacial water molecules is effectively activated in a manner similar to hydrogen *** work not only identifies a high-performance and low-cost electrocatalyst but also provides new insights into the chemical processes underlying water dissociation,thus benefiting the rational design of electrocatalysts.

摘要：The overall water splitting for hydrogen production is an effective strategy to resolve the environmental and energy crisis. Here, we report a facile approach to synthesize the Ir-based multimetallic, hierarchical, double-coreshelled architecture(HCSA) assisted by oil bath reaction for boosting overall water splitting in acidic environment. The Ir Ni Cu HCSA shows superior electrocatalytic activity for hydrogen evolution reaction(HER) and oxygen evolution reaction(OER), which are comparable to commercial Pt/C and better than IrO2. The Ir Ni Cu HCSA exhibits remarkably catalytic efficiency as bifunctional catalyst for overall water splitting where a low cell voltage of 1.53 V is enough to drive a current density of 10 mA cm^-2 and maintains stable for at least 20 h. The presented work for the design and synthesis of novel Ir-based multimetallic architecture paves the way for highperformance overall water splitting catalysis.

摘要：The rational design and synthesis of hybrid-type electrode nanomaterials are significant for their diverse applications,including their potential usage as high-efficiency nanoarchitectures for supercapacitors(SCs)as a class of promising energy-storage systems for powering next-generation electric vehicles and electronic ***,we reported a facile and controllable synthesis of core-shell Ni_(3)S_(2)@NiWO_(4)nanoarrays to fabricate a freestanding electrode for hybrid ***,the as-prepared freestanding Ni_(3)S_(2)@NiWO_(4)electrode presents an ultrahigh areal capacity of 2032μA h cm^(-2)at 5 mA cm^(-2),and a capacity retention of 63.6%even when the current density increased up to 50 mA cm^(-2).Remarkably,the Ni_(3)S_(2)@NiWO_(4)nanoarraybased hybrid SC delivers a maximum energy density of 1.283 mW h cm^(-2)at 3.128 mW cm^(-2)and a maximum power density of 41.105 mW cm^(-2)at 0.753 mW h cm^(-2).Furthermore,the hybrid SC exhibits a capacity retention of 89.6%even after continuous 10,000 cycles,proving its superior *** study provides a facile pathway to rationally design a variety of core-shell metal nanostructures for high-performance energy storage devices.